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NorLeu3-A(1-7) 促进糖尿病足溃疡愈合:一项随机、平行分组、双盲、安慰剂对照的 2 期临床试验结果。

NorLeu3-A(1-7) stimulation of diabetic foot ulcer healing: results of a randomized, parallel-group, double-blind, placebo-controlled phase 2 clinical trial.

机构信息

Olive View-UCLA Medical Center, University of California, Los Angeles, Sylmar, California, USA.

出版信息

Wound Repair Regen. 2012 Jul-Aug;20(4):482-90. doi: 10.1111/j.1524-475X.2012.00804.x. Epub 2012 Jun 7.

DOI:10.1111/j.1524-475X.2012.00804.x
PMID:22672145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6314814/
Abstract

This randomized, double-blind, placebo-controlled Phase 2 clinical trial explored NorLeu(3)-A(1-7) (DSC127) safety and healing efficacy in diabetic foot ulcers. Patients with chronic, noninfected, neuropathic, or neuroischemic plantar Wagner Grade 1 or 2 foot ulcers (n = 172) were screened for nonhealing. Subjects were randomized to receive 4 weeks' once-daily topical treatment with 0.03% DSC127 (n = 26), 0.01% DSC127 (n = 27), or Placebo (n = 24), followed by 20 weeks' standard of care. DSC127 was assessed for safety (including laboratory values and adverse events), primary efficacy (% ulcers completely epithelialized at Week 12), and durability of effect. Baseline, demography, and safety parameters were compared between intent-to-treat groups and were comparable. Dose-response curves for DSC127 effect on % area reduction from baseline at Week 12 (40% placebo; 67% 0.01% DSC127; 80% 0.03% DSC127) and 24 (23% placebo; 53% 0.01% DSC127; 95% 0.03% DSC127) followed a log-linear pattern for both intent-to-treat and per-protocol populations. Covariate analysis compared reduction in ulcer area, depth, and volume from baseline; reductions in the 0.03% DSC127 group were greater at Weeks 12 and 24. Placebo-treated ulcers healed in a median 22 weeks vs. 8.5 weeks for 0.03%DSC127 (p = 0.04). This study provides preliminary evidence that DSC127 is safe and effective in accelerating the healing of diabetic foot ulcers.

摘要

这项随机、双盲、安慰剂对照的 2 期临床试验探讨了 NorLeu(3)-A(1-7)(DSC127)在糖尿病足溃疡中的安全性和愈合疗效。筛选出慢性、非感染、神经病变或神经缺血性足底 Wagner 1 级或 2 级溃疡(n = 172)且存在不愈合的患者。受试者随机接受 4 周的每日一次局部治疗,分别给予 0.03% DSC127(n = 26)、0.01% DSC127(n = 27)或安慰剂(n = 24),然后进行 20 周的标准治疗。评估 DSC127 的安全性(包括实验室值和不良事件)、主要疗效(第 12 周时完全上皮化的溃疡百分比)和疗效持久性。意向治疗组之间比较了基线、人口统计学和安全性参数,结果具有可比性。第 12 周时,DSC127 对溃疡面积从基线减少的效果呈剂量反应曲线(安慰剂组为 40%;0.01% DSC127 组为 67%;0.03% DSC127 组为 80%),24 周时的曲线(安慰剂组为 23%;0.01% DSC127 组为 53%;0.03% DSC127 组为 95%)呈对数线性模式,适用于意向治疗和符合方案人群。协变量分析比较了从基线开始溃疡面积、深度和体积的减少,0.03% DSC127 组在第 12 周和第 24 周的减少更为显著。安慰剂治疗的溃疡愈合中位时间为 22 周,而 0.03% DSC127 组为 8.5 周(p = 0.04)。这项研究初步证明了 DSC127 可安全、有效地加速糖尿病足溃疡的愈合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e0a/6314814/edfdd86cb39b/nihms371823f6.jpg
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