CT-007 is under clinical development by First Condor Group 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 CT-007’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.
CT-007 overview
CT-007 is under development for the treatment of claudin 18.2 (CLDN18.2) positive solid tumors. The therapeutic candidate comprises of T-cells genetically modified to express chimeric antigen receptor (CAR) and acts by targeting cells expressing claudin 18.2. It is being developed based on second generation CAR-T technology.
First Condor Group overview
First Condor Group is a biotechnology company that is involved in cell storage, production, research and development, and promotion in the fields of cell therapy. The company is headquartered in Dongguan, Guangdong, China.
For a complete picture of CT-007’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.
