欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Omvoh
适用类别Human
治疗领域Colitis, Ulcerative
通用名/非专利名称mirikizumab
活性成分Mirikizumab
产品号EMEA/H/C/005122
患者安全信息no
授权状态Authorised
ATC编码L04AC
是否额外监管yes
是否仿制药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
批准上市日期2023/05/26
上市许可持有人/公司名称Eli Lilly Nederland B.V.
人用药物治疗分组Immunosuppressants
审评意见发布日期2023/03/30
决定日期2023/07/28
修订号1
适应症Omvoh is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a biologic treatment.
首次发布日期2023/03/27
修订日期2023/07/31
产品信息https://www.ema.europa.eu/en/documents/product-information/omvoh-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/omvoh
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