欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Nemluvio
适用类别Human
治疗领域Dermatitis, Atopic;Prurigo
通用名/非专利名称nemolizumab
活性成分nemolizumab
产品号EMEA/H/C/006149
患者安全信息No
许可状态Authorised
ATC编码D11AH12
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2025/02/12
上市许可开发者/申请人/持有人Galderma International
人用药物治疗学分组Other dermatological preparations
兽用药物治疗学分组
审评意见日期2024/12/12
欧盟委员会决定日期2025/11/10
修订号3
治疗适应症Atopic dermatitis (AD) Nemluvio is indicated for the treatment of moderate-to-severe atopic dermatitis in patients aged 12 years and older who are candidates for systemic therapy. Prurigo nodularis (PN) Nemluvio is indicated for the treatment of adults with moderate-to-severe prurigo nodularis who are candidates for systemic therapy.
适用物种
兽用药物ATC编码
首次发布日期2024/12/13
最后更新日期2025/11/10
产品说明书https://www.ema.europa.eu/en/documents/product-information/nemluvio-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/nemluvio
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