Phase 2/3 Efficacy and Safety of PP405 in Adult Males

Recruiting Phase 2 Phase 3 Interventional Study
Androgenetic Alopecia
Pivotal Trial This treatment is in the last trial phase before FDA approval. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 55
Sex
Male
Trial phase
Phase 2/3
Study type
Interventional
Purpose
Treatment
Participants needed
600 (estimated)
Sponsor
Pelage Pharmaceuticals, Inc. · Industry
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About This Trial

The study is designed to validate efficacy and long term safety of PP405.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Males (assigned at birth) aged 18 to 55 years, inclusive at time of consent. 2. Able and willing to provide written informed consent 3. Must have been experiencing Androgenetic Alopecia (AGA) for at least 6 months prior to screening. 4. Have a modified Norwood-Hamilton score …
Contacts

Lisa Sherman

213-218-3830

clinicaltrials@pelagepharma.com

CONTACT