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Fordadistrogene movaparvovec - Pfizer

Drug Profile

Fordadistrogene movaparvovec - Pfizer

Alternative Names: BMB-D-001; PF 06939926

Latest Information Update: 14 Nov 2023

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At a glance

  • Originator Bamboo Therapeutics
  • Developer Pfizer
  • Class Gene therapies
  • Mechanism of Action Dystrophin replacements; Gene transference
  • 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 No

Highest Development Phases

  • Phase III Duchenne muscular dystrophy

Most Recent Events

  • 14 Nov 2023 US FDA granted Rare Pediatric Disease for Duchenne muscular dystrophy, prior to November 2023 (Pfizer website, November 2023)
  • 13 Mar 2023 Pfizer initiates a phase III trial for Duchenne Muscular Dystrophy (In children, In adolescents, In adults, In the elderly) in USA (NCT05689164)
  • 19 Jan 2023 Pfizer plans a phase III trial for Duchenne Muscular Dystrophy(In children, In adolescents, In adults, In the elderly) in April 2023(NCT05689164)
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