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Subjects continued treatment until an unacceptable toxicity, disease progression, or death.","id":"EG001","otherNumAffected":43,"otherNumAtRisk":43,"seriousNumAffected":17,"seriousNumAtRisk":43,"title":"Biliary Tract Cancer (BTC) (On-Treatment)"},{"deathsNumAffected":0,"deathsNumAtRisk":1,"description":"All subjects enrolled received oral dabrafenib 150 mg bid in combination with oral trametinib 2 mg once daily. Subjects continued treatment until an unacceptable toxicity, disease progression, or death.","id":"EG002","otherNumAffected":1,"otherNumAtRisk":1,"seriousNumAffected":1,"seriousNumAtRisk":1,"title":"Gastrointestinal Stromal Tumor (GIST) (On-Treatment)"},{"deathsNumAffected":1,"deathsNumAtRisk":13,"description":"All subjects enrolled received oral dabrafenib 150 mg bid in combination with oral trametinib 2 mg once daily. Subjects continued treatment until an unacceptable toxicity, disease progression, or death.","id":"EG003","otherNumAffected":12,"otherNumAtRisk":13,"seriousNumAffected":3,"seriousNumAtRisk":13,"title":"Low Grade (WHO G1/G2) Glioma (LGG) (On-Treatment)"},{"deathsNumAffected":2,"deathsNumAtRisk":45,"description":"All subjects enrolled received oral dabrafenib 150 mg bid in combination with oral trametinib 2 mg once daily. Subjects continued treatment until an unacceptable toxicity, disease progression, or death.","id":"EG004","otherNumAffected":42,"otherNumAtRisk":45,"seriousNumAffected":16,"seriousNumAtRisk":45,"title":"High Grade (WHO G3/G4) Glioma (HGG) (On-Treatment)"},{"deathsNumAffected":0,"deathsNumAtRisk":3,"description":"All subjects enrolled received oral dabrafenib 150 mg bid in combination with oral trametinib 2 mg once daily. Subjects continued treatment until an unacceptable toxicity, disease progression, or death.","id":"EG005","otherNumAffected":3,"otherNumAtRisk":3,"seriousNumAffected":0,"seriousNumAtRisk":3,"title":"Adenocarcinoma of the Small Intestine (ASI) (On-Treatment)"},{"deathsNumAffected":4,"deathsNumAtRisk":55,"description":"All subjects enrolled received oral dabrafenib 150 mg bid in combination with oral trametinib 2 mg once daily. Subjects continued treatment until an unacceptable toxicity, disease progression, or death.","id":"EG006","otherNumAffected":55,"otherNumAtRisk":55,"seriousNumAffected":32,"seriousNumAtRisk":55,"title":"Hairy Cell Leukemia (HCL) (On-Treatment)"},{"deathsNumAffected":1,"deathsNumAtRisk":10,"description":"All subjects enrolled received oral dabrafenib 150 mg bid in combination with oral trametinib 2 mg once daily. Subjects continued treatment until an unacceptable toxicity, disease progression, or death.","id":"EG007","otherNumAffected":9,"otherNumAtRisk":10,"seriousNumAffected":4,"seriousNumAtRisk":10,"title":"Multiple Myeloma (MM) (On-Treatment)"},{"deathsNumAffected":18,"deathsNumAtRisk":30,"description":"Deaths collected in the post- treatment survival follow-up period (starting from day 31 post- treatment). No AEs were collected during this period.","id":"EG008","otherNumAffected":0,"otherNumAtRisk":0,"seriousNumAffected":0,"seriousNumAtRisk":0,"title":"Anaplastic Thyroid Cancer (ATC) (Post-treatment Survival Follow-up)"},{"deathsNumAffected":28,"deathsNumAtRisk":37,"description":"Deaths collected in the post- treatment survival follow-up period (starting from day 31 post- treatment). No AEs were collected during this