A Study of TDM-105795 in Male Subjects With Androgenetic Alopecia (AGA)

  • STATUS
    Recruiting
  • days left to enroll
    63
  • participants needed
    32
  • sponsor
    Technoderma Medicines Inc.
Updated on 17 May 2022
androgenic alopecia
Accepts healthy volunteers

Summary

Multi-center, randomized, double-blind, vehicle-controlled, parallel group, multi-dose escalation study of TDM-105795 in male subjects, 18 to 55 years old, with Androgenetic Alopecia (AGA).

Description

Protocol 239-11651-102 is a planned Phase 1 study entitled "A Randomized, Double-Blind, Vehicle-Controlled, Parallel Group, Multi-Dose Escalation Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of TDM-105795 in Healthy Male Subjects with Androgenetic Alopecia". Eligible subjects will be assigned to a sequential treatment cohort and will receive either one of the TDM-105795 solutions or the Placebo. The assigned test article will be applied once daily onto the scalp in the hair loss area (e.g., top of head and temple areas). All subjects will be treated with 1 mL/dose of test article with application to the scalp focusing on the regions that are bald and thinning.

Details
Condition Alopecia, Androgenetic
Treatment Placebo, TDM-105795
Clinical Study IdentifierNCT05244980
SponsorTechnoderma Medicines Inc.
Last Modified on17 May 2022

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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