(Dexborneol + edaravone) is under clinical development by Simcere Pharmaceutical Group and currently in Phase I for Acute Ischemic Stroke. According to GlobalData, Phase I drugs for Acute Ischemic Stroke have an 86% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how (Dexborneol + edaravone)’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.
(Dexborneol + edaravone) overview
Dexborneol and Edaravone (Sanbexin) is a fixed dose combination product, acts as a cerebro protective agent. It is formulated as concentrated solution for intravenous route of administration. Sanbexin is indicated for the improvement of neurological symptoms and dysfunction of activities of daily living caused by acute cerebral infarction.
It is also under development for the treatment of intracerebral hemorrhage and acute ischemic stroke. It is administered through sublingual route as a tablet.
Simcere Pharmaceutical Group overview
Simcere Pharmaceutical Group (Simcere) is a pharmaceutical company that discovers, develops, and markets branded generic and prescription pharmaceutical products. The company offers services in therapeutic areas such as anti-tumor, anti-infection, central nervous, cardiovascular, skeletal muscle and others. Simcere’s products are used for the treatment of oncology, infectious diseases, neurology, anti-inflammation and also cardiovascular diseases. The company conducts research and development focused on low-end generics and APIs for innovative medicines. Simcere is headquartered in Nanjing, Jiangsu, China
For a complete picture of (Dexborneol + edaravone)’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.
