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RGX 202- REGENXBIO

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Drug Profile

RGX 202- REGENXBIO

Alternative Names: RGX-202 - REGENXBIO

Latest Information Update: 07 Aug 2024

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At a glance

  • Originator REGENXBIO
  • 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 I/II Duchenne muscular dystrophy

Most Recent Events

  • 02 Aug 2024 Updated pharmacodynamics data from a phase I/II AFFINITY DUCHENNE trial in Duchenne Muscular Dystrophy released by REGENXBIO
  • 01 Aug 2024 REGENXBIO completes an end-of-Phase II (EOP2) meeting with the US FDA for Duchenne muscular dystrophy
  • 01 Aug 2024 REGENXBIO plans to initiate a pivotal dose determination trial for Duchenne muscular dystrophy in the second half of 2024

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