欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Trelegy 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/004363
患者安全信息No
许可状态Authorised
ATC编码R03AL08
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2025/04/25
修订号12
治疗适应症Trelegy 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2025/05/05
产品说明书https://www.ema.europa.eu/en/documents/product-information/trelegy-ellipta-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/trelegy-ellipta
©2006-2025 DrugFuture->European Medicines Agency Authorisation of Medicines DataBase