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CTA 301

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Drug Profile

CTA 301

Alternative Names: CTA-301

Latest Information Update: 28 Sep 2024

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At a glance

  • Originator Nanjing Bioheng Biotech
  • Class Antineoplastics; 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
  • Available For Licensing Yes

Highest Development Phases

  • No development reported Non-Hodgkin's lymphoma; Precursor B-cell lymphoblastic leukaemia-lymphoma

Most Recent Events

  • 28 Sep 2024 No recent reports of development identified for preclinical development in Non-Hodgkin's-lymphoma in China (Parenteral)
  • 28 Sep 2024 No recent reports of development identified for preclinical development in Precursor-B-cell-lymphoblastic-leukaemia-lymphoma in China (Parenteral)
  • 28 Aug 2020 CTA 301 is available for licensing as of 28 Aug 2020. https://www.bioheng.com/en/index.php/contact/investment.html

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