Research programme: gene editing based therapeutics - Casebia Therapeutics

Drug Profile

Research programme: gene editing based therapeutics - Casebia Therapeutics

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

Latest Information Update: 20 Nov 2017

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At a glance

  • Originator Casebia Therapeutics
  • Class 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

  • Preclinical Blindness; Congenital heart defects; Haemophilia; Immunodeficiency disorders

Most Recent Events

  • 14 Nov 2017 CureVac and Casebia Therapeutics enter into a collaboration agreement for the development of gene-editing programmes
  • 25 Jul 2017 University of California, University of Vienna and Charpentier submit appellate brief seeking reversal of decision by PTAB, which dismissed interference proceedings against Broad Institute, MIT and Harvard University for a patent related to CRISPR-Cas9 genome editing technology, in USA
  • 17 Apr 2017 Casebia Therapeutics signs a collaboration agreement with StrideBio to develop gene editing based therapeutics
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