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SPR3 is a preclinical-stage small molecule inhibitor of the C-C chemokine receptor type 2 (CCR2), being developed by Sporos BioDiscovery. CCR2 is a critical signaling node that facilitates the recruitment of myeloid-derived suppressor cells (MDSCs) and the conversion of neutrophils into immunosuppressive MDSCs, which can lead to resistance against MAPK pathway inhibitors and immunotherapy. By blocking CCR2, SPR3 aims to prevent these bypass mechanisms, particularly in KRAS-mutant cancers, thereby restoring or enhancing the efficacy of standard-of-care treatments.
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