Rademikibart is under clinical development by Suzhou Connect Biopharmaceuticals and currently in Phase II for Asthma. According to GlobalData, Phase II drugs for Asthma have a 27% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Rademikibart’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.
Rademikibart overview
CBP-201 is under development for the treatment of allergic inflammation such as asthma, atopic dermatitis, chronic obstructive pulmonary disease (COPD). The drug candidate is a human monoclonal IgG4 monoclonal antibody that binds to IL-4R alpha. It is administered as subcutaneous or intravenous injection. It was also under development for nasal polyps.
It was also under development for the treatment of chronic rhinosinusitis with with nasal polyps, food allergy, eosinophilic esophagitis.
Suzhou Connect Biopharmaceuticals overview
Suzhou Connect Biopharmaceuticals (Connect Biopharmaceuticals) is a Bio pharmaceutical company that discovers and develops next-generation immune modulators for the treatment of autoimmune diseases and inflammation. The company’s pipeline Product portfolio includes CBP-307 is an orally-active small molecule used for the treatment of ulcerative colitis (UC) and Crohn’s disease (CD); CBP-201 is an antibody for asthma and atopic dermatitis; and CBP-174 is a small molecule inhibitor for the treatment of chronic skin inflammation. Connect Biopharmaceuticals serves in the therapeutic areas of inflammatory bowel disease, psoriasis, multiple sclerosis and other autoimmune diseases. Connect Biopharmaceuticals is headquartered in Taicang, Jiangsu, China.
For a complete picture of Rademikibart’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.
