Cardiac safety of indacaterol in healthy subjects: a randomized, multidose, placebo- and positive-controlled, parallel-group thorough QT study

<p>Abstract</p> <p>Background</p> <p>Indacaterol is a novel once-daily ultra long-acting β<sub>2</sub>-agonist for the treatment of chronic obstructive pulmonary disease. It is known that β<sub>2</sub>-agonists, like other adrenergic compounds, c...

Full description

Bibliographic Details
Main Authors: Woessner Ralph, Harris Stuart, Sabo Ronald, Khindri Sanjeev, Jennings Simon, Drollmann Anton F
Format: Article
Language:English
Published: BMC 2011-05-01
Series:BMC Pulmonary Medicine
Online Access:http://www.biomedcentral.com/1471-2466/11/31
id doaj-443017adf1b64ab7adcd2f63672b1efb
record_format Article
spelling doaj-443017adf1b64ab7adcd2f63672b1efb2020-11-25T00:43:33ZengBMCBMC Pulmonary Medicine1471-24662011-05-011113110.1186/1471-2466-11-31Cardiac safety of indacaterol in healthy subjects: a randomized, multidose, placebo- and positive-controlled, parallel-group thorough QT studyWoessner RalphHarris StuartSabo RonaldKhindri SanjeevJennings SimonDrollmann Anton F<p>Abstract</p> <p>Background</p> <p>Indacaterol is a novel once-daily ultra long-acting β<sub>2</sub>-agonist for the treatment of chronic obstructive pulmonary disease. It is known that β<sub>2</sub>-agonists, like other adrenergic compounds, can prolong the QT-interval. This thorough QT/QTc study (as per ICH E14 guideline) evaluated the effect of indacaterol on the QT interval in healthy subjects.</p> <p>Methods</p> <p>In this randomized, double-blind, parallel-group, placebo- and positive-controlled (open-label moxifloxacin) study, non-smoking healthy subjects (18-55 years, body mass index: 18.5-32.0 kg/m<sup>2</sup>) were randomized (4:4:2:4:1) to 14-day treatment with once-daily indacaterol (150 μg, 300 μg, or 600 μg), placebo, or placebo/moxifloxacin (double-blind 14-day treatment with placebo and a single open-label dose of 400 mg moxifloxacin on Day 14). The primary endpoint was the change from baseline on Day 14 in QTcF (QT interval corrected for heart rate using Fridericia's formula).</p> <p>Results</p> <p>In total, 404 subjects were randomized to receive indacaterol (150 [n = 108], 300 [n = 108], 600 μg [n = 54]), placebo (n = 107), or placebo/moxifloxacin (n = 27); 388 subjects completed the study. Maximal time-matched mean (90% confidence intervals) treatment differences from placebo in QTcF change from baseline on Day 14 were 2.66 (0.55, 4.77), 2.98 (1.02, 4.93) and 3.34 (0.86, 5.82) ms for indacaterol 150 μg, 300 μg and 600 μg, respectively. Study sensitivity was confirmed with moxifloxacin demonstrating a significant maximal time-matched QTcF prolongation of 13.90 (10.58, 17.22) ms compared to placebo. All indacaterol doses were well tolerated.</p> <p>Conclusion</p> <p>Indacaterol, at doses up to 600 μg once daily (2-4 times the therapeutic dose) does not have any clinically relevant effect on the QT interval.</p> <p>Trial Registration</p> <p>ClinicalTrials.gov: <a href="http://www.clinicaltrials.gov/ct2/show/NCT01263808">NCT01263808</a></p> http://www.biomedcentral.com/1471-2466/11/31
collection DOAJ
language English
format Article
sources DOAJ
author Woessner Ralph
Harris Stuart
Sabo Ronald
Khindri Sanjeev
Jennings Simon
Drollmann Anton F
spellingShingle Woessner Ralph
Harris Stuart
Sabo Ronald
Khindri Sanjeev
Jennings Simon
Drollmann Anton F
Cardiac safety of indacaterol in healthy subjects: a randomized, multidose, placebo- and positive-controlled, parallel-group thorough QT study
BMC Pulmonary Medicine
author_facet Woessner Ralph
Harris Stuart
Sabo Ronald
Khindri Sanjeev
Jennings Simon
Drollmann Anton F
author_sort Woessner Ralph
title Cardiac safety of indacaterol in healthy subjects: a randomized, multidose, placebo- and positive-controlled, parallel-group thorough QT study
