A Study to Evaluate the Safety and Efficacy of FB102 in Patients With Non-segmental Vitiligo

Recruiting Phase 1 Interventional Study
Vitiligo
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At a Glance
Age
18 – 75
Sex
Any
Trial phase
Phase 1
Study type
Interventional
Purpose
Treatment
Participants needed
64 (estimated)
Sponsor
Forte Biosciences, Inc. · Industry
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About This Trial

A Randomized, Double-Blind, Placebo Controlled, Multi-center Study to Evaluate the Safety and Efficacy of FB102 in Patients with Non-Segmental Vitiligo.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Males and females aged ≥ 18 to 75 years at time of Screening. 2. Must have confirmed non-segmental vitiligo criteria at the Screening Visit and the Baseline Visit, as assessed by the study investigator. 3. If receiving concomitant medications for any reason other than vitilig…
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