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近期治疗难治性抑郁症临床试验中的研究性药物。

Investigational drugs in recent clinical trials for treatment-resistant depression.

作者信息

Garay Ricardo P, Zarate Carlos A, Charpeaud Thomas, Citrome Leslie, Correll Christoph U, Hameg Ahcène, Llorca Pierre-Michel

机构信息

a Pharmacology and Therapeutics, Craven , Villemoisson-sur-Orge , France.

b Experimental Therapeutics and Pathophysiology Branch , National Institute of Mental Health, National Institutes of Health , Bethesda , MD , USA.

出版信息

Expert Rev Neurother. 2017 Jun;17(6):593-609. doi: 10.1080/14737175.2017.1283217. Epub 2017 Jan 29.

DOI:10.1080/14737175.2017.1283217
PMID:28092469
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5418088/
Abstract

The authors describe the medications for treatment-resistant depression (TRD) in phase II/III of clinical development in the EU and USA and provide an opinion on how current treatment can be improved in the near future. Areas covered: Sixty-two trials were identified in US and EU clinical trial registries that included six investigational compounds in recent phase III development and 12 others in recent phase II clinical trials. Glutamatergic agents have been the focus of many studies. A single intravenous dose of the glutamatergic modulator ketamine produces a robust and rapid antidepressant effect in persons with TRD; this effect continues to remain significant for 1 week. This observation was a turning point that opened the way for other, more selective glutamatergic modulators (intranasal esketamine, AVP-786, AVP-923, AV-101, and rapastinel). Of the remaining compounds, monoclonal antibodies open highly innovative therapeutic options, based on new pathophysiological approaches to depression. Expert commentary: Promising new agents are emerging for TRD treatment. Glutamatergic modulators likely represent a very promising alternative to monoaminergic antidepressant monotherapy. We could see the arrival of the first robust and rapid acting antidepressant drug in the near future, which would strongly facilitate the ultimate goal of recovery in persons with TRD.

摘要

作者描述了在美国和欧盟处于临床开发II/III期的难治性抑郁症(TRD)治疗药物,并就近期如何改进当前治疗提供了见解。涵盖领域:在美国和欧盟临床试验注册库中识别出62项试验,其中包括6种处于近期III期开发的研究性化合物和12种处于近期II期临床试验的其他化合物。谷氨酸能药物一直是许多研究的重点。单次静脉注射谷氨酸能调节剂氯胺酮可在TRD患者中产生强大而快速的抗抑郁作用;这种作用在1周内仍持续显著。这一观察结果是一个转折点,为其他更具选择性的谷氨酸能调节剂(鼻内艾司氯胺酮、AVP - 786、AVP - 923、AV - 101和瑞帕斯汀)开辟了道路。在其余化合物中,单克隆抗体基于抑郁症新的病理生理学方法开辟了极具创新性的治疗选择。专家评论:TRD治疗正在出现有前景的新药物。谷氨酸能调节剂可能是单胺能抗抑郁单药治疗非常有前景的替代方案。在不久的将来,我们可能会看到首款强大且起效迅速的抗抑郁药物问世,这将极大地推动TRD患者康复的最终目标。

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