欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Tezspire
适用类别Human
治疗领域Asthma;Sinusitis
通用名/非专利名称tezepelumab
活性成分tezepelumab
产品号EMEA/H/C/005588
患者安全信息No
许可状态Authorised
ATC编码R03DX11
是否额外监管Yes
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2022/09/19
上市许可开发者/申请人/持有人AstraZeneca AB
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2022/07/21
欧盟委员会决定日期2025/10/20
修订号13
治疗适应症AsthmaTezspire is indicated as an add-on maintenance treatment in adults and adolescents 12 years and older with severe asthma who are inadequately controlled despite high dose inhaled corticosteroids plus another medicinal product for maintenance treatment. Chronic rhinosinusitis with nasal polyps (CRSwNP) Tezspire is indicated as an add-on therapy with intranasal corticosteroids for the treatment of adult patients with severe CRSwNP for whom therapy with systemic corticosteroids, and/or surgery do not provide adequate disease control.
适用物种
兽用药物ATC编码
首次发布日期2022/09/21
最后更新日期2025/10/22
产品说明书https://www.ema.europa.eu/en/documents/product-information/tezspire-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/tezspire
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