Trial Outcomes & Findings for A Study to Test the Effect of Different Doses of BI 1358894 and Quetiapine in People With Depression (NCT NCT04521478)
NCT ID: NCT04521478
Last Updated: 2025-03-06
Results Overview
Change from baseline in MADRS total score at Week 6 is reported. The MADRS evaluates core symptoms of depression and consists of 10 items. Nine of them are based upon participant reports, and one is on the rater's observation (apparent sadness) during the rating interview. MADRS items are rated on a 0-6 continuum (0=no abnormality, 6=severe). The possible total score could range from 0 (normal with absence of symptoms) to 60 (severe depression). Least squares mean and adjusted standard error were estimated by Restricted Maximum Likelihood (REML)-based Mixed effects model for repeated measures (MMRM) including the fixed categorical effects of treatment, concomitant psychotherapy use (yes vs. no), and the fixed continuous effect of baseline MADRS total score. Visit was treated as a repeated measure with an unstructured covariance matrix. The Kenward-Roger approximation was used to estimate the denominator degrees of freedom and adjust standard errors.
COMPLETED
PHASE2
389 participants
MMRM included measurements from baseline (Week 0) and at Weeks 1, 2, 4 and 6 after first drug administration. MMRM estimates of change from baseline to Week 6 is reported.
2025-03-06
Participant Flow
This was a Phase II, 6-week parallel-group multicenter, randomized, double blind, doubledummy, placebo-controlled trial with a Quetiapine arm in participants with Major Depressive Disorder (MDD) with inadequate response to ongoing treatment with a Selective Serotonin Reuptake Inhibitor (SSRI) or a Serotonin Norepinephrine Reuptake Inhibitor (SNRI) or bupropion.
All patients were screened for eligibility prior to participation in the trial, to ensure that they met all inclusion and none of the exclusion criteria. One patient was randomized to the placebo arm but treated with 125 mg BI 1358894.
Participant milestones
| Measure |
Placebo
Participants with an established diagnosis of Major Depressive Disorder (MDD) administered one dose of placebo matching BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their Ongoing Antidepressants (OAD).
|
5 mg BI 1358894
Participants with an established diagnosis of MDD administered one 5 milligram (mg) dose of BI 1358894 in the morning as film-coated tablet, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
25 mg BI 1358894
Participants with an established diagnosis of MDD administered one 25 mg dose of BI 1358894 in the morning as film-coated tablet, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
75 mg BI 1358894
Participants with an established diagnosis of MDD administered one 75 mg dose of BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
125 mg BI 1358894
Participants with an established diagnosis of MDD administered one 125 mg dose of BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
Quetiapine
Participants with an established diagnosis of MDD administered one dose of placebo matching BI 1358894 in the morning as film-coated tablets, and one 150 or 300 mg dose of quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
The daily active dose at the start of therapy was 50 mg on Day 1, 100 mg at Day 2 and 150 mg on Day 3 and 4. Beginning with Day 5, the recommended daily dose of 300 mg was taken. If not tolerated by a participant, the dose was reduced to 150 mg in Week 1. Thereafter, this finally chosen dose had to be stable until end of treatment at Week 6.
During the trial, participants also continued treatment with their OAD.
|
|---|---|---|---|---|---|---|
|
Overall Study
STARTED
|
129
|
36
|
39
|
39
|
74
|
72
|
|
Overall Study
Treated
|
129
|
36
|
39
|
39
|
74
|
71
|
|
Overall Study
COMPLETED
|
116
|
31
|
33
|
34
|
67
|
59
|
|
Overall Study
NOT COMPLETED
|
13
|
5
|
6
|
5
|
7
|
13
|
Reasons for withdrawal
| Measure |
Placebo
Participants with an established diagnosis of Major Depressive Disorder (MDD) administered one dose of placebo matching BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their Ongoing Antidepressants (OAD).
