欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Topotecan Teva
适用类别Human
治疗领域Ovarian Neoplasms;Uterine Cervical Neoplasms;Small Cell Lung Carcinoma
通用名/非专利名称topotecan
活性成分topotecan
产品号EMEA/H/C/001071
患者安全信息No
许可状态Withdrawn
ATC编码L01CE01
是否额外监管Nei
是否仿制药或hybrid药物
是否生物类似药Nei
是否附条件批准Nei
是否特殊情形Nei
是否加速审评Nei
是否罕用药Nei
上市许可日期2009/09/21
上市许可开发者/申请人/持有人Teva B.V.
人用药物治疗学分组Antineoplastic agents
兽用药物治疗学分组
欧盟委员会决定日期2018/06/22
修订号8
治疗适应症Topotecan monotherapy is indicated for the treatment of: patients with metastatic carcinoma of the ovary after failure of first line or subsequent therapy; patients with relapsed small cell lung cancer [SCLC] for whom re-treatment with the first-line regimen is not considered appropriate. Topotecan in combination with cisplatin is indicated for patients with carcinoma of the cervix recurrent after radiotherapy and for patients with Stage IVB disease. Patients with prior exposure to cisplatin require a sustained treatment free interval to justify treatment with the combination.
适用物种
兽用药物ATC编码
首次发布日期2018/06/22
最后更新日期2018/07/13
产品说明书https://www.ema.europa.eu/en/documents/product-information/topotecan-teva-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/topotecan-teva
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