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A Phase I, Open Label, Multicenter Study to Evaluate the Safety and Efficacy of PUR001 Administered Intravenously in Adult Patients With Advanced Solid Tumors
This is a Phase I, First-In-Human, open label, dose escalation study to evaluate the safety, tolerability, pharmacokinetics, and preliminary anti-cancer activity of PUR001, an anti-CD39 monoclonal antibody, in adult patients with advanced solid tumors, as monotherapy. A "3+3" design will be used to determine MTD and RP2D. .
100 Clinical Results associated with Purinomia Biotech, Inc.
0 Patents (Medical) associated with Purinomia Biotech, Inc.
100 Deals associated with Purinomia Biotech, Inc.
100 Translational Medicine associated with Purinomia Biotech, Inc.