欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Deltyba
适用类别Human
治疗领域Tuberculosis, Multidrug-Resistant
通用名/非专利名称delamanid
活性成分Delamanid
产品号EMEA/H/C/002552
患者安全信息No
许可状态Authorised
ATC编码J04AK06
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Yes
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2014/04/27
拒绝上市许可日期2013/07/25
上市许可开发者/申请人/持有人Otsuka Novel Products GmbH
人用药物治疗学分组Antimycobacterials
兽用药物治疗学分组
审评意见日期2013/11/21
欧盟委员会决定日期2025/04/25
修订号27
治疗适应症Deltyba is indicated for use as part of an appropriate combination regimen for pulmonary multi-drug resistant tuberculosis (MDR-TB) in adults, adolescents, children and infants with a body weight of at least 10 kg when an effective treatment regimen cannot otherwise be composed for reasons of resistance or tolerability (see sections 4.2, 4.4 and 5.1). Consideration should be given to official guidance on the appropriate use of antibacterial agents.
适用物种
兽用药物ATC编码
首次发布日期2018/06/11
最后更新日期2025/05/05
产品说明书https://www.ema.europa.eu/en/documents/product-information/deltyba-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/deltyba
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