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Efficacy and safety of twice-daily glycopyrrolate in patients with stable, symptomatic COPD with moderate-to-severe airflow limitation: the GEM1 study.
LaForce, Craig; Feldman, Gregory; Spangenthal, Selwyn; Eckert, Joerg H; Henley, Michelle; Patalano, Francesco; D'Andrea, Peter.
Afiliação
  • LaForce C; North Carolina Clinical Research, Raleigh, NC, USA.
  • Feldman G; South Carolina Pharmaceutical Research, Spartanburg, SC, USA.
  • Spangenthal S; American Health Research, Charlotte, NC, USA.
  • Eckert JH; Novartis Pharma AG, Basel, Switzerland.
  • Henley M; Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
  • Patalano F; Novartis Pharma AG, Basel, Switzerland.
  • D'Andrea P; Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
Article em En | MEDLINE | ID: mdl-27354782
BACKGROUND: The purpose of this study was to confirm the efficacy and safety of twice-daily glycopyrrolate 15.6 µg, a long-acting muscarinic antagonist, in patients with stable, symptomatic, chronic obstructive pulmonary disease (COPD) with moderate-to-severe airflow limitation. METHODS: The GEM1 study was a 12-week, multicenter, double-blind, parallel-group, placebo-controlled study that randomized patients with stable, symptomatic COPD with moderate-to-severe airflow limitation to twice-daily glycopyrrolate 15.6 µg or placebo (1:1) via the Neohaler(®) device. The primary objective was to demonstrate superiority of glycopyrrolate versus placebo in terms of forced expiratory volume in 1 second area under the curve between 0 and 12 hours post morning dose at week 12. Other outcomes included additional spirometric end points, transition dyspnea index, St George's Respiratory Questionnaire, COPD Assessment Test, rescue medication use, and symptoms reported by patients via electronic diary. Safety was also assessed during the study. RESULTS: Of the 441 patients randomized (glycopyrrolate, n=222; placebo, n=219), 96% of patients completed the planned treatment phase. Glycopyrrolate demonstrated statistically significant (P<0.001) improvements in lung function versus placebo. Glycopyrrolate showed statistically significant improvement in the transition dyspnea index focal score, St George's Respiratory Questionnaire total score, COPD Assessment Test score, rescue medication use, and daily total symptom score versus placebo at week 12. Safety was comparable between the treatment groups. CONCLUSION: Significant improvement in lung function, dyspnea, COPD symptoms, health status, and rescue medication use suggests that glycopyrrolate is a safe and effective treatment option as maintenance bronchodilator in patients with stable, symptomatic COPD with moderate-to-severe airflow limitation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Broncodilatadores / Antagonistas Muscarínicos / Doença Pulmonar Obstrutiva Crônica / Glicopirrolato / Pulmão Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies Aspecto: Patient_preference Limite: Aged / Female / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: Int J Chron Obstruct Pulmon Dis Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Broncodilatadores / Antagonistas Muscarínicos / Doença Pulmonar Obstrutiva Crônica / Glicopirrolato / Pulmão Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies Aspecto: Patient_preference Limite: Aged / Female / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: Int J Chron Obstruct Pulmon Dis Ano de publicação: 2016 Tipo de documento: Article