Trial Outcomes & Findings for Study on Olaparib Plus Abiraterone as First-line Therapy in Men With Metastatic Castration-resistant Prostate Cancer (NCT NCT03732820)

NCT ID: NCT03732820

Last Updated: 2026-01-29

Results Overview

An rPFS event is defined as progression determined by Response Evaluation Criteria in Solid Tumours version 1.1 \[RECIST 1.1\] and/or Prostate Cancer Working Group 3 \[PCWG-3\] or death (by any cause in the absence of progression), regardless of whether the patient withdraws from randomised therapy or receives another anticancer therapy prior to progression. Per RECIST v1.1, progression is defined as the sum of TLs has a 20% and absolute ≥ 5mm increase from nadir, and/or unequivocal progression in any non target lesions, and/or any new lesion identified. Per PCWG3, progression on a bone scan is defined as 2 or more new lesions observed from the first visit after baseline compared to baseline, or from all other visits compared to first visit after baseline. A confirmatory scan is required.

Recruitment status

ACTIVE_NOT_RECRUITING

Study phase

PHASE3

Target enrollment

895 participants

Primary outcome timeframe

Assessed from date of randomisation to data cut off (DCO1): 30Jul2021 (Approx. 2 years 9 months)

Results posted on

2026-01-29

Participant Flow

Participant milestones

Participant milestones
Measure
Olaparib 300 mg bd + Abiraterone 1000 mg qd
Patients receive oral treatment with olaparib 300mg twice daily in combination with abiraterone 1000mg once daily
Placebo bd + Abiraterone 1000 mg qd
Patients receive oral treatment with placebo twice daily in combination with abiraterone 1000mg once daily.
Overall Study
STARTED
399
397
Overall Study
COMPLETED
0
0
Overall Study
NOT COMPLETED
399
397

Reasons for withdrawal

Reasons for withdrawal
Measure
Olaparib 300 mg bd + Abiraterone 1000 mg qd
Patients receive oral treatment with olaparib 300mg twice daily in combination with abiraterone 1000mg once daily
Placebo bd + Abiraterone 1000 mg qd
Patients receive oral treatment with placebo twice daily in combination with abiraterone 1000mg once daily.
Overall Study
Death
168
203
Overall Study
Other
2
2
Overall Study
Failure to meet randomisation criteria
1
1
Overall Study
Patient decision
14
10
Overall Study
Screen failure
0
1
Overall Study
Patients ongoing study at data cut off
210
178
Overall Study
Lost to Follow-up
4
2

Baseline Characteristics

Study on Olaparib Plus Abiraterone as First-line Therapy in Men With Metastatic Castration-resistant Prostate Cancer

