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tralokinumab

2020-05-29

小小医者 (审核中...)

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全文收起全球领先的皮肤病医疗机构#LEO Pharma# A/S今天宣布，#欧洲药品管理局#(EMA)人用医药产品委员会(CHMP)已采纳积极意见，建议扩大Adtralza® (#tralokinumab#)在欧盟的批准使用范围，将12至17岁的中重度#特应性皮炎#的青少年纳入系统治疗的对象。青少年患者的推荐初始剂量为600 mg，然后每隔一周使用300 mg，与成年患者的剂量相同。

LEO Pharma获得人用医药产品委员会关于Adtralza® (tralokinumab)治疗青少年中度至重度特应性皮炎的积极意见

2022-09-20

丁鹏鹏 (审核中...)

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#tralokinumab#

LEO Pharma宣布FDA核准Adbry™ (tralokinumab)作为特异性靶向作用于中度至重度特应性皮炎成人IL-13的治疗药物

2022-01-01

丁鹏鹏 (审核中...)

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#tralokinumab#

FDA接受Tralokinumab治疗中重度特应性皮炎的BLA

2020-07-12

丁鹏鹏 (审核中...)

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#tralokinumab#

欧盟监管机构开始审查LEO的IL-13单抗tralokinumab，治疗特应性皮炎

2020-06-15

丁鹏鹏 (审核中...)

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#tralokinumab#

Lancet respir med：临床3期试验：Tralokinumab，抗白介素13单克隆抗体，用于重度哮喘发作的效果和安全性评估

2018-05-23

丁鹏鹏 (审核中...)

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#tralokinumab#

Gut：Tralokinumab能有效缓解中重度溃疡性结肠炎

2014-10-29

丁鹏鹏 (审核中...)

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#tralokinumab#

阿斯利康启动哮喘生物药tralokinumab III期项目

2014-08-20

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