IMPT-514 is under clinical development by ImmPACT Bio USA and currently in Phase II for Lupus Nephritis. According to GlobalData, Phase II drugs for Lupus Nephritis have a 50% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how IMPT-514’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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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.
IMPT-514 overview
IMPT-514 is under development for the treatment of systemic lupus erythematosus (SLE) multiple sclerosis (MS) and refractory lupus nephritis. The therapeutic candidate comprises of allogenic T-cells that are genetically modified by transposon transduction to express chimeric antigen receptor (CAR) that targets CD19 and CD20 expressing cells. It uses logic-gate-based CAR T platforms technology. It is administered through intravenous route.
ImmPACT Bio USA overview
ImmPACT-Bio USA Inc (ImmPACT-Bio) is a clinical-stage company that discovers and transforms chimeric antigen receptor (CAR) T-cell therapies to address biological challenges in treating cancer and autoimmune diseases using CAR T-cell platforms. The company’s pipeline products include IMPT-314, IMPT- 514 and TBD. Its pipeline candidates treat aggressive B-cell lymphoma, lupus nephritis, and gastric cancer. The company was funded by Decheng Capital, Foresite Capital, JVC investment partners, Takeda and others. ImmPACT Bio is headquartered in Los Angeles, California, the US.
For a complete picture of IMPT-514’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.
