欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Thalidomide Lipomed
适用类别Human
治疗领域Multiple Myeloma
通用名/非专利名称thalidomide
活性成分thalidomide
产品号EMEA/H/C/005715
患者安全信息No
许可状态Authorised
ATC编码L04AX02
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No
上市许可日期2022/09/19
上市许可开发者/申请人/持有人Lipomed GmbH
人用药物治疗学分组Immunosuppressants
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2024/05/10
修订号2
治疗适应症Thalidomide Lipomed in combination with melphalan and prednisone is indicated as first line treatment of patients with untreated multiple myeloma, aged ? 65 years or ineligible for high dose chemotherapy. Thalidomide Lipomed is prescribed and dispensed in accordance with the Thalidomide Lipomed Pregnancy Prevention Programme (see section 4.4).
适用物种
兽用药物ATC编码
首次发布日期2022/07/18
最后更新日期2025/09/15
产品说明书https://www.ema.europa.eu/en/documents/product-information/thalidomide-lipomed-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/thalidomide-lipomed
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