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Participants were to receive study drug until discontinuation due to PD, toxicity, or choice. (Up to \\~66 months)","id":"EG005","otherNumAffected":48,"otherNumAtRisk":53,"seriousNumAffected":18,"seriousNumAtRisk":53,"title":"ICC→Pembrolizumab 2 mg/kg (After Switch to Pembrolizumab)"},{"deathsNumAffected":37,"deathsNumAtRisk":45,"description":"Participants who were initiall randomized to ICC, subsequently experienced confirmed progressive disease (PD) and met all switching criteria at study treatment Week 12, had the opportunity to switch to receive pembrolizumab 2 mg/kg or 10 mg/kg. Participants received pembrolizumab 10 mg/kg IV Q3W. With Amendment 03, this dosing was discontinued and all study participants were to be treated with fixed-dose open label pembrolizumab 200 mg IV Q3W. Participants were to receive study drug until discontinuation due to PD, toxicity, or choice. 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