period.","id":"EG009","otherNumAffected":0,"otherNumAtRisk":0,"seriousNumAffected":0,"seriousNumAtRisk":0,"title":"Biliary Tract Cancer (BTC) (Post-treatment Survival Follow-up)"},{"deathsNumAffected":1,"deathsNumAtRisk":1,"description":"Deaths collected in the post- treatment survival follow-up period (starting from day 31 post- treatment). No AEs were collected during this period.","id":"EG010","otherNumAffected":0,"otherNumAtRisk":0,"seriousNumAffected":0,"seriousNumAtRisk":0,"title":"Gastrointestinal Stromal Tumor (GIST) (Post-treatment Survival Follow-up)"},{"deathsNumAffected":3,"deathsNumAtRisk":12,"description":"Deaths collected in the post- treatment survival follow-up period (starting from day 31 post- treatment). No AEs were collected during this period.","id":"EG011","otherNumAffected":0,"otherNumAtRisk":0,"seriousNumAffected":0,"seriousNumAtRisk":0,"title":"Low Grade (WHO G1/G2) Glioma (LGG) (Post-treatment Survival Follow-up)"},{"deathsNumAffected":26,"deathsNumAtRisk":43,"description":"Deaths collected in the post- treatment survival follow-up period (starting from day 31 post- treatment). No AEs were collected during this period.","id":"EG012","otherNumAffected":0,"otherNumAtRisk":0,"seriousNumAffected":0,"seriousNumAtRisk":0,"title":"High Grade (WHO G3/G4) Glioma (HGG) (Post-treatment Survival Follow-up)"},{"deathsNumAffected":3,"deathsNumAtRisk":3,"description":"Deaths collected in the post- treatment survival follow-up period (starting from day 31 post- treatment). No AEs were collected during this period.","id":"EG013","otherNumAffected":0,"otherNumAtRisk":0,"seriousNumAffected":0,"seriousNumAtRisk":0,"title":"Adenocarcinoma of the Small Intestine (ASI) (Post-treatment Survival Follow-up)"},{"deathsNumAffected":4,"deathsNumAtRisk":51,"description":"Deaths collected in the post- treatment survival follow-up period (starting from day 31 post- treatment). No AEs were collected during this period.","id":"EG014","otherNumAffected":0,"otherNumAtRisk":0,"seriousNumAffected":0,"seriousNumAtRisk":0,"title":"Hairy Cell Leukemia (HCL) (Post-treatment Survival Follow-up)"},{"deathsNumAffected":8,"deathsNumAtRisk":9,"description":"Deaths collected in the post- treatment survival follow-up period (starting from day 31 post- treatment). 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(24.1)","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":36},{"groupId":"EG001","numAffected":1,"numAtRisk":43},{"groupId":"EG002","numAffected":0,"numAtRisk":1},{"groupId":"EG003","numAffected":0,"numAtRisk":13},{"groupId":"EG004","numAffected":0,"numAtRisk":45},{"groupId":"EG005","numAffected":0,"numAtRisk":3},{"groupId":"EG006","numAffected":0,"numAtRisk":55},{"groupId":"EG007","numAffected":0,"numAtRisk":10},{"groupId":"EG008","numAtRisk":0},{"groupId":"EG009","numAtRisk":0},{"groupId":"EG010","numAtRisk":0},{"groupId":"EG011","numAtRisk":0},{"groupId":"EG012","numAtRisk":0},{"groupId":"EG013","numAtRisk":0},{"groupId":"EG014","numAtRisk":0},{"groupId":"EG015","numAtRisk":0}],"term":"Thrombophlebitis"}],"timeFrame":"Adverse events were reported from first dose of study treatment until end of study treatment plus 30 days, up to a maximum duration of approximately 85 months. Deaths were collected in the post treatment survival follow up period from 31 days after last dose of study medication until the end of the study, up to approximately 92 months. These are not considered Adverse Events."}