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NCT05802173 · ClinicalTrials.gov registry record · Phase 2

Study of TDM-105795 Following Topical Administration in Male Subjects With Androgenetic Alopecia

A Phase 2 study of Alopecia, Androgenetic, sponsored by Technoderma Medicines.

Completed
Registry status
Phase 2
Development phase
71
Enrollment target
13
Study locations

NCT05802173 is a Phase 2 study of Alopecia, Androgenetic that has completed, run by Technoderma Medicines. The registered enrollment target is 71 participants, below the 326-participant average among 3 other Alopecia, Androgenetic trials with a reported enrollment target (78% lower). The trial reports 13 study locations across 9 states.

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The verdict

NCT05802173, a Phase 2 study of Alopecia, Androgenetic, has completed, sponsored by Technoderma Medicines.

COMPLETED
Registry status
Phase 2
Development phase
71 participants
Enrollment target
13
Study locations

Study Summary

Randomized, double-blind, vehicle-controlled, parallel group, multi-dose study of TDM-105795 in male subjects with androgenetic alopecia

Conditions Studied

Interventions

  • DRUG TDM-105795, 0.0025%
  • DRUG TDM-105795, 0.02%
  • DRUG TDM-105795 topical vehicle solution

Study Locations (13)

Louisiana

  • Site 11 - Baton Rouge
  • Site 13 - New Orleans

Minnesota

  • Site 10 - Minneapolis
  • Site 9 - New Brighton

Tennessee

  • Site 5 - Knoxville
  • Site 8 - Murfreesboro

Texas

  • Site 1 - Austin
  • Site 6 - College Station

Arkansas

  • Site 12 - North Little Rock

Illinois

  • Site 4 - Rolling Meadows

Indiana

  • Site 7 - Plainfield

Oregon

  • Site 3 - Portland

Trial Details

FieldValue
Enrollment Target 71 participants
Start Date 2023-03-06
Est. Completion 2024-01-29
Phase Phase 2

Sponsor

Technoderma Medicines

5 total trials

What the Registry Record Tells You About NCT05802173

The ClinicalTrials.gov registry entry for NCT05802173 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 71 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 326-participant average among 3 other Alopecia, Androgenetic trials with a reported enrollment target (78% lower). The listed sponsor is Technoderma Medicines, which has 5 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Alopecia, Androgenetic appearing as the primary indexed condition, and to 3 interventions - of which TDM-105795, 0.0025% is the first listed.

NCT05802173 reports 13 study locations spanning 9 distinct geographic areas - top geographies include Louisiana, Minnesota, Tennessee.

Frequently Asked Questions

What is clinical trial NCT05802173 about?

NCT05802173 is a clinical study titled "Study of TDM-105795 Following Topical Administration in Male Subjects With Androgenetic Alopecia". Randomized, double-blind, vehicle-controlled, parallel group, multi-dose study of TDM-105795 in male subjects with androgenetic alopecia

What is the current status of trial NCT05802173?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 71 participants. The study started on 2023-03-06. Estimated completion is 2024-01-29.

What conditions does trial NCT05802173 study?

This clinical trial studies the following conditions: Alopecia, Androgenetic.

What interventions are being tested in trial NCT05802173?

The interventions under investigation include: TDM-105795, 0.0025% (DRUG), TDM-105795, 0.02% (DRUG), TDM-105795 topical vehicle solution (DRUG).

Who is sponsoring clinical trial NCT05802173?

This trial is sponsored by Technoderma Medicines, which has 5 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05802173 being conducted?

This trial has 13 study locations across Arkansas, Illinois, Indiana, Louisiana, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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