UTAA-17 is under clinical development by PersonGen BioTherapeutics (Suzhou) and currently in Phase II for Refractory Multiple Myeloma. According to GlobalData, Phase II drugs for Refractory Multiple Myeloma have a 35% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how UTAA-17’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.
UTAA-17 overview
UTAA-17 is under development for the treatment of relapsed and refractory multiple myeloma and autoimmune disorders. The therapeutic candidate comprises gamma delta T cells genetically modified to express universal chimeric antigen receptor (UCAR), which acts by targeting B-cell mature antigen (BCMA). It is administered through parenteral route.
PersonGen BioTherapeutics (Suzhou) overview
PersonGen BioTherapeutics (Suzhou) (PersonGen) is a biotechnology company focused on developing CAR-related therapies, analytical antibodies, novel CAR-T therapeutics, and allogeneic cellular therapies. PersonGen is headquartered in Suzhou, Jiangsu, China.
For a complete picture of UTAA-17’s drug-specific PTSR and LoA scores, buy the report here.
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