drugset / Trial / NCT04530344

Assess the Long Term Efficacy and Safety of Ruxolitinib Cream in Participants With Vitiligo

NCT04530344

Phase 3 Completed 458 enrolled Incyte Corporation
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the duration of response following withdrawal of ruxolitinib cream (Cohort A vehicle group), safety and maintenance of response with continued use of ruxolitinib cream in participants who have completed either Study NCT04052425 or NCT04057573 (parent studies) in which the participants will have been using ruxolitinib cream BID for the previous 28 to 52 weeks depending on their initial randomization in the parent study.

Timeline

Start
2020-09-24
Primary completion
2022-11-14
Completion
2022-11-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Ruxolitinib Small molecule Topical

Indications