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Clinical Trial · NCT04939610
A Study of 177Lu-FAP-2286 in Advanced Solid Tumors (LuMIERE)
Overview
Brief Summary: Phase 1 of this study will evaluate the safety and tolerability of 177Lu-FAP-2286 and determine the recommended Phase 2 dose (RP2D) in patients with advanced solid tumors. Phase 2 of this study is designed to evaluate objective response rate (ORR) in patients with specific solid tumors.
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