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Olaparib 300 mg bd + Abiraterone 1000 mg qd
n=399 Participants
Patients receive oral treatment with olaparib 300mg twice daily in combination with abiraterone 1000mg once daily
Placebo bd + Abiraterone 1000 mg qd
n=397 Participants
Patients receive oral treatment with placebo twice daily in combination with abiraterone 1000mg once daily.
Total
n=796 Participants
Total of all reporting groups
Age, Customized
>=65
269 Participants
n=41 Participants
300 Participants
n=1581 Participants
569 Participants
n=4626 Participants
Age, Customized
<65
130 Participants
n=41 Participants
97 Participants
n=1581 Participants
227 Participants
n=4626 Participants
Age, Continuous
68.5 Years
STANDARD_DEVIATION 8.5 • n=41 Participants
69.8 Years
STANDARD_DEVIATION 7.9 • n=1581 Participants
69.1 Years
STANDARD_DEVIATION 8.2 • n=4626 Participants
Sex/Gender, Customized
Male
399 Participants
n=41 Participants
397 Participants
n=1581 Participants
796 Participants
n=4626 Participants
Race/Ethnicity, Customized
HISPANIC OR LATINO
68 Participants
n=41 Participants
63 Participants
n=1581 Participants
131 Participants
n=4626 Participants
Race/Ethnicity, Customized
NOT HISPANIC OR LATINO
310 Participants
n=41 Participants
305 Participants
n=1581 Participants
615 Participants
n=4626 Participants
Race/Ethnicity, Customized
NOT REPORTED
22 Participants
n=41 Participants
30 Participants
n=1581 Participants
52 Participants
n=4626 Participants
Race/Ethnicity, Customized
AMERICAN INDIAN OR ALASKA NATIVE
1 Participants
n=41 Participants
0 Participants
n=1581 Participants
1 Participants
n=4626 Participants
Race/Ethnicity, Customized
ASIAN
66 Participants
n=41 Participants
72 Participants
n=1581 Participants
138 Participants
n=4626 Participants
Race/Ethnicity, Customized
BLACK OR AFRICAN AMERICAN
14 Participants
n=41 Participants
11 Participants
n=1581 Participants
25 Participants
n=4626 Participants
Race/Ethnicity, Customized
NATIVE HAWAIIAN OR OTHER PACIFIC ISLANDER
2 Participants
n=41 Participants
0 Participants
n=1581 Participants
2 Participants
n=4626 Participants
Race/Ethnicity, Customized
UNKNOWN
12 Participants
n=41 Participants
9 Participants
n=1581 Participants
21 Participants
n=4626 Participants
Race/Ethnicity, Customized
WHITE
282 Participants
n=41 Participants
275 Participants
n=1581 Participants
557 Participants
n=4626 Participants
Region of Enrollment
USA
40 Participants
n=41 Participants
34 Participants
n=1581 Participants
74 Participants
n=4626 Participants
Region of Enrollment
Turkey
39 Participants
n=41 Participants
33 Participants
n=1581 Participants
72 Participants
n=4626 Participants
Region of Enrollment
Slovakia
5 Participants
n=41 Participants
13 Participants
n=1581 Participants
18 Participants
n=4626 Participants
Region of Enrollment
Netherlands
16 Participants
n=41 Participants
12 Participants
n=1581 Participants
28 Participants
n=4626 Participants
Region of Enrollment
Korea, Republic Of
27 Participants
n=41 Participants
29 Participants
n=1581 Participants
56 Participants
n=4626 Participants
Region of Enrollment
Japan
36 Participants
n=41 Participants
41 Participants
n=1581 Participants
77 Participants
n=4626 Participants
Region of Enrollment
Italy
22 Participants
n=41 Participants
18 Participants
n=1581 Participants
40 Participants
n=4626 Participants
Region of Enrollment
United Kingdom
27 Participants
n=41 Participants
22 Participants
n=1581 Participants
49 Participants
n=4626 Participants
Region of Enrollment
France
14 Participants
n=41 Participants
25 Participants
n=1581 Participants
39 Participants
n=4626 Participants
Region of Enrollment
Spain
19 Participants
n=41 Participants
24 Participants
n=1581 Participants
43 Participants
n=4626 Participants
Region of Enrollment
Germany
14 Participants
n=41 Participants
11 Participants
n=1581 Participants
25 Participants
n=4626 Participants
Region of Enrollment
Czech Republic
18 Participants
n=41 Participants
13 Participants
n=1581 Participants
31 Participants
n=4626 Participants
Region of Enrollment
Chile
19 Participants
n=41 Participants
25 Participants
n=1581 Participants
44 Participants
n=4626 Participants
Region of Enrollment
Canada
17 Participants
n=41 Participants
16 Participants
n=1581 Participants
33 Participants
n=4626 Participants
Region of Enrollment
Brazil
54 Participants
n=41 Participants
46 Participants
n=1581 Participants
100 Participants
n=4626 Participants
Region of Enrollment
Belgium
4 Participants
n=41 Participants
1 Participants
n=1581 Participants
5 Participants
n=4626 Participants
Region of Enrollment
Australia
28 Participants
n=41 Participants
34 Participants
n=1581 Participants
62 Participants
n=4626 Participants

PRIMARY outcome

Timeframe: Assessed from date of randomisation to data cut off (DCO1): 30Jul2021 (Approx. 2 years 9 months)

Population: Full Analysis Set (FAS)

An rPFS event is defined as progression determined by Response Evaluation Criteria in Solid Tumours version 1.1 \[RECIST 1.1\] and/or Prostate Cancer Working Group 3 \[PCWG-3\] or death (by any cause in the absence of progression), regardless of whether the patient withdraws from randomised therapy or receives another anticancer therapy prior to progression. Per RECIST v1.1, progression is defined as the sum of TLs has a 20% and absolute ≥ 5mm increase from nadir, and/or unequivocal progression in any non target lesions, and/or any new lesion identified. Per PCWG3, progression on a bone scan is defined as 2 or more new lesions observed from the first visit after baseline compared to baseline, or from all other visits compared to first visit after baseline. A confirmatory scan is required.

Outcome measures

Outcome measures
Measure
Placebo bd + Abiraterone 1000 mg qd
n=397 Participants
Patients receive oral treatment with placebo twice daily in combination with abiraterone 1000mg once daily.
Olaparib 300 mg bd + Abiraterone 1000 mg qd
n=399 Participants
Patients receive oral treatment with olaparib 300mg twice daily in combination with abiraterone 1000mg once daily
Number of Participants With Radiological Progression Free Survival (rPFS) Event by Investigator Assessment
226 Participants
168 Participants

SECONDARY outcome

Timeframe: Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months). DCO3 is the final data cut-off for the OS analysis and therefore no further updates will be made.