|
5 mg BI 1358894
Participants with an established diagnosis of MDD administered one 5 milligram (mg) dose of BI 1358894 in the morning as film-coated tablet, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
25 mg BI 1358894
Participants with an established diagnosis of MDD administered one 25 mg dose of BI 1358894 in the morning as film-coated tablet, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
75 mg BI 1358894
Participants with an established diagnosis of MDD administered one 75 mg dose of BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
125 mg BI 1358894
Participants with an established diagnosis of MDD administered one 125 mg dose of BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
Quetiapine
Participants with an established diagnosis of MDD administered one dose of placebo matching BI 1358894 in the morning as film-coated tablets, and one 150 or 300 mg dose of quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
The daily active dose at the start of therapy was 50 mg on Day 1, 100 mg at Day 2 and 150 mg on Day 3 and 4. Beginning with Day 5, the recommended daily dose of 300 mg was taken. If not tolerated by a participant, the dose was reduced to 150 mg in Week 1. Thereafter, this finally chosen dose had to be stable until end of treatment at Week 6.
During the trial, participants also continued treatment with their OAD.
|
|---|---|---|---|---|---|---|
|
Overall Study
Protocol Violation
|
2
|
0
|
1
|
0
|
0
|
0
|
|
Overall Study
Technical Problems
|
0
|
0
|
0
|
1
|
0
|
0
|
|
Overall Study
Burden of Study Procedures
|
1
|
0
|
0
|
1
|
0
|
1
|
|
Overall Study
Lack of Efficacy
|
0
|
0
|
0
|
0
|
1
|
1
|
|
Overall Study
Adverse Event
|
7
|
0
|
2
|
1
|
2
|
7
|
|
Overall Study
No Reason Available
|
0
|
2
|
0
|
0
|
1
|
0
|
|
Overall Study
Other than listed
|
3
|
3
|
3
|
2
|
3
|
3
|
|
Overall Study
Not treated
|
0
|
0
|
0
|
0
|
0
|
1
|
Baseline Characteristics
A Study to Test the Effect of Different Doses of BI 1358894 and Quetiapine in People With Depression
Baseline characteristics by cohort
| Measure |
Placebo
n=128 Participants
Participants with an established diagnosis of Major Depressive Disorder (MDD) administered one dose of placebo matching BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their Ongoing Antidepressants (OAD).
|
5 mg BI 1358894
n=36 Participants
Participants with an established diagnosis of MDD administered one 5 milligram (mg) dose of BI 1358894 in the morning as film-coated tablet, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
25 mg BI 1358894
n=39 Participants
Participants with an established diagnosis of MDD administered one 25 mg dose of BI 1358894 in the morning as film-coated tablet, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
75 mg BI 1358894
n=39 Participants
Participants with an established diagnosis of MDD administered one 75 mg dose of BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
125 mg BI 1358894
n=75 Participants
Participants with an established diagnosis of MDD administered one 125 mg dose of BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
Quetiapine
n=71 Participants
Participants with an established diagnosis of MDD administered one dose of placebo matching BI 1358894 in the morning as film-coated tablets, and one 150 or 300 mg dose of quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
The daily active dose at the start of therapy was 50 mg on Day 1, 100 mg at Day 2 and 150 mg on Day 3 and 4. Beginning with Day 5, the recommended daily dose of 300 mg was taken. If not tolerated by a participant, the dose was reduced to 150 mg in Week 1. Thereafter, this finally chosen dose had to be stable until end of treatment at Week 6.
During the trial, participants also continued treatment with their OAD.
