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Trial · NCT04052425

Results by group90

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

OutcomeGroupCategoryValueSpreadUnits
Percentage of Participants Achieving a ≥ 75% Improvement From Baseline in the Face Vitiligo Area Scoring Index (F-VASI75) Score at Week 24Double-Blind Period: Ruxolitinib Cream 1.5% BID29.8percentage of participants
Percentage of Participants Achieving a ≥ 75% Improvement From Baseline in the Face Vitiligo Area Scoring Index (F-VASI75) Score at Week 24Double-Blind Period: Vehicle Cream BID7.4percentage of participants
Percentage of Participants Achieving a ≥ 50% Improvement From Baseline in the Face Vitiligo Area Scoring Index (F-VASI50) Score at Week 24Double-Blind Period: Ruxolitinib Cream 1.5% BID51.2percentage of participants
Percentage of Participants Achieving a ≥ 50% Improvement From Baseline in the Face Vitiligo Area Scoring Index (F-VASI50) Score at Week 24Double-Blind Period: Vehicle Cream BID16.9percentage of participants
Percentage of Participants Achieving a ≥ 90% Improvement From Baseline in the Face Vitiligo Area Scoring Index (F-VASI90) Score at Week 24Double-Blind Period: Ruxolitinib Cream 1.5% BID15.3percentage of participants
Percentage of Participants Achieving a ≥ 90% Improvement From Baseline in the Face Vitiligo Area Scoring Index (F-VASI90) Score at Week 24Double-Blind Period: Vehicle Cream BID2.2percentage of participants
Percentage of Participants Achieving a ≥ 50% Improvement From Baseline in the Total Body Vitiligo Area Scoring Index (T-VASI50) Score at Week 24Double-Blind Period: Ruxolitinib Cream 1.5% BID20.6percentage of participants
Percentage of Participants Achieving a ≥ 50% Improvement From Baseline in the Total Body Vitiligo Area Scoring Index (T-VASI50) Score at Week 24Double-Blind Period: Vehicle Cream BID5.1percentage of participants
Percentage of Participants Achieving a Vitiligo Noticeability Scale (VNS) of 4 or 5 at Week 24Double-Blind Period: Ruxolitinib Cream 1.5% BID24.5percentage of participants
Percentage of Participants Achieving a Vitiligo Noticeability Scale (VNS) of 4 or 5 at Week 24Double-Blind Period: Vehicle Cream BID3.3percentage of participants
Percentage Change From Baseline in Facial Body Surface Area (F-BSA) at Week 24Double-Blind Period: Ruxolitinib Cream 1.5% BID-28.9Standard Error 2.22percentage change
Percentage Change From Baseline in Facial Body Surface Area (F-BSA) at Week 24Double-Blind Period: Vehicle Cream BID-9.5Standard Error 3.25percentage change
Number of Participants With Treatment-emergent Adverse Events (TEAEs) During the Double-Blind PeriodDouble-Blind Period: Ruxolitinib Cream 1.5% BID101Participants
Number of Participants With Treatment-emergent Adverse Events (TEAEs) During the Double-Blind PeriodDouble-Blind Period: Vehicle Cream BID42Participants
Number of Participants With Treatment-emergent Adverse Events (TEAEs) During the Treatment-Extension PeriodTreatment-Extension Period: Ruxolitinib Cream 1.5% BID65Participants
Number of Participants With Treatment-emergent Adverse Events (TEAEs) During the Treatment-Extension PeriodTreatment-Extension Period: Vehicle Cream to Ruxolitinib Cream 1.5% BID31Participants
Percentage of Participants Achieving a ≥ 25% Improvement in the Face Vitiligo Area Scoring Index (F-VASI25) Score at Week 24Double-Blind Period: Ruxolitinib Cream 1.5% BID69.8percentage of participants
Percentage of Participants Achieving a ≥ 25% Improvement in the Face Vitiligo Area Scoring Index (F-VASI25) Score at Week 24Double-Blind Period: Vehicle Cream BID30.0percentage of participants
Percentage of Participants Achieving a ≥ %25, ≥ %50, ≥ 75%, and ≥ 90% Improvement in the Face Vitiligo Area Scoring Index (F-VASI25/50/75/90) Score at Week 52Treatment-Extension Period: Ruxolitinib Cream 1.5% BIDF-VASI2589.6percentage of participants
Percentage of Participants Achieving a ≥ %25, ≥ %50, ≥ 75%, and ≥ 90% Improvement in the Face Vitiligo Area Scoring Index (F-VASI25/50/75/90) Score at Week 52Treatment-Extension Period: Vehicle Cream to Ruxolitinib Cream 1.5% BIDF-VASI2574.4percentage of participants

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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