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Active Not RecruitingNCT06493578

A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of VYN201 Gel in Subjects With Non-segmental Vitiligo.

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 Not Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
Vyne Therapeutics Inc. · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the efficacy, safety, and pharmacokinetics of VYN201 Gel in subjects with non-segmental vitiligo.

Conditions

Interventions

TypeNameDescription
DRUGVYN201 GelVYN201 Gel is a topical formulation applied as a thin layer to affected areas.
DRUGVehicle GelVehicle gel (placebo) is matching in appearance to VYN201 gel and is to be applied in the same manner as VYN201 gel.

Timeline

Start date
2024-06-04
Primary completion
2025-07-10
Completion
2026-01-30
First posted
2024-07-10
Last updated
2025-09-16

Locations

49 sites across 2 countries: United States, Canada

Regulatory

Source: ClinicalTrials.gov record NCT06493578. Inclusion in this directory is not an endorsement.

A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of VYN201 Gel in Subjects With Non-segmental Vitiligo. (NCT06493578) · Clinical Trials Directory