|
Total
n=388 Participants
Total of all reporting groups
|
|---|---|---|---|---|---|---|---|
|
Age, Continuous
|
42.9 Years
STANDARD_DEVIATION 13.0 • n=99 Participants
|
39.7 Years
STANDARD_DEVIATION 13.8 • n=107 Participants
|
44.7 Years
STANDARD_DEVIATION 12.1 • n=206 Participants
|
42.7 Years
STANDARD_DEVIATION 12.2 • n=7 Participants
|
47.7 Years
STANDARD_DEVIATION 11.7 • n=31 Participants
|
43.6 Years
STANDARD_DEVIATION 12.4 • n=30 Participants
|
43.8 Years
STANDARD_DEVIATION 12.7 • n=3 Participants
|
|
Sex: Female, Male
Female
|
82 Participants
n=99 Participants
|
27 Participants
n=107 Participants
|
28 Participants
n=206 Participants
|
26 Participants
n=7 Participants
|
51 Participants
n=31 Participants
|
49 Participants
n=30 Participants
|
263 Participants
n=3 Participants
|
|
Sex: Female, Male
Male
|
46 Participants
n=99 Participants
|
9 Participants
n=107 Participants
|
11 Participants
n=206 Participants
|
13 Participants
n=7 Participants
|
24 Participants
n=31 Participants
|
22 Participants
n=30 Participants
|
125 Participants
n=3 Participants
|
|
Ethnicity (NIH/OMB)
Hispanic or Latino
|
19 Participants
n=99 Participants
|
5 Participants
n=107 Participants
|
2 Participants
n=206 Participants
|
5 Participants
n=7 Participants
|
8 Participants
n=31 Participants
|
12 Participants
n=30 Participants
|
51 Participants
n=3 Participants
|
|
Ethnicity (NIH/OMB)
Not Hispanic or Latino
|
109 Participants
n=99 Participants
|
31 Participants
n=107 Participants
|
37 Participants
n=206 Participants
|
34 Participants
n=7 Participants
|
67 Participants
n=31 Participants
|
59 Participants
n=30 Participants
|
337 Participants
n=3 Participants
|
|
Ethnicity (NIH/OMB)
Unknown or Not Reported
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
0 Participants
n=7 Participants
|
0 Participants
n=31 Participants
|
0 Participants
n=30 Participants
|
0 Participants
n=3 Participants
|
|
Race (NIH/OMB)
American Indian or Alaska Native
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
0 Participants
n=7 Participants
|
0 Participants
n=31 Participants
|
0 Participants
n=30 Participants
|
0 Participants
n=3 Participants
|
|
Race (NIH/OMB)
Asian
|
24 Participants
n=99 Participants
|
5 Participants
n=107 Participants
|
6 Participants
n=206 Participants
|
6 Participants
n=7 Participants
|
15 Participants
n=31 Participants
|
12 Participants
n=30 Participants
|
68 Participants
n=3 Participants
|
|
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
0 Participants
n=7 Participants
|
0 Participants
n=31 Participants
|
0 Participants
n=30 Participants
|
0 Participants
n=3 Participants
|
|
Race (NIH/OMB)
Black or African American
|
6 Participants
n=99 Participants
|
2 Participants
n=107 Participants
|
3 Participants
n=206 Participants
|
1 Participants
n=7 Participants
|
7 Participants
n=31 Participants
|
6 Participants
n=30 Participants
|
25 Participants
n=3 Participants
|
|
Race (NIH/OMB)
White
|
98 Participants
n=99 Participants
|
29 Participants
n=107 Participants
|
30 Participants
n=206 Participants
|
32 Participants
n=7 Participants
|
53 Participants
n=31 Participants
|
53 Participants
n=30 Participants
|
295 Participants
n=3 Participants
|
|
Race (NIH/OMB)
More than one race
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
0 Participants
n=7 Participants
|
0 Participants
n=31 Participants
|
0 Participants
n=30 Participants
|
0 Participants
n=3 Participants
|
|
Race (NIH/OMB)
Unknown or Not Reported
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
0 Participants
n=7 Participants
|
0 Participants
n=31 Participants
|
0 Participants
n=30 Participants
|
0 Participants
n=3 Participants
|
|
Montgomery-Åsberg Depression Rating Scale (MADRS) total score
|
32.0 Score on a scale
STANDARD_DEVIATION 6.4 • n=99 Participants
|
34.0 Score on a scale
STANDARD_DEVIATION 4.8 • n=107 Participants
|
34.1 Score on a scale
STANDARD_DEVIATION 5.6 • n=206 Participants
|
32.1 Score on a scale
STANDARD_DEVIATION 6.4 • n=7 Participants
|
33.1 Score on a scale
STANDARD_DEVIATION 6.0 • n=31 Participants
|
33.6 Score on a scale
STANDARD_DEVIATION 5.6 • n=30 Participants
|
32.9 Score on a scale
STANDARD_DEVIATION 6.0 • n=3 Participants
|
PRIMARY outcome
Timeframe: MMRM included measurements from baseline (Week 0) and at Weeks 1, 2, 4 and 6 after first drug administration. MMRM estimates of change from baseline to Week 6 is reported.Population: Full analysis set (FAS): all participants in TS that have a baseline and at least one evaluable post-baseline measurement. As per protocol, data from participants assigned to the quetiapine arm were not included in the primary endpoint.
