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Treatment was continued until disease progression, unacceptable toxicity, or treatment discontinuation for other reasons.","id":"EG001","otherNumAffected":10,"otherNumAtRisk":10,"seriousNumAffected":8,"seriousNumAtRisk":10,"title":"Phase 1: 20 mg Selpercatinib BID"},{"deathsNumAffected":0,"deathsNumAtRisk":16,"description":"Participants received Selpercatinib 40 milligrams (mg) administered orally twice daily (BID), in a 28-day treatment cycle. Treatment was continued until disease progression, unacceptable toxicity, or treatment discontinuation for other reasons.","id":"EG002","otherNumAffected":16,"otherNumAtRisk":16,"seriousNumAffected":9,"seriousNumAtRisk":16,"title":"Phase 1: 40 mg Selpercatinib BID"},{"deathsNumAffected":0,"deathsNumAtRisk":12,"description":"Participants received Selpercatinib 60 milligrams (mg) administered orally twice daily (BID), in a 28-day treatment cycle. Treatment was continued until disease progression, unacceptable toxicity, or treatment discontinuation for other reasons.","id":"EG003","otherNumAffected":12,"otherNumAtRisk":12,"seriousNumAffected":7,"seriousNumAtRisk":12,"title":"Phase 1: 60 mg Selpercatinib BID"},{"deathsNumAffected":0,"deathsNumAtRisk":1,"description":"Participants received Selpercatinib 160 milligrams (mg) administered orally once daily (QD), in a 28-day treatment cycle. Treatment was continued until disease progression, unacceptable toxicity, or treatment discontinuation for other reasons.","id":"EG004","otherNumAffected":1,"otherNumAtRisk":1,"seriousNumAffected":1,"seriousNumAtRisk":1,"title":"Phase 1: 160 mg Selpercatinib QD"},{"deathsNumAffected":0,"deathsNumAtRisk":20,"description":"Participants received Selpercatinib 80 milligrams (mg) administered orally twice daily (BID), in a 28-day treatment cycle. Treatment was continued until disease progression, unacceptable toxicity, or treatment discontinuation for other reasons.","id":"EG005","otherNumAffected":20,"otherNumAtRisk":20,"seriousNumAffected":13,"seriousNumAtRisk":20,"title":"Phase 1: 80 mg Selpercatinib BID"},{"deathsNumAffected":0,"deathsNumAtRisk":19,"description":"Participants received Selpercatinib 120 milligrams (mg) administered orally twice daily (BID), in a 28-day treatment cycle. Treatment was continued until disease progression, unacceptable toxicity, or treatment discontinuation for other reasons.","id":"EG006","otherNumAffected":19,"otherNumAtRisk":19,"seriousNumAffected":11,"seriousNumAtRisk":19,"title":"Phase 1: 120 mg Selpercatinib BID"},{"deathsNumAffected":0,"deathsNumAtRisk":764,"description":"Participants received Selpercatinib 160 milligrams (mg) administered orally twice daily (BID), in a 28-day treatment cycle. Treatment was continued until disease progression, unacceptable toxicity, or treatment discontinuation for other reasons.","id":"EG007","otherNumAffected":764,"otherNumAtRisk":764,"seriousNumAffected":380,"seriousNumAtRisk":764,"title":"Phase 1: 160 mg Selpercatinib BID"},{"deathsNumAffected":0,"deathsNumAtRisk":3,"description":"Participants received Selpercatinib 200 milligrams (mg) administered orally twice daily (BID), in a 28-day treatment cycle. Treatment was continued until disease progression, unacceptable toxicity, or treatment discontinuation for other reasons.","id":"EG008","otherNumAffected":3,"otherNumAtRisk":3,"seriousNumAffected":3,"seriousNumAtRisk":3,"title":"Phase 1: 200 mg Selpercatinib BID"},{"deathsNumAffected":0,"deathsNumAtRisk":6,"description":"Participants received Selpercatinib 240 milligrams (mg) administered orally twice daily (BID), in a 28-day treatment cycle. Treatment was continued until disease progression, unacceptable toxicity, or treatment discontinuation for other