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

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Drug Profile

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

Alternative Names: Allogeneic CAR T-cell therapy - CRISPR Therapeutics; Anti-CD33 CAR-T cells - CRISPR Therapeutics; CRISPR-based CAR-T cell therapies - CRISPR Therapeutics

Latest Information Update: 28 May 2022

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At a glance

  • Originator CRISPR Therapeutics
  • Class CAR-T cell therapies; Gene therapies; Immunotherapies
  • Mechanism of Action Immunologic cytotoxicity; 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

  • No development reported Haematological malignancies; Solid tumours

Most Recent Events

  • 28 May 2022 No recent reports of development identified for preclinical development in Solid-tumours in Switzerland (Parenteral)
  • 28 Dec 2021 No recent reports of development identified for preclinical development in Haematological-malignancies in Switzerland (Parenteral)
  • 22 Jun 2020 Pharmacodynamics data from a preclinical trial in cancer presented at the 111th Annual Meeting of the American Association for Cancer Research - II (AACR-II-2020)

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