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2025年5月、再発又は難治性の多発性骨髄腫に対し、BCMA（B細胞成熟抗原）を標的とした本邦初のADC（抗体薬物複合体）として、ブーレンレップ点滴静注用 100mgが承認されました。
PM-JP-NA-WCNT-190010 2025.02
