Your browser doesn't support javascript.
loading
Absence of QTc prolongation in a thorough QT study with subcutaneous liraglutide, a once-daily human GLP-1 analog for treatment of type 2 diabetes.
Chatterjee, Dhruba J; Khutoryansky, Naum; Zdravkovic, Milan; Sprenger, Craig R; Litwin, Jeffrey S.
Affiliation
  • Chatterjee DJ; Clinical Research, Novo Nordisk, Inc, Princeton, NJ 08540, USA. dcee@novonordisk.com
J Clin Pharmacol ; 49(11): 1353-62, 2009 Nov.
Article de En | MEDLINE | ID: mdl-19737980
The objective of this study was to establish effects of liraglutide on the QTc interval. In this randomized, placebo-controlled, double-blind crossover study, 51 healthy participants were administered placebo, 0.6, 1.2, and 1.8 mg liraglutide once daily for 7 days each. Electrocardiograms were recorded periodically over 24 hours at the end of placebo and highest dosing periods. Four different models for QT correction were used: QTci, as the primary endpoint, and QTciL, QTcF, and QTcB as secondary endpoints. The upper bound of the 1-sided 95% confidence interval for time-matched, baseline-corrected, placebo-subtracted QTc intervals was <10 ms for all 4 correction methods. Moxifloxacin (400 mg) increased QTc intervals by 10.6 to 12.3 ms at 2 hours. There was no concentration-exposure dependency on QTc interval changes by liraglutide and no QTc thresholds above 500 ms or QTc increases >60 ms. The authors conclude that liraglutide caused no clinically relevant increases in the QTc interval.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Électrocardiographie / Glucagon-like peptide 1 Type d'étude: Clinical_trials / Prognostic_studies / Risk_factors_studies Limites: Adolescent / Adult / Female / Humans / Male / Middle aged Langue: En Journal: J Clin Pharmacol Année: 2009 Type de document: Article Pays d'affiliation: États-Unis d'Amérique Pays de publication: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Électrocardiographie / Glucagon-like peptide 1 Type d'étude: Clinical_trials / Prognostic_studies / Risk_factors_studies Limites: Adolescent / Adult / Female / Humans / Male / Middle aged Langue: En Journal: J Clin Pharmacol Année: 2009 Type de document: Article Pays d'affiliation: États-Unis d'Amérique Pays de publication: Royaume-Uni