Change from baseline in MADRS total score at Week 6 is reported. The MADRS evaluates core symptoms of depression and consists of 10 items. Nine of them are based upon participant reports, and one is on the rater's observation (apparent sadness) during the rating interview. MADRS items are rated on a 0-6 continuum (0=no abnormality, 6=severe). The possible total score could range from 0 (normal with absence of symptoms) to 60 (severe depression). Least squares mean and adjusted standard error were estimated by Restricted Maximum Likelihood (REML)-based Mixed effects model for repeated measures (MMRM) including the fixed categorical effects of treatment, concomitant psychotherapy use (yes vs. no), and the fixed continuous effect of baseline MADRS total score. Visit was treated as a repeated measure with an unstructured covariance matrix. The Kenward-Roger approximation was used to estimate the denominator degrees of freedom and adjust standard errors.
Outcome measures
| Measure |
Placebo
n=126 Participants
Participants with an established diagnosis of Major Depressive Disorder (MDD) administered one dose of placebo matching BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their Ongoing Antidepressants (OAD).
|
5 mg BI 1358894
n=36 Participants
Participants with an established diagnosis of MDD administered one 5 milligram (mg) dose of BI 1358894 in the morning as film-coated tablet, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
25 mg BI 1358894
n=39 Participants
Participants with an established diagnosis of MDD administered one 25 mg dose of BI 1358894 in the morning as film-coated tablet, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
75 mg BI 1358894
n=39 Participants
Participants with an established diagnosis of MDD administered one 75 mg dose of BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
125 mg BI 1358894
n=72 Participants
Participants with an established diagnosis of MDD administered one 125 mg dose of BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
|---|---|---|---|---|---|
|
Change From Baseline in Montgomery-Åsberg Depression Rating Scale (MADRS) Total Score at Week 6
|
-13.0 Units on a scale
Standard Error 1.0
|
-12.4 Units on a scale
Standard Error 2.0
|
-10.8 Units on a scale
Standard Error 1.9
|
-10.8 Units on a scale
Standard Error 1.9
|
-11.5 Units on a scale
Standard Error 1.4
|
SECONDARY outcome
Timeframe: Prior to the first intake of the trial medication (week 0, baseline) and after 6 weeks of treatment.Population: Full analysis set (FAS): all participants in TS that have a baseline and at least one evaluable post-baseline measurement. As per protocol, data from participants assigned to the quetiapine arm were not included in the secondary endpoints.
Number of participants with response defined as ≥ 50% MADRS reduction from baseline at Week 6 is reported. Percent reduction from baseline was calculated as follows: \[(MADRS total score at baseline - MADRS total score at week 6)/ MADRS total score at baseline\] \*100.
Outcome measures
| Measure |
Placebo
n=126 Participants
Participants with an established diagnosis of Major Depressive Disorder (MDD) administered one dose of placebo matching BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their Ongoing Antidepressants (OAD).
