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A Randomized, Double-Blind, Vehicle-Controlled Phase 2b Trial Evaluating the Efficacy, Safety & Pharmacokinetics of VYN201 Gel in the Treatment of Non Segmental Vitiligo

Trial Profile

A Randomized, Double-Blind, Vehicle-Controlled Phase 2b Trial Evaluating the Efficacy, Safety & Pharmacokinetics of VYN201 Gel in the Treatment of Non Segmental Vitiligo

Status: Active, no longer recruiting
Phase of Trial: Phase II

Latest Information Update: 11 Jun 2025

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At a glance

  • Drugs VYN 201 (Primary)
  • Indications Vitiligo
  • Focus Therapeutic Use
  • Sponsors VYNE Therapeutics

Most Recent Events

  • 04 Jun 2025 Planned number of patients changed from 160 to 200.
  • 08 May 2025 According to a VYNE Therapeutics media release, following the 24-week treatment period, subjects who have been randomized in the three active dose cohorts will continue treatment with their respective dose concentrations for an additional 28-week active treatment extension. Subjects who have been randomized in the vehicle group during the initial 24-week treatment period will be equally re-randomized into one of the three active dose cohorts for an additional 28 weeks.
  • 06 Mar 2025 According to a VYNE Therapeutics media release, topline results from this trial is expected in mid-2025.

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