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.

Recruitment status

COMPLETED

Study phase

PHASE2

Target enrollment

389 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.

Results posted on

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

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

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

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

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

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

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

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

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

Serious events: 7 serious events
Other events: 32 other events
Deaths: 0 deaths

5 mg BI 1358894

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

25 mg BI 1358894

Serious events: 2 serious events
Other events: 22 other events
Deaths: 0 deaths

75 mg BI 1358894

Serious events: 2 serious events
Other events: 24 other events
Deaths: 0 deaths

125 mg BI 1358894

Serious events: 1 serious events
Other events: 34 other events
Deaths: 0 deaths

Quetiapine

Serious events: 1 serious events
Other events: 43 other events
Deaths: 0 deaths

Serious adverse events

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

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

Phone: 1-800-243-0127

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