BRB-002 is under clinical development by Bitterroot Bio and currently in Phase I for Atherosclerosis. According to GlobalData, Phase I drugs for Atherosclerosis have a 64% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how BRB-002’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.

BRB-002 overview

BRB-002 is under development for the treatment of atherosclerotic cardiovascular disease (ASCVD) and vascular inflammation. The therapeutic candidate acts by targeting CD47. It is administered through subcutaneous route.

Bitterroot Bio overview

Bitterroot Bio focuses on developing and delivering novel immunotherapies for the treatment of cardiovascular diseases. The company is headquartered in Palo Alto, California, the US.

For a complete picture of BRB-002’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.