|
5 mg BI 1358894
n=36 Participants
Participants with an established diagnosis of MDD administered one 5 milligram (mg) dose of BI 1358894 in the morning as film-coated tablet, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
25 mg BI 1358894
n=39 Participants
Participants with an established diagnosis of MDD administered one 25 mg dose of BI 1358894 in the morning as film-coated tablet, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
75 mg BI 1358894
n=39 Participants
Participants with an established diagnosis of MDD administered one 75 mg dose of BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
125 mg BI 1358894
n=72 Participants
Participants with an established diagnosis of MDD administered one 125 mg dose of BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
|---|---|---|---|---|---|
|
Number of Participants With Response Defined as ≥ 50% Montgomery-Åsberg Depression Rating Scale (MADRS) Reduction From Baseline at Week 6
|
40 Participants
|
10 Participants
|
9 Participants
|
12 Participants
|
23 Participants
|
SECONDARY outcome
Timeframe: MMRM included measurements from baseline (Week 0) and at Weeks 1, 2, 4 and 6 after first drug administration. MMRM estimates of change from baseline to Week 6 is reported.Population: Full analysis set (FAS): all participants in TS that have a baseline and at least one evaluable post-baseline measurement. As per protocol, data from participants assigned to the quetiapine arm were not included in the secondary endpoints.
Change from baseline in STAI State and Trait version scores at Week 6 is reported. The STAI comprises separate self-report scales for measuring state and trait anxiety. Both consist of 20 statements. The S-Anxiety scale evaluates how respondents feel "right now, at this moment." The T-Anxiety scale assesses how people generally feel. Each STAI item is given a weighted score of 1 to 4. Scores for both scales can vary from 20 (minimum) to 80 (maximum). Higher scores indicate greater anxiety. Least squares mean and adjusted standard error were estimated by REML-based MMRM including the fixed categorical effects of treatment, concomitant psychotherapy use (yes vs. no), and the fixed continuous effect of baseline score. Visit was treated as a repeated measure with an unstructured covariance matrix. The Kenward-Roger approximation was used to estimate the denominator degrees of freedom and adjust standard errors.
Outcome measures
| Measure |
Placebo
n=126 Participants
Participants with an established diagnosis of Major Depressive Disorder (MDD) administered one dose of placebo matching BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their Ongoing Antidepressants (OAD).
|
5 mg BI 1358894
n=36 Participants
Participants with an established diagnosis of MDD administered one 5 milligram (mg) dose of BI 1358894 in the morning as film-coated tablet, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
25 mg BI 1358894
n=39 Participants
Participants with an established diagnosis of MDD administered one 25 mg dose of BI 1358894 in the morning as film-coated tablet, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
75 mg BI 1358894
n=39 Participants
Participants with an established diagnosis of MDD administered one 75 mg dose of BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
125 mg BI 1358894
n=72 Participants
Participants with an established diagnosis of MDD administered one 125 mg dose of BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
|---|---|---|---|---|---|
|
Change From Baseline in State-Trait Anxiety Inventory (STAI) State and Trait Version Scores at Week 6
T-Anxiety
|
-11.0 Units on a scale
Standard Error 1.1
|
-6.9 Units on a scale
Standard Error 2.1
|
-10.2 Units on a scale
Standard Error 2.1
|
-9.9 Units on a scale
Standard Error 2.1
|
-7.2 Units on a scale
Standard Error 1.5
|
|
Change From Baseline in State-Trait Anxiety Inventory (STAI) State and Trait Version Scores at Week 6
S-Anxiety
|
-11.3 Units on a scale
Standard Error 1.2
|
-7.0 Units on a scale
Standard Error 2.3
|
-8.9 Units on a scale
Standard Error 2.3
|
-12.3 Units on a scale
Standard Error 2.2
|
-8.6 Units on a scale
Standard Error 1.6
|
SECONDARY outcome
Timeframe: MMRM included measurements from baseline (Week 0) and at Weeks 1, 2, 4 and 6 after first drug administration. MMRM estimates of change from baseline to Week 6 is reported.Population: Full analysis set (FAS): all participants in TS that have a baseline and at least one evaluable post-baseline measurement. As per protocol, data from participants assigned to the quetiapine arm were not included in the secondary endpoints.
