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NCT07011485Phase 2Active, not recruiting

A Safety and Efficacy Study of PDFE-2304 Topical Solution for the Treatment of Androgenic Alopecia.

A Triple-Blind, Randomized, Efficacy and Tolerability Comparison Study of PDFE-2304 Topical Solution Versus Minoxidil 5% Topical Solution for the Treatment of Androgenic Alopecia (AGA).

In the register

The register attaches this trial to PDFE-2304 (Neopili) (PDFE Pharma Innovations), currently at “Phase 2” in the register. The programme's phase is checked by hand; the trial's is declared by its sponsor.

What the registry records

Status
Active, not recruiting
Declared phase
Phase 2
Sponsor
PDFE Pharma Innovations FZCO
Participants (registry)
15
Start
May 2025
Primary completion
August 2025
Study completion
September 2025
Last registry update
June 2025
Countries
India

Conditions studied: Alopecia, Androgenetic, Baldness, Androgenetic Alopecia (AGA)

Interventions: Minoxidil 5% Topical Solution, PDFE-2304 Topical Solution

Full record on ClinicalTrials.gov ↗

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.