跳至主要内容
临床试验/JPRN-jRCT2080221435
JPRN-jRCT2080221435未知3 期

A Randomised, Double-blind, Double-dummy, Parallel Group, International (Asian), Multicenter, Phase 3 Study to Assess Safety and Efficacy of AZD6140 on Top of Low Dose Acetyl Salicylic Acid (ASA) Versus Clopidogrel on Top of Low Dose ASA in Asian/Japanese Patients With Non-ST or ST Elevation Acute Coronary Syndromes(ACS) for Whom PCI is Planned

AstraZeneca0 个研究点开始时间: 2011年4月18日最近更新:
适应症

试验速览

阶段
3 期
发起方
AstraZeneca

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • Provision of signed informed consent
  • - Index event of non-ST or ST segment elevation ACS

排除标准

  • - Index event is an acute complication of percutaneous coronary intervention
  • - Patient has undergone Percutaneous Coronary Intervention (PCI) after the index event before the first dose of study treatment
  • - Oral anticoagulation therapy that cannot be stopped
  • - The conditions associated with increased risk of bradycardiac events

研究者

发起方
AstraZeneca

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