| 商品名称 | Tecartus |
|---|---|
| 适用类别 | Human |
| 治疗领域 | Lymphoma, Mantle-Cell |
| 通用名/非专利名称 | brexucabtagene autoleucel |
| 活性成分 | autologous peripheral blood T cells CD4 and CD8 selected and CD3 and CD28 activated transduced with retroviral vector expressing anti-CD19 CD28/CD3-zeta chimeric antigen receptor and cultured (brexucabtagene autoleucel) |
| 产品号 | EMEA/H/C/005102 |
| 患者安全信息 | No |
| 许可状态 | Authorised |
| ATC编码 | L01X |
| 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 | Yes |
| 是否特殊情形 | No |
| 是否加速审评 | No |
| 是否罕用药 | Yes |
| 上市许可日期 | 2020/12/14 |
| 上市许可开发者/申请人/持有人 | Kite Pharma EU B.V. |
| 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 | 2020/10/15 |
| 欧盟委员会决定日期 | 2025/11/13 |
| 修订号 | 16 |
| 治疗适应症 | Mantle cell lymphoma Tecartus is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (MCL) after two or more lines of systemic therapy including a Bruton’s tyrosine kinase (BTK) inhibitor. Acute lymphoblastic leukaemia Tecartus is indicated for the treatment of adult patients 26 years of age and above with relapsed or refractory B-cell precursor acute lymphoblastic leukaemia (ALL). |
| 适用物种 | |
| 兽用药物ATC编码 | |
| 首次发布日期 | 2021/01/25 |
| 最后更新日期 | 2025/12/08 |
| 产品说明书 | https://www.ema.europa.eu/en/documents/product-information/tecartus-epar-product-information_en.pdf |
| 公共评估报告 | https://www.ema.europa.eu/en/medicines/human/EPAR/tecartus |