WTX-212 is under clinical development by West Lake Biomedical Technology (Hangzhou) and currently in Phase I for Hodgkin Lymphoma (B-Cell Hodgkin Lymphoma). According to GlobalData, Phase I drugs for Hodgkin Lymphoma (B-Cell Hodgkin Lymphoma) have a 74% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how WTX-212’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.
WTX-212 overview
WTX-212 is under development for the treatment of lung cancer, Hodgkin lymphoma (cHL), primary mediastinal large B-cell lymphoma PMBCL , extranodal NK/T-cell lymphoma ENKTCL, mycosis fungoides/Sezari syndrome MF/SS. The therapy comprises of autologous engineered red blood cells administered as infusion, it is being developed based on red blood cell drug technology platform REDx. It acts by expressing serine protein kinase B-Raf-g469v mutated protein.
West Lake Biomedical Technology (Hangzhou) overview
Westlake Therapeutics a developer of cell therapy intended to treat diseases through cellular medicine, a cell therapy company. It is headquartered in Hangzhou City, Zhejiang, China.
For a complete picture of WTX-212’s drug-specific PTSR and LoA scores, buy the report here.