RecruitingPhase 3NCT07435012

Androgenic Alopecia TH07 Clinical Trial

Phase III, Parallel Design, Triple-Blind, Randomized, Multicenter Clinical Trial to Evaluate Safety & Efficacy of TH07 Topical Treatment in Male Patients With Androgenic Alopecia.


Sponsor

Triple Hair Inc

Enrollment

420 participants

Start Date

Apr 1, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this clinical trial is to learn whether a new topical solution, TH07, can help treat androgenic alopecia in men and to learn more about its safety. Participants will be asked to apply either the TH07 solution, a standard hair growth treatment (Minoxidil 5%), or a placebo every day for 24 weeks. At the end of the study, hair growth will be compared in each group to determine which treatment is most effective at increasing hair count.


Eligibility

Sex: MALEMin Age: 18 YearsMax Age: 49 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Minoxidil 5% Topical Solution, Placebo, and others for people with androgenic alopecia. The study is currently recruiting participants at 1 location. People eligible for this study include men aged 18 Years to 49 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGTH07

TH07 (5%Minoxidil, 0.1%Finasteride, 0.03%Latanoprost); topical solution; twice a day

DRUGTH07

* TH07 (5%Minoxidil, 0.1%Finasteride, 0.03%Latanoprost); topical solution; once a day * Placebo; topical solution; once a day

DRUGMinoxidil 5% Topical Solution

Minoxidil 5%; topical solution; twice a day

OTHERPlacebo

Placebo; topical solution; twice a day


Locations(1)

YVR Aesthetic Training and Study Centre.

Vancouver, British Columbia, Canada

View Full Details on ClinicalTrials.gov

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NCT07435012


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