Change from baseline in CGI-S score at Week 6 is reported. The CGI-S rating scale evaluates the severity of psychopathology on a scale of 1 to 7. Considering total clinical experience with the depression population, a participant is assessed on severity of illness at the time of rating according to: 1=normal (not at all ill); 2=borderline ill; 3=mildly ill; 4=moderately ill; 5=markedly ill; 6=severely ill; 7=among the most extremely ill participants. Least squares mean and adjusted standard error were estimated by REML-based MMRM including the fixed categorical effects of treatment, concomitant psychotherapy use (yes vs. no), and the fixed continuous effect of the baseline score. Visit was treated as a repeated measure with an unstructured covariance matrix. The Kenward-Roger approximation was used to estimate the denominator degrees of freedom and adjust standard errors.
Outcome measures
| Measure |
Placebo
n=126 Participants
Participants with an established diagnosis of Major Depressive Disorder (MDD) administered one dose of placebo matching BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their Ongoing Antidepressants (OAD).
|
5 mg BI 1358894
n=36 Participants
Participants with an established diagnosis of MDD administered one 5 milligram (mg) dose of BI 1358894 in the morning as film-coated tablet, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
25 mg BI 1358894
n=39 Participants
Participants with an established diagnosis of MDD administered one 25 mg dose of BI 1358894 in the morning as film-coated tablet, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
75 mg BI 1358894
n=39 Participants
Participants with an established diagnosis of MDD administered one 75 mg dose of BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
125 mg BI 1358894
n=72 Participants
Participants with an established diagnosis of MDD administered one 125 mg dose of BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
|---|---|---|---|---|---|
|
Change From Baseline in Clinical Global Impression Severity Scale (CGI-S) Score at Week 6
|
-1.3 Units on a scale
Standard Error 0.1
|
-1.2 Units on a scale
Standard Error 0.2
|
-1.2 Units on a scale
Standard Error 0.2
|
-1.1 Units on a scale
Standard Error 0.2
|
-1.1 Units on a scale
Standard Error 0.2
|
SECONDARY outcome
Timeframe: MMRM included measurements from baseline (Week 0) and at Weeks 1, 2, 4 and 6 after first drug administration. MMRM estimates of change from baseline to Week 6 is reported.Population: Full analysis set (FAS): all participants in TS that have a baseline and at least one evaluable post-baseline measurement. As per protocol, data from participants assigned to the quetiapine arm were not included in the secondary endpoints.
Change from baseline in SMDDS total score at Week 6 is reported. The SMDDS is a 16-item, patient-reported outcome measure developed to capture the core symptoms of MDD. The SMDDS uses a recall of "over the past 7 days" and participants respond to each question using a rating scale between 0 ("Not at all" or "Never") to 4 ("Extremely" or "Always"). The total score ranges from 0 to 60 with a higher score indicating more severe depressive symptomatology. Least squares mean and adjusted standard error were estimated by REML-based MMRM including the fixed categorical effects of treatment, concomitant psychotherapy use (yes vs. no), and the fixed continuous effect of the baseline score. Visit was treated as a repeated measure with an unstructured covariance matrix. The Kenward-Roger approximation was used to estimate the denominator degrees of freedom and adjust standard errors.
Outcome measures
| Measure |
Placebo
n=126 Participants
Participants with an established diagnosis of Major Depressive Disorder (MDD) administered one dose of placebo matching BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their Ongoing Antidepressants (OAD).
|
5 mg BI 1358894
n=36 Participants
Participants with an established diagnosis of MDD administered one 5 milligram (mg) dose of BI 1358894 in the morning as film-coated tablet, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
25 mg BI 1358894
n=39 Participants
Participants with an established diagnosis of MDD administered one 25 mg dose of BI 1358894 in the morning as film-coated tablet, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
75 mg BI 1358894
n=39 Participants
Participants with an established diagnosis of MDD administered one 75 mg dose of BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
125 mg BI 1358894
n=72 Participants
Participants with an established diagnosis of MDD administered one 125 mg dose of BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
|---|---|---|---|---|---|
|
Change From Baseline in Symptoms of Major Depressive Disorder Scale (SMDDS) Total Score at Week 6
|
-13.3 Units on a scale
Standard Error 1.2
|
-9.9 Units on a scale
Standard Error 2.2
|
-8.9 Units on a scale
Standard Error 2.2
|
-12.3 Units on a scale
Standard Error 2.1
|
-10.5 Units on a scale
Standard Error 1.6
|
Adverse Events
Placebo
5 mg BI 1358894
25 mg BI 1358894
75 mg BI 1358894
125 mg BI 1358894
Quetiapine
Serious adverse events
| Measure |
Placebo
n=128 participants at risk
Participants with an established diagnosis of Major Depressive Disorder (MDD) administered one dose of placebo matching BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their Ongoing Antidepressants (OAD).
