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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

Status: Recruiting

The research study will compare VDPHL01 with placebo (no active ingredient) to learn about the safety and how VDPHL01 works for women who have androgenetic alopecia (AGA). AGA is a genetic disorder caused by an excessive (too much) hair follicle response to androgens resulting in hair loss. VDPHL01 is an extended release (ER) oral (taken by mouth) form of minoxidil.

I'm interested

Sex: Female
Age Group: 18 years and over
This study is NOT accepting healthy volunteers
Inclusion Criteria:

• women
• 18-65 years of age
• mild to moderate Androgenetic Alopecia (AGA)
Exclusion Criteria:

• history of organ transplant
• history of heart disease
Interventions:

Drug: Placebo, Drug: Placebo, Drug: VDPHL01 BID, Drug: VDPHL01 QD

Conditions:

Dermatology (Skin, Hair & Nails)

Keywords:

AGA, Androgenetic Alopecia, dermatology, women's health

Study Contact: John Meisenheimer - jmeisenh@umn.edu
Principal Investigator: Maria Hordinsky
Phase: PHASE3
IRB Number: STUDY00025450
See this study on ClinicalTrials.gov

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