The primary objective of this research project is to assess the effects on walking distance of SR33589B administered orally for one month to patients with left ventricular dysfunction and in NYHA class I-II. Secondary objectives are to assess the effects of SR33589B on ejection fraction, NYHA status, cardiothoracic ration, liver and renal function. Holter parameters with respect to PVC counts, arrhythmic events, heart rate and QT variability will be measured as well as the relationship between plasma concentration of SR33589B and its metabolite and changes in hemodynamic and electrophysiological parameters. Because of the potency of SR33589B as compared to amiodarone (proven to be 3 to 10 times more potent in several animal models) and the fact that it appears to be less toxic, SR33589B may provide a more effetive, yet less toxic treatment for patients with left ventricular dysfunction.

Project Start
1997-02-10
Project End
1997-11-30
Budget Start
1996-10-01
Budget End
1997-09-30
Support Year
37
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of Alabama Birmingham
Department
Type
DUNS #
004514360
City
Birmingham
State
AL
Country
United States
Zip Code
35294
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