Population: Full Analysis Set (FAS)

An OS event is defined as death by any cause, regardless of whether the patient withdraws from randomised therapy or receives another anticancer therapy.

Outcome measures

Outcome measures
Measure
Placebo bd + Abiraterone 1000 mg qd
n=397 Participants
Patients receive oral treatment with placebo twice daily in combination with abiraterone 1000mg once daily.
Olaparib 300 mg bd + Abiraterone 1000 mg qd
n=399 Participants
Patients receive oral treatment with olaparib 300mg twice daily in combination with abiraterone 1000mg once daily
Number of Participants With Overall Survival (OS) Event
205 Participants
176 Participants

SECONDARY outcome

Timeframe: Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)

Population: Full Analysis Set (FAS)

A TFST (excluding radiotherapy) event is defined as the start of the first subsequent anticancer therapy after discontinuation of randomised treatment or death from any cause.

Outcome measures

Outcome measures
Measure
Placebo bd + Abiraterone 1000 mg qd
n=397 Participants
Patients receive oral treatment with placebo twice daily in combination with abiraterone 1000mg once daily.
Olaparib 300 mg bd + Abiraterone 1000 mg qd
n=399 Participants
Patients receive oral treatment with olaparib 300mg twice daily in combination with abiraterone 1000mg once daily
Number of Participants With Time to First Subsequent Anticancer Therapy or Death (TFST) Event
285 Participants
255 Participants

SECONDARY outcome

Timeframe: Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)

Population: Full Analysis Set (FAS)

A TTPP event is defined as pain progression based on the Brief Pain Inventory-Short Form (BPI-SF) Item 3 (range 0-10, a higher score indicates worse pain) and opiate analgesic use (Analgesic quantification algorithm \[AQA\] score, range 0-7, a higher score indicates increased opioid use). For patients who are asymptomatic at baseline (average worst pain score of 0 and not taking opioids): A ≥2 point change from baseline in average (4-7 days) worst pain score observed at 2 consecutive visits or initiation of opioid use; For patients who are symptomatic at baseline (average worst pain score \>0 and/or receiving opioids): A ≥2 point change from baseline in average (4-7 days) worst pain score observed at 2 consecutive visits and an average worst pain score ≥4, and no decrease in average opioid use (≥1-point decrease in AQA score from a starting value of ≥2), or increase in opioid use (≥1-point increase, or ≥2-point increase if the starting value is 0) at 2 consecutive follow-up visits.

Outcome measures

Outcome measures
Measure
Placebo bd + Abiraterone 1000 mg qd
n=397 Participants
Patients receive oral treatment with placebo twice daily in combination with abiraterone 1000mg once daily.
Olaparib 300 mg bd + Abiraterone 1000 mg qd
n=399 Participants
Patients receive oral treatment with olaparib 300mg twice daily in combination with abiraterone 1000mg once daily
Number of Participants With Time to Pain Progression (TTPP) Event
60 Participants
68 Participants

SECONDARY outcome

Timeframe: Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)

Population: Randomised patients who are not on opiates at baseline

An event for opiate use is defined as the first opiate use for cancer related pain.

Outcome measures

Outcome measures
Measure
Placebo bd + Abiraterone 1000 mg qd
n=353 Participants
Patients receive oral treatment with placebo twice daily in combination with abiraterone 1000mg once daily.
Olaparib 300 mg bd + Abiraterone 1000 mg qd
n=344 Participants
Patients receive oral treatment with olaparib 300mg twice daily in combination with abiraterone 1000mg once daily
Number of Participants With Opiate Use
45 Participants
58 Participants

SECONDARY outcome

Timeframe: Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)

Population: Full Analysis Set (FAS)

An SSRE event is defined as the first sympomatic skeletal-related event defined by * Use of radiation therapy to prevent or relieve skeletal symptoms. * Occurrence of new symptomatic pathological bone fractures (vertebral or non-vertebral).

Outcome measures

Outcome measures
Measure
Placebo bd + Abiraterone 1000 mg qd
n=397 Participants
Patients receive oral treatment with placebo twice daily in combination with abiraterone 1000mg once daily.
Olaparib 300 mg bd + Abiraterone 1000 mg qd
n=399 Participants
Patients receive oral treatment with olaparib 300mg twice daily in combination with abiraterone 1000mg once daily
Number of Participants With First Symptomatic Skeletal Related Event (SSRE)
51 Participants
46 Participants

SECONDARY outcome

Timeframe: Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)

Population: Full Analysis Set (FAS)

An event for PFS2 is defined as the second progression on next-line anticancer therapy or death, whichever occurs earlier.

