Trial Outcomes & Findings for Evaluation of Safety and Effectiveness of Fostamatinib Compared to Placebo in Patients in Asia With Rheumatoid Arthritis (NCT NCT01569074)

NCT ID: NCT01569074

Last Updated: 2014-04-07

Results Overview

ACR20: American College of Rheumatology 20% response criteria, based on count of swollen and tender joints (out of 28 joints), blood test measures of inflammation (such as C-Reactive Protein) and the physician and patient's own assessments of disease activity, pain and physical function. BID = twice daily, DMARD = disease-modifying anti-rheumatic drug, PO = orally, QD = once a day.

Recruitment status

TERMINATED

Study phase

PHASE2

Target enrollment

163 participants

Primary outcome timeframe

12 weeks

Results posted on

2014-04-07

Participant Flow

A total of 298 patients were enrolled: 31, 33, 33, 33 \& 33 were randomised to Groups A, B, C, D \& E respectively (all received at least 1 dose of investigational product).

A total of 135 patients failed screening.

Participant milestones

Participant milestones
Measure
FOSTA 100 MG BID PO
Dosing Group A
FOSTA 100 MG BID (4 WKS) THEN 150 MG QD PO
Dosing Group B
FOSTA 75 MG BID PO
Dosing Group C
FOSTA 50 MG BID PO
Dosing Group D
PLACEBO PO
Dosing Group E
Overall Study
STARTED
31
33
33
33
33
Overall Study
Randomised But Did Not Receive Treatment
0
0
0
0
0
Overall Study
COMPLETED
24
24
21
25
25
Overall Study
NOT COMPLETED
7
9
12
8
8

Reasons for withdrawal

Reasons for withdrawal
Measure
FOSTA 100 MG BID PO
Dosing Group A
FOSTA 100 MG BID (4 WKS) THEN 150 MG QD PO
Dosing Group B
FOSTA 75 MG BID PO
Dosing Group C
FOSTA 50 MG BID PO
Dosing Group D
PLACEBO PO
Dosing Group E
Overall Study
Study stopped
6
6
8
7
7
Overall Study
Study-specific discontinuation criteria
0
1
0
0
0
Overall Study
Severe non-compliance to protocol
0
0
1
0
0
Overall Study
eg change in circumstances
0
2
0
1
1
Overall Study
Adverse Event
1
0
3
0
0

Baseline Characteristics

Evaluation of Safety and Effectiveness of Fostamatinib Compared to Placebo in Patients in Asia With Rheumatoid Arthritis

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
FOSTA 100 MG BID PO
n=31 Participants
Dosing Group A
FOSTA 100 MG BID (4 WKS) THEN 150 MG QD PO
n=33 Participants
Dosing Group B
FOSTA 75 MG BID PO
n=33 Participants
Dosing Group C
FOSTA 50 MG BID PO
n=33 Participants
Dosing Group D
PLACEBO PO
n=33 Participants
Dosing Group E
Total
n=163 Participants
Total of all reporting groups
Age, Continuous
51 years
STANDARD_DEVIATION 14.3 • n=39 Participants
55 years
STANDARD_DEVIATION 10.4 • n=41 Participants
56 years
STANDARD_DEVIATION 11.5 • n=35 Participants
50 years
STANDARD_DEVIATION 11.4 • n=31 Participants
53 years
STANDARD_DEVIATION 11.3 • n=146 Participants
53 years
STANDARD_DEVIATION 11.9 • n=19 Participants
Sex: Female, Male
Female
31 Participants
n=39 Participants
25 Participants
n=41 Participants
27 Participants
n=35 Participants
31 Participants
n=31 Participants
28 Participants
n=146 Participants
142 Participants
n=19 Participants
Sex: Female, Male
Male
0 Participants
n=39 Participants
8 Participants
n=41 Participants
6 Participants
n=35 Participants
2 Participants
n=31 Participants
5 Participants
n=146 Participants
21 Participants
n=19 Participants
Race/Ethnicity, Customized
Asian
31 Participants
n=39 Participants
33 Participants
n=41 Participants
33 Participants
n=35 Participants
33 Participants
n=31 Participants
33 Participants
n=146 Participants
163 Participants
n=19 Participants
Race/Ethnicity, Customized
White
0 Participants
n=39 Participants
0 Participants
n=41 Participants
0 Participants
n=35 Participants
0 Participants
n=31 Participants
0 Participants
n=146 Participants
0 Participants
n=19 Participants
Race/Ethnicity, Customized
Black or African American
0 Participants
n=39 Participants
0 Participants
n=41 Participants
0 Participants
n=35 Participants
0 Participants
n=31 Participants
0 Participants
n=146 Participants
0 Participants
n=19 Participants
Race/Ethnicity, Customized
American Indian or Alaska Native
0 Participants
n=39 Participants
0 Participants
n=41 Participants
0 Participants
n=35 Participants
0 Participants
n=31 Participants
0 Participants
n=146 Participants
0 Participants
n=19 Participants
Race/Ethnicity, Customized
Indian or Pakistani
0 Participants
n=39 Participants
0 Participants
n=41 Participants
0 Participants
n=35 Participants
0 Participants
n=31 Participants
0 Participants
n=146 Participants
0 Participants
n=19 Participants
Race/Ethnicity, Customized
Native Hawaiian or Other Pacific Islander
0 Participants
n=39 Participants
0 Participants
n=41 Participants
0 Participants
n=35 Participants
0 Participants
n=31 Participants
0 Participants
n=146 Participants
0 Participants
n=19 Participants

