欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Prolia
适用类别Human
治疗领域Bone Resorption;Osteoporosis, Postmenopausal;Osteoporosis
通用名/非专利名称denosumab
活性成分denosumab
产品号EMEA/H/C/001120
患者安全信息No
许可状态Authorised
ATC编码M05BX04
是否额外监管No
是否仿制药或hybrid药物No
是否生物类似药No
是否附条件批准No
是否特殊情形No
是否加速审评No
是否罕用药No
上市许可日期2010/05/26
上市许可开发者/申请人/持有人Amgen Europe B.V.
人用药物治疗学分组Drugs for treatment of bone diseases
兽用药物治疗学分组
欧盟委员会决定日期2025/07/17
修订号34
治疗适应症Treatment of osteoporosis in postmenopausal women and in men at increased risk of fractures. In postmenopausal women Prolia significantly reduces the risk of vertebral, non vertebral and hip fractures. Treatment of bone loss associated with hormone ablation in men with prostate cancer at increased risk of fractures. In men with prostate cancer receiving hormone ablation, Prolia significantly reduces the risk of vertebral fractures.
适用物种
兽用药物ATC编码
首次发布日期2018/06/04
最后更新日期2025/10/22
产品说明书https://www.ema.europa.eu/en/documents/product-information/prolia-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/prolia
©2006-2025 DrugFuture->European Medicines Agency Authorisation of Medicines DataBase