Study design and rationale of a comparison of prasugrel and clopidogrel in medically managed patients with unstable angina/non–ST-segment elevation myocardial infarction: The TaRgeted platelet Inhibition to cLarify the Optimal strateGy to medicallY manage Acute Coronary Syndromes (TRILOGY ACS) trial

Practice guidelines recommend dual antiplatelet therapy with aspirin and clopidogrel for patients with non–ST-segment elevation acute coronary syndromes (NSTE ACS) regardless of in-hospital management strategy. Prasugrel—a thienopyridine adenosine diphosphate receptor antagonist that provides higher...

Full description

Saved in:
Bibliographic Details
Published inThe American heart journal Vol. 160; no. 1; pp. 16 - 22.e1
Main Authors Chin, Chee Tang, Roe, Matthew T., Fox, Keith A.A., Prabhakaran, Dorairaj, Marshall, Debra A., Petitjean, Helene, Lokhnygina, Yuliya, Brown, Eileen, Armstrong, Paul W., White, Harvey D., Ohman, E. Magnus
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Inc 01.07.2010
Mosby
Elsevier Limited
Subjects
Online AccessGet full text
ISSN0002-8703
1097-6744
1097-6744
DOI10.1016/j.ahj.2010.04.022

Cover

More Information
Summary:Practice guidelines recommend dual antiplatelet therapy with aspirin and clopidogrel for patients with non–ST-segment elevation acute coronary syndromes (NSTE ACS) regardless of in-hospital management strategy. Prasugrel—a thienopyridine adenosine diphosphate receptor antagonist that provides higher and less variable levels of platelet inhibition than clopidogrel—has demonstrated benefit when used to treat ACS patients undergoing percutaneous coronary intervention. However, the optimal approach to antiplatelet therapy for high-risk, medically managed NSTE ACS patients remains uncertain, as these patients have not been the focus of previous clinical trials of these therapies. TRILOGY ACS is a phase 3, randomized, double-blind trial enrolling approximately 10,300 NSTE ACS patients within 10 days of presentation with either unstable angina or NSTE myocardial infarction who are not intended to undergo revascularization procedures for their index event. Patients will be randomly allocated to prasugrel + aspirin versus clopidogrel + aspirin for a median duration of 18 months. A reduction in the maintenance dose of prasugrel for elderly patients (age ≥75 years) and those with body weight <60 kg is planned. The primary composite efficacy end point will be time to first occurrence of cardiovascular death, myocardial infarction, or stroke in patients aged <75 years. If the superiority of prasugrel is established in patients aged <75 years, the treatment arms will then be compared for all subjects (including those aged ≥75 years). TRILOGY ACS is the largest randomized clinical trial to date focusing exclusively on medically managed NSTE ACS patients and will provide important information regarding the optimal approach to oral antiplatelet therapy for this high-risk, understudied population.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ObjectType-Undefined-3
ISSN:0002-8703
1097-6744
1097-6744
DOI:10.1016/j.ahj.2010.04.022