Lorundrostat hydrobromide is under clinical development by Mineralys Therapeutics and currently in Phase III for Hypertension. According to GlobalData, Phase III drugs for Hypertension have a 49% phase transition success rate (PTSR) indication benchmark for progressing into Pre-Registration. GlobalData’s report assesses how Lorundrostat hydrobromide’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.
Lorundrostat hydrobromide overview
Mineralys Therapeutics overview
Mineralys Therapeutics. (Mineralys Therapeutics) is a private, clinical-stage biopharmaceutical company that develops novel therapy for the treatment of hypertension. Mineralys Therapeutics is headquartered in Radnor, Pennsylvania, the US.
For a complete picture of Lorundrostat hydrobromide’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.
