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Clinical Trial Summary

The purpose of this study is to evaluate the pharmacodynamics, safety, tolerability, pharmacokinetics, and efficacy of RO7204239, a humanized monoclonal antibody that binds to human latent myostatin, in ambulant adult participants with facioscapulohumeral muscular dystrophy (FSHD).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Facioscapulohumeral Muscular Dystrophy (FSHD)
  • Muscular Dystrophies
  • Muscular Dystrophy, Facioscapulohumeral

NCT number NCT05548556
Study type Interventional
Source Hoffmann-La Roche
Contact
Status Active, not recruiting
Phase Phase 2
Start date February 7, 2023
Completion date October 30, 2026

See also
  Status Clinical Trial Phase
Completed NCT02239224 - Safety, Tolerability, Pharmacokinetics, and Biological Activity of ATYR1940 in Adult Participants With Muscular Dystrophy Phase 1/Phase 2
Completed NCT02603562 - Evaluate Safety and Biological Activity of ATYR1940 in Participants With Early Onset Facioscapulohumeral Muscular Dystrophy Phase 1/Phase 2
Active, not recruiting NCT05397470 - Efficacy and Safety of Losmapimod in Treating Participants With Facioscapulohumeral Muscular Dystrophy (FSHD) (REACH) Phase 3
Active, not recruiting NCT04264442 - Efficacy and Safety of Losmapimod in Treating Subjects With Facioscapulohumeral Muscular Dystrophy (FSHD) With Open-Label Extension (OLE) Phase 2
Completed NCT04003974 - Efficacy and Safety of Losmapimod in Subjects With Facioscapulohumeral Muscular Dystrophy (FSHD) Phase 2