RecruitingNot ApplicableNCT07107841

Autologous Hair Follicle Secretome for Androgenic Alopecia (Single Site)

Blinded, Randomized, Controlled, Trial to Evaluate the Efficacy and Safety of Autologous Hair Follicle Secretome for the Treatment of Androgenic Alopecia (Single Site)


Sponsor

Acorn Biolabs Inc.

Enrollment

60 participants

Start Date

Oct 16, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

(SINGLE SITE Study) The purpose of this clinical trial is to evaluate the safety and efficacy of the use of an autologous hair follicle derived secretome for androgenous alopecia. The secretome will be injected into the scalp at baseline, and days 30, 90, 180, 270 and 365. Hair growth will be quantitatively measured for density and thickness. PROs will also be collected from participants. This study will be run at a SINGLE SITE.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Autologous Hair Follicle-Derived Secretome and Placebo Control for people with alopecia, androgenic alopecia, and other related conditions. The study is currently recruiting participants at 1 location.

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

OTHERAutologous Hair Follicle-Derived Secretome

Hair follicles are plucked, cultured and the product is the resulting cell secretions (secretome) collected from the conditioned media.

OTHERPlacebo Control

The same saline used for diluting the active treatment in will be used as a control.


Locations(1)

Ziering Medical

West Hollywood, California, United States

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NCT07107841


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