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Research programme: T-cell therapies - CRISPR Therapeutics

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Drug Profile

Research programme: T-cell therapies - CRISPR Therapeutics

Latest Information Update: 28 Sep 2021

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At a glance

  • Originator CRISPR Therapeutics
  • Developer CRISPR Therapeutics; Massachusetts General Hospital
  • Class Gene therapies; Immunotherapies; T lymphocyte 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

  • No development reported Haematological malignancies; Solid tumours

Most Recent Events

  • 28 Sep 2021 No recent reports of development identified for research development in Haematological-malignancies in USA (Parenteral)
  • 28 Sep 2021 No recent reports of development identified for research development in Solid-tumours in USA (Parenteral)
  • 22 Aug 2017 CRISPR Therapeutics enters into a two-year research collaboration and license option agreement with Massachusetts General Hospital to develop novel T-cell therapies for Cancer

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