drugset / Trial / NCT06905873

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

NCT06905873 ↗

Phase 1 Recruiting 64 enrolled Forte Biosciences, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

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

Timeline

Start
2025-03-25
Primary completion
2026-12-31
Completion
2026-12-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator FB102 Unknown — Intravenous

Indications