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Active, not recruiting Phase 3 Interventional

Safety and Efficacy of VDPHL01 in Males With AGA

ClinicalTrials.gov ID: NCT06972264

Public ClinicalTrials.gov record NCT06972264. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 4, 2026, 6:10 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multi-dose Study to Evaluate the Efficacy and Safety of VDPHL01 in Male Subjects With Androgenetic Alopecia

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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).

Study identification

NCT ID
NCT06972264
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Veradermics, Inc.
Industry
Enrollment
480 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 11, 2025 (Actual)
Primary completion
Dec 2026 (Estimated)
Completion
Jul 2027 (Estimated)
Last update posted
Feb 12, 2026

2025 – 2027

United States locations

U.S. sites
44
U.S. states
22
U.S. cities
40
Facility City State ZIP Site status
Site 73 Birmingham Alabama 35209 —
Site 89 Birmingham Alabama 35244 —
Site 77 Phoenix Arizona 85006 —
Site 69 Encino California 91436 —
Site 64 Manhattan Beach California 90266 —
Site 93 Northridge California 91324 —
Site 66 Santa Monica California 90404 —
Site 94 Thousand Oaks California 91320 —
Site 71 Boca Raton Florida 33486 —
Site 86 Coral Gables Florida 33134 —
Site 62 Coral Gables Florida 33146 —
Site 99 Miami Florida 33173 —
Site 54 Ocala Florida 34470 —
Site 96 Tamarac Florida 33321 —
Site 90 Sandy Springs Georgia 30328 —
Site 61 Chicago Illinois 60611 —
Site 53 Clarksville Indiana 47129 —
Site 55 Plainfield Indiana 46168 —
Site 79 Leawood Kansas 66211 —
Site 52 Louisville Kentucky 40241 —
Site 75 New Orleans Louisiana 70124 —
Site 84 Glenn Dale Maryland 20769 —
Site 87 Rockville Maryland 20850 —
Site 80 Chestnut Hill Massachusetts 02467 —
Site 59 Quincy Massachusetts 02169 —
Site 68 Clinton Township Michigan 48038 —
Site 83 Troy Michigan 48084 —
Site 82 Hickory North Carolina 28602 —
Site 92 Huntersville North Carolina 28078 —
Site 72 Cincinnati Ohio 45236 —
Site 57 Portland Oregon 97210 —
Site 81 East Greenwich Rhode Island 02818 —
Site 60 Anderson South Carolina 29625 —
Site 95 Hermitage Tennessee 37076 —
Site 76 Austin Texas 78746 —
Site 51 Austin Texas 78759 —
Site 74 College Station Texas 77845 —
Site 67 Dallas Texas 75230 —
Site 78 Plano Texas 75024 —
Site 88 San Antonio Texas 78218 —
Site 91 Sugarland Texas 77479 —
Site 63 Norfolk Virginia 23502 —
Site 85 Norfolk Virginia 23502 —
Site 70 Mill Creek Washington 98012 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06972264, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 12, 2026 · Synced Nov 4, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06972264 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →