欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Elebrato Ellipta
适用类别Human
治疗领域Pulmonary Disease, Chronic Obstructive
通用名/非专利名称fluticasone furoate;umeclidinium;vilanterol
活性成分fluticasone furoate;umeclidinium bromide;vilanterol trifenatate
产品号EMEA/H/C/004781
患者安全信息No
许可状态Authorised
ATC编码R03AL08
是否额外监管Nei
是否仿制药或hybrid药物Nei
是否生物类似药Nei
是否附条件批准Nei
是否特殊情形Nei
是否加速审评Nei
是否罕用药Nei
上市许可日期2017/11/15
上市许可开发者/申请人/持有人GlaxoSmithKline Trading Services Limited
人用药物治疗学分组Drugs for obstructive airway diseases
兽用药物治疗学分组
审评意见日期2017/09/14
欧盟委员会决定日期2023/08/31
修订号13
治疗适应症Elebrato Ellipta is indicated as a maintenance treatment in adult patients with moderate to severe chronic obstructive pulmonary disease (COPD) who are not adequately treated by a combination of an inhaled corticosteroid and a long-acting ?2-agonist.
适用物种
兽用药物ATC编码
首次发布日期2018/05/30
最后更新日期2025/05/06
产品说明书https://www.ema.europa.eu/en/documents/product-information/elebrato-ellipta-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/elebrato-ellipta
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