Research programme: Duchenne muscular dystrophy therapeutics - RASRx

Drug Profile

Research programme: Duchenne muscular dystrophy therapeutics - RASRx

Alternative Names: MMX 1902; RASRx 1902

Latest Information Update: 23 Jun 2017

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At a glance

  • Originator RASRx
  • Class
  • Mechanism of Action Angiotensin modulators; Renin modulators
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    Yes - Duchenne muscular dystrophy
  • New Molecular Entity Yes

Highest Development Phases

  • Preclinical Duchenne muscular dystrophy

Most Recent Events

  • 15 Jun 2017 MMX 1902 receives Orphan Drug status for Duchenne muscular dystrophy in USA
  • 15 Jun 2017 RASRx plans clinical trials for Duchenne muscular dystrophy
  • 01 Mar 2017 Preclinical trials in Duchenne muscular dystrophy in USA (PO) before March 2017 (CureDuchenne pipeline, February 2017)
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