University of Washington, Seattle, WA, USA
University of Utah, Salt Lake City, UT, USA.
Eur Respir J. 2016 May;47(5):1481-91. doi: 10.1183/13993003.01030-2015. Epub 2016 Mar 10.
FG-3019 is a fully human monoclonal antibody that interferes with the action of connective tissue growth factor, a central mediator in the pathogenesis of fibrosis.This open-label phase 2 trial evaluated the safety and efficacy of two doses of FG-3019 administered by intravenous infusion every 3 weeks for 45 weeks in patients with idiopathic pulmonary fibrosis (IPF). Subjects had a diagnosis of IPF within the prior 5 years defined by either usual interstitial pneumonia (UIP) pattern on a recent high-resolution computed tomography (HRCT) scan, or a possible UIP pattern on HRCT scan and a recent surgical lung biopsy showing UIP pattern. Pulmonary function tests were performed every 12 weeks, and changes in the extent of pulmonary fibrosis were measured by quantitative HRCT scans performed at baseline and every 24 weeks.FG-3019 was safe and well-tolerated in IPF patients participating in the study. Changes in fibrosis were correlated with changes in pulmonary function.Further investigation of FG-3019 in IPF with a placebo-controlled clinical trial is warranted and is underway.
FG-3019 是一种全人源单克隆抗体,可干扰结缔组织生长因子的作用,该因子是纤维化发病机制中的主要介质。这项开放标签的 2 期临床试验评估了 FG-3019 两种剂量的安全性和疗效,每 3 周静脉输注一次,共 45 周,用于特发性肺纤维化(IPF)患者。受试者在过去 5 年内有 IPF 的诊断,定义为最近高分辨率计算机断层扫描(HRCT)扫描上有寻常型间质性肺炎(UIP)模式,或 HRCT 扫描上可能有 UIP 模式,最近的外科肺活检显示 UIP 模式。每 12 周进行一次肺功能检查,通过基线和每 24 周进行的定量 HRCT 扫描测量肺纤维化程度的变化。FG-3019 在参与研究的 IPF 患者中安全且耐受良好。纤维化的变化与肺功能的变化相关。进一步在 IPF 患者中开展 FG-3019 的安慰剂对照临床试验是合理的,且正在进行中。