欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Oxbryta
适用类别Human
治疗领域Anemia; Anemia, Hemolytic; Anemia, Sickle Cell
通用名/非专利名称Voxelotor
活性成分Voxelotor
产品号EMEA/H/C/004869
患者安全信息no
授权状态Authorised
ATC编码B06AX03
是否额外监管yes
是否仿制药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yes
批准上市日期2022/02/14
上市许可持有人/公司名称Pfizer Europe MA EEIG 
人用药物治疗分组Other hematological agents
审评意见发布日期2021/12/16
决定日期2023/06/08
修订号4
适应症Oxbryta is indicated for the treatment of haemolytic anaemia due to sickle cell disease (SCD) in adults and paediatric patients 12 years of age and older as monotherapy or in combination with hydroxycarbamide.
首次发布日期2021/12/14
修订日期2023/07/06
产品信息https://www.ema.europa.eu/en/documents/product-information/oxbryta-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/oxbryta
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