Ropeginterferon alfa-2b LA is under clinical development by PharmaEssentia and currently in Phase II for Myelofibrosis. According to GlobalData, Phase II drugs for Myelofibrosis have a 40% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Ropeginterferon alfa-2b LA’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.
Ropeginterferon alfa-2b LA overview
Ropeginterferon alpha-2b (Besremi) is a long acting interferon. It is formulated as pegylated solution for subcutaneous route of administration. Besremi is indicated as monotherapy in adults for the treatment of polycythaemia vera without symptomatic splenomegaly.
PharmaEssentia overview
PharmaEssentia is a biotechnology company. It operates as a developer of therapeutic products for the treatment of human diseases. The company’s pipeline product includes P1101, a new generation PEG-Interferon-alpha-2b which is developed using the PEGylation technology platform. Its pegylation technology platform is designed to increase the protein drug’s efficacy by prolonging its circulation in the bloodstream. PharmaEssentia’s products are used in the therapeutic areas of dermatology, hematology, infectious diseases and oncology. The company also develops oncology drugs for leukemia, gastric, esophageal, liver, and breast cancer. It collaborates with biotechnology companies, university research institutes and pharmaceutical companies. The company operates in Taiwan, Japan, Hong Kong, Korea, Singapore and China. PharmaEssentia is headquartered in Taipei, Taiwan.
For a complete picture of Ropeginterferon alfa-2b LA’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.
