| 商品名称 | Blenrep |
|---|---|
| 适用类别 | Human |
| 治疗领域 | Multiple Myeloma |
| 通用名/非专利名称 | belantamab mafodotin |
| 活性成分 | belantamab mafodotin |
| 产品号 | EMEA/H/C/006511 |
| 患者安全信息 | No |
| 许可状态 | Authorised |
| ATC编码 | L01FX15 |
| 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 | 2025/07/23 |
| 上市许可开发者/申请人/持有人 | GlaxoSmithKline Trading Services Limited |
| 人用药物治疗学分组 | Antineoplastic agents |
| 兽用药物治疗学分组 | |
| 审评意见日期 | 2025/05/22 |
| 欧盟委员会决定日期 | 2025/09/01 |
| 修订号 | 1 |
| 治疗适应症 | Blenrep is indicated in adults for the treatment of relapsed or refractory multiple myeloma: in combination with bortezomib and dexamethasone in patients who have received at least one prior therapy; and in combination with pomalidomide and dexamethasone in patients who have received at least one prior therapy including lenalidomide. |
| 适用物种 | |
| 兽用药物ATC编码 | |
| 首次发布日期 | 2025/05/23 |
| 最后更新日期 | 2025/09/02 |
| 产品说明书 | https://www.ema.europa.eu/en/documents/product-information/blenrep-epar-product-information_en.pdf |
| 公共评估报告 | https://www.ema.europa.eu/en/medicines/human/EPAR/blenrep |