Anumigilimab is under clinical development by CSL and currently in Phase I for Coronavirus Disease 2019 (COVID-19). According to GlobalData, Phase I drugs for Coronavirus Disease 2019 (COVID-19) have a 94% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Anumigilimab’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.
Anumigilimab overview
Anumigilimab (CSL324) is under development for the treatment of Coronavirus disease 2019 (COVID-19), cancer, inflammatory diseases associated with neutrophil infiltration including chronic obstructive pulmonary disease (COPD), rheumatoid arthritis, neutrophilic dermatoses, sickle cell disease and palmoplantar pustulosis. It is administered intravenous and subcutaneous route. It is a recombinant monoclonal antibody against the cytokine granulocyte colony stimulating factor receptor.
It was under development for the treatment of community-acquired pneumonia acute respiratory distress syndrome (CAP ARDS) and hidradenitis suppurativa.
CSL overview
CSL is a biotechnology company. It discovers, develops, manufactures, commercializes and distributes biopharmaceuticals. The company’s product portfolio comprises treatments for hemophilia and immune deficiency, vaccines to prevent influenza and therapies for iron deficiency and kidney conditions. CSL‘s proprietary platform consists of plasma and recombinant protein technology, cell and gene therapy and adjuvant cell-based egg-based mRNA. CSL focuses on conditions related to hematology, respiratory, cardiovascular and metabolic, nephrology and transplant, immunology and vaccines, among others. The company operates in various countries including Australia, China, Germany, Switzerland, the US, Hungary, Puerto Rico, the UK, Italy, Japan, the Netherlands and Spain. CSL is headquartered in Melbourne, Victoria, Australia.
For a complete picture of Anumigilimab’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.
