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Use of laquinimod in high doses for the treatment of Multiple sclerosis

机译:高剂量拉喹莫德在治疗多发性硬化症中的用途

摘要

Methods for treating a Human Patient affected by multiple sclerosis or presents a clinically isolated Syndrome, Methods for treating a Human subject by providing neuroprotection to the Human subject.And Methods for treating a Human Patient affected by multiple sclerosis or presents a clinically isolated syndrome by increasing the time to progression of disease is confirmed, the increased time to Relapse or confirmed the reduction in brain atrophy Human patient,Which comprises administering to the Human Patient or subject orally Daily doses of approximately 1.2 mg laquinimod or a pharmaceutically acceptable Salt thereof.This also provides an oral pharmaceutical dosage Unit of approximately 1.2 mg laquinimod or a pharmaceutically acceptable Salt thereof and a pharmaceutically acceptable vehicle for use in the treatment of a Human Patient affected by multiple sclerosis or P Introduced a clinically isolated Syndrome,For use in the treatment of a Human subject by providing neuroprotection to the Human subject, or for use in the treatment of a Human Patient affected by multiple sclerosis or presents a clinically isolated Syndrome through the increased time to progression Disease was confirmed,The increased time to Relapse or confirmed the reduction of Brain atrophy in the Human patient.
机译:治疗患有多发性硬化症或呈现临床孤立综合症的人类患者的方法,通过对人类受试者提供神经保护来治疗人类受试者的方法以及治疗患有多发性硬化症或呈现临床孤立综合症的人类患者的方法证实疾病发展的时间,复发时间的增加或证实脑萎缩的减少人类患者,这包括向人类患者或受试者口服每天约1.2mg拉喹莫德或其药学上可接受的盐的剂量。提供了约1.2mg拉喹莫德或其药学上可接受的盐和药学上可接受的媒介物的口服药物剂量单位,用于治疗患有多发性硬化症或P的人患者引入了临床分离的综合症,用于治疗通过提供神经保护作用的人类受试者o证实了人类受试者,或用于治疗患有多发性硬化症或通过增加疾病进展时间表现出临床孤立综合症的人类患者的疾病,增加了复发时间或证实了人类脑萎缩的减少患者。

著录项

  • 公开/公告号AR090885A1

    专利类型

  • 公开/公告日2014-12-10

    原文格式PDF

  • 申请/专利权人 TEVA PHARMACEUTICAL INDUSTRIES LTD.;

    申请/专利号AR2013P101459

  • 发明设计人 DAN BAR-ZOHAR;

    申请日2013-04-29

  • 分类号A61K31/47;A61P37/02;

  • 国家 AR

  • 入库时间 2022-08-21 15:16:32

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