Int. Journal of Clinical Pharmacology and Therapeutics, Volume 53 - April (301 - 316)

A thorough QT study of guanfacine
Patrick Martin1, Lawrence Satin2, Robert S. Kahn3, Antoine Robinson1, Mary Corcoran1, Jaideep Purkayastha1, Sharon Youcha4, James C. Ermer1
1 Shire Development LLC, Wayne, PA, 2 Independent Consultant in Cardiac Safety, Wellington, FL, 3 Genentech, San Francisco, CA, and 4 Drexel University College of Medicine, Philadelphia, PA, USA

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DOI 10.5414/CP202065

Abstract

Objectives: Guanfacine extended- release (GXR) is approved for the treatment of attention-deficit/hyperactivity disorder in children and adolescents. As part of the clinical development of GXR, and to further explore the effect of guanfacine on QT intervals, a thorough QT study of guanfacine was conducted (ClinicalTrials. gov identifier: NCT00672984). Methods: In this double-blind, 3-period, crossover trial, healthy adults (n = 83) received immediaterelease guanfacine (at therapeutic (4 mg) and supra-therapeutic (8 mg) doses), placebo, and 400 mg moxifloxacin (positive control) in 1 of 6 randomly assigned sequences. Continuous 12-lead electrocardiograms were extracted, and guanfacine plasma concentrations were assessed pre-dose and at intervals up to 24 hours post-dose. QT intervals were corrected using 2 methods: subject-specific (QTcNi) and Fridericia (QTcF). Time-matched analyses examined the largest, baseline-adjusted, drug-placebo difference in QTc intervals. Results: In the QTcNi analysis, the largest 1-sided 95% upper confidence bound (UCB) through hour 12 was 1.94 ms (12 hours postdose). For the 12-hour QTcF analysis, the largest 1-sided 95% UCB was 10.34 ms (12 hours post-supratherapeutic dose), representing the only 1-sided 95% UCB > 10 ms. Following the supra-therapeutic dose, maximum guanfacine plasma concentration was attained at 5.0 hours (median) post-dose. Assay sensitivity was confirmed by moxifloxacin results. Among guanfacine-treated subjects, most treatment-emergent adverse events were mild (78.9%); dry mouth (65.8%) and dizziness (61.8%) were most common. Conclusions: Neither therapeutic nor supra-therapeutic doses of guanfacine prolonged QT interval after adjusting for heart rate using individualized correction, QTcNi, through 12 hours postdose. Guanfacine does not appear to interfere with cardiac repolarization of the form associated with pro-arrhythmic drugs.

Author Details

Authors

Departments

  • 1 Shire Development LLC, Wayne, PA,
  • 2 Independent Consultant in Cardiac Safety, Wellington, FL,
  • 3 Genentech, San Francisco, CA, and
  • 4 Drexel University College of Medicine, Philadelphia, PA, USA

Address

Patrick Martin, MD, Vice President
Global Clinical Pharmacology and Pharmacokinetics
Shire Development LLC
725 Chesterbrook Blvd., Wayne, PA 19087, USA
Email: [email protected]

Citation

Patrick Martin, Lawrence Satin, Robert S. Kahn, Antoine Robinson, Mary Corcoran, Jaideep Purkayastha, Sharon Youcha, and James C. Ermer.A thorough QT study of guanfacine. 2015; 53: 301-316. doi: 10.5414/CP202065.

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