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Trial · NCT02106195

Results by group53

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Number of Subjects Experiencing Adverse Events as a Measure of Safety and TolerabilityBelumosudil 200 mg PO QDAll AEs4Participants
Number of Subjects Experiencing Adverse Events as a Measure of Safety and TolerabilityBelumosudil 200 mg PO QDRelated AEs1Participants
Number of Subjects Experiencing Adverse Events as a Measure of Safety and TolerabilityBelumosudil 200 mg PO QDGrade ≥3 AEs1Participants
Number of Subjects Experiencing Adverse Events as a Measure of Safety and TolerabilityBelumosudil 200 mg PO QDGrade ≥3 Related AEs0Participants
Number of Subjects Experiencing Adverse Events as a Measure of Safety and TolerabilityBelumosudil 200 mg PO QDGrade 4 AEs0Participants
Number of Subjects Experiencing Adverse Events as a Measure of Safety and TolerabilityBelumosudil 200 mg PO QDDeaths0Participants
Number of Subjects Experiencing Adverse Events as a Measure of Safety and TolerabilityBelumosudil 200 mg PO QDSAEs1Participants
Number of Subjects Experiencing Adverse Events as a Measure of Safety and TolerabilityBelumosudil 200 mg PO QDRelated SAEs0Participants
Number of Subjects Experiencing Adverse Events as a Measure of Safety and TolerabilityBelumosudil 200 mg PO QDAEs leading to discontinuation2Participants
Efficacy: Change in Overall PASI (Psoriasis Area and Severity Index) From Baseline to Week 4 and Week 8Belumosudil 200 mg PO QDBaseline (Day 1)17.5Standard Deviation 8.41Score on a scale
Efficacy: Change in Overall PASI (Psoriasis Area and Severity Index) From Baseline to Week 4 and Week 8Belumosudil 200 mg PO QDWeek 4 (Day 28)16.3Standard Deviation 9.49Score on a scale
Efficacy: Change in Overall PASI (Psoriasis Area and Severity Index) From Baseline to Week 4 and Week 8Belumosudil 200 mg PO QDChange from Baseline to Week 4-1.1Standard Deviation 3.04Score on a scale
Efficacy: Change in Overall PASI (Psoriasis Area and Severity Index) From Baseline to Week 4 and Week 8Belumosudil 200 mg PO QDWeek 8 (Day 56)14.7Standard Deviation 3.41Score on a scale
Efficacy: Change in Overall PASI (Psoriasis Area and Severity Index) From Baseline to Week 4 and Week 8Belumosudil 200 mg PO QDChange from Baseline to Week 80.0Standard Deviation 1.54Score on a scale
Efficacy: Physician Global Assessment (PGA) at Week 4 and Week 8Belumosudil 200 mg PO QD4 weeks: 75% to 100%0Participants
Efficacy: Physician Global Assessment (PGA) at Week 4 and Week 8Belumosudil 200 mg PO QD4 weeks: 50% to 74% clearing1Participants
Efficacy: Physician Global Assessment (PGA) at Week 4 and Week 8Belumosudil 200 mg PO QD4 weeks: 25% to 49% clearing1Participants
Efficacy: Physician Global Assessment (PGA) at Week 4 and Week 8Belumosudil 200 mg PO QD4 weeks: 0 to 24% clearing4Participants
Efficacy: Physician Global Assessment (PGA) at Week 4 and Week 8Belumosudil 200 mg PO QD4 weeks: Worse2Participants
Efficacy: Physician Global Assessment (PGA) at Week 4 and Week 8Belumosudil 200 mg PO QD8 weeks: 75% to 100%0Participants

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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