Drug intelligence / Profile preview

tedisamil

Development stage
Phase 3
Lead developer
Abbott
Modality
Small Molecules
Administration
Intravenous
01

Overview

Tedisamil is an investigational class III antiarrhythmic small molecule developed primarily for the treatment of atrial fibrillation and atrial flutter. It acts as a potassium channel blocker, prolonging action potential duration and the QT interval in cardiac tissue. Tedisamil blocks multiple types of potassium channels in the heart, resulting in slowed heart rate and more efficient repolarization in atrial muscle compared to ventricular muscle. It also exhibits significant anti-ischemic properties and was initially investigated for angina pectoris before its antiarrhythmic effects were discovered. Tedisamil is administered intravenously and has a half-life of approximately 8–13 hours[1][2][4][5][6].

Brand names
Pulzium
Other names
tedisamil
02

Targets

SCN5A (Sodium channel protein type 5 subunit alpha)KCND2 (Transient outward potassium channel subunit Kv4.2)KCNH2 (Voltage-gated potassium channel subfamily H member 2)SUR2A (ATP-binding cassette sub-family C member 9)

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