|
5 mg BI 1358894
n=36 participants at risk
Participants with an established diagnosis of MDD administered one 5 milligram (mg) dose of BI 1358894 in the morning as film-coated tablet, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
25 mg BI 1358894
n=39 participants at risk
Participants with an established diagnosis of MDD administered one 25 mg dose of BI 1358894 in the morning as film-coated tablet, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
75 mg BI 1358894
n=39 participants at risk
Participants with an established diagnosis of MDD administered one 75 mg dose of BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
125 mg BI 1358894
n=75 participants at risk
Participants with an established diagnosis of MDD administered one 125 mg dose of BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
Quetiapine
n=71 participants at risk
Participants with an established diagnosis of MDD administered one dose of placebo matching BI 1358894 in the morning as film-coated tablets, and one 150 or 300 mg dose of quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
The daily active dose at the start of therapy was 50 mg on Day 1, 100 mg at Day 2 and 150 mg on Day 3 and 4. Beginning with Day 5, the recommended daily dose of 300 mg was taken. If not tolerated by a participant, the dose was reduced to 150 mg in Week 1. Thereafter, this finally chosen dose had to be stable until end of treatment at Week 6.
During the trial, participants also continued treatment with their OAD.
|
|---|---|---|---|---|---|---|
|
Infections and infestations
Genital herpes
|
0.00%
0/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
2.6%
1/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Investigations
Blood creatinine increased
|
0.78%
1/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Myeloproliferative neoplasm
|
0.00%
0/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
1.3%
1/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Psychiatric disorders
Emotional distress
|
0.00%
0/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
2.6%
1/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Psychiatric disorders
Suicidal ideation
|
4.7%
6/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.1%
2/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
1.4%
1/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Respiratory, thoracic and mediastinal disorders
Pulmonary fibrosis
|
0.00%
0/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
2.6%
1/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
Other adverse events
| Measure |
Placebo
n=128 participants at risk
Participants with an established diagnosis of Major Depressive Disorder (MDD) administered one dose of placebo matching BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their Ongoing Antidepressants (OAD).
|
5 mg BI 1358894
n=36 participants at risk
Participants with an established diagnosis of MDD administered one 5 milligram (mg) dose of BI 1358894 in the morning as film-coated tablet, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
25 mg BI 1358894
n=39 participants at risk
Participants with an established diagnosis of MDD administered one 25 mg dose of BI 1358894 in the morning as film-coated tablet, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
75 mg BI 1358894
n=39 participants at risk
Participants with an established diagnosis of MDD administered one 75 mg dose of BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
125 mg BI 1358894
n=75 participants at risk
Participants with an established diagnosis of MDD administered one 125 mg dose of BI 1358894 in the morning as film-coated tablets, and one dose of placebo matching quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
During the trial, participants also continued treatment with their OAD.
|
Quetiapine
n=71 participants at risk
Participants with an established diagnosis of MDD administered one dose of placebo matching BI 1358894 in the morning as film-coated tablets, and one 150 or 300 mg dose of quetiapine in the evening as tablets. Each administration was performed orally once daily, for 6 weeks.
The daily active dose at the start of therapy was 50 mg on Day 1, 100 mg at Day 2 and 150 mg on Day 3 and 4. Beginning with Day 5, the recommended daily dose of 300 mg was taken. If not tolerated by a participant, the dose was reduced to 150 mg in Week 1. Thereafter, this finally chosen dose had to be stable until end of treatment at Week 6.
