Your browser doesn't support javascript.
loading
Efficacy and safety of a 12-week treatment with twice-daily aclidinium bromide in COPD patients (ACCORD COPD I).
Kerwin, Edward M; D'Urzo, Anthony D; Gelb, Arthur F; Lakkis, Hassan; Garcia Gil, Esther; Caracta, Cynthia F.
Afiliação
  • Kerwin EM; Clinical Research Institute, Medford, OR 97504, USA. ekerwin@criresearch.com
COPD ; 9(2): 90-101, 2012 Apr.
Article em En | MEDLINE | ID: mdl-22320148
ABSTRACT

BACKGROUND:

This Phase III study evaluated the efficacy and safety of twice-daily aclidinium 200 µg and 400 µg versus placebo in the treatment of moderate-to-severe COPD.

METHODS:

In this 12-week, double-blind, multicenter trial, patients were randomized (111) to inhaled twice-daily aclidinium 200 µg, aclidinium 400 µg, or placebo. Primary and secondary endpoints were changes from baseline in trough FEV1 and peak FEV1 at Week 12, respectively. Health status (St. George's Respiratory Questionnaire [SGRQ]), COPD symptoms (Transitional Dyspnea Index [TDI], night and early morning symptoms), and safety were also assessed.

RESULTS:

A total of 561 patients (mean age, 64 ± 9 years) with a mean baseline FEV1 of 1.36 ± 0.54 L (47.2% of predicted value) were randomized. At Week 12, aclidinium 200 µg and 400 µg showed significant improvements from baseline in mean (95% CI) trough FEV1 compared with placebo by 86 (45, 127) mL and 124 (83,164) mL, respectively, and in peak FEV1 by 146 (101, 190) mL and 192 (148, 236) mL, respectively (p ≤ 0.0001 for all). Both aclidinium doses also provided significant improvements in SGRQ, TDI and almost all COPD symptom scores compared with placebo (p < 0.05 for all). Incidences of adverse events (AEs) were similar across treatment groups. The incidence of anticholinergic AEs was low and similar across groups (dry mouth 0.5%-1.6%; constipation 0%-1.1%).

CONCLUSIONS:

Treatment of moderate-to-severe COPD patients with twice-daily aclidinium 200 µg and 400 µg was associated with significant improvements in bronchodilation, health status, and COPD symptoms. Both doses were well tolerated and had safety profiles similar to placebo. TRIAL REGISTRATION This ACCORD I study (AClidinium in Chronic Obstructive Respiratory Disease I) was registered on clinicaltrials.gov (NCT00891462) as "Efficacy and Safety of Aclidinium Bromide for Treatment of Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD)".
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tropanos / Antagonistas Muscarínicos / Doença Pulmonar Obstrutiva Crônica Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2012 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tropanos / Antagonistas Muscarínicos / Doença Pulmonar Obstrutiva Crônica Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2012 Tipo de documento: Article