Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
Efficacy and Safety of VDPHL01 in Males With AGA
NCT06724614 · View on ClinicalTrials.gov ↗
Study Summary
This study will evaluate the safety and efficacy of VDPHL01 in male subjects with Androgenetic Alopecia (AGA). AGA (or male pattern baldness) is a genetic disorder caused by an excessive (too much) hair follicle response to androgens (hormone) that causes hair loss. VDPHL01 8.5 mg Tablet is an investigational oral drug to treat male pattern baldness. This multi-center, double blind, 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). The first 7 visits will be part of the placebo-controlled period. The next 3 visits will be part of the treatment extension phase. All subjects will receive active drug in the treatment extension phase.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG VDPHL01
Study Locations (20)
California
- Site 07 — Fountain Valley
- Site 02 — Fremont
- Site 34 — Sherman Oaks
- Site 21 — Vista
Florida
- Site 17 — Aventura
- Site 25 — Brandon
- Site 42 — Hollywood
- Site 03 — Tampa
Indiana
- Site 15 — Indianapolis
- Site 32 — New Albany
- Site 27 — West Lafayette
Arkansas
- Site 30 — Fort Smith
- Site 35 — Rogers
Colorado
- Site 05 — Castle Rock
- Site 24 — Englewood
Alabama
- Site 36 — Birmingham
Arizona
- Site 28 — Phoenix
Georgia
- Site 43 — Atlanta
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 480 participants |
| Start Date | 2024-11-06 |
| Est. Completion | 2026-09 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06724614
The ClinicalTrials.gov registry entry for NCT06724614 describes a study currently listed as active not recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 480 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Veradermics, which has 4 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 3 conditions, with Androgenetic Alopecia appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06724614 reports 20 study locations spanning 10 distinct geographic areas — top geographies include California, Florida, Indiana. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06724614 about?
NCT06724614 is a clinical study titled "Efficacy and Safety of VDPHL01 in Males With AGA". This study will evaluate the safety and efficacy of VDPHL01 in male subjects with Androgenetic Alopecia (AGA). AGA (or male pattern baldness) is a genetic disorder caused by an excessive (too much) hair follicle response to androgens (hormone) that causes hair loss. VDPHL01 8.5 mg Tablet is an inve...
What is the current status of trial NCT06724614?
This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 480 participants. The study started on 2024-11-06. Estimated completion is 2026-09.
What conditions does trial NCT06724614 study?
This clinical trial studies the following conditions: Androgenetic Alopecia, AGA, Male Pattern Baldness. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06724614?
The interventions under investigation include: Placebo (DRUG), VDPHL01 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06724614?
This trial is sponsored by Veradermics, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06724614 being conducted?
This trial has 20 study locations across Alabama, Arizona, Arkansas, California, Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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