VS-105 is under clinical development by Vidasym and currently in Phase I for Osteoporosis. According to GlobalData, Phase I drugs for Osteoporosis have a 65% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how VS-105’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.
VS-105 overview
VS-105 is under development for the treatment of osteoporosis, secondary hyperparathyroidism in chronic kidney disease, inflammatory bowel disease, psoriasis. It is administered through oral route. VS-105 acts by targeting vitamin D receptor.
It was under development for diabetic nephropathy, non-alcoholic steatohepatitis (NASH), non alcoholic fatty liver disease (NAFLD).
Vidasym overview
Vidasym operates in pharmaceutical and healthcare industry. It is headquartered in United States.
For a complete picture of VS-105’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.
