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RP2 + durvalumab is an investigational combination therapy consisting of RP2, an oncolytic herpes simplex virus type 1 (HSV-1) engineered to express a fusogenic glycoprotein and the immune co-stimulator GM-CSF, combined with durvalumab, a human monoclonal antibody targeting PD-L1. RP2 is designed to selectively replicate in and lyse tumor cells, promoting immunogenic cell death and recruiting immune cells to the tumor microenvironment, while durvalumab blocks PD-L1–mediated immune evasion, thereby enhancing antitumor immune response. This combination aims to synergize direct tumor cell killing with checkpoint blockade immunotherapy to improve clinical outcomes in solid tumors.
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