PRIMARY outcome

Timeframe: 12 weeks

Population: The full analysis set includes those patients who received at least 1 dose of investigational product. Patients were analysed by randomised treatment in accordance with the intention to treat principle.

ACR20: American College of Rheumatology 20% response criteria, based on count of swollen and tender joints (out of 28 joints), blood test measures of inflammation (such as C-Reactive Protein) and the physician and patient's own assessments of disease activity, pain and physical function. BID = twice daily, DMARD = disease-modifying anti-rheumatic drug, PO = orally, QD = once a day.

Outcome measures

Outcome measures
Measure
FOSTA 100 MG BID PO
n=26 Participants
Dosing Group A
FOSTA 100 MG BID (4 WKS) THEN 150 MG QD PO
n=29 Participants
Dosing Group B
FOSTA 75 MG BID PO
n=27 Participants
Dosing Group C
FOSTA 50 MG BID PO
n=28 Participants
Dosing Group D
PLACEBO PO
n=28 Participants
Dosing Group E
Proportion of Patients Achieving ACR20 at Week 12, Comparison Between Fostamatinib and Placebo
53.8 Percentage of responders
55.2 Percentage of responders
25.9 Percentage of responders
46.4 Percentage of responders
32.1 Percentage of responders

SECONDARY outcome

Timeframe: 1 week

Population: The full analysis set includes those patients who received at least 1 dose of investigational product. Patients were analysed by randomised treatment in accordance with the intention to treat principle. The fostamatinib 100 mg BID combined group contains 31 patients from Dosing Group A and 33 patients from Dosing Group B.

ACR20: American College of Rheumatology 20% response criteria, based on count of swollen and tender joints (out of 28 joints), blood test measures of inflammation (such as C-Reactive Protein) and the physician and patient's own assessments of disease activity, pain and physical function. BID = twice daily, DMARD = disease-modifying anti-rheumatic drug, PO = orally.

Outcome measures

Outcome measures
Measure
FOSTA 100 MG BID PO
n=33 Participants
Dosing Group A
FOSTA 100 MG BID (4 WKS) THEN 150 MG QD PO
n=33 Participants
Dosing Group B
FOSTA 75 MG BID PO
n=33 Participants
Dosing Group C
FOSTA 50 MG BID PO
n=64 Participants
Dosing Group D
PLACEBO PO
Dosing Group E
Proportion of Patients Achieving ACR20 at Week 1, Comparison Between Fostamatinib and Placebo
21.2 Percentage of responders
18.2 Percentage of responders
15.2 Percentage of responders
25.0 Percentage of responders

SECONDARY outcome

Timeframe: 12 weeks

Population: The full analysis set includes those patients who received at least 1 dose of investigational product. Patients were analysed by randomised treatment in accordance with the intention to treat principle.

