欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Orkambi
适用类别Human
治疗领域Cystic Fibrosis
通用名/非专利名称lumacaftor;ivacaftor
活性成分Lumacaftor;ivacaftor
产品号EMEA/H/C/003954
患者安全信息No
许可状态Authorised
ATC编码R07AX30
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2015/11/19
上市许可开发者/申请人/持有人Vertex Pharmaceuticals (Ireland) Limited
人用药物治疗学分组Other respiratory system products
兽用药物治疗学分组
审评意见日期2015/09/23
欧盟委员会决定日期2025/10/30
修订号38
治疗适应症Orkambi tablets are indicated for the treatment of cystic fibrosis (CF) in patients aged 6 years and older who are homozygous for the F508del mutation in the CFTR gene. Orkambi granules are indicated for the treatment of cystic fibrosis (CF) in children aged 1 year and older who are homozygous for the F508del mutation in the CFTR gene.
适用物种
兽用药物ATC编码
首次发布日期2023/03/09
最后更新日期2025/10/30
产品说明书https://www.ema.europa.eu/en/documents/product-information/orkambi-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/orkambi
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