Science and Research

Effects of roflumilast in COPD patients receiving inhaled corticosteroid/long-acting beta2-agonist fixed-dose combination: RE(2)SPOND rationale and study design

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
Publication details
DOI: 10.2147/COPD.S109661
Journal: International journal of chronic obstructive pulmonary disease
Pages: 1921-8 
Work Type: Original
Location: ARCN
Disease Area: COPD
Partner / Member: Ghd
Access-Number: 27574416
See publication on PubMed

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