IBI-334 is under clinical development by Innovent Biologics and currently in Phase I for Head And Neck Cancer Squamous Cell Carcinoma. According to GlobalData, Phase I drugs for Head And Neck Cancer Squamous Cell Carcinoma have a 79% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how IBI-334’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.

IBI-334 overview

IBI-334 is under development for the treatment of unresectable, locally advanced or metastatic solid tumors including non-small cell lung cancer, head and neck cancer squamous cell carcinoma, metastatic colorectal cancer and unspecified indication. The drug candidate acts by targeting epidermal growth factor receptor (EGFR) and CD276 antigen (B7 homolog 3 or B7H3). It is a bi-specific monoclonal antibody.

Innovent Biologics overview

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Innovent Biologics is a biopharmaceutical company that carries out the research, development and manufacturing of monoclonal antibodies. It provides products for various diseases such as metabolic, cancer, autoimmune diseases and other therapeutic areas. The company’s oncology products include sintilimab injection, bevacizumab injection, rituximab injection, pemigatinib, olverembatinib, ramucirumab, and others. Its autoimmune drugs are adalimumab injection, IBI-353, IBI-112 and IBI-314, among others. The company’s metabolic and ophthalmology products include IBI-306, IBI-362, IBI-302, IBI-324, IBI-311

For a complete picture of IBI-334’s drug-specific PTSR and LoA scores, buy the report here.