drugset / Trial / NCT06924632

Efficacy & Safety of Minoxidil SL Tablets in Men With AGA

NCT06924632

Phase 3 Completed 142 enrolled Samson Clinical Operations Pty Ltd
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a phase 3, multicentre, randomised, double-blinded, placebo-controlled study examining the safety and efficacy of 2.5 mg sublingual (SL) minoxidil tablets taken twice daily in the treatment of androgenetic alopecia (AGA) in men. The duration of study participation is 32 weeks including screening and safety follow up. The primary efficacy objective is to determine whether treatment with 2.5 mg SL tablets twice daily increases the number of hairs in men with AGA over 24 weeks. The primary safety objective is to evaluate the safety and tolerability of 2.5 mg SL tablets administered twice daily over 24 weeks.

Timeline

Start
2025-07-14
Primary completion
2026-05-15
Completion
2026-05-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Minoxidil Small molecule 2.5 mg Other