Phillips Bradley, O'Connor Colin, St Onge Erin
Department of Pharmacotherapy and Translational Research, University of Florida College of Pharmacy, Orlando, FL, USA.
J Pharm Technol. 2024 Oct;40(5):230-235. doi: 10.1177/87551225241269179. Epub 2024 Aug 13.
To evaluate the safety, efficacy, and tolerability of gepirone (Exxua) in the treatment of adult patients with major depressive disorder. A literature search was performed through PubMed, Embase, and PsycINFO using the following terms: Exxua, gepirone, depression, major depressive disorder, anxiety, and anxiety disorders. Articles that were selected included English-language dominant studies, or studies that could be translated into English by the authors, with terms associated with the safety, efficacy, and/or tolerability of gepirone. Gepirone exhibits its antidepressant activity through agonism of 5HT serotonin receptors. Phase 3 clinical trials showed that gepirone at a dose of 20 to 80 mg was proven to be effective in the treatment of major depressive disorder in adult patients. Common adverse effects reported in clinical trials included dizziness, nausea, headache, fatigue, and insomnia. This review evaluates the pharmacokinetic, pharmacologic, efficacy, and safety profile of gepirone and includes a discussion on its place in therapy for the treatment of major depressive disorder. Most clinical guidelines recommend second-generation antidepressants consisting of selective serotonin reuptake inhibitors or serotonin norepinephrine reuptake inhibitors as first-line therapy options. Gepirone is expected to receive greater clinical relevance and recommendations when compared to other azapirone medications (buspirone) within practice guidelines. Gepirone could be considered as either an alternative option for patients failing first-line therapies or for initial use to avoid unwanted side effects of other therapy options in the treatment of adult patients with major depressive disorder.
评估吉哌隆(Exxua)治疗成年重度抑郁症患者的安全性、有效性和耐受性。通过PubMed、Embase和PsycINFO进行文献检索,使用以下检索词:Exxua、吉哌隆、抑郁症、重度抑郁症、焦虑症和焦虑障碍。入选的文章包括以英语为主的研究,或作者可翻译成英语的研究,且与吉哌隆的安全性、有效性和/或耐受性相关。吉哌隆通过激动5HT血清素受体发挥其抗抑郁活性。3期临床试验表明,20至80毫克剂量的吉哌隆被证明对治疗成年重度抑郁症患者有效。临床试验报告的常见不良反应包括头晕、恶心、头痛、疲劳和失眠。本综述评估了吉哌隆的药代动力学、药理学、有效性和安全性概况,并讨论了其在重度抑郁症治疗中的治疗地位。大多数临床指南推荐由选择性5-羟色胺再摄取抑制剂或5-羟色胺去甲肾上腺素再摄取抑制剂组成的第二代抗抑郁药作为一线治疗选择。与实践指南中的其他氮杂螺环酮类药物(丁螺环酮)相比,吉哌隆有望获得更大的临床相关性和推荐。在治疗成年重度抑郁症患者时,吉哌隆可被视为一线治疗失败患者的替代选择,或作为初始用药以避免其他治疗选择的不良副作用。