跳至主要内容
临床试验/NCT00431782
NCT00431782已完成2 期

An Open-Label Multi-Center Study of ATI-5923 for Anticoagulation in Patients With Atrial Fibrillation

ARYx Therapeutics11 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2006年12月最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
60
试验地点
11
主要终点
INR, Coagulation Factors II, VII, IX and X. Safety Measures: ECG, Laboratory and Adverse Events

研究概览

简要总结

The primary purpose of this study (CLN-504) is to determine the safety and develop a dosing regimen of an investigational anticoagulant drug (ATI-5923) in patients with atrial fibrillation.

详细描述

ATI-5923 is a structural analog of warfarin that is being developed as an oral anticoagulant. It has a similar pharmacological profile to warfarin but was designed to provide more uniform and stable anticoagulation. ATI-5923 is a selective, non-competitive inhibitor of vitamin K epoxide reductase. ATI-5923 is metabolized by esterase to a single inactive metabolite and thus is expected to have less variable metabolism, drug-drug interactions and reduced instances of under/over coagulation, making the response safer and more predictable. The primary purpose of this study is to develop a dosing regimen and INR monitoring schedule that can be applied in an outpatient setting to safely and conveniently anticoagulate patients with atrial fibrillation to a therapeutic INR. Patients with atrial fibrillation (AF) were chosen for the study population of this trial because they require anticoagulation if they have risk factors for stroke.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Documented atrial fibrillation
  • Candidate for anticoagulation or currently receiving warfarin at screening
  • Males or females greater than 18 years of age
  • Males or females with a CHADS2 score of 0 to 2

排除标准

  • Contraindications to anticoagulation e.g., active bleeding
  • Taking other anticoagulant or antiplatelet agents other than low-dose aspirin
  • History of myocardial infarction, acute coronary syndrome, or coronary revascularization procedure within the past 3 months prior to Day 1
  • History of laboratory values suggestive of anemia (i.e., Hb <10 gm/dL)
  • Women of childbearing potential

结局指标

主要结局

INR, Coagulation Factors II, VII, IX and X. Safety Measures: ECG, Laboratory and Adverse Events

次要结局

未报告次要终点

研究者

申办方类型
Industry

研究点 (11)

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