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SGS-742 治疗琥珀酸半醛脱氢酶缺乏症的随机对照试验:一种 γ-氨基丁酸 B(GABA-B)受体拮抗剂。

A Randomized Controlled Trial of SGS-742, a γ-aminobutyric acid B (GABA-B) Receptor Antagonist, for Succinic Semialdehyde Dehydrogenase Deficiency.

机构信息

Clinical Epilepsy Section, National Institute of Neurological Disorders and Stroke, 35053National Institutes of Health (NIH), Bethesda, MD, USA.

Division of Epilepsy, Neurophysiology, and Critical Care Neurology, 8404Children's National Hospital, Washington, DC, USA.

出版信息

J Child Neurol. 2021 Nov;36(13-14):1189-1199. doi: 10.1177/08830738211012804. Epub 2021 May 20.

Abstract

We examined safety, tolerability, and efficacy of SGS-742, a γ-aminobutyric acid B (GABA-B) receptor antagonist, in patients with succinic semialdehyde dehydrogenase deficiency. This was a single-center randomized, double-blind crossover phase II clinical trial of SGS-742 versus placebo in patients with succinic semialdehyde dehydrogenase deficiency. Procedures included transcranial magnetic stimulation and the Adaptive Behavior Assessment Scale. Nineteen subjects were consented and enrolled; the mean age was 14.0 ± 7.5 years and 11 (58%) were female. We did not find a significant effect of SGS-742 on the Adaptive Behavior Assessment Scale score, motor threshold, and paired-pulse stimulation. The difference in recruitment curve slopes between treatment groups was 0.003 ( = .09). There was no significant difference in incidence of adverse effects between drug and placebo arms. SGS-742 failed to produce improved cognition and normalization of cortical excitability as measured by the Adaptive Behavior Assessment Scale and transcranial magnetic stimulation. Our data do not support the current use of SGS-742 in succinic semialdehyde dehydrogenase deficiency.Trial registry number NCT02019667. Phase 2 Clinical Trial of SGS-742 Therapy in Succinic Semialdehyde Dehydrogenase Deficiency. https://clinicaltrials.gov/ct2/show/NCT02019667.

摘要

我们研究了 SGS-742(γ-氨基丁酸 B(GABA-B)受体拮抗剂)在琥珀酸半醛脱氢酶缺乏症患者中的安全性、耐受性和疗效。这是一项在琥珀酸半醛脱氢酶缺乏症患者中进行的 SGS-742 与安慰剂的单中心随机、双盲交叉 II 期临床试验。程序包括经颅磁刺激和适应性行为评估量表。19 名患者同意并入组;平均年龄为 14.0 ± 7.5 岁,11 名(58%)为女性。我们没有发现 SGS-742 对适应性行为评估量表评分、运动阈值和成对脉冲刺激有显著影响。治疗组之间募集曲线斜率的差异为 0.003(=.09)。药物组和安慰剂组不良反应的发生率无显著差异。SGS-742 未能改善认知功能,也未能使经颅磁刺激测量的皮质兴奋性正常化。我们的数据不支持目前在琥珀酸半醛脱氢酶缺乏症中使用 SGS-742。试验注册号 NCT02019667。琥珀酸半醛脱氢酶缺乏症的 SGS-742 治疗的 II 期临床试验。https://clinicaltrials.gov/ct2/show/NCT02019667。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1d7/8605041/b1b094df94a2/nihms-1692640-f0001.jpg

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