Outcome measures

Outcome measures
Measure
Placebo bd + Abiraterone 1000 mg qd
n=397 Participants
Patients receive oral treatment with placebo twice daily in combination with abiraterone 1000mg once daily.
Olaparib 300 mg bd + Abiraterone 1000 mg qd
n=399 Participants
Patients receive oral treatment with olaparib 300mg twice daily in combination with abiraterone 1000mg once daily
Number of Participants With Second Progression or Death (PFS2) Event
126 Participants
103 Participants

SECONDARY outcome

Timeframe: Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)

Population: Full Analysis Set (FAS), only patients with baseline assessment and at least one post treatment assessment are included in the analysis.

The BPI-SF is a validated, 15-item domain-specific instrument designed to assess the severity of pain and the impact/interference of pain on daily functions. BPI-SF worst pain, pain severity and pain interference score changes can be a minimum of -10 and a maximum of 10. A negative change from baseline value indicates improvement.

Outcome measures

Outcome measures
Measure
Placebo bd + Abiraterone 1000 mg qd
n=333 Participants
Patients receive oral treatment with placebo twice daily in combination with abiraterone 1000mg once daily.
Olaparib 300 mg bd + Abiraterone 1000 mg qd
n=330 Participants
Patients receive oral treatment with olaparib 300mg twice daily in combination with abiraterone 1000mg once daily
Brief Pain Inventory-Short Form (BPI-SF)
Change from baseline in BPI-SF worst pain
0.03 Score
Standard Error 0.099
-0.09 Score
Standard Error 0.093
Brief Pain Inventory-Short Form (BPI-SF)
Change from baseline in BPI-SF pain severity score
-0.02 Score
Standard Error 0.076
-0.08 Score
Standard Error 0.071
Brief Pain Inventory-Short Form (BPI-SF)
Change from baseline in BPI-SF pain interference score
0.13 Score
Standard Error 0.079
0.01 Score
Standard Error 0.074

SECONDARY outcome

Timeframe: Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)

Population: Full Analysis Set (FAS), only patients with baseline assessment and at least one post treatment assessment are included in the analysis.

Functional Assessment of Cancer Therapy-Prostate Cancer (FACT-P) total score and Functional Assessment of Cancer Therapy-General (FACT-G) total score. Total FACT-P score is the sum of Physical Well-being (PWB), Social Well-being (SWB), Emotional Well-being (EWB), Functional Well-being (FWB) and Prostate cancer subscale (PCS). FACT-P total score change from baseline values can be a minimum of -156 and a maximum of 156. A positive value indicates improvement. FACT-G total score is the sum of PWB, SWB, EWB and FWB. FACT-G Total score change from baseline values can be a minimum of -108 and a maximum of 108. A positive value indicates improvement.

Outcome measures

Outcome measures
Measure
Placebo bd + Abiraterone 1000 mg qd
n=295 Participants
Patients receive oral treatment with placebo twice daily in combination with abiraterone 1000mg once daily.
Olaparib 300 mg bd + Abiraterone 1000 mg qd
n=278 Participants
Patients receive oral treatment with olaparib 300mg twice daily in combination with abiraterone 1000mg once daily
Functional Assessment of Cancer Therapy- Prostate Cancer (FACT-P)
Change from baseline in FACT-P Total
-5.30 Score
Standard Error 1.060
-5.84 Score
Standard Error 1.031
Functional Assessment of Cancer Therapy- Prostate Cancer (FACT-P)
Change from baseline in FACT-G Total
-4.35 Score
Standard Error 0.787
-5.06 Score
Standard Error 0.766

Adverse Events

Olaparib 300 mg bd + Abiraterone 1000 mg qd

Serious events: 161 serious events
Other events: 374 other events
Deaths: 176 deaths

Placebo bd + Abiraterone 1000 mg qd

Serious events: 126 serious events
Other events: 346 other events
Deaths: 205 deaths