reasons.","id":"EG009","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":3,"seriousNumAtRisk":6,"title":"Phase 1: 240 mg Selpercatinib BID"},{"deathsNumAffected":147,"deathsNumAtRisk":307,"description":"Participants with Rearranged during transfection (RET) Fusion solid tumor progressed on/intolerant to standard first line therapy received Selpercatinib 160 milligrams (mg) administered orally twice daily (BID), in a continuous 28-day treatment cycle. Treatment was continued until disease progression, unacceptable toxicity, or treatment discontinuation for other reasons.","id":"EG010","otherNumAffected":307,"otherNumAtRisk":307,"seriousNumAffected":187,"seriousNumAtRisk":307,"title":"Phase 2, Cohort 1: RET Fusion Solid Tumor"},{"deathsNumAffected":27,"deathsNumAtRisk":74,"description":"Participants with RET Fusion solid tumor without standard first line therapy received Selpercatinib 160 milligrams (mg) administered orally twice daily (BID), in a continuous 28-day treatment cycle. Treatment was continued until disease progression, unacceptable toxicity, or treatment discontinuation for other reasons.","id":"EG011","otherNumAffected":74,"otherNumAtRisk":74,"seriousNumAffected":39,"seriousNumAtRisk":74,"title":"Phase 2, Cohort 2: RET Fusion Solid Tumor Without Standard Therapy"},{"deathsNumAffected":67,"deathsNumAtRisk":143,"description":"Participants with RET mutant medullary thyroid cancer (MTC) progressed on/intolerant to standard first line therapy received Selpercatinib 160 milligrams (mg) administered orally twice daily (BID), in a continuous 28-day treatment cycle. Treatment was continued until disease progression, unacceptable toxicity, or treatment discontinuation for other reasons.","id":"EG012","otherNumAffected":143,"otherNumAtRisk":143,"seriousNumAffected":93,"seriousNumAtRisk":143,"title":"Phase 2, Cohort 3: RET Mutant MTC"},{"deathsNumAffected":18,"deathsNumAtRisk":116,"description":"Participants with RET mutant MTC without prior standard first line therapy or other kinase inhibitor(s) with anti-RET activity received Selpercatinib 160 milligrams (mg) administered orally twice daily (BID), in a continuous 28-day treatment cycle. Treatment was continued until disease progression, unacceptable toxicity, or treatment discontinuation for other reasons.","id":"EG013","otherNumAffected":116,"otherNumAtRisk":116,"seriousNumAffected":65,"seriousNumAtRisk":116,"title":"Phase 2, Cohort 4: RET Mutant MTC Without Standard Therapy"},{"deathsNumAffected":83,"deathsNumAtRisk":201,"description":"Participants with RET altered solid tumor (cohorts 1-4, disease not measurable; MTC not eligible for Cohort 3 or 4; MTC syndrome spectrum cancer; circulating free tumor DNA \\[cfDNA+\\] for RET alteration not known to be present in tumor) received Selpercatinib 160 milligrams (mg) administered orally twice daily (BID), in a continuous 28-day treatment cycle. Treatment was continued until disease progression, unacceptable toxicity, or treatment discontinuation for other reasons.","id":"EG014","otherNumAffected":201,"otherNumAtRisk":201,"seriousNumAffected":114,"seriousNumAtRisk":201,"title":"Phase 2, Cohort 5: Advanced RET Altered Solid Tumor"},{"deathsNumAffected":8,"deathsNumAtRisk":16,"description":"Participants otherwise eligible for Cohorts 1-5 who discontinued other RET inhibitors received Selpercatinib 160 milligrams (mg) administered orally twice daily (BID), in a continuous 28-day treatment cycle. Treatment was continued until disease progression, unacceptable toxicity, or treatment discontinuation for other reasons.","id":"EG015","otherNumAffected":16,"otherNumAtRisk":16,"seriousNumAffected":8,"seriousNumAtRisk":16,"title":"Phase 2, Cohort 6: RET Inhibitor-Discontinued Participants"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 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