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Clinical Trial Summary

This Phase 2 proof-of-concept, dose range finding study aims to evaluate the safety and efficacy of 3 dose levels of NMD670 vs placebo in adult patients with MG with antibodies against AChR or MuSK, administered twice a day (BID) for 21 days.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06414954
Study type Interventional
Source NMD Pharma A/S
Contact NMD Pharma A/S
Phone contact@nmdpharma.com
Email contact@nmdpharma.com
Status Not yet recruiting
Phase Phase 2
Start date May 2024
Completion date November 2025

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