Serious adverse events

Serious adverse events
Measure
Olaparib 300 mg bd + Abiraterone 1000 mg qd
n=398 participants at risk
Patients receive oral treatment with olaparib 300mg twice daily in combination with abiraterone 1000mg once daily
Placebo bd + Abiraterone 1000 mg qd
n=396 participants at risk
Patients receive oral treatment with placebo twice daily in combination with abiraterone 1000mg once daily.
Cardiac disorders
Acute myocardial infarction
1.0%
4/398 • Number of events 5 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.76%
3/396 • Number of events 3 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Urinary tract infection
2.3%
9/398 • Number of events 17 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.76%
3/396 • Number of events 3 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Urinary tract infection pseudomonal
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Urosepsis
1.3%
5/398 • Number of events 5 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.51%
2/396 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Wound infection staphylococcal
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Cervical vertebral fracture
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Craniocerebral injury
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Extra-axial haemorrhage
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Fall
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Cardiac disorders
Angina pectoris
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Femoral neck fracture
0.50%
2/398 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Femur fracture
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Gun shot wound
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Hand fracture
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Head injury
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Hip fracture
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Injury
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Limb crushing injury
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Post procedural complication
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Post procedural haematoma
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Cardiac disorders
Atrial fibrillation
1.0%
4/398 • Number of events 6 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
1.0%
4/396 • Number of events 5 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Post procedural haemorrhage
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Post procedural hypotension
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Radiation pneumonitis
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Radiation proctitis
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Radius fracture
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Rib fracture
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Spinal fracture
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Sternal fracture
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Subdural haematoma
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Thermal burn
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Cardiac disorders
Atrioventricular block complete
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Tibia fracture
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Toxicity to various agents
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Investigations
Alanine aminotransferase increased
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Investigations
Aspartate aminotransferase increased
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Investigations
Blood creatinine increased
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Investigations
Electrocardiogram qt prolonged
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Investigations
Lymphocyte count decreased
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Investigations
Neutrophil count decreased
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Cardiac disorders
Cardiac failure
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Investigations
White blood cell count decreased
0.75%
3/398 • Number of events 3 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Metabolism and nutrition disorders
Cachexia
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Metabolism and nutrition disorders
Dehydration
0.50%
2/398 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Metabolism and nutrition disorders
Diabetes mellitus inadequate control
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Metabolism and nutrition disorders
Diabetic ketoacidosis
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.51%
2/396 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Metabolism and nutrition disorders
Hyperglycaemia
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Metabolism and nutrition disorders
Hypoalbuminaemia
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Metabolism and nutrition disorders
Hypocalcaemia
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Cardiac disorders
Cardiac failure acute
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Metabolism and nutrition disorders
Hypokalaemia
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Metabolism and nutrition disorders
Hyponatraemia
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.51%
2/396 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Metabolism and nutrition disorders
Hypophagia
0.50%
2/398 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Musculoskeletal and connective tissue disorders
Back pain
1.3%
5/398 • Number of events 6 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.76%
3/396 • Number of events 3 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Musculoskeletal and connective tissue disorders
Bone pain
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.51%
2/396 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Musculoskeletal and connective tissue disorders
Intervertebral disc protrusion
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Musculoskeletal and connective tissue disorders
Muscular weakness
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Cardiac disorders
Coronary artery disease
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Musculoskeletal and connective tissue disorders
Neck pain
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Musculoskeletal and connective tissue disorders
Osteitis
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Musculoskeletal and connective tissue disorders
Osteoarthritis
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Musculoskeletal and connective tissue disorders
Osteonecrosis of jaw
0.50%
2/398 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Musculoskeletal and connective tissue disorders
Osteoporosis
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Musculoskeletal and connective tissue disorders
Osteoporotic fracture
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Musculoskeletal and connective tissue disorders
Spinal pain
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Bladder cancer
0.50%
2/398 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Cardiac disorders
Left ventricular failure
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Colon cancer
0.75%
3/398 • Number of events 3 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Colorectal adenoma
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Colorectal cancer
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Diffuse large b-cell lymphoma
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Gastric adenoma
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Gastric cancer
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.51%
2/396 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Lung adenocarcinoma
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Malignant melanoma
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Myelodysplastic syndrome
