欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Revlimid
适用类别Human
治疗领域Multiple Myeloma;Lymphoma, Mantle-Cell;Myelodysplastic Syndromes
通用名/非专利名称lenalidomide
活性成分lenalidomide
产品号EMEA/H/C/000717
患者安全信息No
许可状态Authorised
ATC编码L04AX04
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2007/06/14
上市许可开发者/申请人/持有人Bristol-Myers Squibb Pharma EEIG
人用药物治疗学分组Immunosuppressants
兽用药物治疗学分组
欧盟委员会决定日期2025/06/05
修订号54
治疗适应症Multiple myeloma Revlimid as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. Revlimid as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4.2) is indicated for the treatment of adult patients with previously untreated multiple myeloma who are not eligible for transplant. Revlimid in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. Myelodysplastic syndromes Revlimid as monotherapy is indicated for the treatment of adult patients with transfusion-dependent anemia due to low- or intermediate-1-risk myelodysplastic syndromes associated with an isolated deletion 5q cytogenetic abnormality when other therapeutic options are insufficient or inadequate. Mantle cell lymphoma Revlimid as monotherapy is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma. Follicular lymphoma Revlimid in combination with rituximab (anti-CD20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (Grade 1 – 3a).
适用物种
兽用药物ATC编码
首次发布日期2018/06/29
最后更新日期2025/09/09
产品说明书https://www.ema.europa.eu/en/documents/product-information/revlimid-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/revlimid
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