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Safety and tolerability of montelukast in placebo-controlled pediatric studies and their open-label extensions.

机译:孟鲁司特在安慰剂对照的儿科研究及其开放标签扩展中的安全性和耐受性。

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BACKGROUND: Montelukast is a potent leukotriene-receptor antagonist administered once daily that provides clinical benefit in the treatment of asthma and allergic rhinitis in children and adults. Because of its wide use as a pediatric controller, there is a need for a further review of the safety and tolerability of montelukast in children. OBJECTIVE: To summarize safety and tolerability data for montelukast from previously reported as well as from unpublished placebo-controlled, double-blind, pediatric studies and their active-controlled open-label extension/extended studies. METHODS: These studies evaluated 2,751 pediatric patients 6 months to 14 years of age with persistent asthma, intermittent asthma associated with upper respiratory infection, or allergic rhinitis. These patients were enrolled in seven randomized, placebo-controlled, double-blind registration and post-registration studies and three active-controlled open-label extension/extended studies conducted by Merck Research Laboratories between 1995 and 2004. RESULTS: Montelukast was well tolerated in all studies. Clinical and laboratory adverse experiences for patients treated with montelukast were generally mild and transient. The most frequent clinical adverse events for all treatments (placebo, montelukast, active control/usual care) in virtually all studies were upper respiratory infection, worsening asthma, pharyngitis, and fever. CONCLUSION: The clinical and laboratory safety profile for montelukast was similar to that observed for placebo or active control/usual care therapies. The safety profile of montelukast did not change with long-term use.
机译:背景:孟鲁司特是一种有效的白三烯受体拮抗剂,每天给药一次,在治疗儿童和成人的哮喘和过敏性鼻炎方面具有临床益处。由于它广泛用作儿科控制器,因此需要进一步评估孟鲁司特在儿童中的安全性和耐受性。目的:总结先前报道的孟鲁司特的安全性和耐受性数据,以及未发表的安慰剂对照,双盲,儿科研究及其活性药物对照开放标签扩展/扩展研究的数据。方法:这些研究评估了2 751名6个月至14岁的患有持续性哮喘,间歇性哮喘并伴有上呼吸道感染或过敏性鼻炎的儿科患者。这些患者参加了1995年至2004年间由默克研究实验室进行的7项随机,安慰剂对照,双盲注册和注册后研究以及3项主动控制的开放标签扩展/扩展研究。结果:孟鲁司特在下列药物中的耐受性良好所有研究。接受孟鲁司特治疗的患者的临床和实验室不良反应通常是轻微和短暂的。在几乎所有研究中,所有治疗(安慰剂,孟鲁司特,主动控制/日常护理)最常见的临床不良事件是上呼吸道感染,哮喘,咽炎和发烧加重。结论:孟鲁司特的临床和实验室安全性与安慰剂或主动对照/日常护理疗法相似。孟鲁司特的安全性不会随长期使用而改变。

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