0.50%
2/398 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Neuroendocrine carcinoma of the skin
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Cardiac disorders
Mitral valve disease
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Non-small cell lung cancer
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.51%
2/396 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Penile squamous cell carcinoma
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Pituitary tumour benign
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Plasma cell myeloma
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Rectal cancer
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Small intestine adenocarcinoma
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Squamous cell carcinoma
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Squamous cell carcinoma of skin
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Squamous cell carcinoma of the tongue
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Transitional cell carcinoma
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Cardiac disorders
Myocardial infarction
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.76%
3/396 • Number of events 3 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Nervous system disorders
Cerebral ischaemia
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Nervous system disorders
Cerebrovascular accident
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Nervous system disorders
Depressed level of consciousness
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Nervous system disorders
Dizziness
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Nervous system disorders
Embolic stroke
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Nervous system disorders
Epilepsy
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Nervous system disorders
Hemiparesis
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Nervous system disorders
Hypoglycaemic unconsciousness
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Blood and lymphatic system disorders
Anaemia
5.8%
23/398 • Number of events 29 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.76%
3/396 • Number of events 3 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Cardiac disorders
Myocardial ischaemia
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Nervous system disorders
Intraventricular haemorrhage
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Nervous system disorders
Ischaemic stroke
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
1.0%
4/396 • Number of events 4 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Nervous system disorders
Loss of consciousness
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.51%
2/396 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Nervous system disorders
Neuralgia
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Nervous system disorders
Optic neuritis
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Nervous system disorders
Partial seizures
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Nervous system disorders
Syncope
1.3%
5/398 • Number of events 5 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.51%
2/396 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Nervous system disorders
Thalamic infarction
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Nervous system disorders
Transient ischaemic attack
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Product Issues
Device occlusion
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Cardiac disorders
Palpitations
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Psychiatric disorders
Alcohol withdrawal syndrome
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Psychiatric disorders
Depression
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Renal and urinary disorders
Acute kidney injury
0.75%
3/398 • Number of events 3 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
1.0%
4/396 • Number of events 4 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Renal and urinary disorders
Calculus bladder
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Renal and urinary disorders
Dysuria
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Renal and urinary disorders
Haematuria
0.50%
2/398 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Renal and urinary disorders
Hydronephrosis
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Renal and urinary disorders
Nephrolithiasis
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Renal and urinary disorders
Postrenal failure
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Cardiac disorders
Prinzmetal angina
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Renal and urinary disorders
Ureteric obstruction
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Renal and urinary disorders
Ureterolithiasis
0.50%
2/398 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Renal and urinary disorders
Urethral stenosis
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Renal and urinary disorders
Urinary incontinence
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Renal and urinary disorders
Urinary retention
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Renal and urinary disorders
Urinary tract obstruction
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Renal and urinary disorders
Urinary tract pain
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Reproductive system and breast disorders
Prostatitis
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Respiratory, thoracic and mediastinal disorders
Acute pulmonary oedema
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.51%
2/396 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Respiratory, thoracic and mediastinal disorders
Chronic obstructive pulmonary disease
0.50%
2/398 • Number of events 3 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Ear and labyrinth disorders
Vertigo
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Respiratory, thoracic and mediastinal disorders
Dyspnoea
0.50%
2/398 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Respiratory, thoracic and mediastinal disorders
Interstitial lung disease
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Respiratory, thoracic and mediastinal disorders
Nasal polyps
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Respiratory, thoracic and mediastinal disorders
Pneumonitis
0.50%
2/398 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Respiratory, thoracic and mediastinal disorders
Pneumothorax
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Respiratory, thoracic and mediastinal disorders
Pulmonary embolism
3.8%
15/398 • Number of events 15 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.76%
3/396 • Number of events 3 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Respiratory, thoracic and mediastinal disorders
Respiratory failure
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Skin and subcutaneous tissue disorders
Cutaneous vasculitis
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Skin and subcutaneous tissue disorders
Dermatitis
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Ear and labyrinth disorders
Vestibular disorder
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Skin and subcutaneous tissue disorders
Drug eruption
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Vascular disorders
Adventitial cystic disease
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Vascular disorders
Aortic dissection
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Vascular disorders
Aortic stenosis
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Vascular disorders
Deep vein thrombosis
0.50%
2/398 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Vascular disorders
Giant cell arteritis
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Vascular disorders
Hypotension
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Vascular disorders
