Overview

Safety and Efficacy of NMD670 in Adult Patients With Type 1 and Type 2 Charcot-Marie-Tooth Disease

Status:
RECRUITING
Trial end date:
2026-03-16
Target enrollment:
Participant gender:
Summary
This Phase 2a study aims to evaluate the efficacy, safety and tolerability of NMD670 vs placebo administered twice a day (BID) for 21 days in ambulatory adult patients with Charcot-Marie-Tooth disease type 1 and type 2.
Phase:
PHASE2
Details
Lead Sponsor:
NMD Pharma A/S