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Bidridistrogene xeboparvovec - Myonexus Therapeutics

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Drug Profile

Bidridistrogene xeboparvovec - Myonexus Therapeutics

Alternative Names: MYO-101; rAAVrh74.MHCK7.hSGCB; rAAVrh74.MHCK7.SGCB; scAAVrh74.MHCK7.hSGCB; scAAVrh74.tMCK.hSGCB; SRP-9003

Latest Information Update: 17 Oct 2025

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At a glance

  • Originator Nationwide Children's Hospital
  • Developer Myonexus Therapeutics; Nationwide Children's Hospital; Sarepta Therapeutics
  • Class Gene therapies
  • Mechanism of Action Sarcoglycan expression stimulants
  • Orphan Drug Status

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

    Yes - Limb girdle muscular dystrophies
  • New Molecular Entity No

Highest Development Phases

  • Phase III Limb girdle muscular dystrophies

Most Recent Events

  • 03 Sep 2025 Sarepta Therapeutics terminates a phase I/II trial in Limb girdle muscular dystrophies (In children, In adolescents) in USA due to a business decision.(IV) (NCT03652259)
  • 18 Jul 2025 US FDA places clinical hold on all clinical trials for limb girdle muscular dystrophy using AAVrh74 gene therapies
  • 04 Jun 2025 US FDA grants platform technology designation for rAAVrh74 viral vector used in bidridistrogene xeboparvovec for Limb-girdle muscular dystrophy

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