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.
TERMINATED
PHASE2
163 participants
12 weeks
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
| 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
| 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
| 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 weeksPopulation: 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
| 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 weekPopulation: 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
| 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 weeksPopulation: 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
| 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 weeksPopulation: 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
| 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 weeksPopulation: 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
| 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 weeksPopulation: 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
| 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 weeksPopulation: 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
| 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 weeksPopulation: 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
| 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 weeksPopulation: 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
| 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 weeksPopulation: 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
| 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
FOSTA 100 MG BID (4 WKS) THEN 150 MG QD PO
FOSTA 50 MG BID PO
FOSTA 75 MG BID PO
PLACEBO PO
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
| 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
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place
Restriction type: GT60