{"denoms":[{"counts":[{"groupId":"OG000","value":"0"},{"groupId":"OG001","value":"0"}],"units":"Participants"}],"description":"An Adverse Event (AE) is defined as any new untoward medical occurrence or worsening of a preexisting medical condition in a clinical investigation participant administered study treatment and that does not necessarily have a causal relationship with this treatment.","groups":[{"description":"Part 2A were planned to evaluate BMS-986466 in combination with adagrasib in KRAS G12C-mutant (G12C inhibitor treatment-naïve) NSCLC participants.","id":"OG000","title":"Part 2A"},{"description":"Part 2B were planned to evaluate BMS-986466 in combination with adagrasib with or without cetuximab in KRAS G12C-mutant(G12C inhibitor treatment-naïve) CRC participants.","id":"OG001","title":"Part 2B"}],"populationDescription":"Participants were not enrolled in Part 2 arm, hence participants analyzed is 0. Prespecified to be collected for Part 2 only","reportingStatus":"POSTED","timeFrame":"From first dose until 100 days after last dose (Up to approximately 5 months)","title":"Part 2- Number of Participants With Adverse Events (AEs)","type":"SECONDARY"}