Adis, Auckland, New Zealand.
Drugs. 2014 Jul;74(10):1147-52. doi: 10.1007/s40265-014-0249-x.
The anti-interleukin-6 (IL-6) chimeric monoclonal antibody siltuximab is the first drug to be approved for the treatment of multicentric Castleman's disease (MCD) in the US and European union (EU), having gained approval under the FDA priority review program in the US and from an accelerated assessment and recommendation by the Committee for Medicinal Products for Human Use (CHMP) in the EU. Development of the drug is continuing in smoldering multiple myeloma. This article summarizes the milestones in the development of siltuximab leading to this first approval for MCD.
抗白细胞介素-6(IL-6)嵌合单克隆抗体西妥昔单抗是第一种获得美国食品药品监督管理局(FDA)优先审查程序和欧盟人用医药产品委员会(CHMP)加速评估和推荐批准,用于治疗多发性骨髓瘤(MM)的药物。本文总结了导致该药首次获批用于治疗 MCD 的里程碑事件。