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Cosibelimab - Checkpoint Therapeutics

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Drug Profile

Cosibelimab - Checkpoint Therapeutics

Alternative Names: Anti PDL1 monoclonal antibody; CK 301; Cosibelimab-ipdl; TG 1501; UNLOXCYT

Latest Information Update: 18 Dec 2024

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At a glance

  • Originator Dana-Farber Cancer Institute
  • Developer Checkpoint Therapeutics; TG Therapeutics Inc
  • Class Antineoplastics; Immunotherapies; Monoclonal antibodies
  • Mechanism of Action Antibody-dependent cell cytotoxicity; Programmed cell death-1 ligand-1 inhibitors; T lymphocyte stimulants
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    No
  • New Molecular Entity Yes

Highest Development Phases

  • Registered Squamous cell cancer
  • Phase III Non-small cell lung cancer
  • Phase I Cancer
  • Discontinued Chronic lymphocytic leukaemia; Lymphoma; Richter's syndrome

Most Recent Events

  • 17 Dec 2024 Phase-I development in Cancer (Inoperable/Unresectable, Late-stage disease, Metastatic disease, Monotherapy, Recurrent, Treatment-naive) is ongoing in Australia, New Zealand, Poland, Russia, Thailand, South Africa, Ukraine, Spain, France (NCT03212404)
  • 17 Dec 2024 Phase-I development in Squamous-cell-cancer (Metastatic disease) is ongoing in Australia, France (IV), New Zealand (IV), Thailand (IV), Spain (IV), Poland (IV), Russia (IV), Ukraine (IV), South Africa (IV) (NCT03212404)
  • 17 Dec 2024 Planned Prescription Drug User Fee Act (PDUFA) date for Squamous cell cancer (Late-stage disease, Metastatic disease) in USA (IV) is 2024-01-03

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