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Tislelizumab - BeiGene

Drug Profile

Tislelizumab - BeiGene

Alternative Names: BGB-A317

Latest Information Update: 24 Jan 2020

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At a glance

  • Originator BeiGene
  • Developer BeiGene; Celgene Corporation
  • Class Antineoplastics; Immunotherapies; Monoclonal antibodies
  • Mechanism of Action Antibody-dependent cell cytotoxicity; Programmed cell death-1 receptor antagonists; T lymphocyte stimulants
  • Orphan Drug Status

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

  • New Molecular Entity Yes

Highest Development Phases

  • Registered Hodgkin's disease
  • Preregistration Urogenital cancer
  • Phase III Cancer; Gastric cancer; Liver cancer; Nasopharyngeal cancer; Non-small cell lung cancer; Oesophageal cancer; Small cell lung cancer
  • Phase II Chronic lymphocytic leukaemia; Lung cancer; Lymphoma; Solid tumours
  • Phase I Ovarian cancer; Renal cancer

Most Recent Events

  • 24 Feb 2020 BeiGene plans a phase I/II trial for BGB 10188 and tislelizumab in mature B-cell lymphoma and Solid tumours (Combination therapy, Monotherapy, Metastatic disease, Second-line therapy) (PO) in March 2020 (NCT04282018)
  • 21 Jan 2020 BeiGene intends to file sNDA for Non-small cell lung cancer (First-line therapy) with NMPA in China
  • 21 Jan 2020 BeiGene intends to meet with Center for Drug Evaluation (CDE) at the National Medical Products Administration (NMPA) in China to discuss the possibility of a supplemental new drug application (sNDA) submission for tislelizumab for Non-small cell lung cancer (First-line therapy)
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