ACR50: American College of Rheumatology 50% response criteria, based on count of swollen and tender joints (out of 28 joints), blood test measures of inflammation (such as C-Reactive Protein) and the physician and patient's own assessments of disease activity, pain and physical function, BID = twice daily, DMARD = disease-modifying anti-rheumatic drug, PO = orally, QD = once a day.

Outcome measures

Outcome measures
Measure
FOSTA 100 MG BID PO
n=26 Participants
Dosing Group A
FOSTA 100 MG BID (4 WKS) THEN 150 MG QD PO
n=29 Participants
Dosing Group B
FOSTA 75 MG BID PO
n=27 Participants
Dosing Group C
FOSTA 50 MG BID PO
n=28 Participants
Dosing Group D
PLACEBO PO
n=28 Participants
Dosing Group E
Proportion of Patients Achieving ACR50 at Week 12, Comparison Between Fostamatinib and Placebo
30.8 Percentage of responders
34.5 Percentage of responders
7.4 Percentage of responders
10.7 Percentage of responders
14.3 Percentage of responders

SECONDARY outcome

Timeframe: 12 weeks

Population: The full analysis set includes those patients who received at least 1 dose of investigational product. Patients were analysed by randomised treatment in accordance with the intention to treat principle.

ACR70: American College of Rheumatology 70% response criteria, based on count of swollen and tender joints (out of 28 joints), blood test measures of inflammation (such as C-Reactive Protein) and the physician and patient's own assessments of disease activity, pain and physical function. BID = twice daily, DMARD = disease-modifying anti-rheumatic drug, PO = orally, QD = once a day.

Outcome measures

Outcome measures
Measure
FOSTA 100 MG BID PO
n=26 Participants
Dosing Group A
FOSTA 100 MG BID (4 WKS) THEN 150 MG QD PO
n=29 Participants
Dosing Group B
FOSTA 75 MG BID PO
n=27 Participants
Dosing Group C
FOSTA 50 MG BID PO
n=28 Participants
Dosing Group D
PLACEBO PO
n=28 Participants
Dosing Group E
Proportion of Patients Achieving ACR70 at Week 12, Comparison Between Fostamatinib and Placebo
11.5 Percentage of responders
13.8 Percentage of responders
0 Percentage of responders
0 Percentage of responders
0 Percentage of responders

SECONDARY outcome

Timeframe: Baseline and 12 weeks

Population: The full analysis set includes those patients who received at least 1 dose of investigational product. Patients were analysed by randomised treatment in accordance with the intention to treat principle.

ACRn: American College of Rheumatology index of RA improvement, based on smallest percentage improvement in the count of swollen joints (out of 28 joints), count of tender joints (out of 28 joints), or in blood test measures of inflammation (such as C-Reactive Protein) or the physician or patient's own assessments of disease activity, pain and physical function. Scores are reported as a percentage improvement on a scale of -100 to +100, with larger values representing a better clinical outcome. Mean refers to change at Week 12. BID = twice daily, DMARD = disease-modifying anti-rheumatic drug, PO = orally, QD = once a day.

Outcome measures

Outcome measures
Measure
FOSTA 100 MG BID PO
n=26 Participants
Dosing Group A
FOSTA 100 MG BID (4 WKS) THEN 150 MG QD PO
n=29 Participants
Dosing Group B
FOSTA 75 MG BID PO
n=27 Participants
Dosing Group C
FOSTA 50 MG BID PO
n=28 Participants
Dosing Group D
PLACEBO PO
n=28 Participants
Dosing Group E
ACRn - Comparison Between Fostamatinib and Placebo at Week 12
25.52 Percentage improvement from baseline
Standard Deviation 37.029
24.18 Percentage improvement from baseline
Standard Deviation 39.925
3.59 Percentage improvement from baseline
Standard Deviation 29.774
15.88 Percentage improvement from baseline
Standard Deviation 24.354
10.94 Percentage improvement from baseline
Standard Deviation 28.302

SECONDARY outcome

Timeframe: 12 weeks

Population: The full analysis set includes those patients who received at least 1 dose of investigational product. Patients were analysed by randomised treatment in accordance with the intention to treat principle.

