欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Bildyos
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/006434
患者安全信息No
许可状态Authorised
ATC编码M05BX04
是否额外监管Yes
是否仿制药或hybrid药物No
是否生物类似药Yes
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2025/09/17
上市许可开发者/申请人/持有人Sciencepharma Sp. z o.o
人用药物治疗学分组Drugs for treatment of bone diseases
兽用药物治疗学分组
审评意见日期2025/07/24
欧盟委员会决定日期2025/11/06
修订号1
治疗适应症Treatment of osteoporosis in postmenopausal women and in men at increased risk of fractures. Inpostmenopausal women, denosumab significantly reduces the risk of vertebral, non-vertebral and hipfractures. Treatment of bone loss associated with hormone ablation in men with prostate cancer at increased riskof fractures. In men with prostate cancer receiving hormone ablation, denosumabsignificantly reduces the risk of vertebral fractures. Treatment of bone loss associated with long-term systemic glucocorticoid therapy in adult patients atincreased risk of fracture.
适用物种
兽用药物ATC编码
首次发布日期2025/07/25
最后更新日期2025/11/27
产品说明书https://www.ema.europa.eu/en/documents/product-information/bildyos-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/bildyos
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