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一项为期 78 周、单臂、开放标签的 2 期研究的结果,旨在评估 UX007 在患有严重长链脂肪酸氧化障碍(LC-FAOD)的儿科和成年患者中的疗效。

Results from a 78-week, single-arm, open-label phase 2 study to evaluate UX007 in pediatric and adult patients with severe long-chain fatty acid oxidation disorders (LC-FAOD).

机构信息

School of Medicine and Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Children's Hospital of Pittsburgh, UPMC, 4401 Penn Avenue, Pittsburgh, Pennsylvania, 15224, USA.

出版信息

J Inherit Metab Dis. 2019 Jan;42(1):169-177. doi: 10.1002/jimd.12038.

Abstract

Long-chain fatty acid oxidation disorders (LC-FAOD) are rare disorders characterized by acute crises of energy metabolism and severe energy deficiency that may present with cardiomyopathy, hypoglycemia, and/or rhabdomyolysis, which can lead to frequent hospitalizations and early death. An open-label Phase 2 study evaluated the efficacy of UX007, an investigational odd-carbon medium-chain triglyceride, in 29 subjects with severe LC-FAOD. UX007 was administered over 78 weeks at a target dose of 25-35% total daily caloric intake (mean 27.5%). The frequency and duration of major clinical events (hospitalizations, emergency room visits, and emergency home interventions due to rhabdomyolysis, hypoglycemia, and cardiomyopathy) occurring during 78 weeks of UX007 treatment was compared with the frequency and duration of events captured retrospectively from medical records for 78 weeks before UX007 initiation. The mean annualized event rates decreased from 1.69 to 0.88 events/year following UX007 initiation (p = 0.021; 48.1% reduction). The mean annualized duration rate decreased from 5.96 to 2.96 days/year (p = 0.028; 50.3% reduction). Hospitalizations due to rhabdomyolysis, the most common event, decreased from 1.03 to 0.63 events/year (p = 0.104; 38.7% reduction). Initiation of UX007 eliminated hypoglycemia events leading to hospitalization (from 11 pre-UX007 hospitalizations, 0.30 events/year vs. 0; p = 0.067) and intensive care unit (ICU) care (from 2 pre-UX007 ICU admissions, 0.05 events/year vs. 0; p = 0.161) and reduced cardiomyopathy events (3 events vs. 1 event; 0.07 to 0.02 events/year; 69.7% decrease). The majority of treatment-related adverse events (AEs) were mild to moderate gastrointestinal symptoms, including diarrhea, vomiting, and abdominal or gastrointestinal pain, which can be managed with smaller, frequent doses mixed with food.

摘要

长链脂肪酸氧化障碍(LC-FAOD)是一种罕见的疾病,其特征为能量代谢急性危机和严重能量不足,可能表现为心肌病、低血糖和/或横纹肌溶解症,这可能导致频繁住院和早期死亡。一项开放标签的 2 期研究评估了 UX007 的疗效,UX007 是一种研究用奇数碳中链甘油三酯,用于 29 例严重 LC-FAOD 患者。在 78 周内,以 25-35%的总日热量摄入(平均 27.5%)为目标剂量给予 UX007。比较了 78 周 UX007 治疗期间主要临床事件(因横纹肌溶解症、低血糖和心肌病而住院、急诊室就诊和紧急家庭干预)的频率和持续时间与 UX007 开始前 78 周回顾性记录的事件频率和持续时间。起始 UX007 后,年化事件发生率从 1.69 降至 0.88 事件/年(p = 0.021;48.1%减少)。年化持续时间率从 5.96 降至 2.96 天/年(p = 0.028;50.3%减少)。横纹肌溶解症导致的住院率最高,从 1.03 降至 0.63 事件/年(p = 0.104;38.7%减少)。UX007 的起始消除了导致住院的低血糖事件(从 11 例 UX007 前住院,0.30 事件/年降至 0;p = 0.067)和重症监护病房(ICU)治疗(从 2 例 UX007 前 ICU 入院,0.05 事件/年降至 0;p = 0.161),减少了心肌病事件(3 例对 1 例;0.07 至 0.02 事件/年;69.7%减少)。大多数与治疗相关的不良事件(AE)为轻度至中度胃肠道症状,包括腹泻、呕吐、腹痛和胃肠道疼痛,可通过较小剂量、频繁剂量与食物混合来治疗。

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