Research programme: chimeric antigen receptor T cell therapy - CRISPR Therapeutics

Drug Profile

Research programme: chimeric antigen receptor T cell therapy - CRISPR Therapeutics

Alternative Names: Allogeneic CAR T-cell therapy - CRISPR Therapeutics; CTX 101 - CRISPR Therapeutics

Latest Information Update: 13 Nov 2017

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At a glance

  • Originator CRISPR Therapeutics
  • Class Antineoplastics; CAR-T cell therapies
  • Mechanism of Action T lymphocyte replacements
  • 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 Haematological malignancies

Most Recent Events

  • 10 Nov 2017 CRISPR Therapeutics announces intention to submit IND application for CTX 101 for Haematological malignancies in late 2018
  • 10 Nov 2017 CRISPR Therapeutics plans clinical development of CTX 101 for Haematological malignancies in early 2019
  • 19 Jun 2017 CRISPR Therapeutics has patent protection for CRISPR-Cas9 genome editing technology
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