| Abstrakt: |
In an open-label study, electrophysiology and pharmacokinetics of TYB-3823, a new antiarrhythmic compound, were investigated. Sixteen patients underwent an electrophysiologic study before and after intravenous (i.v.) administration of TYB-3823. Two patients each received the following increasing doses: 0.2, 0.4, 0.8, and 1 mg/kg. Eight patients received 1.2-mg/kg. TYB-3823 concentrations followed a biexponential decrease with a terminal half-life (t1/2) of 3.88 ± 0.87 h. Clearance was 47.2 ± 18.5 L/h, and volume of distribution was 250 ± 77 L. Dose-dependent pharmacokinetics were evident. Significant effects of TYB-3823 were apparent at doses ≥0.8 mg/kg (n = 12), including increase in the AH and HV interval from 92 ± 17 to 105 ± 19 ms (p < 0.002) and 47 ± 7 to 60 ± 12 ms (p < 0.005), respectively. QRS duration was prolonged from 100 ± 16 to 126 ± 22 ms (p < 0.001), accompanied by an increase of the corrected QT interval from 425 ± 28 to 465 ± 37 ms (p < 0.002). The corrected JT interval remained unchanged, however, refractoriness did not change, but monophasic action potential duration (APD) tended to decrease. TYB-3823 appeared effective against reinduction of all arrhythmias observed during the control study [atrial fibrillation, atrioventricular (AV) nodal tachycardias]. TYB-3823 depresses conduction velocity significantly without prolonging refractoriness. Therefore, TYB-3823 may be classified as a class 1C antiarrhythmic. On the basis of the present results, additional class 1B activity cannot be excluded. TYB-3823 has antiarrhythmic properties, appears to be devoid of proarrhythmic effects, and is well tolerated. |
