(Clofutriben + prednisolone) is under clinical development by Sparrow Pharmaceuticals and currently in Phase II for Polymyalgia Rheumatica (PMR). According to GlobalData, Phase II drugs for Polymyalgia Rheumatica (PMR) have a 75% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how (Clofutriben + prednisolone)’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.
(Clofutriben + prednisolone) overview
Sparrow Pharmaceuticals overview
Sparrow Pharmaceuticals is a clinical-stage biopharmaceutical company that develops novel therapies for endocrinology and rheumatology diseases. The company’s pipeline products include SPI-62 and SPI-47. Its SPI-62 is an oral, small molecule, highly potent and selective new chemical entity HSD-1 inhibitor that treats conditions of excess cortisol including endogenous Cushing’s syndrome and autonomous cortisol secretion (ACS). The company’s SPI-47 is an HSD-1 inhibitor that treats polymyalgia rheumatica (PMR). Sparrow Pharmaceuticals is headquartered in Portland, Oregon, the US.
For a complete picture of (Clofutriben + prednisolone)’s drug-specific PTSR and LoA scores, buy the report here.
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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.
