CT-0525 is under clinical development by CTx Operations 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-0525’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-0525 overview

CT-0525 is under development for the treatment of solid tumors, HER2 positive breast cancer and gastroesophageal junction carcinomas. The drug candidate is being developed based on CAR-M technology that combines chimeric antigen receptor targeting with macrophages to tackle solid tumors. It acts by targeting HER2. The drug candidate is administered through intravenous route.

CTx Operations overview

CTx Operations, formerly Carisma Therapeutics Inc, is a biotechnology service provider that discovers and develops macrophage-based immunotherapeutic for the treatment of cancer. The company product CAR-macrophage platform to provide human macrophages the capability to identify relevant targets to exterminate cancer cells in solid tumors. CTx Operations technology harnesses the latest developments in macrophage biology, chimeric antigen receptor engineering and adoptive cellular therapy to treat multiple diseases in humans. Its portfolio includes CT – 0508 (CAR-Macrophage), CT – 0508 + Pembro (CAR-Macrophage), CT – 1119 (CAR-Monocyte) and CT – 0525 (CAR-Monoctye) which treat mesothelin-positive solid tumors, prostate cancer, neurodegeneration, liver fibrosis and others. CTx Operations is headquartered in Philadelphia, Pennsylvania, the US.

For a complete picture of CT-0525’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 18 April 2024

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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.