Peripheral arterial occlusive disease
0.50%
2/398 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Endocrine disorders
Adrenal insufficiency
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Vascular disorders
Peripheral ischaemia
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Vascular disorders
Vasculitis
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Eye disorders
Cataract
0.50%
2/398 • Number of events 3 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.51%
2/396 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Eye disorders
Limbal stem cell deficiency
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Abdominal pain
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.51%
2/396 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Blood and lymphatic system disorders
Febrile neutropenia
1.3%
5/398 • Number of events 5 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.51%
2/396 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Colitis
0.50%
2/398 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Colitis ulcerative
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Diarrhoea
0.75%
3/398 • Number of events 3 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Duodenal ulcer
0.50%
2/398 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Gastric ulcer perforation
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Gastroduodenal ulcer
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Gastrointestinal angiodysplasia
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Haematochezia
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Blood and lymphatic system disorders
Leukocytosis
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Hypoaesthesia oral
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Ileus
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Inguinal hernia
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Intestinal obstruction
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Intestinal ulcer
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Large intestine polyp
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.51%
2/396 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Lower gastrointestinal haemorrhage
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Nausea
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Rectal haemorrhage
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Small intestinal obstruction
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Umbilical hernia, obstructive
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Vomiting
1.0%
4/398 • Number of events 4 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
General disorders
Asthenia
0.50%
2/398 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
General disorders
Death
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
1.0%
4/396 • Number of events 4 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
General disorders
Fatigue
0.75%
3/398 • Number of events 3 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
General disorders
General physical health deterioration
0.50%
2/398 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
General disorders
Malaise
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
General disorders
Non-cardiac chest pain
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
General disorders
Pyrexia
0.75%
3/398 • Number of events 3 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.51%
2/396 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Blood and lymphatic system disorders
Myelosuppression
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
General disorders
Sudden death
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Hepatobiliary disorders
Bile duct stone
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Hepatobiliary disorders
Cholangitis acute
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Hepatobiliary disorders
Cholecystitis
0.50%
2/398 • Number of events 3 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Hepatobiliary disorders
Cholecystitis acute
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Hepatobiliary disorders
Drug-induced liver injury
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.51%
2/396 • Number of events 3 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Hepatobiliary disorders
Portal vein thrombosis
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Immune system disorders
Anaphylactic shock
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Acute sinusitis
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Anal abscess
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Blood and lymphatic system disorders
Neutropenia
0.50%
2/398 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Appendicitis
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.51%
2/396 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Atypical pneumonia
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Bacterial sepsis
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Covid-19
3.8%
15/398 • Number of events 16 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
2.5%
10/396 • Number of events 10 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Covid-19 pneumonia
1.8%
7/398 • Number of events 7 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.76%
3/396 • Number of events 3 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Cellulitis
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Diverticulitis
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Gastroenteritis
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Gastroenteritis viral
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Hepatitis b reactivation
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Blood and lymphatic system disorders
Thrombocytopenia
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Infection
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Lower respiratory tract infection
0.75%
3/398 • Number of events 3 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Lung abscess
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Oral infection
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Osteomyelitis
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.51%
2/396 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Perirectal abscess
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Pneumococcal sepsis
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Pneumocystis jirovecii pneumonia
1.0%
4/398 • Number of events 4 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Pneumonia
2.8%
11/398 • Number of events 13 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
1.3%
5/396 • Number of events 5 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Pneumonia aspiration
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Cardiac disorders
Acute coronary syndrome
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Pneumonia bacterial
0.50%
2/398 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Pneumonia cryptococcal
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Pneumonia viral
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Pyelonephritis
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Pyelonephritis acute
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Sepsis
1.3%
5/398 • Number of events 5 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.76%
3/396 • Number of events 3 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Septic shock
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Skin infection
0.25%
1/398 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Staphylococcal sepsis
0.00%
0/398 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.25%
1/396 • Number of events 1 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Suspected covid-19
0.50%
2/398 • Number of events 2 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
0.00%
0/396 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).

