Lemon Michael D, Strain Joe D, Hegg Annie M, Farver Debra K
Department of Pharmacy Practice, South Dakota State University College of Pharmacy, VA Black Hills Health Care System, 13 Comanche Road, Fort Meade, SD 57741, USA.
Drug Des Devel Ther. 2009 Sep 21;3:131-42. doi: 10.2147/dddt.s3207.
Indiplon is a novel pyrazolopyrimidine, nonbenzodiazepine gamma-aminobutyric acid (GABA) agonist studied for the treatment of insomnia. This article reviews the chemistry, pharmacology, clinical pharmacokinetics, drug interactions, clinical trials, safety, tolerability, contraindications, use in special populations, and dosing of indiplon. OVID, International Pharmaceutical Abstracts (IPA), and PubMed databases were searched (1966 to February 2009) for the keywords indiplon, NBI-34060, and insomnia. References of key articles were also reviewed to identify additional publications. Only English language articles were selected for review. Indiplon has been shown to have high affinity and selectivity for the GABAalpha(1) receptor subunit associated with sedation. In clinical studies, indiplon has demonstrated efficacy in improving latency to sleep onset, latency to persistent sleep, total sleep time, wake time after sleep onset, number of awakenings after sleep onset, and overall sleep quality when compared to placebo. Indiplon has a favorable safety profile with limited rebound insomnia and no tolerance. Neurocrine Biosciences, Incorporated received an Approvable Letter from the United States Food and Drug Administration in December 2007 for the indiplon IR 5 mg and 10 mg capsules based on meeting three additional requirements. At the time of this writing, indiplon remains unapproved.
因地普隆是一种新型的吡唑并嘧啶类非苯二氮䓬γ-氨基丁酸(GABA)激动剂,用于失眠治疗的研究。本文综述了因地普隆的化学性质、药理学、临床药代动力学、药物相互作用、临床试验、安全性、耐受性、禁忌证、特殊人群用药及剂量。检索了OVID、国际药学文摘(IPA)和PubMed数据库(1966年至2009年2月),以查找关键词因地普隆、NBI-34060和失眠。还查阅了关键文章的参考文献以确定其他出版物。仅选择英文文章进行综述。已证明因地普隆对与镇静相关的GABAα(1)受体亚基具有高亲和力和选择性。在临床研究中,与安慰剂相比,因地普隆在改善入睡潜伏期、持续睡眠潜伏期、总睡眠时间、睡眠起始后觉醒时间、睡眠起始后觉醒次数及总体睡眠质量方面已显示出疗效。因地普隆具有良好的安全性,反弹性失眠有限且无耐受性。Neurocrine Biosciences公司于2007年12月收到美国食品药品监督管理局的一封批准信,基于满足另外三项要求,批准了因地普隆5毫克和10毫克速释胶囊。在撰写本文时,因地普隆仍未获批。