DAS28-CRP: Disease Activity Score based on a count of swollen and tender joints (out of 28 joints), blood test measures of inflammation (CRP) and the patient's own assessment. Scores can take any positive value with a lower value indicating a better clinical condition. DAS28-CRP score of \<=3.2 indicates low disease activity. BID = twice daily, CRP = C-reactive protein, , DMARD = disease modifying anti-rheumatic drug, OR = odds ratio, PO = orally, QD = once daily.

Outcome measures

Outcome measures
Measure
FOSTA 100 MG BID PO
n=26 Participants
Dosing Group A
FOSTA 100 MG BID (4 WKS) THEN 150 MG QD PO
n=29 Participants
Dosing Group B
FOSTA 75 MG BID PO
n=27 Participants
Dosing Group C
FOSTA 50 MG BID PO
n=28 Participants
Dosing Group D
PLACEBO PO
n=28 Participants
Dosing Group E
Proportion of Patients Achieving DAS28-CRP<=3.2 at Week 12, Comparison Between Fostamatinib and Placebo
34.6 Percentage of responders
0.81
34.5 Percentage of responders
0.82
22.2 Percentage of responders
0.77
17.9 Percentage of responders
0.75
10.7 Percentage of responders

SECONDARY outcome

Timeframe: 12 weeks

Population: The full analysis set includes those patients who received at least 1 dose of investigational product. Patients were analysed by randomised treatment in accordance with the intention to treat principle.

Change from baseline in DAS28-CRP at Week 12 was derived and categorised using the European League Against Rheumatism (EULAR) response criteria. BID = twice a day, DMARD = disease-modifying anti-rheumatic drug, OR = odds ratio, PO = orally, QD = once a day.

Outcome measures

Outcome measures
Measure
FOSTA 100 MG BID PO
n=26 Participants
Dosing Group A
FOSTA 100 MG BID (4 WKS) THEN 150 MG QD PO
n=29 Participants
Dosing Group B
FOSTA 75 MG BID PO
n=27 Participants
Dosing Group C
FOSTA 50 MG BID PO
n=28 Participants
Dosing Group D
PLACEBO PO
n=28 Participants
Dosing Group E
Proportion of Patients With DAS28-CRP EULAR Response at Week 12, Comparison Between Fostamatinib and Placebo
Good response
34.6 Percentage of responders
34.5 Percentage of responders
22.2 Percentage of responders
17.9 Percentage of responders
10.7 Percentage of responders
Proportion of Patients With DAS28-CRP EULAR Response at Week 12, Comparison Between Fostamatinib and Placebo
No response
30.8 Percentage of responders
1.46 • Interval 0.2 to 0.68
41.4 Percentage of responders
1.34 • Interval 0.26 to 0.89
48.1 Percentage of responders
1.30 • Interval 0.2 to 0.65
17.9 Percentage of responders
1.58
35.7 Percentage of responders
Proportion of Patients With DAS28-CRP EULAR Response at Week 12, Comparison Between Fostamatinib and Placebo
Moderate response
34.6 Percentage of responders
24.1 Percentage of responders
29.6 Percentage of responders
64.3 Percentage of responders
53.6 Percentage of responders

SECONDARY outcome

Timeframe: 12 weeks

Population: The full analysis set includes those patients who received at least 1 dose of investigational product. Patients were analysed by randomised treatment in accordance with the intention to treat principle.

HAQ-DI: Health Assessment Questionnaire - Disability Index, a measure of physical function. The HAQ-DI score is calculated by summing scores from 8 sub-categories (ie, scores for patient ability in dressing and grooming, rising, eating, walking, hygiene, reach, grip and common daily activities) and dividing by the number of categories completed. The HAQ-DI score takes values between 0 and 3, with higher score indicating greater disability. HAQ-DI response is a reduction from baseline in HAQ-DI greater than or equal to the minimally important difference (0.22). BID = twice daily, DMARD = disease-modifying anti-rheumatic drug, OR = odds ratio, PO = orally, QD = once a day.

