首页> 外文期刊>Expert opinion on pharmacotherapy >Aclidinium bromide/formoterol fumarate fixed-dose combination for the treatment of chronic obstructive pulmonary disease.
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Aclidinium bromide/formoterol fumarate fixed-dose combination for the treatment of chronic obstructive pulmonary disease.

机译:溴氰化铵/富马酸福莫特罗固定剂量联合用药治疗慢性阻塞性肺疾病。

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摘要

Combining a long-acting β(2)-agonist (LABA) and a long-acting antimuscarinic agent (LAMA) is potentially a good pharmacological approach to improve clinical results in stable moderate chronic obstructive pulmonary disease (COPD) patients when symptoms are not adequately controlled with tiotropium monotherapy. Consequently, there is a strong interest in developing a LABA/LAMA fixed-dose combination therapy in an attempt to simplify the treatment. AREAS COVERED: An aclidinium bromide/formoterol fumarate fixed-dose combination is under development. The few clinical data at our disposal suggest that the addition of formoterol fumarate to aclidinium bromide results in greater bronchodilation than formoterol fumarate or aclidinium bromide alone. However, a large Phase III program is involving a huge number of patients with moderate-to-severe COPD and consists of large long-term (from 24 to 52 weeks) pivotal clinical trials that have been designed to fulfil both European Medicines Agency (EMA) and Food and Drug Administration (FDA) requirements and are evaluating the efficacy and safety of this fixed-dose combination. EXPERT OPINION: Studies assessing the impact of aclidinium bromide/formoterol fumarate fixed-dose combination on COPD exacerbations, exercise capacity and hospitalisations are clearly needed to better detect its potential effects of disease modification in COPD. Moreover, it seems pragmatic to proceed with its introduction in the market at a highly competitive price.
机译:长效β(2)-激动剂(LABA)和长效抗毒蕈碱剂(LAMA)的组合可能是一种良好的药理方法,可以改善症状不充分的稳定的中度慢性阻塞性肺疾病(COPD)患者的临床结果噻托溴铵单一疗法可控制。因此,强烈希望开发一种LABA / LAMA固定剂量联合疗法,以简化治疗。涉及的领域:溴氰菊酯/富马酸福莫特罗固定剂量组合正在开发中。我们掌握的一些临床数据表明,将富马酸福莫特罗添加到溴化阿地铵中比单独使用富马酸福莫特罗或溴化阿地铵导致更大的支气管扩张作用。但是,大型的III期计划涉及大量患有中度至重度COPD的患者,并且由旨在满足欧洲药品管理局(EMA)的大型长期(24至52周)关键性临床试验组成)和食品药品管理局(FDA)的要求,并正在评估这种固定剂量组合的疗效和安全性。专家意见:评估溴氰化铵/富马酸福莫特罗固定剂量联合用药对COPD病情加重,运动能力和住院治疗的影响的研究显然需要更好地检测其在COPD中改变疾病的潜在作用。此外,以极具竞争力的价格将其引入市场似乎很实用。

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