Futibatinib is under clinical development by Otsuka Pharmaceutical and currently in Phase II for Esophageal Squamous Cell Carcinoma (ESCC). According to GlobalData, Phase II drugs for Esophageal Squamous Cell Carcinoma (ESCC) have a 56% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Futibatinib’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
Smarter leaders trust GlobalData
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.
Futibatinib overview
Futibatinib (Lytgobi) is an anticancer agent. It is formulated as a film-coated tablets for oral route of administration, Lytgobi is indicated for the treatment of adult patients with previously treated, unresectable, locally advanced, or metastatic intrahepatic cholangiocarcinoma harboring fibroblast growth factor receptor 2 (FGFR2) gene fusions or other rearrangements.
TAS-120 (futibatinib) is under development for the treatment of solid tumors including advanced or metastatic urothelial carcinoma, intrahepatic cholangiocarcinoma (icca), extrahepatic cholangiocarcinoma, unspecified cancer (FGFR aberrations cancer), HER2-negative metastatic breast cancer, HR positive metastatic breast cancer and triple-negative breast cancer, breast cancer, urothelial carcinoma, metastatic gastric cancer, gastro esophageal junction cancer, pancreatic ductal adenocarcinoma (PDAC), esophageal squamous cell carcinoma, metastatic hepatocellular carcinoma, metastatic microsatellite stable endometrial carcinoma, myeloid and lymphoid neoplasms. The drug candidate is administered orally. It is a small molecule acts by targeting fibroblast growth factor receptors (FGFRs).
It was also under development for squamous cell lung cancer harboring FGFR1 gene amplification, multiple myeloma, glioblastoma, anaplastic astrocytoma, anaplastic oligodendroglioma, non-small cell lung cancer
Otsuka Pharmaceutical overview
Otsuka Pharmaceutical (OPC), a subsidiary of Otsuka Holdings Co Ltd, is a manufacturer and supplier of pharmaceuticals, food products, clinical testing, and medical equipment. The company develops formulations for the diagnosis and treatment of central nervous system, oncology, cardiovascular and renal, gastrointestinal, ophthalmology disorders and infectious diseases through its pharmaceutical business. Its nutraceutical segment offers rehydration, nutrition, vitamin supplements and cosmetics. OPC is investigating drugs for psychiatry and neurology; oncology; cardiovascular and other therapeutic indications in collaboration with academia and venture companies. The company operates branch offices, research facilities and factories in Japan. OPC is headquartered in Chiyoda-ku, Tokyo, Japan.
For a complete picture of Futibatinib’s drug-specific PTSR and LoA scores, buy the report here.
Data Insights
From
The gold standard of business intelligence.
Blending expert knowledge with cutting-edge technology, GlobalData’s unrivalled proprietary data will enable you to decode what’s happening in your market. You can make better informed decisions and gain a future-proof advantage over your competitors.
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.