Outcome measures

Outcome measures
Measure
FOSTA 100 MG BID PO
n=26 Participants
Dosing Group A
FOSTA 100 MG BID (4 WKS) THEN 150 MG QD PO
n=29 Participants
Dosing Group B
FOSTA 75 MG BID PO
n=27 Participants
Dosing Group C
FOSTA 50 MG BID PO
n=28 Participants
Dosing Group D
PLACEBO PO
n=28 Participants
Dosing Group E
Proportion of Patients With HAQ-DI Response at Week 12, Comparison Between Fostamatinib and Placebo
69.2 Percentage of responders
48.3 Percentage of responders
44.4 Percentage of responders
46.4 Percentage of responders
50.0 Percentage of responders

SECONDARY outcome

Timeframe: Baseline and 12 weeks

Population: The full analysis set includes those patients who received at least 1 dose of investigational product. Patients were analysed by randomised treatment in accordance with the intention to treat principle.

SF-36 = 36-item Short Form Health Survey, as a measure of health related quality of life. Scores for 8 sub-domains (Physical Functioning, Role-Physical, Bodily Pain, General Health, Vitality, Social Function, Role-Emotional and Mental Health) are derived and normalised to a scale of 0 to 100. The physical and mental component scores (PCS and MCS) are derived by multiplying each of these 8 scores by a constant, summing them and standardising against a population with mean of 50, standard deviation of 10. A higher score represents better quality of life. Mean changes from baseline are presented as increases from baseline (defined as post-baseline minus baseline); larger changes indicate a better clinical condition. Mean refers to change in scores at Week 12. ANCOVA = analysis of covariance, BID = twice daily, DMARD = disease-modifying anti-rheumatic drug, PO = orally, QD = once a day.

Outcome measures

Outcome measures
Measure
FOSTA 100 MG BID PO
n=25 Participants
Dosing Group A
FOSTA 100 MG BID (4 WKS) THEN 150 MG QD PO
n=29 Participants
Dosing Group B
FOSTA 75 MG BID PO
n=26 Participants
Dosing Group C
FOSTA 50 MG BID PO
n=27 Participants
Dosing Group D
PLACEBO PO
n=27 Participants
Dosing Group E
SF-36 - Comparison of the Change in PCS From Baseline Between Fostamatinib and Placebo at Week 12
7 Units on a scale
Standard Deviation 7.5
4 Units on a scale
Standard Deviation 7.4
3 Units on a scale
Standard Deviation 6.8
5 Units on a scale
Standard Deviation 5.6
3 Units on a scale
Standard Deviation 5.1

SECONDARY outcome

Timeframe: Baseline and 12 weeks

Population: The full analysis set includes those patients who received at least 1 dose of investigational product. Patients were analysed by randomised treatment in accordance with the intention to treat principle.

SF-36 = 36-item Short Form Health Survey, as a measure of health related quality of life. Scores for 8 sub-domains (Physical Functioning, Role-Physical, Bodily Pain, General Health, Vitality, Social Function, Role-Emotional and Mental Health) are derived and normalised to a scale of 0 to 100. The physical and mental component scores (PCS and MCS) are derived by multiplying each of these 8 scores by a constant, summing them and standardising against a population with mean of 50, standard deviation of 10. A higher score represents better quality of life. Mean changes from baseline are presented as increases from baseline (defined as post-baseline minus baseline); larger changes indicate a better clinical condition. Mean refers to change in scores at Week 12. ANCOVA = analysis of covariance, BID = twice daily, DMARD = disease-modifying anti-rheumatic drug, PO = orally, QD = once a day.

