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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 Sep 6, 2026, 2:16 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 24, 2025
Primary completion
May 31, 2027
Completion
Dec 31, 2027
Last update posted
Aug 16, 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 16, 2026 · Synced Sep 6, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07146022 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →