Flonoltinib maleate is under clinical development by Chengdu Zenitar Biomedical Technology and currently in Phase II for Coronavirus Disease 2019 (COVID-19). According to GlobalData, Phase II drugs for Coronavirus Disease 2019 (COVID-19) have a 76% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Flonoltinib maleate’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.
Flonoltinib maleate overview
Flonoltinib maleate is under development for the treatment essential thrombocythemia (ET), primary myelofibrosis, post-essential thrombocythemia myelofibrosis (Post-ET MF), post-polycythemia vera myelofibrosis (PPV-MF), graft vs host disease and covid-19. It is administered by oral route in the form of tablet. The therapeutic candidate acts by targeting Janus Kinase 2 gene, receptor type tyrosine protein kinase FLT3 and cyclin dependent kinase 6 (CDK6).
It was also under development for the treatment of alopecia areata and Hemophagocytic Lymphohistiocytosis.
For a complete picture of Flonoltinib maleate’s drug-specific PTSR and LoA scores, buy the report here.
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