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双可变区免疫球蛋白ABT-981对健康受试者和膝骨关节炎患者体内白细胞介素-1α和白细胞介素-1β的药代动力学及耐受性研究

Pharmacokinetics and Tolerability of a Dual Variable Domain Immunoglobulin ABT-981 Against IL-1α and IL-1β in Healthy Subjects and Patients With Osteoarthritis of the Knee.

作者信息

Kosloski Matthew P, Goss Sandra, Wang Susanne X, Liu Jia, Loebbert Ralf, Medema Jeroen K, Liu Wei, Dutta Sandeep

机构信息

AbbVie Inc, North Chicago, IL, USA.

AbbVie Deutschland GmbH and Co KG, Wiesbaden, Hesse, Germany.

出版信息

J Clin Pharmacol. 2016 Dec;56(12):1582-1590. doi: 10.1002/jcph.764. Epub 2016 Jun 2.

Abstract

The interleukin (IL)-1 family of proinflammatory cytokines are thought to play a significant role in the structural progression of osteoarthritis and its associated symptoms. IL-1α and IL-1β are 2 distinct cytokines found in the cartilage, synovial membrane, and synovial fluid of patients with osteoarthritis. The aim of these studies was to evaluate the pharmacokinetics of ABT-981, a dual variable domain immunoglobulin (DVD-Ig) capable of simultaneously binding IL-1α and IL-1β, in healthy subjects and patients with osteoarthritis of the knee. Fifty-six healthy adult subjects were randomized to receive single doses of ABT-981 intravenously (0.3, 1, 3, or 10 mg/kg), subcutaneously (0.3, 1, 3 mg/kg), or matching placebo in a 3:1 ratio. Thirty-six patients with osteoarthritis of the knee were randomized to receive 4 subcutaneous ABT-981 doses of 0.3, 1, or 3 mg/kg administered every 2 weeks, 3 subcutaneous doses of ABT-981 3 mg/kg every 4 weeks, or matching placebo in a 7:2 active:placebo ratio. ABT-981 behaved similarly to conventional monoclonal antibodies following single or multiple doses with mean maximum serum concentrations 2 to 9 days after subcutaneous doses, mean terminal half-lives of 10 to 14 days, and an absolute subcutaneous bioavailability of 46%. Exposure of ABT-981 was approximately linear following single or multiple doses every 2 weeks with monoexponential decline of terminal-phase concentrations. The most common adverse events associated with ABT-981 were diarrhea and headache in healthy subjects and injection site erythema in subjects with osteoarthritis of the knee. Decreased absolute neutrophil counts were observed in response to ABT-981 administration.

摘要

促炎细胞因子白细胞介素(IL)-1家族被认为在骨关节炎的结构进展及其相关症状中起重要作用。IL-1α和IL-1β是在骨关节炎患者的软骨、滑膜和滑液中发现的两种不同细胞因子。这些研究的目的是评估ABT-981(一种能够同时结合IL-1α和IL-1β的双可变域免疫球蛋白(DVD-Ig))在健康受试者和膝骨关节炎患者中的药代动力学。56名健康成年受试者被随机分为接受静脉注射单剂量ABT-981(0.3、1、3或10mg/kg)、皮下注射(0.3、1、3mg/kg)或匹配安慰剂,比例为3:1。36名膝骨关节炎患者被随机分为接受每2周皮下注射4剂0.3、1或3mg/kg的ABT-981、每4周皮下注射3剂3mg/kg的ABT-981或匹配安慰剂,活性:安慰剂比例为7:2。单剂量或多剂量给药后,ABT-981的表现与传统单克隆抗体相似,皮下给药后2至9天平均最大血清浓度出现,平均终末半衰期为10至14天,绝对皮下生物利用度为46%。每2周单剂量或多剂量给药后,ABT-981的暴露量近似呈线性,终末相浓度呈单指数下降。与ABT-981相关的最常见不良事件在健康受试者中为腹泻和头痛,在膝骨关节炎受试者中为注射部位红斑。接受ABT-981给药后观察到绝对中性粒细胞计数下降。

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