Study of a New Anticoagulant Drug in Patients With Atrial Fibrillation
Completed · Phase 2
Conditions studied: Atrial Fibrillation
In brief
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.
Key facts
- Study ID
- NCT00431782
- Run by
- ARYx Therapeutics
- People needed
- 60
- Starts
- 2006-12-01
- Expected to finish
- 2007-10-01
- Last updated by the study team
- 2007-11-08
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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
You may not qualify if…
- 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
Where it is running
- ARYx Investigational Site — Anaheim, California, United States
- ARYx Investigational Site — Yuba City, California, United States
- ARYx Investigational Site — Deerfield Beach, Florida, United States
- ARYx Investigational Site — Winfield, Illinois, United States
- ARYx Investigational Site — Oklahoma City, Oklahoma, United States
- ARYx Investigational Site — Wellsboro, Pennsylvania, United States
- ARYx Investigational Site — Wynnewood, Pennsylvania, United States
- ARYx Investigational Site — Greer, South Carolina, United States
- ARYx Investigational Site — Spartanburg, South Carolina, United States
- ARYx Investigational Site — Memphis, Tennessee, United States
- ARYx Investigational Site — San Antonio, Texas, United States
Full record on ClinicalTrials.gov
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