欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Signifor
适用类别Human
治疗领域Acromegaly;Pituitary ACTH Hypersecretion
通用名/非专利名称pasireotide
活性成分pasireotide
产品号EMEA/H/C/002052
患者安全信息No
许可状态Authorised
ATC编码H01CB05
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2012/04/24
上市许可开发者/申请人/持有人Recordati Rare Diseases
人用药物治疗学分组Pituitary and hypothalamic hormones and analogues
兽用药物治疗学分组
欧盟委员会决定日期2024/12/16
修订号16
治疗适应症Signifor is indicated for the treatment of adult patients with Cushing’s disease for whom surgery is not an option or for whom surgery has failed. Signifor is indicated for the treatment of adult patients with acromegaly for whom surgery is not an option or has not been curative and who are inadequately controlled on treatment with another somatostatin analogue.
适用物种
兽用药物ATC编码
首次发布日期2018/04/12
最后更新日期2024/12/18
产品说明书https://www.ema.europa.eu/en/documents/product-information/signifor-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/signifor
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