IM-96 is under clinical development by Beijing Immunochina Pharmaceuticals and currently in Phase I for Metastatic Colorectal Cancer. According to GlobalData, Phase I drugs for Metastatic Colorectal Cancer have an 84% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how IM-96’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.

IM-96 overview

IM-96 is under development for the treatment of colorectal cancer, metastatic colorectal cancer, metastatic pancreatic cancer, gastric cancer, esophageal cancer and small intestinal cancer. The therapeutic candidate comprises of T-cells genetically modified to express a chimeric antigen receptor (CAR). The drug candidate is administered through parenteral route.

Beijing Immunochina Pharmaceuticals overview

Beijing Immunochina Pharmaceuticals (Immunochina) develops chimeric antigen receptor (CAR-T) cell molecules for the treatment of cancer. The company’s pipeline products include IM19, IM21, INS21(InstanCART), IM83, IM18, IM92, IM96. Its pipeline candidates treat diffuse large B cell lymphoma, B-cell acute lymphoblastic leukemia, mantle cell lymphoma (MCL), multiple myeloma, hepatocellular carcinoma, melanoma, gastric cancer & pancreatic cancer and carcinoma of colon and rectum. Immunochina utilizes its proprietary CAR-T technology platform to develop novel CAR-T therapeutics. Immunochina is headquartered in Beijing, China.

For a complete picture of IM-96’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 16 July 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.