Clinical Trials Logo

Clinical Trial Summary

The purpose of this study is to assess the safety and biological activity of ATYR1940 in participants with early onset FSHD.


Clinical Trial Description

A Phase 1b/2 open-label, intraparticipant dose-escalation study aiming to evaluate the safety, tolerability, immunogenicity, biological and pharmacodynamic activity of intravenous ATYR1940, administered once weekly for 12 weeks, in early onset FSHD participants with signs or symptoms prior to 10 years of age. ;


Study Design


Related Conditions & MeSH terms

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

NCT number NCT02603562
Study type Interventional
Source aTyr Pharma, Inc.
Contact
Status Completed
Phase Phase 1/Phase 2
Start date March 30, 2016
Completion date December 12, 2016

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
Active, not recruiting NCT05397470 - Efficacy and Safety of Losmapimod in Treating Participants With Facioscapulohumeral Muscular Dystrophy (FSHD) (REACH) Phase 3
Active, not recruiting NCT05548556 - A Study to Evaluate RO7204239 in Participants With Facioscapulohumeral Muscular Dystrophy Phase 2
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