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Clinical Trial Summary

BLS-M22 is being developed as an anti-myostatin agent for the treatment of Duchenne Muscular Dystrophy (Muscular Dystrophy). A total of 37 subjects participated in this study to confirm the safety of BLS-M22.


Clinical Trial Description

This study is a dose Block-randomized, Double-blind, Placebo-controlled and Dose-escalation Phase I Clinical Trial to Evaluate Safety of BLS-M22. The single ascending dose group participated in 9 patients in each group(500mg, 1,000mg, 2000mg/BLS-M22 or Placebo(n=7:2)). The multiple ascending dose group participated in 10 patients(determined dose in SAD/BLS-M22 or Placebo(n=8:2)). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03789734
Study type Interventional
Source BioLeaders Corporation
Contact
Status Completed
Phase Phase 1
Start date June 4, 2019
Completion date November 27, 2020

See also
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