欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Mimpara
适用类别Human
治疗领域Hypercalcemia;Parathyroid Neoplasms;Hyperparathyroidism
通用名/非专利名称cinacalcet
活性成分cinacalcet hydrochloride
产品号EMEA/H/C/000570
患者安全信息No
许可状态Authorised
ATC编码H05BX01
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2004/10/22
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Calcium homeostasis
兽用药物治疗学分组
欧盟委员会决定日期2024/06/03
修订号26
治疗适应症Secondary hyperparathyroidism Adults Treatment of secondary hyperparathyroidism (HPT) in adult patients with end stage renal disease (ESRD) on maintenance dialysis therapy. Paediatric population Treatment of secondary hyperparathyroidism (HPT) in children aged 3 years and older with end stage renal disease (ESRD) on maintenance dialysis therapy in whom secondary HPT is not adequately controlled with standard of care therapy. Mimpara may be used as part of a therapeutic regimen including phosphate binders and/or Vitamin D sterols, as appropriate. Parathyroid carcinoma and primary hyperparathyroidism in adults. Reduction of hypercalcaemia in adult patients with: parathyroid carcinoma; primary HPT for whom parathyroidectomy would be indicated on the basis of serum calcium levels (as defined by relevant treatment guidelines), but in whom parathyroidectomy is not clinically appropriate or is contraindicated.
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2024/06/06
产品说明书https://www.ema.europa.eu/en/documents/product-information/mimpara-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/mimpara
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