Outcome measures

Outcome measures
Measure
FOSTA 100 MG BID PO
n=25 Participants
Dosing Group A
FOSTA 100 MG BID (4 WKS) THEN 150 MG QD PO
n=29 Participants
Dosing Group B
FOSTA 75 MG BID PO
n=26 Participants
Dosing Group C
FOSTA 50 MG BID PO
n=27 Participants
Dosing Group D
PLACEBO PO
n=27 Participants
Dosing Group E
SF-36 - Comparison of the Change in MCS From Baseline Between Fostamatinib and Placebo at Week 12
7 Units on a scale
Standard Deviation 8.7
6 Units on a scale
Standard Deviation 7.7
2 Units on a scale
Standard Deviation 7.0
5 Units on a scale
Standard Deviation 8.9
4 Units on a scale
Standard Deviation 7.9

Adverse Events

FOSTA 100 MG BID PO

Serious events: 1 serious events
Other events: 21 other events
Deaths: 0 deaths

FOSTA 100 MG BID (4 WKS) THEN 150 MG QD PO

Serious events: 1 serious events
Other events: 17 other events
Deaths: 0 deaths

FOSTA 50 MG BID PO

Serious events: 3 serious events
Other events: 17 other events
Deaths: 0 deaths

FOSTA 75 MG BID PO

Serious events: 0 serious events
Other events: 16 other events
Deaths: 0 deaths

PLACEBO PO

Serious events: 1 serious events
Other events: 15 other events
Deaths: 0 deaths

Serious adverse events

Serious adverse events
Measure
FOSTA 100 MG BID PO
n=31 participants at risk
Dosing Group A
FOSTA 100 MG BID (4 WKS) THEN 150 MG QD PO
n=33 participants at risk
Dosing Group B
FOSTA 50 MG BID PO
n=33 participants at risk
Dosing Group D
FOSTA 75 MG BID PO
n=33 participants at risk
Dosing Group C
PLACEBO PO
n=33 participants at risk
Dosing Group E
Gastrointestinal disorders
DIARRHOEA
0.00%
0/31
3.0%
1/33 • Number of events 1
0.00%
0/33
0.00%
0/33
0.00%
0/33
Infections and infestations
LARYNGITIS VIRAL
3.2%
1/31 • Number of events 1
0.00%
0/33
0.00%
0/33
0.00%
0/33
0.00%
0/33
Musculoskeletal and connective tissue disorders
OSTEOPOROSIS
0.00%
0/31
0.00%
0/33
3.0%
1/33 • Number of events 1
0.00%
0/33
0.00%
0/33
Musculoskeletal and connective tissue disorders
RHEUMATOID ARTHRITIS
0.00%
0/31
0.00%
0/33
3.0%
1/33 • Number of events 1
0.00%
0/33
3.0%
1/33 • Number of events 1
Nervous system disorders
CARPAL TUNNEL SYNDROME
0.00%
0/31
0.00%
0/33
3.0%
1/33 • Number of events 1
0.00%
0/33
0.00%
0/33
Vascular disorders
HYPERTENSION
3.2%
1/31 • Number of events 1
0.00%
0/33
0.00%
0/33
0.00%
0/33
0.00%
0/33

