Cetrelimab is under clinical development by Johnson & Johnson and currently in Phase III for Muscle Invasive Bladder Cancer (MIBC). According to GlobalData, Phase III drugs for Muscle Invasive Bladder Cancer (MIBC) have a 50% phase transition success rate (PTSR) indication benchmark for progressing into Pre-Registration. GlobalData’s report assesses how Cetrelimab’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.
Cetrelimab overview
Cetrelimab (JNJ-63723283) is under development for the treatment of metastatic or surgically unresectable urothelial cancer, chronic hepatitis B, muscle-invasive bladder cancer (MIBC), metastatic castration-resistant prostate cancer (second line and third line) advanced cancers such as colorectal cancer, non-small-cell lung cancer (NSCLC), melanoma, renal cancer, bladder cancer, small-cell lung cancer (SCLC) gastric and esophageal cancer. It is administered through intravenous and subcutaneous route. The therapeutic candidate is a monoclonal antibody and targets programmed cell death protein 1 (PD1). It is a new molecular entity (NME). It was also under development for relapsed and refractory multiple myeloma.
Johnson & Johnson overview
Johnson & Johnson (J&J) researches, develops, manufactures, and sells pharmaceutical products and medical devices. The company conducts business through its operating companies. It provides pharmaceuticals for immune disorders, cancer, neurological disorders, infectious, cardiovascular, and metabolic diseases; and medical devices for use in cardiovascular, orthopaedic, neurovascular care, general surgery and vision care fields. J&J distributes pharmaceutical and medical products to retailers, wholesalers, healthcare professionals and hospitals. The company offers its products in the US; Europe; Asia-Pacific and Africa; and Western Hemisphere (excluding the US) and Latin America. J&J is headquartered in New Brunswick, New Jersey, the US.
For a complete picture of Cetrelimab’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.
