{"title":"Indacaterol: a new once daily long-acting beta(2) adrenoceptor agonist.","authors":"Kai M Beeh, Jutta Beier","doi":"10.2147/ce.s6013","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Indacaterol is a novel once daily long-acting beta agonist (LABA) developed for the treatment of chronic obstructive pulmonary disease (COPD) and asthma.</p><p><strong>Aims: </strong>This review summarizes preclinical and clinical data of indacaterol, including all data generated during the phase II trial program, and further discusses the outlook and potential of the drug in the future treatment of COPD and asthma.</p><p><strong>Evidence review: </strong>Clinical studies suggest that indacaterol produces rapid and sustained bronchodilation in COPD patients and asthmatics of different severities. Until now, clinical studies of up to 28 days' duration have been published that have confirmed the suitability of indacaterol for once daily dosing, along with a favorable overall safety and tolerability profile.</p><p><strong>Outcomes summary: </strong>Indacaterol monotherapy has potential in COPD, where antiinflammatory treatment is not fully established and issues about a potential risk of LABA use causing excess mortality have not been raised. In addition, indacaterol represents an option for future combination therapies in both asthma and COPD. However, more data are required, particularly in COPD, to fully assess the therapeutic potential of indacaterol in improving symptoms, quality of life, exacerbation rates, disease progression, exercise capacity, and hyperinflation. The currently ongoing phase III clinical trial program will add knowledge in respect to many long-term efficacy outcomes and gather further safety and tolerability data in both asthma and COPD.</p>","PeriodicalId":10764,"journal":{"name":"Core Evidence","volume":"4 ","pages":"37-41"},"PeriodicalIF":0.0000,"publicationDate":"2010-06-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2899782/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Core Evidence","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2147/ce.s6013","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: Indacaterol is a novel once daily long-acting beta agonist (LABA) developed for the treatment of chronic obstructive pulmonary disease (COPD) and asthma.
Aims: This review summarizes preclinical and clinical data of indacaterol, including all data generated during the phase II trial program, and further discusses the outlook and potential of the drug in the future treatment of COPD and asthma.
Evidence review: Clinical studies suggest that indacaterol produces rapid and sustained bronchodilation in COPD patients and asthmatics of different severities. Until now, clinical studies of up to 28 days' duration have been published that have confirmed the suitability of indacaterol for once daily dosing, along with a favorable overall safety and tolerability profile.
Outcomes summary: Indacaterol monotherapy has potential in COPD, where antiinflammatory treatment is not fully established and issues about a potential risk of LABA use causing excess mortality have not been raised. In addition, indacaterol represents an option for future combination therapies in both asthma and COPD. However, more data are required, particularly in COPD, to fully assess the therapeutic potential of indacaterol in improving symptoms, quality of life, exacerbation rates, disease progression, exercise capacity, and hyperinflation. The currently ongoing phase III clinical trial program will add knowledge in respect to many long-term efficacy outcomes and gather further safety and tolerability data in both asthma and COPD.
简介茚达特罗是一种新型的每日一次长效β受体激动剂(LABA),用于治疗慢性阻塞性肺疾病(COPD)和哮喘。目的:本综述总结了茚达特罗的临床前和临床数据,包括II期试验项目中产生的所有数据,并进一步讨论了该药物在未来治疗COPD和哮喘方面的前景和潜力:临床研究表明,茚达特罗可对不同严重程度的慢性阻塞性肺疾病患者和哮喘患者产生快速、持续的支气管扩张作用。迄今为止,已发表的长达 28 天的临床研究证实,茚达特罗适用于每日一次给药,且总体安全性和耐受性良好。结果总结:茚达特罗单药治疗在慢性阻塞性肺病中具有潜力,因为该病的抗炎治疗尚未完全确立,且尚未提出使用 LABA 会导致过高死亡率的潜在风险问题。此外,茚达特罗也是未来哮喘和慢性阻塞性肺病联合疗法的一种选择。然而,要全面评估茚达特罗在改善症状、生活质量、恶化率、疾病进展、运动能力和过度充气方面的治疗潜力,还需要更多的数据,尤其是慢性阻塞性肺病方面的数据。目前正在进行的 III 期临床试验计划将增加对许多长期疗效结果的了解,并进一步收集哮喘和慢性阻塞性肺病的安全性和耐受性数据。
期刊介绍:
Core Evidence evaluates the evidence underlying the potential place in therapy of drugs throughout their development lifecycle from preclinical to postlaunch. The focus of each review is to evaluate the case for a new drug or class in outcome terms in specific indications and patient groups The emerging evidence on new drugs is reviewed at key stages of development and evaluated against unmet needs