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Flibanserin Efficacy and Safety in Premenopausal Women With Generalized Acquired Hypoactive Sexual Desire Disorder

机译:全身血液妇女的Flibanserin疗效和安全性具有广义获得的嗜不血性的性欲障碍

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Introduction: Flibanserin is a postsynaptic 5-HT-1A agonist and 5-HT-2A antagonist for the treatment of generalized acquired hypoactive sexual desire disorder in premenopausal women. Aim: To review and evaluate the efficacy and safety of flibanserin. Methods: We review and critique the appropriateness of the co-primary and secondary end points used in the flibanserin pivotal trial research program. We review the efficacy and safety parameters of this drug based on the published literature and related sources. Main Outcome Measures: Pivotal trial primary and secondary end points and safety profile data from the flibanserin development program. Results: Our review identified instances of poor fit of two primary trial pivotal trial end points with the hypoactive sexual desire disorder construct: satisfying sexual events and electronic daily diary assessments of the most intense level of sexual desire experienced each day. Efficacy findings of the flibanserin pivotal trials program were positive for satisfying sexual events, not positive for electronic daily diary assessments of the most intense level of sexual desire experienced, and positive for secondary end points of the Female Sexual Function Index desire domain and overall measurements and the Female Sexual Distress Scale—Revised desire-specific and overall measurements. Safety data from the clinical trial program showed a reasonable safety profile. Conclusion: Flibanserin has demonstrated efficacy on appropriate measurements of the hallmarks of hypoactive sexual desire disorder—experience of absent or decreased sexual desire that is persistent over time and distressing—and the safety profile of flibanserin is acceptable.
机译:介绍:Flibanserin是一种突触后的5-HT-1A激动剂和5-HT-2A拮抗剂,用于治疗前辈妇女的广义获得的嗜不血性的性欲障碍。目的:审查和评估氟氯甲烷的疗效和安全性。方法:我们审查并批评氟哌猴枢轴试验研究计划中使用的共进次级和二次终点的适当性。我们根据发表的文献和相关来源审查该药物的疗效和安全参数。主要观察措施:来自Flibanserin开发计划的关键试验初级和次要终点和安全配置文件数据。结果:我们的评论鉴定了两个主要试验枢轴试验端的难度的情况,具有低速性的性欲障碍构建:满足性事件和电子每日日记评估每天都有最强烈的性欲水平。霉素的疗效结果表现为满足性事件的阳性,对于最强烈的性欲望水平的电子每日日记评估,以及女性性功能指数欲望域和整体测量的次要终点积极女性性痛苦规模修正的欲望特定和整体测量。来自临床试验计划的安全数据显示了合理的安全性。结论:Flibanserin在适当测量的疗效上表现出对缺乏或减少的性欲,随着时间的推移和痛苦的缺陷或减少的性欲,以及Flibanserin的安全性曲线是可以接受的。

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