drugset / Trial / NCT05368103

Study of DAXDILIMAB for the Treatment of Moderate-to-Severe Alopecia Areata

NCT05368103 ↗

Phase 2 Completed 30 enrolled Amgen
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the preliminary efficacy, safety, tolerability, PK, and PD of Daxdilimab in participants with moderate to severe AA, with ≥50% and ≤95% total scalp hair loss as defined by the SALT score at Screening and Day 1.

Timeline

Start
2022-04-27
Primary completion
2023-08-07
Completion
2024-01-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Daxdilimab Monoclonal antibody — Subcutaneous

Indications