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    • 118. 发明授权
    • Use of pirfenidone in therapeutic regimens
    • 吡非尼酮在治疗方案中的应用
    • US07407973B2
    • 2008-08-05
    • US10574631
    • 2004-10-21
    • Osman N. OzesLawrence M. BlattScott D. Seiwert
    • Osman N. OzesLawrence M. BlattScott D. Seiwert
    • A61K31/445
    • A61K31/47A61K31/4412A61K38/212A61K38/217A61K45/06G01N33/5091Y02A50/411A61K2300/00
    • The present invention provides methods for treating a disorder, and methods for inhibiting a stress-activated protein kinase (SAPK) in a cell in an individual, the methods generally involving administering to an individual in need thereof an effective amount of pirfenidone or a pirfenidone analog; comparing a post-treatment SAPK activity level in a biological sample from the individual with a pre-treatment SAPK activity level; and adjusting the dose of the pirfenidone or pirfenidone analog based on the results of the comparison step. The present invention provides methods for treating a disorder, and methods for inhibiting a SAPK in a cell in an individual, the methods generally involving administering to an individual in need thereof an effective amount of pirfenidone or a pirfenidone analog; comparing a second post-treatment SAPK activity level in a biological sample from the individual with a first post-treatment SAPK activity level; and adjusting the dose of the pirfenidone or pirfenidone analog based on the results of the comparison step.
    • 本发明提供了治疗病症的方法以及在个体细胞中抑制应激活化蛋白激酶(SAPK)的方法,所述方法通常涉及向有需要的个体施用有效量的吡非尼酮或吡非尼酮类似物 ; 将来自个体的生物样品中的后处理SAPK活性水平与预处理SAPK活性水平进行比较; 并根据比较步骤的结果调整吡非尼酮或吡非尼酮类似物的剂量。 本发明提供了治疗病症的方法以及在个体细胞中抑制SAPK的方法,所述方法通常涉及向有需要的个体施用有效量的吡非尼酮或吡非尼酮类似物; 将来自个体的生物样品中的第二后处理SAPK活性水平与第一后处理SAPK活性水平进行比较; 并根据比较步骤的结果调整吡非尼酮或吡非尼酮类似物的剂量。