欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Axumin
适用类别Human
治疗领域Prostatic Neoplasms;Radionuclide Imaging
通用名/非专利名称fluciclovine (18F)
活性成分fluciclovine (18F)
产品号EMEA/H/C/004197
患者安全信息No
许可状态Authorised
ATC编码V09IX12
是否额外监管No
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2017/05/21
上市许可开发者/申请人/持有人Blue Earth Diagnostics Ireland Ltd
人用药物治疗学分组Diagnostic radiopharmaceuticals
兽用药物治疗学分组
审评意见日期2017/03/22
欧盟委员会决定日期2025/07/11
修订号19
治疗适应症This medicinal product is for diagnostic use only. Axumin is indicated for Positron Emission Tomography (PET) imaging to detect recurrence of prostate cancer in adult men with a suspected recurrence based on elevated blood prostate specific antigen (PSA) levels after primary curative treatment.
适用物种
兽用药物ATC编码
首次发布日期2018/06/11
最后更新日期2025/07/14
产品说明书https://www.ema.europa.eu/en/documents/product-information/axumin-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/axumin
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