VIP-943 is under clinical development by Vincerx Pharma and currently in Phase I for Refractory Acute Myeloid Leukemia. According to GlobalData, Phase I drugs for Refractory Acute Myeloid Leukemia have a 68% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how VIP-943’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.
VIP-943 overview
VIP-943 is under development for the treatment of acute myelocytic leukemia, relapsed and refractory acute myeloid leukemia, B-cell acute lymphoblastic leukemia and myelodysplastic syndrome. It is a next generation antibody drug conjugate (ADC) consisting of a humanized anti-IL3RA (CD123) antibody (Ab) linked to kinesin spindle protein inhibitor (KSPi). It acts by targeting cells expressing CD123 on cancer tumors. It is being developed based on VersAptx platform. It is administered through intravenous route.
It was also under development for the treatment of chronic myelocytic leukemia, T-cell acute lymphocytic leukemia and Hodgkin lymphoma.
Vincerx Pharma overview
Vincerx Pharma (Vincera) is a clinical-stage biopharmaceutical company. It focuses on the discovery and development of oncology therapeutics. The company’s products include ENITOCICLIB, a CDK9 inhibitor, and several antibody-drug conjugates (ADCs) such as VIP236, VIP943, VIP924, and others targeting solid tumors. Vincera’s products are also used for the treatment of various types of cancers including diffuse large B-cell lymphoma (DLBCL), non-GCB DLBCL, peripheral T-cell lymphoma, leukemias, myelodysplastic syndrome (MDS), and multiple solid tumors. The company operates in the US. Vincera is headquartered in Santa Clara, California, the US.
For a complete picture of VIP-943’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.
