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The results presented are based on data cut-off date 30 Jan 2025 and additional safety results will be updated within a year of study completion.","eventGroups":[{"deathsNumAffected":23,"deathsNumAtRisk":40,"description":"Participants with Relapsed or Refractory Multiple Myeloma (RRMM) received belantamab mafodotin as 2.5 milligram (mg)/kilogram (kg) dose on Day 1 of every 3 weeks (Q3W) as a 30-60 minute intravenous (IV) infusion until confirmed disease progression, unacceptable toxicity or death.","id":"EG000","otherNumAffected":38,"otherNumAtRisk":39,"seriousNumAffected":17,"seriousNumAtRisk":39,"title":"Arm A: Belantamab Mafodotin 2.5 Milligram (mg)/Kilogram (kg) Every 3 Weeks (Q3W)"},{"deathsNumAffected":23,"deathsNumAtRisk":40,"description":"Participants with RRMM received belantamab mafodotin as 1.9 mg/kg dose on Day 1 of Q3W as a 30-60 minute IV infusion until confirmed disease progression, unacceptable toxicity or death.","id":"EG001","otherNumAffected":36,"otherNumAtRisk":40,"seriousNumAffected":17,"seriousNumAtRisk":40,"title":"Arm B: Belantamab Mafodotin 1.9 mg/kg Q3W"},{"deathsNumAffected":25,"deathsNumAtRisk":40,"description":"Participants with RRMM received belantamab mafodotin as 2.5 mg/kg dose on Day 1 of every 6 weeks (Q6W) as a 30-60 minute IV infusion until confirmed disease progression, unacceptable toxicity or death.","id":"EG002","otherNumAffected":36,"otherNumAtRisk":39,"seriousNumAffected":21,"seriousNumAtRisk":39,"title":"Arm C: Belantamab Mafodotin 2.5 mg/kg Every 6 Weeks (Q6W)"},{"deathsNumAffected":21,"deathsNumAtRisk":40,"description":"Participants with RRMM received belantamab mafodotin as 1.9 mg/kg dose on Day 1 of Q6W as a 30-60 minute IV infusion until confirmed disease progression, unacceptable toxicity or death.","id":"EG003","otherNumAffected":40,"otherNumAtRisk":40,"seriousNumAffected":16,"seriousNumAtRisk":40,"title":"Arm D: Belantamab Mafodotin 1.9 mg/kg Q6W"},{"deathsNumAffected":5,"deathsNumAtRisk":17,"description":"Participants with RRMM received belantamab mafodotin as 1.9 mg/kg dose on Day 1 of Q6W as a 30-60 minute IV infusion until confirmed disease progression, unacceptable toxicity or death. 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