Irodanoprost is under clinical development by Mesentech and currently in Phase I for Duchenne Muscular Dystrophy. According to GlobalData, Phase I drugs for Duchenne Muscular Dystrophy have an 81% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Irodanoprost’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.
Irodanoprost overview
Irodanoprost is under development for the treatment of osteogenesis imperfecta, duchenne muscular dystrophy, facioscapulohumeral muscular dystrophy and osteoporosis. The drug candidate acts by targeting PGE2 receptor 4 (EP4).
Mesentech overview
Mesentech is a Pharmaceuticals and Healthcare company that provides Health care and drug Development services. The company is Headquartered in Vancouver, British Columbia, Canada.
For a complete picture of Irodanoprost’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.
