欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Kiovig
适用类别Human
治疗领域Purpura, Thrombocytopenic, Idiopathic;Bone Marrow Transplantation;Immunologic Deficiency Syndromes;Guillain-Barre Syndrome;Mucocutaneous Lymph Node Syndrome
通用名/非专利名称human normal immunoglobulin
活性成分human normal immunoglobulin (IVIg)
产品号EMEA/H/C/000628
患者安全信息No
许可状态Authorised
ATC编码J06BA02
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2006/01/19
上市许可开发者/申请人/持有人Takeda Manufacturing Austria AG
人用药物治疗学分组Immune sera and immunoglobulins
兽用药物治疗学分组
欧盟委员会决定日期2022/06/24
修订号26
治疗适应症Replacement therapy in adults, and children and adolescents (0-18 years) in: primary immunodeficiency syndromes with impaired antibody production; hypogammaglobulinaemia and recurrent bacterial infections in patients with chronic lymphocytic leukaemia, in whom prophylactic antibiotics have failed; hypogammaglobulinaemia and recurrent bacterial infections in plateau-phase-multiple-myeloma patients who have failed to respond to pneumococcal immunisation; hypogammaglobulinaemia in patients after allogeneic haematopoietic-stem-cell transplantation (HSCT); congenital AIDS and recurrent bacterial infections. Immunomodulation in adults, and children and adolescents (0-18 years) in: primary immune thrombocytopenia (ITP), in patients at high risk of bleeding or prior to surgery to correct the platelet count; Guillain Barré syndrome; Kawasaki disease; multifocal motor neuropathy (MMN).
适用物种
兽用药物ATC编码
首次发布日期2017/06/07
最后更新日期2022/06/27
产品说明书https://www.ema.europa.eu/en/documents/product-information/kiovig-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/kiovig
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