YSON-001 is under clinical development by Yisheng Biopharma and currently in Phase I for Solid Tumor. According to GlobalData, Phase I drugs for Solid Tumor have a 54% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how YSON-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.
YS-ON-001 is under development for the treatment of hepatocellular carcinoma, pancreatic cancer, breast cancer, metastatic breast cancer, lung cancer, liver cancer, melanoma, colorectal cancer, prostate cancer and other solid tumors. It is administered as an intramuscular injection. It is developed based on PIKA adjuvant technology. Vaccine composed of inactivated rabies vaccine (RV-V) and polyinosinic-polycytidylic acid (poly IC; poly I-C), an immunostimulant and Toll-like receptor 3 (TLR3) agonist.
Yisheng Biopharma overview
Yisheng Biopharma (Yisheng Biopharma Co) is a global, fully integrated bio-pharmaceutical company. The company is headquartered in Beijing, Beijing, China.
For a complete picture of YSON-001’s drug-specific PTSR and LoA scores, buy the report here.