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Rationale, design, and baseline characteristics in Evaluation of LIXisenatide in Acute Coronary Syndrome, a long-term cardiovascular end point trial of lixisenatide versus placebo

dc.contributor.authorBENTLEY-LEWIS, Rhonda
dc.contributor.authorAGUILAR, David
dc.contributor.authorRIDDLE, Matthew C.
dc.contributor.authorCLAGGETT, Brian
dc.contributor.authorDIAZ, Rafael
dc.contributor.authorDICKSTEIN, Kenneth
dc.contributor.authorGERSTEIN, Hertzel C.
dc.contributor.authorJOHNSTON, Peter
dc.contributor.authorKOBER, Lars V.
dc.contributor.authorLAWSON, Francesca
dc.contributor.authorLEWIS, Eldrin F.
dc.contributor.authorMAGGIONI, Aldo P.
dc.contributor.authorMCMURRAY, John J. V.
dc.contributor.authorPING, Lin
dc.contributor.authorPROBSTFIELD, Jeffrey L.
dc.contributor.authorSOLOMON, Scott D.
dc.contributor.authorTARDIF, Jean-Claude
dc.contributor.authorWU, Yujun
dc.contributor.authorPFEFFER, Marc A.
dc.contributor.authorCATARGI, Bogdan
dc.contributor.authorINVESTIGATORS, Elixa
dc.date.accessioned2020-09-03T08:02:20Z
dc.date.available2020-09-03T08:02:20Z
dc.date.issued2015
dc.identifier.issn0002-8703
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/11016
dc.description.abstractEnBackground Cardiovascular (CV) disease is the leading cause of morbidity andmortality in patients with type 2 diabetes mellitus (T2DM). Furthermore, patients with T2DM and acute coronary syndrome (ACS) have a particularly high risk of CV events. The glucagon-like peptide 1 receptor agonist, lixisenatide, improves glycemia, but its effects on CV events have not been thoroughly evaluated. Methods ELIXA (www.clinicaltrials.govno.NCT01147250) is a randomized, double-blind, placebo-controlled, parallel-group, multicenter study of lixisenatide in patients with T2DM and a recent ACS event. The primary aim is to evaluate the effects of lixisenatide on CV morbidity and mortality in a population at high CV risk. The primary efficacy end point is a composite of time to CV death, nonfatal myocardial infarction, nonfatal stroke, or hospitalization for unstable angina. Data are systematically collected for safety outcomes, including hypoglycemia, pancreatitis, and malignancy. Results Enrollment began in July 2010 and ended in August 2013; 6,068 patients from 49 countries were randomized. Of these, 69% are men and 75% are white; at baseline, the mean +/- SD age was 60.3 +/- 9.7 years, body mass index was 30.2 +/- 5.7 kg/m(2), and duration of T2DM was 9.3 +/- 8.2 years. The qualifying ACS was a myocardial infarction in 83% and unstable angina in 17%. The study will continue until the positive adjudication of the protocol-specified number of primary CV events. Conclusion ELIXA will be the first trial to report the safety and efficacy of a glucagon-like peptide 1 receptor agonist in people with T2DM and high CV event risk.
dc.language.isoen
dc.title.enRationale, design, and baseline characteristics in Evaluation of LIXisenatide in Acute Coronary Syndrome, a long-term cardiovascular end point trial of lixisenatide versus placebo
dc.typeArticle de revue
dc.identifier.doi10.1016/j.ahj.2015.02.002
dc.subject.halChimie/Matériaux
bordeaux.journalAmerican Heart Journal
bordeaux.page631-U75
bordeaux.volume169
bordeaux.hal.laboratoriesInstitut de Chimie & de Biologie des Membranes & des Nano-objets (CBMN) - UMR 5248*
bordeaux.hal.laboratoriesInstitut de Chimie & de Biologie des Membranes & des Nano-objets (CBMN, UMR 5248)
bordeaux.issue5
bordeaux.institutionUniversité de Bordeaux
bordeaux.institutionBordeaux INP
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