欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Cresemba
适用类别Human
治疗领域Aspergillosis
通用名/非专利名称isavuconazole
活性成分isavuconazole
产品号EMEA/H/C/002734
患者安全信息No
许可状态Authorised
ATC编码J02AC05
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Yes
上市许可日期2015/10/15
上市许可开发者/申请人/持有人Basilea Pharmaceutica Deutschland GmbH
人用药物治疗学分组Antimycotics for systemic use;Triazole derivatives
兽用药物治疗学分组
审评意见日期2005/07/23
欧盟委员会决定日期2025/07/17
修订号21
治疗适应症Powder for concentrate for solution for infusion: Cresemba is indicated in patients from 1 year of age and older for the treatment of invasive aspergillosis mucormycosis in patients for whom amphotericin B is inappropriate (see sections 4.4 and 5.1) Consideration should be given to official guidance on the appropriate use of antifungal agents. Hard capsules: Cresemba hard capsules are indicated in adults and in paediatric patients from 6 years of age for the treatment of invasive aspergillosis mucormycosis in patients for whom amphotericin B is inappropriate (see sections 4.4 and 5.1) Consideration should be given to official guidance on the appropriate use of antifungal agents. Cresemba 40 mg hard capsules are intended to be used for paediatric patients.
适用物种
兽用药物ATC编码
首次发布日期2017/08/24
最后更新日期2025/07/24
产品说明书https://www.ema.europa.eu/en/documents/product-information/cresemba-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/cresemba
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