Effect of Eleclazine on QT, Safety, and Tolerability in Adults With Long QT2 Syndrome
Status: | Completed |
---|---|
Conditions: | Cardiology |
Therapuetic Areas: | Cardiology / Vascular Diseases |
Healthy: | No |
Age Range: | 18 - 65 |
Updated: | 7/13/2016 |
Start Date: | July 2015 |
End Date: | June 2016 |
A Double-blind, Placebo-controlled Study to Evaluate the Effect of GS-6615 on QT, Safety and Tolerability in Subjects With Long QT2 Syndrome
This study will evaluate the effect of oral eleclazine (GS-6615) on QTc interval, safety,
and tolerability in adults with long QT2 syndrome.
and tolerability in adults with long QT2 syndrome.
Inclusion Criteria:
- Individuals with an established diagnosis of LQT2 (by genotype testing)
- Mean (of triplicate) QTc interval ≥ 480 msec for at least four out of seven time
points, determined by standard 12-lead ECG, at screening
Exclusion Criteria:
- Known mutations associated with LQT1 or LQT3
- Known or suspected history of seizures or epilepsy
- History of heart failure defined as New York Heart Association (NYHA) Class IV and/or
known left ventricular ejection fraction (EF) ≤ 45%
- Body mass index (BMI) ≥ 36 kg/m^2 at screening
- Severe renal impairment at screening (defined as an estimated glomerular filtration
rate (eGFR) < 30 mL/min/1.73m^2, using the 4 Variable Modification of Diet in Renal
Disease (MDRD) equation), as determined by the study center
- Abnormal liver function tests at screening, defined as alanine aminotransferase (ALT)
or aspartate aminotransferase (AST) > 2 x upper limit of normal (ULN), or total
bilirubin > 1.5 x ULN
- An aborted cardiac arrest (ACA), implantable cardioverter-defibrillator (ICD)
implantation, syncopal episode, or appropriate ICD therapy within 3 months prior to
screening
- Any other condition or circumstance that in the opinion of the investigator would
preclude compliance with the study protocol
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