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Research programme: AAV mediated antibody delivery gene therapies - REGENXBIO

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Drug Profile

Research programme: AAV mediated antibody delivery gene therapies - REGENXBIO

Alternative Names: Gene therapies for hereditary angioedema - REGENXBIO; Hereditary angioedema gene therapy programme - REGENXBIO

Latest Information Update: 16 Jun 2022

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At a glance

  • Originator REGENXBIO
  • Class Gene therapies; Skin disorder therapies; Vascular disorder therapies
  • Mechanism of Action Gene transference
  • Orphan Drug Status

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

    No
  • New Molecular Entity No

Highest Development Phases

  • Discontinued Hereditary angioedema

Most Recent Events

  • 16 Jun 2022 Discontinued - Preclinical for Hereditary angioedema in USA (IV) (REGENXBIO pipeline, June 2022)
  • 31 Dec 2020 REGENXBIO has patents pending for AAV mediated antibody delivery gene therapies in USA and Europe
  • 26 Jul 2019 REGENXBIO plans clinical trials for Hereditary angioedema

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