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A randomized double-blind placebo- and positive-controlled crossover study to evaluate the effects of single doses of SD-809 (deutetrabenazine) and tetrabenazine on the corrected QT interval

D. Stamler, E. Offman, M. Bradbury, L. De Boer (La Jolla, CA, USA)

Meeting: 2016 International Congress

Abstract Number: 1105

Keywords: Chorea (also see specific diagnoses, etc): Treatment, Huntingtons disease

Session Information

Date: Wednesday, June 22, 2016

Session Title: Huntington's disease

Session Time: 12:00pm-1:30pm

Location: Exhibit Hall located in Hall B, Level 2

Objective: Evaluate the pharmacokinetics and pharmacodynamics (QTc) of SD-809 (deutetrabenazine) and tetrabenazine.

Background: SD-809 is a VMAT-2 inhibitor in clinical development for treatment of hyperkinetic movement disorders. In a thorough QT (TQT) study, 50 mg of tetrabenazine (TBZ) prolonged the corrected QT (QTc) interval by approximately 8 msec. QT prolongation predisposes to life-threatening ventricular arrhythmias.

Methods: In this double-blind, placebo- and positive-controlled, six-period crossover study, 48 healthy subjects were randomized to one of six treatment sequences. Treatments were separated by a 5-day washout and included single oral doses of SD-809 12 and 24 mg, TBZ 50 mg, moxifloxacin 400 mg and placebo controls. Triplicate 12-lead ECGs were recorded pre-dose and at 12 time points over 24 hours following drug administration. The primary outcome measures were the placebo-adjusted change from baseline in QTcF (ΔΔQTcF) for each SD-809 dose and TBZ. Moxifloxacin was utilized for assay sensitivity. Safety was assessed with adverse event monitoring and clinical laboratory tests.

Results: Forty-two subjects completed all treatments. The maximal mean (90% CI) ΔΔQTcF for SD-809 12 and 24 mg was 2.8 (0.7, 4.8) and 4.5 (2.4, 6.5) msec, respectively, whereas for TBZ 50 mg it was 7.6 (5.6, 9.5) msec. No subjects treated with SD-809 experienced a QTcF interval > 450 msec whereas one subject treated with TBZ experienced one. SD-809 24 mg provided comparable exposure (AUCinf) to circulating drug as 50 mg of TBZ, but with a lower Cmax. Assay sensitivity was demonstrated with moxifloxacin. Study treatments were generally well tolerated, as no severe or serious adverse events were reported.

Conclusions: In this TQT study, SD-809 up to 24 mg increased QTcF by <5 msec, below the threshold of regulatory concern. These results indicate that a single dose of SD-809 up to 24 mg does not have a clinically relevant effect on cardiac repolarization.

To cite this abstract in AMA style:

D. Stamler, E. Offman, M. Bradbury, L. De Boer. A randomized double-blind placebo- and positive-controlled crossover study to evaluate the effects of single doses of SD-809 (deutetrabenazine) and tetrabenazine on the corrected QT interval [abstract]. Mov Disord. 2016; 31 (suppl 2). https://www.mdsabstracts.org/abstract/a-randomized-double-blind-placebo-and-positive-controlled-crossover-study-to-evaluate-the-effects-of-single-doses-of-sd-809-deutetrabenazine-and-tetrabenazine-on-the-corrected-qt-interval/. Accessed May 14, 2025.
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