欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Pemetrexed Baxter
适用类别Human
治疗领域Carcinoma, Non-Small-Cell Lung;Mesothelioma
通用名/非专利名称pemetrexed
活性成分pemetrexed disodium heptahydrate
产品号EMEA/H/C/005848
患者安全信息No
许可状态Authorised
ATC编码L01BA04
是否额外监管No
是否仿制药或hybrid药物Yes
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2022/12/09
上市许可开发者/申请人/持有人Baxter Holding 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2022/10/13
欧盟委员会决定日期2022/12/09
修订号
治疗适应症Malignant pleural mesotheliomaPemetrexed Baxter in combination with cisplatin is indicated for the treatment of chemotherapy naïve patients with unresectable malignant pleural mesothelioma. Non-small cell lung cancerPemetrexed Baxter in combination with cisplatin is indicated for the first line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology (see section 5.1). Pemetrexed Baxter is indicated as monotherapy for the maintenance treatment of locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology in patients whose disease has not progressed immediately following platinum-based chemotherapy (see section 5.1). Pemetrexed Baxter is indicated as monotherapy for the second line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology (see section 5.1).
适用物种
兽用药物ATC编码
首次发布日期2022/10/12
最后更新日期2023/01/19
产品说明书https://www.ema.europa.eu/en/documents/product-information/pemetrexed-baxter-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/pemetrexed-baxter
©2006-2025 DrugFuture->European Medicines Agency Authorisation of Medicines DataBase