Division of Rheumatology, David Geffen School of Medicine, University of California, Los Angeles, CA, USA.
Rheum Dis Clin North Am. 2011 Aug;37(3):433-52, vi-vii. doi: 10.1016/j.rdc.2011.07.004.
Denosumab (Prolia) is a fully human monoclonal antibody directed against receptor activator of nuclear factor-κB ligand (RANKL), which interferes with the formation, activation, and survival of osteoclasts. It was approved by the Food and Drug Administration in June 2010 as a new treatment for postmenopausal osteoporosis in women who are at high risk for fracture. Given its mechanism of action, it is an antiresorptive therapy that is administered as a 60-mg subcutaneous injection every 6 months. It is the first biologic antiresorptive therapy for osteoporosis, and the first osteoporosis therapy to show efficacy and safety in patients with renal impairment.
地舒单抗(普罗力)是一种针对核因子-κB 受体激活剂配体(RANKL)的全人源单克隆抗体,可干扰破骨细胞的形成、激活和存活。它于 2010 年 6 月获得美国食品和药物管理局批准,作为一种新的治疗方案用于绝经后骨折风险高的女性骨质疏松症。鉴于其作用机制,它是一种抗吸收治疗药物,每 6 个月皮下注射 60 毫克。它是骨质疏松症的第一种生物抗吸收治疗药物,也是第一种在肾功能损害患者中显示疗效和安全性的骨质疏松症治疗药物。