drugset / Trial / NCT03231878

A Clinical Study to Evaluate the Efficacy and Safety of MIN-102 (IMP) in Male AMN Patients.

NCT03231878 ↗

Phase 2/3 Completed 105 enrolled Minoryx Therapeutics, S.L.
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a Phase II/III, randomized, double-blind, placebo-controlled, multicenter, two parallel-group study in male patients with the AMN phenotype of X-linked adrenoleukodystrophy (X-ALD) to assess the efficacy and safety of MIN-102 treatment. Study sites will consist of specialist referral centers experienced in the management of adrenoleukodystrophy (ALD).

Timeline

Start
2017-12-08
Primary completion
2021-06-25
Completion
2025-03-06

Drugs

EvaluationDrugModalityDoseRoute
Comparator Leriglitazone Small molecule 150 mg Oral

Indications