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Roflumilast: the evidence for its clinical potential in the treatment of chronic obstructive pulmonary disease

INTRODUCTION: Chronic obstructive pulmonary disease (COPD), characterized by a progressive deterioration of lung function caused primarily by the inhalation of toxic substances, is a leading cause of morbidity and mortality worldwide. Current treatment options for the management of its symptoms incl...

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Autores principales: Wagner, Linda Timm, Kenreigh, Charlotte A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3321655/
https://www.ncbi.nlm.nih.gov/pubmed/22496674
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author Wagner, Linda Timm
Kenreigh, Charlotte A.
author_facet Wagner, Linda Timm
Kenreigh, Charlotte A.
author_sort Wagner, Linda Timm
collection PubMed
description INTRODUCTION: Chronic obstructive pulmonary disease (COPD), characterized by a progressive deterioration of lung function caused primarily by the inhalation of toxic substances, is a leading cause of morbidity and mortality worldwide. Current treatment options for the management of its symptoms include the use of bronchodilators and glucocorticoid agents that are not universally beneficial and which are associated with limitations. Phosphodiesterase-4 (PDE4) inhibitors are a novel class of antiinflammatory agents being developed for COPD treatment. AIMS: The purpose of this article is to review the clinical potential of roflumilast, a PDE4 inhibitor currently in phase III clinical trials, in the management of patients with COPD. EVIDENCE REVIEW: Phase II studies indicate that roflumilast can be given orally once daily. Preliminary evidence from two phase III, randomized, double-blind, placebo-controlled studies suggest that roflumilast improves or stabilizes lung function, as measured by forced expiratory volume in 1 s and 6 s (FEV(1) and FEV(6)), forced vital capacity (FVC), and peak expiratory flow (PEF) in patients with COPD. Improvements in COPD exacerbation rate were also reported in these trials. Quality of life, as measured by the St George’s Respiratory Questionnaire, also improved with roflumilast treatment. Clinical studies to date suggest that roflumilast is well tolerated. CLINICAL POTENTIAL: Current evidence supports the use of roflumilast in the management of COPD as shown by improvements in patients’ symptoms and quality of life, and good tolerability profile. Its once-daily oral dosing regimen is unique among current therapies for COPD. This potential and the place of roflumilast in the stepwise management of the disease need to be confirmed as further evidence is published. Additional evidence will also be welcome to determine if its mechanism of action moderates the progression of lung function deterioration.
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spelling pubmed-33216552012-04-11 Roflumilast: the evidence for its clinical potential in the treatment of chronic obstructive pulmonary disease Wagner, Linda Timm Kenreigh, Charlotte A. Core Evid Proof of Concept Review INTRODUCTION: Chronic obstructive pulmonary disease (COPD), characterized by a progressive deterioration of lung function caused primarily by the inhalation of toxic substances, is a leading cause of morbidity and mortality worldwide. Current treatment options for the management of its symptoms include the use of bronchodilators and glucocorticoid agents that are not universally beneficial and which are associated with limitations. Phosphodiesterase-4 (PDE4) inhibitors are a novel class of antiinflammatory agents being developed for COPD treatment. AIMS: The purpose of this article is to review the clinical potential of roflumilast, a PDE4 inhibitor currently in phase III clinical trials, in the management of patients with COPD. EVIDENCE REVIEW: Phase II studies indicate that roflumilast can be given orally once daily. Preliminary evidence from two phase III, randomized, double-blind, placebo-controlled studies suggest that roflumilast improves or stabilizes lung function, as measured by forced expiratory volume in 1 s and 6 s (FEV(1) and FEV(6)), forced vital capacity (FVC), and peak expiratory flow (PEF) in patients with COPD. Improvements in COPD exacerbation rate were also reported in these trials. Quality of life, as measured by the St George’s Respiratory Questionnaire, also improved with roflumilast treatment. Clinical studies to date suggest that roflumilast is well tolerated. CLINICAL POTENTIAL: Current evidence supports the use of roflumilast in the management of COPD as shown by improvements in patients’ symptoms and quality of life, and good tolerability profile. Its once-daily oral dosing regimen is unique among current therapies for COPD. This potential and the place of roflumilast in the stepwise management of the disease need to be confirmed as further evidence is published. Additional evidence will also be welcome to determine if its mechanism of action moderates the progression of lung function deterioration. Dove Medical Press 2005 2005-03-31 /pmc/articles/PMC3321655/ /pubmed/22496674 Text en © 2005 Dove Medical Press Limited. All rights reserved
spellingShingle Proof of Concept Review
Wagner, Linda Timm
Kenreigh, Charlotte A.
Roflumilast: the evidence for its clinical potential in the treatment of chronic obstructive pulmonary disease
title Roflumilast: the evidence for its clinical potential in the treatment of chronic obstructive pulmonary disease
title_full Roflumilast: the evidence for its clinical potential in the treatment of chronic obstructive pulmonary disease
title_fullStr Roflumilast: the evidence for its clinical potential in the treatment of chronic obstructive pulmonary disease
title_full_unstemmed Roflumilast: the evidence for its clinical potential in the treatment of chronic obstructive pulmonary disease
title_short Roflumilast: the evidence for its clinical potential in the treatment of chronic obstructive pulmonary disease
title_sort roflumilast: the evidence for its clinical potential in the treatment of chronic obstructive pulmonary disease
topic Proof of Concept Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3321655/
https://www.ncbi.nlm.nih.gov/pubmed/22496674
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