During the trial, participants also continued treatment with their OAD.
|
|---|---|---|---|---|---|---|
|
Ear and labyrinth disorders
Vertigo
|
0.78%
1/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.1%
2/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
4.0%
3/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
1.4%
1/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Gastrointestinal disorders
Abdominal pain
|
0.00%
0/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.1%
2/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
1.4%
1/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Gastrointestinal disorders
Abdominal pain upper
|
0.00%
0/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.1%
2/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
1.4%
1/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Gastrointestinal disorders
Dry mouth
|
3.1%
4/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.1%
2/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
2.6%
1/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
1.3%
1/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.6%
4/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
General disorders
Fatigue
|
3.1%
4/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
13.9%
5/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
7.7%
3/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.1%
2/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.3%
4/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
9.9%
7/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Infections and infestations
COVID-19
|
3.9%
5/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
2.8%
1/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
2.6%
1/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
7.7%
3/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
1.3%
1/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Infections and infestations
Nasopharyngitis
|
1.6%
2/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.1%
2/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.1%
2/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
2.7%
2/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
4.2%
3/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Infections and infestations
Respiratory tract infection
|
0.00%
0/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.6%
2/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
4.2%
3/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Infections and infestations
Upper respiratory tract infection
|
1.6%
2/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
2.8%
1/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.1%
2/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.1%
2/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
4.0%
3/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
2.8%
2/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Musculoskeletal and connective tissue disorders
Pain in extremity
|
0.00%
0/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.1%
2/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
1.3%
1/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Nervous system disorders
Disturbance in attention
|
0.00%
0/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.1%
2/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
2.6%
1/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Nervous system disorders
Dizziness
|
2.3%
3/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.6%
2/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
15.4%
6/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.1%
2/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.3%
4/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
8.5%
6/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Nervous system disorders
Headache
|
10.2%
13/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
25.0%
9/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
10.3%
4/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
10.3%
4/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
17.3%
13/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
2.8%
2/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Nervous system disorders
Sedation
|
0.78%
1/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
2.6%
1/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.1%
2/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
2.7%
2/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
8.5%
6/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Nervous system disorders
Somnolence
|
3.1%
4/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
2.8%
1/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
2.6%
1/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
17.9%
7/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
6.7%
5/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
33.8%
24/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Psychiatric disorders
Aggression
|
0.00%
0/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.6%
2/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Psychiatric disorders
Anxiety
|
0.78%
1/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.6%
2/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
2.7%
2/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
1.4%
1/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Psychiatric disorders
Insomnia
|
0.78%
1/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.1%
2/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
2.6%
1/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
2.7%
2/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
8.5%
6/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Psychiatric disorders
Sleep disorder
|
1.6%
2/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.1%
2/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
1.3%
1/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Reproductive system and breast disorders
Dysmenorrhoea
|
0.00%
0/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.1%
2/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Respiratory, thoracic and mediastinal disorders
Cough
|
0.00%
0/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.1%
2/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
2.6%
1/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
1.3%
1/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Skin and subcutaneous tissue disorders
Rash
|
0.00%
0/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
2.8%
1/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
2.6%
1/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.1%
2/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
1.3%
1/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
1.4%
1/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
|
Vascular disorders
Hypertension
|
0.00%
0/128 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/36 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
5.1%
2/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/39 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/75 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
0.00%
0/71 • From first treatment administration until last treatment administration + 28 days, up to approximately 11 weeks.
Treated Set (TS): all participants that have been randomized and that received at least one administration of study drug. Participants are analysed according to the actual received treatment.
|
Additional Information
Boehringer Ingelheim, Call Center
Boehringer Ingelheim
Results disclosure agreements
- Principal investigator is a sponsor employee Boehringer Ingelheim (BI) acknowledges that investigators have the right to publish the study results. Investigators shall provide BI with a copy of any publication or presentation for review prior to any submission. Such review will be done with regard to proprietary information, information related to patentable inventions, medical, scientific, and statistical accuracy within 60 days. BI may request a delay of the publication in order to protect BI's intellectual property rights.
- Publication restrictions are in place
Restriction type: OTHER