Cadisegliatin is under clinical development by VTv Therapeutics and currently in Phase III for Type 1 Diabetes (Juvenile Diabetes). According to GlobalData, Phase III drugs for Type 1 Diabetes (Juvenile Diabetes) have a 58% phase transition success rate (PTSR) indication benchmark for progressing into Pre-Registration. GlobalData’s report assesses how Cadisegliatin’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.
Cadisegliatin overview
TTP-399 (GK1-399) is under development for the treatment of type 1 diabetes and type 2 diabetes. It is administered through oral route. The drug candidate acts by targeting liver-selective glucokinase (GK). It is developed based on the TTP translational technology.
VTv Therapeutics overview
vTv Therapeutics (vTv) is a pharmaceutical company that discovers, develops, and commercializes human therapeutics. The company’s pipeline product portfolio includes small molecule clinical and pre-clinical drug candidates for the treatment of various human diseases including central nervous system disorders, diabetes and metabolic disorders, inflammation, and cancer. Its products include azeliragon, TTP399, TTP273, HPP593 and HPP737. vTv utilizes TTP translational technology to deliver clinical drug candidates against biological targets including protein-protein interactions, receptor modulators, and enzyme inhibitors. The company collaborates with other pharmaceutical companies to discover and develop small-molecule therapeutics for the treatment of major diseases. vTv is headquartered in High Point, North Carolina, the US.
For a complete picture of Cadisegliatin’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.
