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抗OX40单克隆抗体KHK4083治疗中度活动性溃疡性结肠炎的随机、剂量递增2期研究

Randomized, Ascending Dose, Phase 2 Study of KHK4083, an Anti-OX40 Monoclonal Antibody, in Moderately Active Ulcerative Colitis.

作者信息

Kierkus Jaroslaw, Pesegova Marina, Klopocka Maria, Brankovic Marija, Kasai Noriyuki, Efuni Sergey, Kong Jennifer, Nakajima Yu, Jordan Christina, Matsui Takeshi, Feagan Brian G, Strout Vincent

机构信息

Maternal, Pediatric and Adolescent Healthcare Centre, Gastroenterology Diagnostic Facility for Adults, Warsaw, Poland.

Department of Gastroenterology, Territorial Clinical Hospital, Krasnoyarsk, Russia.

出版信息

Crohns Colitis 360. 2020 Jun 9;2(3):otaa049. doi: 10.1093/crocol/otaa049. eCollection 2020 Jul.

Abstract

BACKGROUND

OX40 (CD134) plays a role in the maintenance of late T-cell proliferation and survival. KHK4083 is a monoclonal antibody directed against OX40. We aimed to assess the safety and preliminary efficacy of KHK4083 in patients with moderately active ulcerative colitis (UC).

METHODS

In this multicenter, double-blind, parallel-group, phase 2 study, patients with moderately active UC patients were randomized to ascending doses of intravenous KHK4083 (1, 3, or 10 mg/kg) or placebo every 2 weeks for 12 weeks. The primary endpoint was safety. The primary efficacy end point was the change from baseline in mean modified Mayo endoscopy subscore at week 12. Treatment with KHK4083 or placebo was continued every 4 weeks for up to 52 weeks in responders.

RESULTS

Long-term treatment with KHK4083 was well tolerated, with treatment-related adverse events being predominantly transient mild-to-moderate infusion-related reactions. Exploratory analysis of biopsy samples showed the virtually complete elimination of OX40+ cells in colon mucosa after 12 weeks of KHK4083 treatment. There were no significant differences between any of the randomized KHK4083 dose groups and placebo for the mean change in Mayo endoscopy subscore from baseline to week 12.

CONCLUSIONS

KHK4083 can be safely administered intravenously at doses up to 10 mg/kg every 2 or 4 weeks for up to 52 weeks. Proof of pharmacodynamic action was confirmed by depletion of the elevated levels of the OX40+ cells associated with UC at all tested doses. Clinical response and mucosal healing (endoscopic improvement) in this population was not correlated with ablation of OX40+ T cells.

摘要

背景

OX40(CD134)在晚期T细胞增殖和存活的维持中发挥作用。KHK4083是一种针对OX40的单克隆抗体。我们旨在评估KHK4083在中度活动性溃疡性结肠炎(UC)患者中的安全性和初步疗效。

方法

在这项多中心、双盲、平行组2期研究中,中度活动性UC患者被随机分为每2周静脉注射递增剂量的KHK4083(1、3或10mg/kg)或安慰剂,共12周。主要终点是安全性。主要疗效终点是第12周时平均改良梅奥内镜亚评分相对于基线的变化。有反应的患者每4周继续接受KHK4083或安慰剂治疗,最长持续52周。

结果

KHK4083的长期治疗耐受性良好,与治疗相关的不良事件主要是短暂的轻度至中度输液相关反应。活检样本的探索性分析显示,KHK4083治疗12周后,结肠黏膜中OX40+细胞几乎完全消除。从基线到第12周,任何随机分组的KHK4083剂量组与安慰剂组在梅奥内镜亚评分的平均变化方面均无显著差异。

结论

KHK4083每2周或4周静脉注射一次,剂量高达10mg/kg,最长持续52周,可安全给药。在所有测试剂量下,与UC相关的OX40+细胞水平升高的消除证实了药效学作用的证据。该人群中的临床反应和黏膜愈合(内镜改善)与OX40+T细胞的消融无关。

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