欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Somavert
适用类别Human
治疗领域Acromegaly
通用名/非专利名称pegvisomant
活性成分pegvisomant
产品号EMEA/H/C/000409
患者安全信息No
许可状态Authorised
ATC编码H01AX01
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2002/11/12
上市许可开发者/申请人/持有人Pfizer Europe MA EEIG
人用药物治疗学分组Pituitary and hypothalamic hormones and analogues
兽用药物治疗学分组
审评意见日期2002/07/25
欧盟委员会决定日期2025/02/25
修订号29
治疗适应症Treatment of adult patients with acromegaly who have had an inadequate response to surgery and/or radiation therapy and in whom an appropriate medical treatment with somatostatin analogues did not normalize IGF-I concentrations or was not tolerated. Treatment of adult patients with acromegaly who have had an inadequate response to surgery and/or radiation therapy and in whom an appropriate medical treatment with somatostatin analogues did not normalize IGF -I concentrations or was not tolerated.
适用物种
兽用药物ATC编码
首次发布日期2018/08/23
最后更新日期2025/02/27
产品说明书https://www.ema.europa.eu/en/documents/product-information/somavert-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/somavert
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