Bronchodilator Efficacy of Single Doses of Indacaterol in Japanese Patients with COPD: A Randomised, Double-Blind, Placebo-Controlled Trial

ABSTRACT: Background: Indacaterol is an investigational, novel, inhaled once-daily ultra-long-acting beta-2 agonist for the treatment of chronic obstructive pulmonary disease (COPD). This study evaluated the 24-h bronchodilatory efficacy and safety of indacaterol in Japanese patients with COPD. Met...

Full description

Bibliographic Details
Main Authors: Motokazu Kato, Hironi Makita, Koji Uemura, Yoshinosuke Fukuchi, Motoi Hosoe, Charlotte Emery, Mark Higgins, Benjamin Kramer
Format: Article
Language:English
Published: Elsevier 2010-01-01
Series:Allergology International
Online Access:http://www.sciencedirect.com/science/article/pii/S1323893015306377
id doaj-0d59abd2b50d43d1ab1860e26cd5dc71
record_format Article
spelling doaj-0d59abd2b50d43d1ab1860e26cd5dc712020-11-24T20:51:04ZengElsevierAllergology International1323-89302010-01-01593285293Bronchodilator Efficacy of Single Doses of Indacaterol in Japanese Patients with COPD: A Randomised, Double-Blind, Placebo-Controlled TrialMotokazu Kato0Hironi Makita1Koji Uemura2Yoshinosuke Fukuchi3Motoi Hosoe4Charlotte Emery5Mark Higgins6Benjamin Kramer7Kishiwada City Hospital, Osaka, JapanMakita Hospital, Hokkaido, JapanKita 13-jo Naika Clinic, Hokkaido, JapanJuntendo University, Tokyo, JapanNovartis Pharma KK, Tokyo, Japan; Correspondence: Motoi Hosoe, Novartis Pharma KK, 4-17-30 Nishi-Azabu, Minato-ku, Tokyo 106-8618, Japan.Novartis Horsham Research Centre, Horsham, West Sussex, UKNovartis Horsham Research Centre, Horsham, West Sussex, UKNovartis Pharmaceuticals Corporation, East Hanover, NJ, USA.ABSTRACT: Background: Indacaterol is an investigational, novel, inhaled once-daily ultra-long-acting beta-2 agonist for the treatment of chronic obstructive pulmonary disease (COPD). This study evaluated the 24-h bronchodilatory efficacy and safety of indacaterol in Japanese patients with COPD. Methods: This Phase-II, randomised, placebo-controlled, crossover study comprised four double-blind, single-dose treatment periods (washout between periods: 14-28 days). Japanese patients aged 40-75 years with moderate-to-severe COPD were randomised to receive single doses of indacaterol (150, 300, or 600 μg) or placebo via a single-dose dry-powder inhaler. Efficacy (primary endpoint: standardised FEV1AUC22-24h) and safety were assessed for 24 h post-dose in each treatment period. Results: Of the 50 patients randomised (92% male; mean age, 67.2 years), 45 completed the study. Standardised FEV1AUC22-24h was significantly higher for all indacaterol doses as compared with placebo, with clinically relevant differences of 130, 160, and 170 mL for 150, 300, and 600 μg, respectively (P < 0.001). The improvement in FEV1 was seen as early as 5 min post-dose with indacaterol and sustained for 24 h (P < 0.001 vs placebo at all time points). All indacaterol doses were well tolerated and showed no clinically meaningful effect on pulse rate, blood pressure, QTc interval, and laboratory parameters when compared with placebo. Conclusions: In the Japanese COPD population studied, single doses of indacaterol (150, 300, and 600 μg) provided sustained 24-h bronchodilation, with onset of action within 5 min post-dose. All doses were well tolerated. These results are consistent with data from Caucasian populations. KEY WORDS: beta2-agonists, bronchodilator, COPD, efficacy, indacaterolhttp://www.sciencedirect.com/science/article/pii/S1323893015306377
collection DOAJ
language English
format Article
sources DOAJ
author Motokazu Kato
Hironi Makita
Koji Uemura
Yoshinosuke Fukuchi
Motoi Hosoe
Charlotte Emery
Mark Higgins
Benjamin Kramer
spellingShingle Motokazu Kato
Hironi Makita
Koji Uemura
Yoshinosuke Fukuchi
Motoi Hosoe
Charlotte Emery
Mark Higgins
Benjamin Kramer
Bronchodilator Efficacy of Single Doses of Indacaterol in Japanese Patients with COPD: A Randomised, Double-Blind, Placebo-Controlled Trial
Allergology International
author_facet Motokazu Kato
Hironi Makita
Koji Uemura
