EBV-Specific Anti-PD1 TCR-T Cells is under clinical development by TCR Cure Biopharma Technology and currently in Phase II for Recurrent Head And Neck Squamous Cell Carcinoma. According to GlobalData, Phase II drugs for Recurrent Head And Neck Squamous Cell Carcinoma have a 33% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how EBV-Specific Anti-PD1 TCR-T Cells’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
EBV-Specific Anti-PD1 TCR-T Cells overview
The therapeutic candidate is under development for the treatment of metastatic or recurrent EBV (Epstein-Barr virus) positive head and neck squamous cell carcinoma (HNSCC). It comprises of autologous T cells genetically engineered to express T cell receptor (TCR) targeting cells expressing programmed cell death protein 1 (PD1). It is administered through parenteral route.
TCR Cure Biopharma Technology overview
TCR Cure Biopharma Technology (Tiankeya), a cutting-edge company in the field of immune cell therapy. The company is headquartered in China.
For a complete picture of EBV-Specific Anti-PD1 TCR-T Cells’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.
