SCP-776 is under clinical development by Silver Creek Pharmaceuticals and currently in Phase I for Myocardial Infarction. According to GlobalData, Phase I drugs for Myocardial Infarction have an 89% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how SCP-776’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.
SCP-776 overview
SCP-776 is under development for the treatment of acute ischemic stroke, post-cardiac arrest brain injury, ST-elevation myocardial infarction (STEMI), chemical-induced lung injury and kidney injury. It is administered through parenteral and intravenous route. The therapeutic candidates act by targeting the insulin-like growth factor-1 receptor. The therapeutic candidates comprise of protein which is modified by fusing them to insulin-like growth factor-1 and Annexin A5 (AnxV).
It was also under development for congestive heart failure.
Silver Creek Pharmaceuticals overview
Silver Creek Pharmaceuticals (Silver Creek) is a clinical-stage biotechnology that discovers and develops targeted protein therapeutics. The company’s pipeline products include scp776, scp787 and scp791. Its pipeline products therapeutic areas include acute ischemic stroke, cosmetic dermatology applications and Parkinson’s disease. The company designs smart growth factors technology (SGF), a new platform of bio-therapeutics with improved pharmacodynamics, pharmacokinetics and accumulation, improving drug-like properties to optimize as cardioprotective therapeutics. Silver Creek is headquartered in San Francisco, California, the US.
For a complete picture of SCP-776’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.
