drugset / Trial / NCT04052425

Topical Ruxolitinib Evaluation in Vitiligo Study 1 (TRuE-V1)

NCT04052425 ↗

Phase 3 Completed 330 enrolled Incyte Corporation
RandomizedCrossoverTriple-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of ruxolitinib cream in adolescent and adult participants with non-segmental vitiligo for whom total body involved vitiligo area (facial and nonfacial) does not exceed 10% body surface area (BSA).

Timeline

Start
2019-09-20
Primary completion
2021-03-18
Completion
2021-10-21

Outcome

Met primary endpoint

paper In TRuE-V1, the percentage of patients with an F-VASI75 response at week 24 was 29.8% in the ruxolitinib-cream group and 7.4% in the vehicle group PMID 36260792 ↗

registry Double-Blind Period: Ruxolitinib Cream 1.5% BID vs Double-Blind Period: Vehicle Cream BID; p < 0.0001 NCT04052425 ↗

release “Both the TRuE-V1 and TRuE-V2 studies met the primary endpoint (p<0.0001 for TRuE-V1; p<.01 for TRuE-V2)” incyte.com ↗

release “Both TRuE-V1 and TRuE-V2 studies met the primary and key secondary endpoints, including patient reported outcomes.” incyte.com ↗

release “resulted in greater improvement to vehicle for the primary and all key secondary endpoints in both the TRuE-V1 and TRuE-V2 studies.” incyte.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Ruxolitinib Small molecule 1.5 % Topical

Indications