This study has 48 locations across the U.S. and Canada - 21 Nov `24A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of VYN201 Gel in Subjects with Non-segmental Vitiligo

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

The VYN201 Gel for Vitiligo clinical trial by Vyne Therapeutics Inc. is a Phase 2 study aimed at evaluating the efficacy, safety, and pharmacokinetics of VYN201 Gel in individuals with non-segmental vitiligo. Participants will apply the gel daily to affected areas over a specified period, with assessments conducted at weeks 24 and 52.

Key Details

  • Study Type: Interventional (Clinical Trial)
  • Phase: Phase 2
  • Estimated Enrollment: Not specified
  • Age Range: 18 to 75 years
  • Duration: Approximately 52 weeks, including treatment and follow-up periods

Eligibility Criteria

  • Adults aged 18 to 75 years
  • Clinical diagnosis of non-segmental vitiligo affecting less than 10% of total body surface area

Exclusion:

  • Dyed hair in treatment areas that could interfere with assessments
  • Inability to maintain facial hair shorter than 5mm during the study
  • Recent major surgery within the last 3 months or planned during the study period
  • Pregnancy or breastfeeding

This study has 48 locations across the U.S. and Canada.

Start date: 2024-03-18

Completion date: 2026-01-30

Contact: Iain Stuart, PhD

Tel.: 1-800-775-7936

Email: clinicaltrials@vynetx.com

Link: https://clinicaltrials.gov/study/NCT06493578

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