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 RE(2)SPOND study is examining whether roflumilast, when added to an inhaled corticosteroid/long-acting beta2-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.
- Rennard, S. I.
- Martinez, F. J.
- Rabe, K. F.
- Sethi, S.
- Pizzichini, E.
- McIvor, A.
- Siddiqui, S.
- Anzueto, A.
- Zhu, H.
Keywords
- Administration, Inhalation
- Adrenal Cortex Hormones/*administration & dosage/adverse effects
- Adrenergic beta-2 Receptor Agonists/*administration & dosage/adverse effects
- Aged
- Aminopyridines/*administration & dosage/adverse effects/pharmacokinetics
- Benzamides/*administration & dosage/adverse effects/pharmacokinetics
- Bronchitis, Chronic/diagnosis/*drug therapy/physiopathology
- Bronchodilator Agents/*administration & dosage/adverse effects
- Budesonide, Formoterol Fumarate Drug Combination/*administration & dosage/adverse
- effects
- Cyclopropanes/administration & dosage/adverse effects/pharmacokinetics
- Disease Progression
- Double-Blind Method
- Female
- Fluticasone-Salmeterol Drug Combination/*administration & dosage/adverse effects
- Forced Expiratory Volume
- Humans
- Lung/*drug effects/physiopathology
- Male
- Middle Aged
- Phosphodiesterase 4 Inhibitors/*administration & dosage/adverse
- effects/pharmacokinetics
- Pulmonary Disease, Chronic Obstructive/diagnosis/*drug therapy/physiopathology
- Research Design
- Severity of Illness Index
- Spirometry
- Surveys and Questionnaires
- Time Factors
- Treatment Outcome
- Vital Capacity
- Ics/laba
- Re2spond
- exacerbation
- methodology
- phosphodiesterase-4
- study design