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A 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
Description:
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: March 18, 2024
Completion date: January 30, 2026
Contact: Iain Stuart, PhD
Tel.: 1-800-775-7936
Email: clinicaltrials@vynetx.com
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