DT-678 is under clinical development by Diapin Therapeutics and currently in Phase I for Peripheral Arterial Disease (PAD)/ Peripheral Vascular Disease (PVD). According to GlobalData, Phase I drugs for Peripheral Arterial Disease (PAD)/ Peripheral Vascular Disease (PVD) have an 89% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how DT-678’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.
DT-678 overview
DT-678 is under development as antiplatelet agents to prevent atherothrombotic events in cardiovascular, cerebrovascular and peripheral vascular disease, peripheral artery disease. The drug candidate is mixed disulphide conjugate of clopidogrel with 3-nitropyridine-2-thiol. It is administered through oral route.
For a complete picture of DT-678’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.
