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An expanded access program of Vamorolone for the patients with Duchenne-muscular-dystrophy in China

Trial Profile

An expanded access program of Vamorolone for the patients with Duchenne-muscular-dystrophy in China

Status: Recruiting
Phase of Trial: Clinical Phase Unknown

Latest Information Update: 14 Jun 2024

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At a glance

  • Drugs Vamorolone (Primary)
  • Indications Duchenne muscular dystrophy
  • Focus Expanded access; Therapeutic Use

Most Recent Events

  • 14 Jun 2024 Status changed from planning to recruiting.
  • 14 Jun 2024 New trial record
  • 10 Jun 2024 According to Santhera Pharmaceuticals media release, In April 2024, the Hainan Medical Products Administration (HMPA) authorized the EAP for AGAMREE based on local policies, AGAMREEs existing overseas approvals (U.S., EU, UK) and its demonstrated ability to address urgent clinical needs in DMD.

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