THN-391 is under clinical development by Therini Bio and currently in Phase I for Dementia. According to GlobalData, Phase I drugs for Dementia have a 77% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how THN-391’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.
THN-391 overview
THN-391 is under development for the treatment of dementia, multiple sclerosis, diabetic macular edema and Alzheimer's disease. The drug candidate targets VEGF and a specific epitope of fibrin that promotes inflammation and oxidation.
Therini Bio overview
Therini Bio, is a biotechnology company that develops novel therapeutics for the treatment of neuroinflammatory diseases. The company is headquartered in United States.
For a complete picture of THN-391’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.
