CBP-1019 is under clinical development by Coherent Biopharma and currently in Phase II for Solid Tumor. According to GlobalData, Phase II drugs for Solid Tumor have a 21% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how CBP-1019’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.

CBP-1019 overview

CBP-1019 is under development for the treatment of lung cancer, non-small cell lung cancer, small-cell lung cancer, colorectal cancer and pancreatic cancer. It is administered through intravenous route. The drug candidate is a FR Alpha/TRPV6 bispecific ligand drug conjugated to exatecan.

Coherent Biopharma overview

Coherent Biopharma is a clinical-stage biopharmaceutical company engaged in development and commercialization of bi-targeting XDC drugs which are targets tumor ligand-mediated drugs and tumor markers. The company is headquartered in Suzhou, Jiangsu, China.

For a complete picture of CBP-1019’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 7 February 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.