Effects of roflumilast in COPD patients receiving inhaled corticosteroid/long-acting β2-agonist fixed-dose combination: RE2SPOND rationale and study design

被引:9
作者
Rennard, Stephen I. [1 ,2 ]
Martinez, Fernando J. [3 ,4 ]
Rabe, Klaus F. [5 ,6 ,7 ]
Sethi, Sanjay [8 ]
Pizzichini, Emilio [9 ]
McIvor, Andrew [10 ]
Siddiqui, Shahid [11 ]
Anzueto, Antonio [12 ]
Zhu, Haiyuan [13 ]
机构
[1] Univ Nebraska Med Ctr, Dept Internal Med, Omaha, NE USA
[2] AstraZeneca, Cambridge, England
[3] Weill Cornell Univ, Joan & Sanford I Weill Dept Med, New York, NY USA
[4] Michigan Hlth Syst, Dept Internal Med, Ann Arbor, MI USA
[5] LungenClinic, Grosshansdorf, Germany
[6] Univ Kiel, Dept Med, Kiel, Germany
[7] German Ctr Lung Res, Airway Res Ctr North, Grosshansdorf, Germany
[8] Univ Buffalo, State Univ New York, Dept Med, Buffalo, NY USA
[9] Univ Fed Santa Catarina, Dept Med, BR-88040900 Florianopolis, SC, Brazil
[10] McMaster Univ, St Josephs Healthcare, Firestone Inst Resp Hlth, Hamilton, ON, Canada
[11] AstraZeneca, Gaithersburg, MD USA
[12] Univ Texas Hlth Sci Ctr San Antonio, South Texas Vet Hlth Care Syst San Antonio, San Antonio, TX 78229 USA
[13] Allergan Plc, Jersey City, NJ USA
关键词
exacerbation; (RESPOND)-S-2; phosphodiesterase-4; ICS/LABA; methodology; study design; OBSTRUCTIVE PULMONARY-DISEASE; PDE4 INHIBITOR ROFLUMILAST; EXACERBATIONS; SALMETEROL; TIOTROPIUM; REDUCTION; COSTS;
D O I
10.2147/COPD.S109661
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Roflumilast, a once-daily, selective phosphodiesterase-4 inhibitor, reduces the risk of COPD exacerbations in patients with severe COPD associated with chronic bronchitis and a history of exacerbations. The (RESPOND)-S-2 study is examining whether roflumilast, when added to an inhaled corticosteroid/long-acting beta(2)-agonist (ICS/LABA) fixed-dose combination (FDC), further reduces exacerbations. The methodology is described herein. Methods: In this Phase IV, multicenter, double-blind, placebo-controlled, parallel-group trial, participants were randomized 1:1 (stratified by long-acting muscarinic antagonist use) to receive roflumilast or placebo, plus ICS/LABA FDC, for 52 weeks. Eligible participants had severe COPD associated with chronic bronchitis, had two or more moderate-severe exacerbations within 12 months, and were receiving ICS/LABA FDC for >= 3 months. The primary efficacy measure is the rate of moderate or severe COPD exacerbations per participant per year. The secondary efficacy outcomes include mean change in prebronchodilator forced expiratory volume in 1 second (FEV1) over 52 weeks, rate of severe exacerbations, and rate of moderate, severe, or antibiotic-treated exacerbations. Additional assessments include spirometry, rescue medication use, the COPD assessment test, daily symptoms using the EXACT-Respiratory symptoms (E-RS) questionnaire, all-cause and COPD-related hospitalizations, and safety and pharmacokinetic measures. Results: Across 17 countries, 2,354 participants were randomized from September 2011 to October 2014. Enrollment goal was met in October 2014, and study completion occurred in June 2016. Conclusion: This study will further characterize the effects of roflumilast added to ICS/LABA on exacerbation rates, lung function, and health of severe-very severe COPD participants at risk of further exacerbations. The results will determine the clinical benefits of roflumilast combined with standard-of-care inhaled COPD treatment.
引用
收藏
页码:1921 / 1928
页数:8
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