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Active, not recruiting Phase 3 Interventional

Safety and Efficacy of VDPHL01 in Females With Androgenetic Alopecia (AGA)

ClinicalTrials.gov ID: NCT07146022

Public ClinicalTrials.gov record NCT07146022. 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 22, 2026, 4:36 PM 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 Female 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 female subjects with Androgenetic Alopecia (AGA). AGA is a genetic disorder caused by an excessive (too much) hair follicle response to androgens (hormones) that causes hair loss. VDPHL01 is an investigational oral drug to treat AGA. 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
NCT07146022
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Veradermics, Inc.
Industry
Enrollment
552 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
Female
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
Jul 25, 2025 (Actual)
Primary completion
Jun 2027 (Estimated)
Completion
Jan 2028 (Estimated)
Last update posted
Aug 17, 2026

2025 – 2028

United States locations

U.S. sites
71
U.S. states
28
U.S. cities
68
Facility City State ZIP Site status
Site 73 Birmingham Alabama 35209 —
Site 89 Birmingham Alabama 35244 —
Site 77 Phoenix Arizona 85006 —
Site 30 Fort Smith Arkansas 72916 —
Site 69 Encino California 91436 —
Site 2 Fremont California 94538 —
Site 64 Manhattan Beach California 90266 —
Site 93 Northridge California 91324 —
Site 66 Santa Monica California 90404 —
Site 34 Sherman Oaks California 91403 —
Site 94 Thousand Oaks California 91320 —
Site 21 Vista California 92083 —
Site 5 Castle Rock Colorado 80109 —
Site 24 Greenwood Village Colorado 80111 —
Site 17 Aventura Florida 33180 —
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 43 Atlanta Georgia 30329 —
Site 90 Sandy Springs Georgia 30328 —
Site 31 Boise Idaho 83704 —
Site 61 Chicago Illinois 60610 —
Site 53 Clarksville Indiana 47129 —
Site 15 Indianapolis Indiana 46250 —
Site 32 New Albany Indiana 47150 —
Site 55 Plainfield Indiana 46168 —
Site 27 West Lafayette Indiana 47906 —
Site 79 Leawood Kansas 66211 —
Site 52 Louisville Kentucky 40241 —
Site 41 Baton Rouge Louisiana 70809 —
Site 13 Covington Louisiana 70433 —
Site 12 Metairie Louisiana 70006 —
Site 75 New Orleans Louisiana 70124 —
Site 84 Glenn Dale Maryland 20769 —
Site 87 Rockville Maryland 20850 —
Site 22 Brighton Massachusetts 02135 —
Site 80 Chestnut Hill Massachusetts 02467 —
Site 59 Quincy Massachusetts 02169 —
Site 26 Clarkston Michigan 48346 —
Site 68 Clinton Township Michigan 48038 —
Site 83 Southfield Michigan 48034 —
Site 98 Medina Minnesota 55340 —
Site 56 Minneapolis Minnesota 55455 —
Site 6 New Brighton Minnesota 55112 —
Site 18 Hackensack New Jersey 07601 —
Site 37 Kew Gardens New York 11415 —
Site 97 New York New York 10003 —
Site 82 Hickory North Carolina 28602 —
Site 92 Huntersville North Carolina 28078 —
Site 39 Boardman Ohio 44512 —
Site 72 Cincinnati Ohio 45236 —
Site 11 Columbus Ohio 43215 —
Site 57 Portland Oregon 97210 —
Site 60 Anderson South Carolina 29621 —
Site 95 Hermitage Tennessee 37076 —
Site 9 Knoxville Tennessee 37909 —
Site 4 Nashville Tennessee 37215 —
Site 76 Austin Texas 78746 —
Site 74 College Station Texas 77845 —
Site 67 Dallas Texas 75230 —
Site 14 Houston Texas 77056 —
Site 88 San Antonio Texas 78218 —
Site 91 Sugar Land Texas 77479 —
Site 19 South Jordan Utah 84095 —
Site 29 Forest Virginia 24551 —
Site 63 Norfolk Virginia 23502 —
Site 85 Norfolk Virginia 23502 —
Site 33 Burien Washington 98168 —
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 NCT07146022, 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 Aug 17, 2026 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT07146022 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →