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An Open-Label, Intrapatient Dose-Escalation Study to Evaluate the Safety, Tolerability, Immunogenicity, and Biological Activity of ATYR1940 in Patients With Early Onset and Other Pediatric Onset Facioscapulohumeral Muscular Dystrophy

Trial Profile

An Open-Label, Intrapatient Dose-Escalation Study to Evaluate the Safety, Tolerability, Immunogenicity, and Biological Activity of ATYR1940 in Patients With Early Onset and Other Pediatric Onset Facioscapulohumeral Muscular Dystrophy

Status: Completed
Phase of Trial: Phase I/II

Latest Information Update: 06 Nov 2021

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At a glance

  • Drugs ATYR 1940 (Primary)
  • Indications Facioscapulohumeral muscular dystrophy
  • Focus Adverse reactions; Pharmacodynamics
  • Sponsors aTyr Pharma

Most Recent Events

  • 13 Aug 2021 This trial has been discontinued in Italy, according to European Clinical Trials Database record.
  • 14 Nov 2017 According to an aTyr Pharma media release, in october data was presented at the 22nd International Annual Congress of the World Muscle Society.
  • 27 Sep 2017 Results presented in an aTyr Pharma Media Release.

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