Recombinant Human Erythropoietin Injection is under clinical development by Angde Biotech Pharmaceutical and currently in Phase II for Anemia in Chronic Kidney Disease (Renal Anemia). According to GlobalData, Phase II drugs for Anemia in Chronic Kidney Disease (Renal Anemia) have a 58% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Recombinant Human Erythropoietin Injection’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. 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.
Recombinant Human Erythropoietin Injection overview
Recombinant protein is under development for the treatment of renal anemia. It is administered through parenteral route. The drug candidate comprises of recombinant human erythropoietin and acts by targeting erythropoietin receptor.
For a complete picture of Recombinant Human Erythropoietin Injection’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.
