CompletedPhase 2NCT06393452
Safety, Pharmacokinetics and Efficacy of PP405 in Adults With AGA
Studying Alopecia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Pelage Pharmaceuticals, Inc.
- Principal Investigator
- Christina WengPelage Pharmaceuticals
- Intervention
- PP405 0.05% Topical Gel(drug)
- Enrollment
- 78 enrolled
- Eligibility
- 18-55 years · All sexes
- Timeline
- 2024 – 2025
Study locations (8)
- California Dermatology & Clinical Research Institute, Encinitas, California, United States
- Clinical Trials Research Institute, Thousand Oaks, California, United States
- Dawes Fretzin Clinical Research Group, LLC, Indianapolis, Indiana, United States
- Minnesota Clinical Study Center, New Brighton, Minnesota, United States
- DermResearch, Austin, Texas, United States
- Stride Clinical Research LLC, Sugar Land, Texas, United States
- Jordan Valley Dermatology Center, South Jordan, Utah, United States
- Virginia Clinical Research, Inc., Norfolk, Virginia, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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