Cellular Immunotherapy for Oncology 1 is under clinical development by GenoImmune Therapeutics Biotechnology and currently in Phase I for Gastric Cancer. According to GlobalData, Phase I drugs for Gastric Cancer have a 74% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Cellular Immunotherapy for Oncology 1’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.
Cellular Immunotherapy for Oncology 1 overview
Cellular immunotherapy is under investigation for the treatment of advanced solid tumors including metastatic melanoma, colorectal cancer, gastric cancer, esophageal cancer, squamous cell carcinoma of the lung, cholangiocarcinoma, non-small cell lung cancer and renal cell carcinoma. It is administered as intravenous infusion in form of suspension. The therapy comprises of tumor specific antigen induced cytotoxic lymphocyte.
The therapeutic candidate was under development for the treatment of triple negative breast cancer.
GenoImmune Therapeutics Biotechnology overview
GenoImmune Therapeutics Biotechnology is a biotechnology company that specialises in the therapy of tumour immune cells. The company is Headquartered in China.
For a complete picture of Cellular Immunotherapy for Oncology 1’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.
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.
