首页> 外国专利> PHARMACEUTICAL COMPOSITION FOR PREVENTION AND/OR TREATMENT OF ATOPIC DERMATITIS, INCLUDING IL-31 ANTAGONIST AS THE ACTIVE INGREDIENT

PHARMACEUTICAL COMPOSITION FOR PREVENTION AND/OR TREATMENT OF ATOPIC DERMATITIS, INCLUDING IL-31 ANTAGONIST AS THE ACTIVE INGREDIENT

机译:用于预防和/或治疗特应性皮炎的药物组合物,包括IL-31拮抗剂作为活性成分

摘要

FIELD: medicine.;SUBSTANCE: group of inventions relates to the field of medicine, namely, to a method for the prevention and/or treatment of atopic dermatitis, containing the introduction of an anti-IL-31RA human neutralizing antibody to a subject suffering from atopic dermatitis or predisposed to its development, in which the said anti-IL-31RA neutralizing antibody is administered according to any of the following (a)-(d): (a) administration several times to an adult subject in equal amounts at the same intervals between administration of 25 to 100 mg / body/4 weeks, 25 to 75 mg / body/4 weeks, 50 to 100 mg / body/4 weeks, or 50 to 75 mg / body/4 weeks; (b) administration several times to an adult subject in equal amounts at the same intervals between administration of 0.5 mg / kg/4 weeks; (с) administration of an initial dose to an adult subject and then constant doses in equal amounts at the same intervals between administration of 25 to 100 mg / body/4 weeks, 25 to 75 mg / body/4 weeks, 50 to 100 mg / body/4 weeks, or 50 to 75 mg / body/4 weeks, with the initial dose being different from the constant dose; and (d) administration several times to the subject child in equal amounts at the same intervals between administration of 10 to 50 mg/body/4 weeks or 10 to 40 mg/body/4 weeks, and in which the specified anti-IL-31RA-neutralizing antibody is an anti-IL-31RA antibody containing an H-chain, as specified in SEQ ID NO: 9, and an L-chain, as specified in SEQ ID NO: 10, and also refers to the use of an anti-IL-31RA human-neutralizing antibody to obtain a drug for prevention and/or treatment of atopic dermatitis.;EFFECT: group of inventions provides the identification of constant doses that effectively and stably suppress atopic dermatitis over a long period of time. ;17 cl, 11 dwg, 4 tbl, 4 ex
机译:现场:医学。物质:本发明组涉及医学领域,即,预防和/或治疗特应性皮炎的方法,含有引入受试者的抗IL-31ra人的中和抗体。从Atopic皮炎或倾向于其发展,其中所述抗IL-31ra中和抗体根据以下任一项(a) - (d):(a)给予成年对象的几次(a)给予成年数量施用25至100毫克/体/ 4周,25至75mg /体/ 4周,50至100mg /体/ 4周,或50至75mg /体/ 4周之间的相同间隔; (b)在0.5mg / kg / 4周的给药之间以相同的间隔施用多次成年对象的数度; (С)将初始剂量施用于成人受试者,然后在25至100mg /体/ 4周,25至75mg /体/ 4周,50至100毫克之间以相同的量持续等量。 /体/ 4周,或50至75 mg /体/ 4周,初始剂量不同于恒定剂量; (d)在给药10至50mg /体/ 4周或10至40mg /体/ 4周内以相同的间隔施用多次对象儿童的若干时间,其中指定的抗IL- 31ra中和抗体是含有H-Chain的抗IL-31RA抗体,如SEQ ID NO:9中所述,如SEQ ID NO:10所示,也指的是使用抗IL-31ra人中和抗体,以获得用于预防和/或治疗特应性皮炎的药物。;效果:发明组在很长一段时间内有效且稳定地抑制了特征性皮炎的恒定剂量。 ; 17 cl,11 dwg,4 tbl,4 ex

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