SRD-002 is under clinical development by Sardocor and currently in Phase II for Diastolic Heart Failure (HFpEF). According to GlobalData, Phase II drugs for Diastolic Heart Failure (HFpEF) does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the SRD-002 LoA Report. 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.
SRD-002 overview
SRD-002 is under development for the treatment of heart failure with preserved ejection fraction (diastolic heart failure/HFpEF). The drug candidate comprises of AAV serotype 1 capsid and the human SERCA2a cDNA flanked by ITRs derived from AAV serotype 2 (AAV1/SERCA2a). It is administered through intracoronary route.
Sardocor overview
Sardocor is developing novel therapeutics for the heart failure. The company is headquartered in Lexington, Massachusetts, the US.
For a complete picture of SRD-002’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.
