Who Can Participate?
Adults 18-75 years with a diagnosis of severe or very severe alopecia areata (AA) may participate.
Eligibility Criteria
What is Included?
How Long Will The Study Last?
Note: Participants may not be engaged in any other kind of systemic, topical, or device-based therapy for AA.
Mason - Dermatologists of Southwest Ohio
Bexley - Bexley Dermatology Research
Waterloo - Alliance Clinical Trials
Peterborough - SKiN Centre for Dermatology
Oakville - The Centre for Clinical Trials
Winnipeg - Wiseman Dermatology Research Inc.
No Doctors Found
Similar Trials
No Similar Trials FoundThe following information is from ClinicalTrials.gov
Last Update Posted: April 16, 2025
NCT06018428
Q32 Bio Inc.
Brief Summary:
Part A is a randomized, double-blind, placebo-controlled, multi-center Proof-of-Concept (POC) Trial in subjects with severe Alopecia Areata. All participants in Part A have completed participation. Part B is a multicenter, open-label study to assess the efficacy, safety, and tolerability of bempikibart (ADX-914) in participants with severe Alopecia Areata.
Condition or Disease:
Alopecia Areata
Intervention/Treatment:
Drug: bempikibart (ADX-914)Phase:
PHASE 2
Ages Eligible for Study:
18 Years and 75 Years (ADULT,OLDER_ADULT)
Sexes Eligible for Study:
ALL
Terms and Conditions – ClinicalTrials.gov
Purpose of ClinicalTrials.gov Database. The U.S. National Institutes of Health, Department of Health and Human Services, through its National Library of Medicine, has developed ClinicalTrials.gov to provide patients, family members, and members of the public current information about clinical research studies.
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Last Revised July 2024
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