CYP-001 is under clinical development by Fujifilm and currently in Phase I for Graft Versus Host Disease (GVHD). According to GlobalData, Phase I drugs for Graft Versus Host Disease (GVHD) have an 89% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how CYP-001’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. 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.

CYP-001 overview

CYP-001 is under development for the treatment of steroid-resistant graft versus host disease, respiratory failure and acute respiratory distress syndrome associated with coronavirus disease 2019 (COVID-19). The therapeutic candidate is administered as an intravenous infusion. It is developed based on Cymerus platform stem cell technology.

Fujifilm overview

Fujifilm designs, manufactures, and markets healthcare solutions, material solutions, document solutions and imaging systems. The company offers document solutions such as office products, office printers, and allied production services and global services. Its major products include color films, color paper and chemicals, photofinishing equipment, electronic imaging and optical devices, TV camera lenses, security lenses, healthcare products, graphic systems, flat panel display materials, recording media and industrial products. Fujifilm also offers equipment and materials for medical systems, cell culture media and reagents, pharmaceuticals, cosmetics, and supplements. The company serves individual consumers and business enterprises. The company has business presence in the Americas, Europe, and Asia-Pacific. Fujifilm is headquartered in Minato-Ku, Tokyo, Japan.

For a complete picture of CYP-001’s drug-specific PTSR and LoA scores, buy the report here.

GlobalData

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 its clinical pathway (PTSR), as well as how likely the drug will be approved (LoA). This is based on a proprietary algorithm built from the drugs’ sales forecast, regulatory milestones, cost forecasts, WACC rate and other proprietary data sources found on GlobalData’s Pharmaceutical Intelligence Center.