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Research programme: gene editing based therapeutics - Casebia Therapeutics

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Drug Profile

Research programme: gene editing based therapeutics - Casebia Therapeutics

Alternative Names: CRISPR/Cas9 gene editing therapies - Bayer-CRISPR Therapeutics

Latest Information Update: 28 May 2024

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At a glance

  • Originator Casebia Therapeutics
  • Class Antihaemorrhagics; Antineoplastics; Cardiovascular therapies; Eye disorder therapies; Gene therapies
  • Mechanism of Action Gene modulators; Gene transference; Immunogenetic modulators
  • 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

  • No development reported Autoimmune disorders; Blindness; Cancer; Congenital heart defects; Haemophilia A; Retinitis pigmentosa; Severe combined immunodeficiency

Most Recent Events

  • 28 May 2024 No recent reports of development identified for preclinical development in Autoimmune-disorders in USA
  • 28 May 2024 No recent reports of development identified for research development in Cancer in USA (Parenteral)
  • 28 May 2024 No recent reports of development identified for research development in Haemophilia-A in USA

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