title_short Cardiac safety of indacaterol in healthy subjects: a randomized, multidose, placebo- and positive-controlled, parallel-group thorough QT study
title_full Cardiac safety of indacaterol in healthy subjects: a randomized, multidose, placebo- and positive-controlled, parallel-group thorough QT study
title_fullStr Cardiac safety of indacaterol in healthy subjects: a randomized, multidose, placebo- and positive-controlled, parallel-group thorough QT study
title_full_unstemmed Cardiac safety of indacaterol in healthy subjects: a randomized, multidose, placebo- and positive-controlled, parallel-group thorough QT study
title_sort cardiac safety of indacaterol in healthy subjects: a randomized, multidose, placebo- and positive-controlled, parallel-group thorough qt study
publisher BMC
series BMC Pulmonary Medicine
issn 1471-2466
publishDate 2011-05-01
description <p>Abstract</p> <p>Background</p> <p>Indacaterol is a novel once-daily ultra long-acting β<sub>2</sub>-agonist for the treatment of chronic obstructive pulmonary disease. It is known that β<sub>2</sub>-agonists, like other adrenergic compounds, can prolong the QT-interval. This thorough QT/QTc study (as per ICH E14 guideline) evaluated the effect of indacaterol on the QT interval in healthy subjects.</p> <p>Methods</p> <p>In this randomized, double-blind, parallel-group, placebo- and positive-controlled (open-label moxifloxacin) study, non-smoking healthy subjects (18-55 years, body mass index: 18.5-32.0 kg/m<sup>2</sup>) were randomized (4:4:2:4:1) to 14-day treatment with once-daily indacaterol (150 μg, 300 μg, or 600 μg), placebo, or placebo/moxifloxacin (double-blind 14-day treatment with placebo and a single open-label dose of 400 mg moxifloxacin on Day 14). The primary endpoint was the change from baseline on Day 14 in QTcF (QT interval corrected for heart rate using Fridericia's formula).</p> <p>Results</p> <p>In total, 404 subjects were randomized to receive indacaterol (150 [n = 108], 300 [n = 108], 600 μg [n = 54]), placebo (n = 107), or placebo/moxifloxacin (n = 27); 388 subjects completed the study. Maximal time-matched mean (90% confidence intervals) treatment differences from placebo in QTcF change from baseline on Day 14 were 2.66 (0.55, 4.77), 2.98 (1.02, 4.93) and 3.34 (0.86, 5.82) ms for indacaterol 150 μg, 300 μg and 600 μg, respectively. Study sensitivity was confirmed with moxifloxacin demonstrating a significant maximal time-matched QTcF prolongation of 13.90 (10.58, 17.22) ms compared to placebo. All indacaterol doses were well tolerated.</p> <p>Conclusion</p> <p>Indacaterol, at doses up to 600 μg once daily (2-4 times the therapeutic dose) does not have any clinically relevant effect on the QT interval.</p> <p>Trial Registration</p> <p>ClinicalTrials.gov: <a href="http://www.clinicaltrials.gov/ct2/show/NCT01263808">NCT01263808</a></p>
url http://www.biomedcentral.com/1471-2466/11/31
work_keys_str_mv AT woessnerralph cardiacsafetyofindacaterolinhealthysubjectsarandomizedmultidoseplaceboandpositivecontrolledparallelgroupthoroughqtstudy
AT harrisstuart cardiacsafetyofindacaterolinhealthysubjectsarandomizedmultidoseplaceboandpositivecontrolledparallelgroupthoroughqtstudy
AT saboronald cardiacsafetyofindacaterolinhealthysubjectsarandomizedmultidoseplaceboandpositivecontrolledparallelgroupthoroughqtstudy
AT khindrisanjeev cardiacsafetyofindacaterolinhealthysubjectsarandomizedmultidoseplaceboandpositivecontrolledparallelgroupthoroughqtstudy
AT jenningssimon cardiacsafetyofindacaterolinhealthysubjectsarandomizedmultidoseplaceboandpositivecontrolledparallelgroupthoroughqtstudy
AT drollmannantonf cardiacsafetyofindacaterolinhealthysubjectsarandomizedmultidoseplaceboandpositivecontrolledparallelgroupthoroughqtstudy
_version_ 1725277875435732992