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An Open-Label Extension Study of Edasalonexent in Pediatric Patients With Duchenne Muscular Dystrophy

Trial Profile

An Open-Label Extension Study of Edasalonexent in Pediatric Patients With Duchenne Muscular Dystrophy

Status: Discontinued
Phase of Trial: Phase III

Latest Information Update: 26 Jul 2022

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At a glance

  • Drugs Edasalonexent (Primary)
  • Indications Duchenne muscular dystrophy
  • Focus Adverse reactions; Registrational
  • Acronyms GalaxyDMD
  • Sponsors Astria Therapeutics

Most Recent Events

  • 14 Nov 2020 This trial has been discontinued in Sweden according to European Clinical Trials Database record.
  • 12 Nov 2020 According to a Catabasis Pharmaceuticals media release, as the PolarisDMD trial did not meet the primary endpoint and secondary endpoint timed function tests also did not show statistically significant improvements, the company is stopping activities related to the development of edasalonexent, including this study.
  • 12 Nov 2020 Status changed from recruiting to discontinued, according to a Catabasis Pharmaceuticals media release.

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