Trial · NCT02852967
Results by group161
Each measurement the trial posted, group by group, in the words and numbers it posted.
1 to 20 of 161
Download this page as JSON| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Efficacy: Percentage of Subjects With a ≥ 75% Decrease in PASI (PASI 75) at Week 16 (Double-blind Period)--LOCF and Observed | Belumosudil 200 mg QD + Placebo | LOCF (%) | 8.7 | 95% Confidence Interval 1.1 to 28.0 | Percentage of participants |
| Efficacy: Percentage of Subjects With a ≥ 75% Decrease in PASI (PASI 75) at Week 16 (Double-blind Period)--LOCF and Observed | Belumosudil 200 mg BID (Twice Daily) + Placebo | LOCF (%) | 9.1 | 95% Confidence Interval 1.1 to 29.2 | Percentage of participants |
| Efficacy: Percentage of Subjects With a ≥ 75% Decrease in PASI (PASI 75) at Week 16 (Double-blind Period)--LOCF and Observed | Belumosudil 400 mg QD + Placebo | LOCF (%) | 19.0 | 95% Confidence Interval 5.4 to 41.9 | Percentage of participants |
| Efficacy: Percentage of Subjects With a ≥ 75% Decrease in PASI (PASI 75) at Week 16 (Double-blind Period)--LOCF and Observed | Belumosudil 600 mg/Day | LOCF (%) | 7.7 | 95% Confidence Interval 0.9 to 25.1 | Percentage of participants |
| Efficacy: Percentage of Subjects With a ≥ 75% Decrease in PASI (PASI 75) at Week 16 (Double-blind Period)--LOCF and Observed | Placebo | LOCF (%) | 16.7 | 95% Confidence Interval 3.6 to 41.4 | Percentage of participants |
| Efficacy: Percentage of Subjects With a ≥ 75% Decrease in PASI (PASI 75) at Week 16 (Double-blind Period)--LOCF and Observed | All Belumosudil | LOCF (%) | 10.9 | 95% Confidence Interval 5.3 to 19.1 | Percentage of participants |
| Efficacy: Percentage of Subjects With a ≥ 75% Decrease in PASI (PASI 75) at Week 16 (Double-blind Period)--LOCF and Observed | Belumosudil 200 mg QD + Placebo | Observed (%) | 7.1 | 95% Confidence Interval 0.2 to 33.9 | Percentage of participants |
| Efficacy: Percentage of Subjects With a ≥ 75% Decrease in PASI (PASI 75) at Week 16 (Double-blind Period)--LOCF and Observed | Belumosudil 200 mg BID (Twice Daily) + Placebo | Observed (%) | 13.3 | 95% Confidence Interval 1.7 to 40.5 | Percentage of participants |
| Efficacy: Percentage of Subjects With a ≥ 75% Decrease in PASI (PASI 75) at Week 16 (Double-blind Period)--LOCF and Observed | Belumosudil 400 mg QD + Placebo | Observed (%) | 23.5 | 95% Confidence Interval 6.8 to 49.9 | Percentage of participants |
| Efficacy: Percentage of Subjects With a ≥ 75% Decrease in PASI (PASI 75) at Week 16 (Double-blind Period)--LOCF and Observed | Belumosudil 600 mg/Day | Observed (%) | 12.5 | 95% Confidence Interval 1.6 to 38.3 | Percentage of participants |
| Efficacy: Percentage of Subjects With a ≥ 75% Decrease in PASI (PASI 75) at Week 16 (Double-blind Period)--LOCF and Observed | Placebo | Observed (%) | 30.0 | 95% Confidence Interval 6.7 to 65.2 | Percentage of participants |
| Efficacy: Percentage of Subjects With a ≥ 75% Decrease in PASI (PASI 75) at Week 16 (Double-blind Period)--LOCF and Observed | All Belumosudil | Observed (%) | 14.5 | 95% Confidence Interval 6.9 to 25.8 | Percentage of participants |
| Efficacy: Mean Change of Raw PASI Score From Baseline to Week 16 and Week 48--LOCF and Observed | Belumosudil 200 mg QD + Placebo | Baseline | 18.93 | Standard Deviation 8.31 | Score on a scale |
| Efficacy: Mean Change of Raw PASI Score From Baseline to Week 16 and Week 48--LOCF and Observed | Belumosudil 200 mg BID (Twice Daily) + Placebo | Baseline | 20.60 | Standard Deviation 8.27 | Score on a scale |
| Efficacy: Mean Change of Raw PASI Score From Baseline to Week 16 and Week 48--LOCF and Observed | Belumosudil 400 mg QD + Placebo | Baseline | 18.82 | Standard Deviation 6.08 | Score on a scale |
| Efficacy: Mean Change of Raw PASI Score From Baseline to Week 16 and Week 48--LOCF and Observed | Belumosudil 600 mg/Day | Baseline | 19.80 | Standard Deviation 9.03 | Score on a scale |
| Efficacy: Mean Change of Raw PASI Score From Baseline to Week 16 and Week 48--LOCF and Observed | Placebo | Baseline | 20.72 | Standard Deviation 8.08 | Score on a scale |
| Efficacy: Mean Change of Raw PASI Score From Baseline to Week 16 and Week 48--LOCF and Observed | All Belumosudil | Baseline | 19.55 | Standard Deviation 7.97 | Score on a scale |
| Efficacy: Mean Change of Raw PASI Score From Baseline to Week 16 and Week 48--LOCF and Observed | Belumosudil 200 mg QD + Placebo | Change at Week 16--LOCF | -5.69 | Standard Deviation 8.59 | Score on a scale |
| Efficacy: Mean Change of Raw PASI Score From Baseline to Week 16 and Week 48--LOCF and Observed | Belumosudil 200 mg BID (Twice Daily) + Placebo | Change at Week 16--LOCF | -4.49 | Standard Deviation 7.44 | Score on a scale |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
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