At a glance
ClinicalIndex Comparison RecordStandardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A PHASE 2B RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTER, DOSE-RANGING STUDY TO EVALUATE THE EFFICACY AND SAFETY PROFILE OF PF-06651600 WITH A PARTIALLY BLINDED EXTENSION PERIOD TO EVALUATE THE EFFICACY AND SAFETY OF PF-06651600 AND PF-06700841 IN SUBJECTS WITH ACTIVE NON-SEGMENTAL VITILIGO
In Brief
A Phase 2 clinical trial evaluating PF-06651600, placebo, and 2 other interventions for Active Non-segmental Vitiligo. Completed, enrolled 366 participants across 92 sites in 10 countries.
Detailed Summary
This is a Phase 2b, randomized, double blind, parallel group, multicenter study with an extension period. The study will have a maximum duration of approximately 60 weeks. This includes an up to 4 weeks Screening Period, a 24 week dose ranging period, an up to 24 week extension period and a 8 week Follow up Period.
Study Details
Timeline
Interventions
Induction dose 1. Oral tablet taken QD
Induction dose 2. Oral tablet taken QD
Maintenance dose A. Oral tablet taken QD
Maintenance Dose B. Oral tablet taken QD
Maintenance Dose C. Oral tablet taken QD
placebo
Oral tablet taken QD
Phototherapy will be combined with PF-06651600