drugset / Trial / NCT07205159

A Study to Evaluate the Safety and Efficacy of FB102 in Patients With Severe to Very Severe Alopecia Areata.

NCT07205159 ↗

Phase 1 Recruiting 32 enrolled Forte Biosciences, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a randomized, double-blind, placebo-controlled study evaluating the safety and efficacy of FB102 in patients with severe to very severe alopecia areata (AA).

Timeline

Start
2025-10-23
Primary completion
2027-03-10
Completion
2027-03-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator FB102 Unknown — Intravenous

Indications