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Upon progression, participants were allowed to receive treatment with cobimetinib and atezolizumab at the recommended Phase II dose of cobimetinib 60 mg PO on Days 1-21 plus atezolizumab intravenous (IV) infusion at a fixed dose of 840 mg on Day 1 and Day 15 of each 28-day cycle. Treatment continued until disease progression, unacceptable toxicity, death, participant or physician decision to withdraw, or pregnancy, whichever occurred first.","id":"EG002","otherNumAffected":5,"otherNumAtRisk":6,"seriousNumAffected":3,"seriousNumAtRisk":6,"title":"A: Cobimetinib"},{"deathsNumAffected":11,"deathsNumAtRisk":16,"description":"Participants received cobimetinib PO daily on Days 1-21 of each 28-day cycle plus venetoclax PO daily on Days 1-28 of each 28-day cycle, at the dose level identified in the safety run-in phase. Treatment continued until disease progression, unacceptable toxicity, death, participant or physician decision to withdraw, or pregnancy, whichever occurred first.","id":"EG003","otherNumAffected":15,"otherNumAtRisk":16,"seriousNumAffected":12,"seriousNumAtRisk":16,"title":"B: Cobimetinib + Venetoclax"},{"deathsNumAffected":8,"deathsNumAtRisk":15,"description":"Participants received cobimetinib PO daily on Days 1-21 of each 28-day cycle plus venetoclax PO daily on Days 1-28 of each 28-day cycle, at the dose level identified in the safety run-in phase plus atezolizumab IV infusion at a fixed dose of 840 mg on Day 1 and Day 15 of each 28-day cycle. 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