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Safety of converting from tetrabenazine to deutetrabenazine for the treatment of chorea

Samuel Frank*, David Stamler, Elise Kayson, Daniel O. Claassen, Amy Colcher, Charles Davis, Andrew Duker, Shirley Eberly, Lawrence Elmer, Erin Furr-Stimming, Mark Gudesblatt, Christine Hunter, Joseph Jankovic, Sandra K. Kostyk, Rajeev Kumar, Clement Loy, William Mallonee, David Oakes, Burton L. Scott, Victor SungJody Goldstein, Christina Vaughan, Claudia M. Testa, for the Huntington Study Group/Alternatives for Reducing Chorea in Huntington Disease Investigators

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

IMPORTANCE: Tetrabenazine is efficacious for chorea control; however, tolerability concerns exist. Deutetrabenazine, a novel molecule that reduces chorea, was well tolerated in a double-blind, placebo-controlled study. OBJECTIVES: To evaluate the safety and explore the efficacy of conversion from tetrabenazine to deutetrabenazine in patients with chorea associated with Huntington disease (HD). DESIGN, SETTING, AND PARTICIPANTS: In this ongoing, open-label, single-arm study that started on December 21, 2013, 37 patients at 13 Huntington Study Group sites in the United States and Australia who were taking stable doses of tetrabenazine that provided a therapeutic benefit were switched overnight to deutetrabenazine therapy. After week 1, the deutetrabenazine dose was titrated on a weekly basis for optimal chorea control. INTERVENTIONS: Deutetrabenazine administration at a dosage thought to provide comparable systemic exposure to the active metabolites of the prior, stable tetrabenazine regimen. MAIN OUTCOMESAND MEASURES: Safety measures included adverse events (AEs), clinical laboratory tests, vital signs, electrocardiograms, and validated scales. Changes in the Unified Huntington's Disease Rating Scale total maximal chorea score and total motor score were efficacy end points. RESULTS: Of the 53 patients with HD screened for the study, 37 ambulatory patients with manifest HD (mean [SD] age, 52.4 [11.5] years; 22 [59%] male and 15 [41%] female; 36 white [97.3%]) were enrolled. Deutetrabenazine was generally well tolerated, with low rates of neuropsychiatric AEs. Safety scales did not reveal subclinical toxicity with deutetrabenazine treatment. Rates of dose reduction or suspension attributable to AEs were also low. Chorea control, as measured by the total maximal chorea score, was maintained at week 1 and significantly improved at week 8 (mean [SD] change from baseline, 2.1 [3.2]; P <.001). CONCLUSIONS AND RELEVANCE: In patients with chorea, overnight conversion to deutetrabenazine therapy provided a favorable safety profile and effectively maintained chorea control.

Original languageEnglish
Pages (from-to)977-982
Number of pages6
JournalJAMA Neurology
Volume74
Issue number8
DOIs
Publication statusPublished - Aug 2017
Externally publishedYes

Bibliographical note

A correction exists for this article, the original has been updated. The correction may be found at doi: 10.1001/jamaneurol.2017.3563

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