CBP-4888 is under clinical development by Comanche Biopharma and currently in Phase I for Pre-Eclampsia. According to GlobalData, Phase I drugs for Pre-Eclampsia does not have sufficient historical data to build an indication benchmark PTSR for Phase I. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the CBP-4888 LoA Report. 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-4888 overview
CBP-4888 is under development for the treatment of pre-eclampsia. They are comprised of conjugated siRNA molecules which act by targeting soluble FLT1 (sFLT1). It is administered by subcutaneous route.
Comanche Biopharma overview
Comanche Biopharma (Comanche) is a preclinical biopharmaceutical company developing novel siRNA molecules for the treatment of preeclampsia. Comanche is headquartered in Concord, Massachusetts, the US.
For a complete picture of CBP-4888’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.
