BBI-825 is under clinical development by Boundless Bio and currently in Phase II for Solid Tumor. According to GlobalData, Phase II drugs for Solid Tumor have a 38% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how BBI-825’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.

BBI-825 overview

BBI-825 is under development for the treatment of solid tumor, gastric and metastatic colorectal cancer. It is administered orally and is being developed based on spyglass platform.

Boundless Bio overview

Boundless Bio is a biopharmaceutical company that discovers and develops drugs for extrachromosomal DNA (ecDNA) based intractable cancer. Its pipeline includes BBI-355, BBI-825, ecDTx 3 and echo. Its pipeline candidates treat extrachromosomal DNA (ecDNA) replication stress, ecDNA assembly and repair, ecDNA segregation, new ecDNA targets and mechanisms, and ecDNA diagnostic It utilizes the spyglass platform, a suite of proprietary ecDNA-driven and pair-matched tumor models with imaging and molecular analytical tools to identify novel oncotargets. The company’s platform technology enables the development of therapies for ecDNA-driven tumors. Boundless Bio is headquartered in San Diego, California, the US.

For a complete picture of BBI-825’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 10 June 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.