This is a Phase Ib study that will evaluate the Safety, Tolerability , Pharmacokinetics and Activity of HS-10370 in Combination With Other Anti-cancer Therapies in patients with KRAS G12C mutation advanced or metastatic solid tumors, especially in non-Small cell lung cancer (NSCLC) .
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Number of Participants with Adverse Event(s) (AEs)
Timeframe: From Cycle 1 Day 1 to first documented progression of disease or death from any cause, approximately 2 years.