UTAA09/17-gammadeltaT is under clinical development by PersonGen BioTherapeutics (Suzhou) and currently in Phase I for Mantle Cell Lymphoma. According to GlobalData, Phase I drugs for Mantle Cell Lymphoma have a 74% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how UTAA09/17-gammadeltaT’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.

UTAA09/17-gammadeltaT overview

UTAA09/17-gammadeltaT is under development for the treatment of relapsed and refractory B-cell Non-Hodgkin Lymphoma, B-cell acute lymphocytic leukemia and autoimmune diseases which include systemic lupus erythematosus, systemic sclerosis, Sjogren's syndrome and rheumatoid arthritis, Idiopathic Inflammatory Myopathy (IIM), Primary Sjogren's Syndrome, Immunoglobulin G4-Related Disease (IgG4-RD), Interstitial Lung Diseases (Diffuse Parenchymal Lung Disease), Thrombocytopenia, Primary Biliary Cholangitis (Primary Biliary Cirrhosis). The therapeutic candidate comprises of allogeneic universal, gamma delta T-cells genetically engineered to express chimeric antigen receptors (CAR) targeting cell expressing CD19. It is administered through intravenous 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 UTAA09/17-gammadeltaT’s drug-specific PTSR and LoA scores, buy the report here.

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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.