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RAG 18

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Drug Profile

RAG 18

Alternative Names: RAG-18

Latest Information Update: 26 Aug 2024

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At a glance

  • Originator Ractigen Therapeutics
  • Class Oligonucleotides; RNA
  • Mechanism of Action Gene expression stimulants
  • 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
  • Available For Licensing Yes

Highest Development Phases

  • Preclinical Duchenne muscular dystrophy

Most Recent Events

  • 22 Aug 2024 RAG 18 receives Orphan Drug status for Duchenne muscular dystrophy in USA
  • 25 Jul 2024 US FDA grants Rare Pediatric Disease Designation (RPDD) to RAG 18 for Duchenne Muscular Dystrophy
  • 02 Nov 2023 Ractigen Therapeutics plans to initiate a phase I trial for Duchenne muscular dystrophy (Parenteral), by early 2025

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