clinical trial · NCT07146022
Safety and Efficacy of VDPHL01 in Females With Androgenetic Alopecia (AGA)
Androgenetic Alopecia (AGA)Androgenetic AlopeciaAGAFemale Androgenetic AlopeciaHair LossVDPHL01 QDPlaceboVDPHL01 BIDPlacebo
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).
started
Jul 25, 2025
primary completion
Jun 1, 2027
completion
Jan 1, 2028
last updated
Nov 24, 2025
detailed description
Not required.
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
sourced from ClinicalTrials.gov · pharmadog mirrors structured fields, not the full protocol