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Study identifier: NCT07317544 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study of ABS-201 Evaluating Single and Multiple Ascending Doses in Healthy Adults With and Without Androgenetic Alopecia

Condition: Androgenetic Alopecia (AGA) · Healthy Volunteers - Male and Female  ·  Sponsor: Absci Pty Ltd.

PhasePhase 1/Phase 2
Planned participants227
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersYes

About this study

The goal of this clinical trial is to learn if ABS-201 (a new medication) is safe and tolerable when used to improve hair growth in men and women. The trial will start with healthy volunteers and if safe, will treat participants with certain types of hair loss. The main questions it aims to answer are: What medical problems, if any, do participants experience when taking a single dose or many doses of ABS-201? How does the medication, ABS-201, compare to placebo (a look alike substance that does not contain any medication). Participants who qualify for the trial will receive either ABS-201 or a placebo, and visit the study clinic for scheduled checkups and tests for approximately 1 year.

This description comes directly from the study's public registry record.

Talk to the study team

Charles Romano, MPH  ·  +1.860.857.4560  ·  cromano@absci.com

Always discuss trial participation with your own doctor first.

Locations (4)

Momentum DarlinghurstSydney, New South Wales, AustraliaRecruiting
Nucleus Network BrisbaneBrisbane, Queensland, AustraliaRecruiting
Sinclair DermatologyMelbourne, Victoria, AustraliaRecruiting
Nucleus NetworkMelbourne, Victoria, AustraliaRecruiting

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Source record: clinicaltrials.gov/study/NCT07317544