Other adverse events

Other adverse events
Measure
FOSTA 100 MG BID PO
n=31 participants at risk
Dosing Group A
FOSTA 100 MG BID (4 WKS) THEN 150 MG QD PO
n=33 participants at risk
Dosing Group B
FOSTA 50 MG BID PO
n=33 participants at risk
Dosing Group D
FOSTA 75 MG BID PO
n=33 participants at risk
Dosing Group C
PLACEBO PO
n=33 participants at risk
Dosing Group E
Infections and infestations
UPPER RESPIRATORY TRACT INFECTION
9.7%
3/31 • Number of events 3
6.1%
2/33 • Number of events 2
0.00%
0/33
3.0%
1/33 • Number of events 1
3.0%
1/33 • Number of events 1
Blood and lymphatic system disorders
ANAEMIA
0.00%
0/31
0.00%
0/33
0.00%
0/33
0.00%
0/33
6.1%
2/33 • Number of events 2
Blood and lymphatic system disorders
LEUKOPENIA
0.00%
0/31
0.00%
0/33
6.1%
2/33 • Number of events 3
3.0%
1/33 • Number of events 1
6.1%
2/33 • Number of events 3
Blood and lymphatic system disorders
NEUTROPENIA
12.9%
4/31 • Number of events 6
6.1%
2/33 • Number of events 2
15.2%
5/33 • Number of events 7
12.1%
4/33 • Number of events 4
9.1%
3/33 • Number of events 5
Cardiac disorders
PALPITATIONS
0.00%
0/31
0.00%
0/33
0.00%
0/33
0.00%
0/33
6.1%
2/33 • Number of events 2
Gastrointestinal disorders
DIARRHOEA
16.1%
5/31 • Number of events 6
15.2%
5/33 • Number of events 5
3.0%
1/33 • Number of events 1
6.1%
2/33 • Number of events 2
0.00%
0/33
Gastrointestinal disorders
GASTRITIS
9.7%
3/31 • Number of events 3
3.0%
1/33 • Number of events 2
3.0%
1/33 • Number of events 2
0.00%
0/33
3.0%
1/33 • Number of events 1
Gastrointestinal disorders
NAUSEA
3.2%
1/31 • Number of events 1
0.00%
0/33
0.00%
0/33
0.00%
0/33
9.1%
3/33 • Number of events 3
Gastrointestinal disorders
VOMITING
6.5%
2/31 • Number of events 2
0.00%
0/33
0.00%
0/33
0.00%
0/33
3.0%
1/33 • Number of events 1
General disorders
PYREXIA
0.00%
0/31
3.0%
1/33 • Number of events 1
6.1%
2/33 • Number of events 2
6.1%
2/33 • Number of events 2
0.00%
0/33
Infections and infestations
CELLULITIS
3.2%
1/31 • Number of events 1
0.00%
0/33
6.1%
2/33 • Number of events 2
0.00%
0/33
0.00%
0/33
Infections and infestations
NASOPHARYNGITIS
6.5%
2/31 • Number of events 2
0.00%
0/33
9.1%
3/33 • Number of events 3
6.1%
2/33 • Number of events 2
0.00%
0/33
Infections and infestations
VIRAL UPPER RESPIRATORY TRACT INFECTION
0.00%
0/31
3.0%
1/33 • Number of events 1
6.1%
2/33 • Number of events 2
0.00%
0/33
0.00%
0/33
Investigations
ALANINE AMINOTRANSFERASE INCREASED
0.00%
0/31
0.00%
0/33
0.00%
0/33
0.00%
0/33
6.1%
2/33 • Number of events 2
Investigations
GAMMA-GLUTAMYLTRANSFERASE INCREASED
0.00%
0/31
0.00%
0/33
0.00%
0/33
0.00%
0/33
6.1%
2/33 • Number of events 2
Nervous system disorders
DIZZINESS
3.2%
1/31 • Number of events 1
0.00%
0/33
3.0%
1/33 • Number of events 2
3.0%
1/33 • Number of events 1
6.1%
2/33 • Number of events 2
Nervous system disorders
HEADACHE
3.2%
1/31 • Number of events 1
6.1%
2/33 • Number of events 2
0.00%
0/33
3.0%
1/33 • Number of events 1
0.00%
0/33
Psychiatric disorders
INSOMNIA
0.00%
0/31
0.00%
0/33
0.00%
0/33
0.00%
0/33
6.1%
2/33 • Number of events 2
Respiratory, thoracic and mediastinal disorders
COUGH
0.00%
0/31
0.00%
0/33
0.00%
0/33
9.1%
3/33 • Number of events 3
0.00%
0/33
Skin and subcutaneous tissue disorders
ALOPECIA
0.00%
0/31
0.00%
0/33
6.1%
2/33 • Number of events 2
0.00%
0/33
0.00%
0/33
Skin and subcutaneous tissue disorders
PRURITUS
0.00%
0/31
0.00%
0/33
0.00%
0/33
0.00%
0/33
6.1%
2/33 • Number of events 2
Vascular disorders
HYPERTENSION
25.8%
8/31 • Number of events 8
18.2%
6/33 • Number of events 6
9.1%
3/33 • Number of events 3
18.2%
6/33 • Number of events 6
6.1%
2/33 • Number of events 2

Additional Information

Dave Goldstraw

AstraZeneca Pharmaceuticals

Phone: +44 (0)1625 512415

Results disclosure agreements

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

Restriction type: GT60