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Research programme: Allogeneic gene-edited chimeric antigen receptors T-cell therapy - Allogene Therapeutics/Cellectis/Servier

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Drug Profile

Research programme: Allogeneic gene-edited chimeric antigen receptors T-cell therapy - Allogene Therapeutics/Cellectis/Servier

Alternative Names: AlloCAR T; UCART 38; UCART CLL1

Latest Information Update: 28 Sep 2023

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At a glance

  • Originator Cellectis
  • Developer Cellectis; Pfizer; Servier
  • 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

Highest Development Phases

  • No development reported Acute myeloid leukaemia; Blastic plasmacytoid dendritic cell neoplasm; Multiple myeloma; Solid tumours

Most Recent Events

  • 28 Sep 2023 No recent reports of development identified for preclinical development in Solid-tumours in France (Parenteral)
  • 28 Mar 2022 No recent reports of development identified for preclinical development in Acute-myeloid-leukaemia in France (Parenteral)
  • 28 Mar 2022 No recent reports of development identified for preclinical development in Blastic-plasmacytoid-dendritic-cell-neoplasm in France (Parenteral)

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