Drug Profile
Tislelizumab - BeiGene
Alternative Names: BGB-A317; TEVIMBRA; Tilelizumab; Tirelizumab - BeiGene; Tizveni; VDT-482Latest Information Update: 29 Mar 2024
Price :
$50
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At a glance
- Originator BeiGene
- Developer Asieris Pharmaceuticals; BeiGene; Celgene Corporation; HUTCHMED; Leap Therapeutics; Novartis; Tianjin Medical University
- Class Antineoplastics; Immunotherapies; Monoclonal antibodies
- Mechanism of Action Antibody-dependent cell cytotoxicity; Programmed cell death-1 receptor antagonists; T lymphocyte stimulants
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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
- Marketed Hodgkin's disease; Liver cancer; Non-small cell lung cancer; Solid tumours; Squamous cell cancer; Urogenital cancer
- Registered Gastric cancer; Nasopharyngeal cancer
- Preregistration Oesophageal cancer; Small cell lung cancer
- Phase III Cancer
- Phase II Bladder cancer; Cervical cancer; Colorectal cancer; Lung cancer; Lymphoma; Rectal cancer
- Phase I/II Endometrial cancer; Haematological malignancies; Triple negative breast cancer
- No development reported Ovarian cancer; Renal cancer
Most Recent Events
- 19 Mar 2024 BeiGene plans to launch Tislelizumab in the second half of 2024
- 15 Mar 2024 Registered for Squamous cell cancer (Inoperable/Unresectable, Metastatic disease, Second-line therapy or greater, Monotherapy, Late-stage disease) in USA (IV)
- 15 Mar 2024 Adverse events data from the phase III RATIONALE 302 trial in Squamous cell cancer released by BeiGene