The purpose of this study is to evaluate the safety and efficacy of two dose levels of ONO-4578 with Opdivo® when added to mFOLFOX6 and bevacizumab versus SOC as first-line treatment for advanced CRC.
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Overall Response Rate (ORR) per Blinded Independent Central Review (BICR)
Timeframe: From randomization to the end of treatment (Up to 39 months)
Number of participants with Adverse Events (AEs)
Timeframe: From first dose to 28 days post last dose
Number of participants with Serious Adverse Events (SAEs)
Timeframe: From first dose to 28 days post last dose
North America Clinical Trial Support Desk