Barzolvolimab is under clinical development by Celldex Therapeutics and currently in Phase II for Prurigo. According to GlobalData, Phase II drugs for Prurigo have a 67% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Barzolvolimab’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.
Barzolvolimab overview
Barzolvolimab (CDX-0159) is under development for the treatment of chronic spontaneous urticaria (CSU), chronic inducible urticaria (CIndU), eosinophilic esophagitis (EoE), prurigo nodularis and atopic dermatitis. The drug candidate is a second generation version of CDX-0158 (fragment crystallizable (Fc) portion of CDX-0158 antibody). It acts by targeting tyrosine protein kinase Kit. It is administered through intravenous and subcutaneous route in the form of suspension or solution.
The drug candidate was also under development for the treatment of unspecified cancer.
Celldex Therapeutics overview
Celldex Therapeutics (Celldex) is a bio-pharmaceutical company that discovers, develops, and commercializes targeted immunotherapy and other biologics for the treatment of various types of cancers. The company’s developmental pipeline comprises therapeutic antibodies, antibody drug conjugates (ADCs), protein-based therapeutics, immune system modulators and vaccine for unmet medical needs. Its key products in development include CDX-1140; CDX-527, CDX-0159. It’s products find application in the treatment of various indications such as brain cancer, triple negative breast cancer, lymphoma/leukemia, melanoma, and renal cell carcinoma. It operates a manufacturing facility in Massachusetts, the US, and research laboratories in Massachusetts, New Jersey, and Connecticut. Celldex is headquartered in Hampton, New Jersey, the US.
For a complete picture of Barzolvolimab’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.
