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NCT06527365 · ClinicalTrials.gov registry record · Phase 2
Safety and Efficacy of VDPHL01 in Males and Females With AGA
A Phase 2 study of Androgenetic Alopecia and AGA, sponsored by Veradermics.
- Active
- Registry status
- Phase 2
- Development phase
- 70
- Enrollment target
- 4
- Study locations
NCT06527365: Active Phase 2 study of Androgenetic Alopecia and AGA, sponsored by Veradermics.
NCT06527365 is a Phase 2 study of Androgenetic Alopecia and AGA that is active but no longer recruiting, run by Veradermics. The registered enrollment target is 70 participants, below the 160-participant average among 16 other Androgenetic Alopecia trials with a reported enrollment target (56% lower). The trial reports 4 study locations across 4 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06527365, a Phase 2 study of Androgenetic Alopecia and AGA, is active but no longer recruiting, sponsored by Veradermics.
- ACTIVE NOT RECRUITING
- Registry status
- Phase 2
- Development phase
- 70 participants
- Enrollment target
- 4
- Study locations
Study Summary
This study will evaluate the safety and efficacy of VDPHL01 in male and female subjects with Androgenetic Alopecia (AGA). AGA (or pattern of hair loss) is a genetic disorder caused by an excessive (too much) hair follicle response to androgens (hormone) that causes hair loss. VDPHL01 8.5 mg Tablets for males and VDPHL01 4.5 mg Tablets for females are an investigational oral drug to treat male and female pattern baldness. This multiple center, open-label, study will last about 13 months and includes 11 study visits (screening, baseline (day 1), week 2, month 1, month 2, month 4, month 6, month 8, month 10, month 12, month 13). Male subjects that meet the study eligibility criteria will be administered VDPHL01 once daily for 12 months. Female subjects that meet the study eligibility criteria will be administered VDPHL01 either once or twice daily for 12 months.
Primary Outcome
Change from baseline in non-vellus TAHC using digital image analysis at Month 12.
Conditions Studied
Interventions
- DRUG VDPHL01
Study Locations (4)
California
- 01 - San Diego
Indiana
- 04 - New Albany
New Jersey
- 03 - Hackensack
Utah
- 02 - South Jordan
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 70 participants |
| Start Date | 2024-07-08 |
| Est. Completion | 2026-08 |
| Phase | Phase 2 |
What the registry record for NCT06527365 still lists
NCT06527365 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 70 participants, a relatively small participant target, below the 160-participant average among 16 other Androgenetic Alopecia trials with a reported enrollment target (56% lower).
The record links to 3 conditions, with Androgenetic Alopecia appearing as the primary indexed condition, and to 1 intervention - of which VDPHL01 is the first listed.
NCT06527365 reports a single indexed study location in California, Indiana, New Jersey.
Frequently Asked Questions
What is clinical trial NCT06527365 about?
NCT06527365 is a clinical study titled "Safety and Efficacy of VDPHL01 in Males and Females With AGA". This study will evaluate the safety and efficacy of VDPHL01 in male and female subjects with Androgenetic Alopecia (AGA). AGA (or pattern of hair loss) is a genetic disorder caused by an excessive (too much) hair follicle response to androgens (hormone) that causes hair loss. VDPHL01 8.5 mg Tablets...
What is the current status of trial NCT06527365?
This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 70 participants. The study started on 2024-07-08. Estimated completion is 2026-08.
What conditions does trial NCT06527365 study?
This clinical trial studies the following conditions: Androgenetic Alopecia, AGA, Male Pattern Baldness.
What interventions are being tested in trial NCT06527365?
The interventions under investigation include: VDPHL01 (DRUG).
Who is sponsoring clinical trial NCT06527365?
This trial is sponsored by Veradermics, which has 5 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06527365 being conducted?
This trial has 4 study locations across California, Indiana, New Jersey, Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT06527365's enrollment target sits among peer trials
70 7th of 16 higher than 10 of 16 other Androgenetic Alopecia trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Androgenetic Alopecia trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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