ART-001 is under clinical development by ARTham Therapeutics and currently in Phase I for Congenital Vascular Malformation. According to GlobalData, Phase I drugs for Congenital Vascular Malformation 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 ART-001 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.
ART-001 overview
ART-001 is under development for the treatment of refractory vascular malformations such as Klippel Trenaunay syndrome. It is administered through oral route. It acts by targeting phosphatidylinositol 3 kinase (PI3K).
ARTham Therapeutics overview
ARTham Therapeutics (ARTham) is a biopharmaceutical company that develops drugs for the treatment of slow-flow vascular transformations. ARTham company is headquartered in Yokohama, Kanagawa, Japan.
For a complete picture of ART-001’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.