Other adverse events

Other adverse events
Measure
Olaparib 300 mg bd + Abiraterone 1000 mg qd
n=398 participants at risk
Patients receive oral treatment with olaparib 300mg twice daily in combination with abiraterone 1000mg once daily
Placebo bd + Abiraterone 1000 mg qd
n=396 participants at risk
Patients receive oral treatment with placebo twice daily in combination with abiraterone 1000mg once daily.
Infections and infestations
Upper respiratory tract infection
5.3%
21/398 • Number of events 22 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
5.6%
22/396 • Number of events 25 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Urinary tract infection
10.6%
42/398 • Number of events 70 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
8.3%
33/396 • Number of events 41 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Contusion
7.8%
31/398 • Number of events 36 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
4.8%
19/396 • Number of events 19 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Injury, poisoning and procedural complications
Fall
7.3%
29/398 • Number of events 35 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
7.1%
28/396 • Number of events 35 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Investigations
Alanine aminotransferase increased
3.8%
15/398 • Number of events 19 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
6.8%
27/396 • Number of events 30 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Investigations
Aspartate aminotransferase increased
4.0%
16/398 • Number of events 18 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
5.6%
22/396 • Number of events 26 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Investigations
Blood alkaline phosphatase increased
5.5%
22/398 • Number of events 25 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
5.3%
21/396 • Number of events 24 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Investigations
Blood creatinine increased
6.8%
27/398 • Number of events 52 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
4.8%
19/396 • Number of events 26 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Investigations
Lymphocyte count decreased
8.5%
34/398 • Number of events 69 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
4.3%
17/396 • Number of events 26 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Investigations
Weight decreased
6.8%
27/398 • Number of events 30 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
3.8%
15/396 • Number of events 16 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Investigations
White blood cell count decreased
5.8%
23/398 • Number of events 48 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
2.5%
10/396 • Number of events 13 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Metabolism and nutrition disorders
Decreased appetite
16.6%
66/398 • Number of events 81 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
7.8%
31/396 • Number of events 33 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Metabolism and nutrition disorders
Hyperglycaemia
7.5%
30/398 • Number of events 45 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
6.8%
27/396 • Number of events 36 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Metabolism and nutrition disorders
Hypertriglyceridaemia
6.0%
24/398 • Number of events 27 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
4.5%
18/396 • Number of events 20 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Metabolism and nutrition disorders
Hypokalaemia
8.3%
33/398 • Number of events 54 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
4.5%
18/396 • Number of events 25 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Musculoskeletal and connective tissue disorders
Arthralgia
14.6%
58/398 • Number of events 84 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
19.4%
77/396 • Number of events 116 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Musculoskeletal and connective tissue disorders
Back pain
20.6%
82/398 • Number of events 111 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
19.7%
78/396 • Number of events 89 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Musculoskeletal and connective tissue disorders
Muscle spasms
8.5%
34/398 • Number of events 44 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
4.8%
19/396 • Number of events 23 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Musculoskeletal and connective tissue disorders
Musculoskeletal chest pain
8.3%
33/398 • Number of events 47 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
7.1%
28/396 • Number of events 31 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Musculoskeletal and connective tissue disorders
Myalgia
5.5%
22/398 • Number of events 28 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
5.8%
23/396 • Number of events 29 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Musculoskeletal and connective tissue disorders
Pain in extremity
9.5%
38/398 • Number of events 46 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
9.6%
38/396 • Number of events 42 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Nervous system disorders
Dizziness
12.3%
49/398 • Number of events 53 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
6.8%
27/396 • Number of events 32 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Nervous system disorders
Dysgeusia
6.0%
24/398 • Number of events 26 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
1.8%
7/396 • Number of events 7 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Nervous system disorders
Headache
9.8%
39/398 • Number of events 44 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
6.6%
26/396 • Number of events 32 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Blood and lymphatic system disorders
Anaemia
46.2%
184/398 • Number of events 293 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
16.9%
67/396 • Number of events 93 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Psychiatric disorders
Insomnia
7.8%
31/398 • Number of events 35 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
7.1%
28/396 • Number of events 30 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Renal and urinary disorders
Dysuria
5.5%
22/398 • Number of events 25 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
4.5%
18/396 • Number of events 19 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Respiratory, thoracic and mediastinal disorders
Cough
11.8%
47/398 • Number of events 59 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
7.3%
29/396 • Number of events 40 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Respiratory, thoracic and mediastinal disorders
Dyspnoea
9.5%
38/398 • Number of events 46 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
6.8%
27/396 • Number of events 33 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Vascular disorders
Hot flush
8.8%
35/398 • Number of events 37 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
12.9%
51/396 • Number of events 52 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Vascular disorders
Hypertension
15.3%
61/398 • Number of events 80 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
18.7%
74/396 • Number of events 97 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Abdominal pain
6.8%
27/398 • Number of events 31 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
3.5%
14/396 • Number of events 14 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Abdominal pain upper
6.5%
26/398 • Number of events 30 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
4.0%
16/396 • Number of events 18 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Constipation
18.6%
74/398 • Number of events 84 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
14.9%
59/396 • Number of events 67 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Diarrhoea
20.1%
80/398 • Number of events 109 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
10.6%
42/396 • Number of events 52 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Dyspepsia
7.3%
29/398 • Number of events 38 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
4.3%
17/396 • Number of events 20 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Nausea
30.7%
122/398 • Number of events 173 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
14.1%
56/396 • Number of events 67 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Blood and lymphatic system disorders
Lymphopenia
6.0%
24/398 • Number of events 37 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
2.5%
10/396 • Number of events 11 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Gastrointestinal disorders
Vomiting
15.1%
60/398 • Number of events 84 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
9.1%
36/396 • Number of events 42 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
General disorders
Asthenia
11.6%
46/398 • Number of events 53 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
10.1%
40/396 • Number of events 55 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
General disorders
Fatigue
28.1%
112/398 • Number of events 131 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
20.5%
81/396 • Number of events 91 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
General disorders
Oedema peripheral
12.3%
49/398 • Number of events 63 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
12.6%
50/396 • Number of events 62 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
General disorders
Pyrexia
6.8%
27/398 • Number of events 35 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
4.8%
19/396 • Number of events 24 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
Infections and infestations
Covid-19
9.0%
36/398 • Number of events 36 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).
6.3%
25/396 • Number of events 26 • Adverse events with an onset date, or worsen, on or after the date of first dose and up to and including 30 days following discontinuation of randomised treatment. Assessed from date of randomisation to data cut off (DCO3): 12Oct2022 (Approx. 3 years 11 months)
Adverse events were assessed based on the Safety population consisting of patients who received treatment (N=794) while all-cause mortality was assessed based on all patients randomized (N=796).

Additional Information

Global Clinical Lead

AstraZeneca

Phone: 1-877-240-9479

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place

Restriction type: GT60