Yoshinosuke Fukuchi
Motoi Hosoe
Charlotte Emery
Mark Higgins
Benjamin Kramer
author_sort Motokazu Kato
title Bronchodilator Efficacy of Single Doses of Indacaterol in Japanese Patients with COPD: A Randomised, Double-Blind, Placebo-Controlled Trial
title_short Bronchodilator Efficacy of Single Doses of Indacaterol in Japanese Patients with COPD: A Randomised, Double-Blind, Placebo-Controlled Trial
title_full Bronchodilator Efficacy of Single Doses of Indacaterol in Japanese Patients with COPD: A Randomised, Double-Blind, Placebo-Controlled Trial
title_fullStr Bronchodilator Efficacy of Single Doses of Indacaterol in Japanese Patients with COPD: A Randomised, Double-Blind, Placebo-Controlled Trial
title_full_unstemmed Bronchodilator Efficacy of Single Doses of Indacaterol in Japanese Patients with COPD: A Randomised, Double-Blind, Placebo-Controlled Trial
title_sort bronchodilator efficacy of single doses of indacaterol in japanese patients with copd: a randomised, double-blind, placebo-controlled trial
publisher Elsevier
series Allergology International
issn 1323-8930
publishDate 2010-01-01
description ABSTRACT: Background: Indacaterol is an investigational, novel, inhaled once-daily ultra-long-acting beta-2 agonist for the treatment of chronic obstructive pulmonary disease (COPD). This study evaluated the 24-h bronchodilatory efficacy and safety of indacaterol in Japanese patients with COPD. Methods: This Phase-II, randomised, placebo-controlled, crossover study comprised four double-blind, single-dose treatment periods (washout between periods: 14-28 days). Japanese patients aged 40-75 years with moderate-to-severe COPD were randomised to receive single doses of indacaterol (150, 300, or 600 μg) or placebo via a single-dose dry-powder inhaler. Efficacy (primary endpoint: standardised FEV1AUC22-24h) and safety were assessed for 24 h post-dose in each treatment period. Results: Of the 50 patients randomised (92% male; mean age, 67.2 years), 45 completed the study. Standardised FEV1AUC22-24h was significantly higher for all indacaterol doses as compared with placebo, with clinically relevant differences of 130, 160, and 170 mL for 150, 300, and 600 μg, respectively (P < 0.001). The improvement in FEV1 was seen as early as 5 min post-dose with indacaterol and sustained for 24 h (P < 0.001 vs placebo at all time points). All indacaterol doses were well tolerated and showed no clinically meaningful effect on pulse rate, blood pressure, QTc interval, and laboratory parameters when compared with placebo. Conclusions: In the Japanese COPD population studied, single doses of indacaterol (150, 300, and 600 μg) provided sustained 24-h bronchodilation, with onset of action within 5 min post-dose. All doses were well tolerated. These results are consistent with data from Caucasian populations. KEY WORDS: beta2-agonists, bronchodilator, COPD, efficacy, indacaterol
url http://www.sciencedirect.com/science/article/pii/S1323893015306377
work_keys_str_mv AT motokazukato bronchodilatorefficacyofsingledosesofindacaterolinjapanesepatientswithcopdarandomiseddoubleblindplacebocontrolledtrial
AT hironimakita bronchodilatorefficacyofsingledosesofindacaterolinjapanesepatientswithcopdarandomiseddoubleblindplacebocontrolledtrial
AT kojiuemura bronchodilatorefficacyofsingledosesofindacaterolinjapanesepatientswithcopdarandomiseddoubleblindplacebocontrolledtrial
AT yoshinosukefukuchi bronchodilatorefficacyofsingledosesofindacaterolinjapanesepatientswithcopdarandomiseddoubleblindplacebocontrolledtrial
AT motoihosoe bronchodilatorefficacyofsingledosesofindacaterolinjapanesepatientswithcopdarandomiseddoubleblindplacebocontrolledtrial
AT charlotteemery bronchodilatorefficacyofsingledosesofindacaterolinjapanesepatientswithcopdarandomiseddoubleblindplacebocontrolledtrial
AT markhiggins bronchodilatorefficacyofsingledosesofindacaterolinjapanesepatientswithcopdarandomiseddoubleblindplacebocontrolledtrial
AT benjaminkramer bronchodilatorefficacyofsingledosesofindacaterolinjapanesepatientswithcopdarandomiseddoubleblindplacebocontrolledtrial
_version_ 1716802773522055168