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Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurs first.","id":"EG001","otherNumAffected":2,"otherNumAtRisk":2,"seriousNumAffected":1,"seriousNumAtRisk":2,"title":"Part A: SEA-BCMA 200mg"},{"deathsNumAffected":2,"deathsNumAtRisk":2,"description":"Participants received SEA-BCMA 400 mg as a monotherapy q2wk IV on Day 1 and 15 of each 28- day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurs first.","id":"EG002","otherNumAffected":2,"otherNumAtRisk":2,"seriousNumAffected":2,"seriousNumAtRisk":2,"title":"Part A: SEA-BCMA 400mg"},{"deathsNumAffected":4,"deathsNumAtRisk":7,"description":"Participants received SEA-BCMA 800 mg as a monotherapy q2wk IV on Day 1 and 15 of each 28- day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurs first.","id":"EG003","otherNumAffected":6,"otherNumAtRisk":7,"seriousNumAffected":3,"seriousNumAtRisk":7,"title":"Part A: SEA-BCMA 800mg"},{"deathsNumAffected":11,"deathsNumAtRisk":22,"description":"Participants received SEA-BCMA 1600 mg as a monotherapy q2wk IV on Day 1 and 15 of each 28- day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurs first.","id":"EG004","otherNumAffected":18,"otherNumAtRisk":22,"seriousNumAffected":8,"seriousNumAtRisk":22,"title":"Part A: SEA-BCMA 1600mg"},{"deathsNumAffected":2,"deathsNumAtRisk":20,"description":"Participants received SEA-BCMA 1600 mg as an IV infusion q1wk as induction dose for the first two cycles, followed by q2wk as maintenance dose in subsequent cycles, of each 28-day cycle. 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