Vorbipiprant sodium is under clinical development by Rottapharm Biotech and currently in Phase II for Gastrointestinal Tumor. According to GlobalData, Phase II drugs for Gastrointestinal Tumor does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Vorbipiprant sodium LoA Report. 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.
Vorbipiprant sodium overview
Vorbipiprant sodium (CR-6086) is under development for the treatment of rheumatoid arthritis and pMMR-MSS Metastatic Colorectal Cancer, adenocarcinoma of the gastroesophageal junction, gastrointestinal tumor.. It is orally administered as a form of capsule. The drug candidate is a prostaglandin E receptor 4 (EP4 or prostaglandin E2 receptor EP4 subtype) antagonist. It was also under development for osteoarthritis.
Rottapharm Biotech overview
Rottapharm Biotech (Rottapharm), a subsidiary of Fidim Srl is a research company focused on the discovery and development of innovative drugs. The company’s pipeline products include CR4056, 12 ligand for analgesia; CR6086 which is a EP4 receptor antagonist for immunomodulation in RA; CR6086 a EP4 receptor antagonist for immuno-oncology; CR13626 for glioblastoma; CR10049 an Inflammatory OA disease modification; CR14629 which is a metabolic OA disease modification. Rottapharm develops therapies based on its proprietary technology platform for the generation and selection of monoclonal antibodies. Rottapharm is headquartered in Monza, Italy.
For a complete picture of Vorbipiprant sodium’s drug-specific PTSR and LoA scores, buy the report here.
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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.
