FIT-003 is under clinical development by Guangzhou FineImmune Biotechnology and currently in Phase I for Solid Tumor. According to GlobalData, Phase I drugs for Solid Tumor have a 70% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how FIT-003’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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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.
FIT-003 overview
FIT-003 is under development for the treatment of metastatic solid tumors and unspecified cancer. It comprises of tumor associated lymph node T cells and is administered through parenteral route.
Guangzhou FineImmune Biotechnology overview
Guangzhou Fanen Biotechnology Co Ltd is engaged in the development of solid tumour immunotherapy medications and associated companies. The company is headquartered in China.
For a complete picture of FIT-003’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.
