欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Abraxane
适用类别Human
治疗领域Breast Neoplasms;Pancreatic Neoplasms;Carcinoma, Non-Small-Cell Lung
通用名/非专利名称paclitaxel
活性成分paclitaxel
产品号EMEA/H/C/000778
患者安全信息No
许可状态Authorised
ATC编码L01CD01
是否额外监管Nei
是否仿制药或hybrid药物Nei
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2008/01/11
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Antineoplastic agents
兽用药物治疗学分组
审评意见日期2007/10/18
欧盟委员会决定日期2024/12/12
修订号31
治疗适应症Abraxane monotherapy is indicated for the treatment of metastatic breast cancer in adult patients who have failed first-line treatment for metastatic disease and for whom standard, anthracycline containing therapy is not indicated. Abraxane in combination with gemcitabine is indicated for the first-line treatment of adult patients with metastatic adenocarcinoma of the pancreas. Abraxane in combination with carboplatin is indicated for the first-line treatment of non-small cell lung cancer in adult patients who are not candidates for potentially curative surgery and/or radiation therapy.
适用物种
兽用药物ATC编码
首次发布日期2018/07/30
最后更新日期2025/01/30
产品说明书https://www.ema.europa.eu/en/documents/product-information/abraxane-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/abraxane
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