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Active, not recruiting Phase 2Phase 3 Interventional

Efficacy and Safety of VDPHL01 in Males With AGA

ClinicalTrials.gov ID: NCT06724614

Public ClinicalTrials.gov record NCT06724614. 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 Oct 21, 2026, 11:00 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. 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). 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.

Study identification

NCT ID
NCT06724614
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2, 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
Nov 6, 2024 (Actual)
Primary completion
Feb 2026 (Estimated)
Completion
Sep 2026 (Estimated)
Last update posted
Nov 6, 2025

2024 – 2026

United States locations

U.S. sites
44
U.S. states
24
U.S. cities
44
Facility City State ZIP Site status
Site 36 Birmingham Alabama 35203 —
Site 28 Phoenix Arizona 85018 —
Site 30 Fort Smith Arkansas 72916 —
Site 35 Rogers Arkansas 72758 —
Site 07 Fountain Valley California 92728 —
Site 02 Fremont California 94538 —
Site 34 Sherman Oaks California 91403 —
Site 21 Vista California 92083 —
Site 05 Castle Rock Colorado 80109 —
Site 24 Englewood Colorado 80111 —
Site 17 Aventura Florida 33180 —
Site 25 Brandon Florida 33511 —
Site 42 Hollywood Florida 33021 —
Site 03 Tampa Florida 33613 —
Site 43 Atlanta Georgia 30329 —
Site 31 Boise Idaho 83704 —
Site 23 Rolling Meadows Illinois 60008 —
Site 15 Indianapolis Indiana 46250 —
Site 32 New Albany Indiana 47150 —
Site 27 West Lafayette Indiana 47906 —
Site 41 Baton Rouge Louisiana 70809 —
Site 13 Covington Louisiana 70433 —
Site 12 Metairie Louisiana 70006 —
Site 22 Brighton Massachusetts 02135 —
Site 26 Clarkston Michigan 48346 —
Site 06 New Brighton Minnesota 55112 —
Site 18 Hackensack New Jersey 07601 —
Site 37 Kew Gardens New York 11415 —
Site 38 New York New York 10075 —
Site 39 Boardman Ohio 44512 —
Site 11 Columbus Ohio 43215 —
Site 08 Broomall Pennsylvania 19073 —
Site 10 Plymouth Meeting Pennsylvania 19462 —
Site 20 Greensville South Carolina 29615 —
Site 09 Knoxville Tennessee 37909 —
Site 16 Murfreesboro Tennessee 37130 —
Site 04 Nashville Tennessee 37215 —
Site 40 Bellaire Texas 77401 —
Site 44 Dallas Texas 75231 —
Site 14 Houston Texas 77056 —
Site 19 West Jordan Utah 84095 —
Site 29 Lynchburg Virginia 24501 —
Site 33 Seattle Washington 98168 —
Site 01 Spokane Washington 99202 —

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 NCT06724614, 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 Nov 6, 2025 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06724614 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →