Who Can Participate?
Women aged 18 to 65 with mild to moderate androgenetic alopecia may participate.
Inclusion Criteria
• have a clinical diagnosis of mild to moderate AGA
• willing to maintain the same hair care regimen with the same hair care products throughout the study
• willing to maintain at least ¼ inch length hair during the study with the same hairstyle, hair length, and hair color throughout the study
Participant Information
• Participate and receive study treatment at no cost
• Regular visits with study doctors who specialise in treating androgenetic alopecia (11 visits)
• Will receive either an investigative oral treatment (study drug) or an inert tablet
• Reimbursement for study-related expenses may be provided
How Long Will The Study Last?
• 62 weeks
Note: Participants will need to stop all other treatments for androgenetic alopecia during clinical trial participation. Some over-the-counter preparations may be deemed acceptable by the doctor performing the study.
Northridge - Quest Dermatology Research
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Similar Trials
No Similar Trials FoundThe following information is from ClinicalTrials.gov
Last Update Posted: October 31, 2025
NCT07146022
Veradermics, Inc.
Brief Summary:
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).
Condition or Disease:
Androgenetic Alopecia (AGA),Androgenetic Alopecia,AGA,Female Androgenetic Alopecia,Hair Loss
Intervention/Treatment:
Drug: VDPHL01 BID Drug: VDPHL01 QD,Drug: Placebo Drug: Placebo Drug: PlaceboPhase:
PHASE3
Ages Eligible for Study:
18 Years and 65 Years (ADULT,OLDER_ADULT)
Sexes Eligible for Study:
FEMALE
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