NVK-004 is under clinical development by Nevakar Injectables and currently in Pre-Registration for Unspecified Cardiovascular Disorders. According to GlobalData, Pre-Registration drugs for Unspecified Cardiovascular Disorders does not have sufficient historical data to build an indication benchmark PTSR for Pre-Registration. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the NVK-004 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.
NVK-004 overview
NVK-004 is under development for the treatment of unspecified cardiovascular disorders. The drug candidate is administered as a sterile injection.
Nevakar Injectables overview
Nevakar Injectables focuses on providing critical patient care, acute pain management, long acting injectables and hospital infections products. Nevakar Injectables is headquartered in Bridgewater, New Jersey, the US.
For a complete picture of NVK-004’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.
