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NCT03742518Phase 2/3Completed

A Study Evaluating the Efficacy and Safety of SM04554 Topical Solution in Male Subjects With Androgenetic Alopecia

Multicenter, Randomized, Double-Blind, Placebo-Controlled Study of the Efficacy and Safety of 0.15% & 0.25% Concentrations of Topical SM04554 Solution in Male Subjects With Androgenetic Alopecia

In the register

The register attaches this trial to Dalosirvat (SM-04554) (Biosplice Therapeutics), currently at “Phase 2/3” in the register. The programme's phase is checked by hand; the trial's is declared by its sponsor.

What the registry records

Status
Completed
Declared phase
Phase 2/3
Sponsor
Biosplice Therapeutics, Inc.
Participants (registry)
675
Start
November 2018
Primary completion
December 2020
Study completion
December 2020
Last registry update
October 2026
Countries
Turkey

Conditions studied: Androgenetic Alopecia

Interventions: Topical SM04554 0.15% solution, Topical SM04554 0.25% solution, Topical vehicle solution

Full record on ClinicalTrials.gov ↗

Other trials of Dalosirvat (SM-04554)

  • NCT02503137Phase 2Completed

    A Study of SM04554 Applied Topically to the Scalp of Male Subjects With Androgenetic Alopecia Analyzed by Biopsy of the Scalp Prior To and Post Dosing

  • NCT02275351Phase 2Completed

    A Study of the Safety, Tolerability, and Efficacy of Topical SM04554 Solution in Male Subjects With Androgenetic Alopecia (AGA)

Listing a trial is not a recommendation to join one. Eligibility, risks and costs vary enormously — discuss any trial with your own doctor first. A registration proves a sponsor declared a study, not that it is progressing or will succeed. We're not doctors.