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A Study to Assess the Safety and Efficacy of Ruxolitinib Cream in Participants With Genital Vitiligo

← catalyst calendar

NCT05750823 · results posted

Sponsored by Incyte Corporation (industry) · INCY — their whole pipeline →.

Phase
Phase 2
Status
Completed
Study type
Interventional
Design
Na · None · Treatment
Enrollment
49actual
Sites
13
Countries
Canada, France, United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-04-11actualWhen the study began enrolling
Primary completion2025-03-06actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-03-06actualThe whole study's end, after follow-up
First posted2023-03-02actualWhen this record first appeared on the registry
Results posted2026-03-20actualWhen the sponsor posted results to the registry
Record updated2026-03-20actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Nonsegmental Vitiligo With Genital Involvement

Intervention

  • Drug: Ruxolitinib Cream — also filed as Opzelura

Primary outcome

what the primary-completion date above is the date OF
Percentage of Participants Achieving a Genital Vitiligo Noticeability Scale (VNS) of "4 - A Lot Less Noticeable" or "5 - No Longer Noticeable" at Week 48
measured Baseline; Week 48

Posted documents

hosted by the registry — we link, never re-serve
Study Protocolposted 2023-02-28 · 732 KB · Prot_000.pdf
Statistical Analysis Planposted 2024-11-06 · 435 KB · SAP_001.pdf

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