{"description":"Adverse events (AEs) for Cohorts A and B were analyzed together as prespecified in SAP. All-Cause Mortality is reported for all enrolled participants, regardless of whether or not they received study drug. SAEs and non-serious AEs are reported only for those participants who received at least one dose of study drug.","eventGroups":[{"deathsNumAffected":54,"deathsNumAtRisk":86,"description":"Participants received Tucatinib 300 mg PO BID on Days 1 to 21 of each 21-day cycle. Trastuzumab 8 mg/kg by IV infusion on Day 1 of Cycle 1 and 6 mg/kg on Day 1 of each subsequent cycle until PD, death, withdrawal of consent, study closure, or alternative therapy.","id":"EG000","otherNumAffected":82,"otherNumAtRisk":86,"seriousNumAffected":20,"seriousNumAtRisk":86,"title":"Tucatinib+Trastuzumab (Cohorts A+B)"},{"deathsNumAffected":2,"deathsNumAtRisk":31,"description":"Participants received Tucatinib 300 mg PO BID on Days 1 to 21 of each 21-day cycle. 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