Effect of Deutetrabenazine on Chorea Among Patients With Huntington Disease: A Randomized Clinical Trial

Authors

Samuel Frank, Harvard Medical School, Boston, Massachusetts.
Claudia M. Testa, Virginia Commonwealth University, Richmond, Virginia.
David Stamler, Teva Pharmaceuticals Ltd, Frazer, Pennsylvania.
Elise Kayson, Center for Human Experimental Therapeutics, University of Rochester, Rochester, New York.
Charles Davis, CSD Biostatistics, Tucson, Arizona.
Mary C. Edmondson, Duke University, Durham, North Carolina.
Shari Kinel, Huntington Study Group, Rochester, New York.
Blair Leavitt, Centre of Molecular Medicine and Therapeutics, University of British Columbia, Vancouver, Canada.
David Oakes, University of Rochester, Rochester, New York.
Christine O'Neill, Wake Forest School of Medicine, Winston-Salem, North Carolina.
Christina Vaughan, Medical University of South Carolina, Charleston, South Carolina.
Jody Goldstein, Center for Human Experimental Therapeutics, University of Rochester, Rochester, New York.
Margaret Herzog, Center for Human Experimental Therapeutics, University of Rochester, Rochester, New York.
Victoria Snively, Center for Human Experimental Therapeutics, University of Rochester, Rochester, New York.
Jacquelyn Whaley, Center for Human Experimental Therapeutics, University of Rochester, Rochester, New York.
Cynthia Wong, Teva Pharmaceuticals Ltd, Frazer, Pennsylvania.
Greg Suter, Hereditary Neurological Disease Centre, Wichita, Kansas.
Joseph Jankovic, Baylor College of Medicine, Houston, Texas.
Joohi Jimenez-Shahed, Baylor College of Medicine, Houston, Texas.
Christine Hunter, Baylor College of Medicine, Houston, Texas.
Daniel O. Claassen, Vanderbilt University Medical Center, Nashville, Tennessee.
Olivia C. Roman, Vanderbilt University Medical Center, Nashville, Tennessee.
Victor Sung, University of Alabama School of Medicine, Birmingham, Alabama.
Jenna Smith, University of Alabama School of Medicine, Birmingham, Alabama.
Sarah Janicki, Columbia University, New York, New York.
Ronda Clouse, Columbia University, New York, New York.
Marie Saint-Hilaire, Boston University Medical Campus, Boston, Massachusetts.
Anna Hohler, Boston University Medical Campus, Boston, Massachusetts.
Denyse Turpin, Boston University Medical Campus, Boston, Massachusetts.
Raymond C. James, Boston University Medical Campus, Boston, Massachusetts.
Ramon Rodriguez, University of Florida College of Medicine, Gainesville, Florida.

Document Type

Article

Abstract

IMPORTANCE: Deutetrabenazine is a novel molecule containing deuterium, which attenuates CYP2D6 metabolism and increases active metabolite half-lives and may therefore lead to stable systemic exposure while preserving key pharmacological activity. OBJECTIVE: To evaluate efficacy and safety of deutetrabenazine treatment to control chorea associated with Huntington disease. DESIGN, SETTING, AND PARTICIPANTS: Ninety ambulatory adults diagnosed with manifest Huntington disease and a baseline total maximal chorea score of 8 or higher (range, 0-28; lower score indicates less chorea) were enrolled from August 2013 to August 2014 and randomized to receive deutetrabenazine (n = 45) or placebo (n = 45) in a double-blind fashion at 34 Huntington Study Group sites. INTERVENTIONS: Deutetrabenazine or placebo was titrated to optimal dose level over 8 weeks and maintained for 4 weeks, followed by a 1-week washout. MAIN OUTCOMES AND MEASURES: Primary end point was the total maximal chorea score change from baseline (the average of values from the screening and day-0 visits) to maintenance therapy (the average of values from the week 9 and 12 visits) obtained by in-person visits. This study was designed to detect a 2.7-unit treatment difference in scores. The secondary end points, assessed hierarchically, were the proportion of patients who achieved treatment success on the Patient Global Impression of Change (PGIC) and on the Clinical Global Impression of Change (CGIC), the change in 36-Item Short Form- physical functioning subscale score (SF-36), and the change in the Berg Balance Test. RESULTS: Ninety patients with Huntington disease (mean age, 53.7 years; 40 women [44.4%]) were enrolled. In the deutetrabenazine group, the mean total maximal chorea scores improved from 12.1 (95% CI, 11.2-12.9) to 7.7 (95% CI, 6.5-8.9), whereas in the placebo group, scores improved from 13.2 (95% CI, 12.2-14.3) to 11.3 (95% CI, 10.0-12.5); the mean between-group difference was -2.5 units (95% CI, -3.7 to -1.3) (P < .001). Treatment success, as measured by the PGIC, occurred in 23 patients (51%) in the deutetrabenazine group vs 9 (20%) in the placebo group (P = .002). As measured by the CGIC, treatment success occurred in 19 patients (42%) in the deutetrabenazine group vs 6 (13%) in the placebo group (P = .002). In the deutetrabenazine group, the mean SF-36 physical functioning subscale scores decreased from 47.5 (95% CI, 44.3-50.8) to 47.4 (44.3-50.5), whereas in the placebo group, scores decreased from 43.2 (95% CI, 40.2-46.3) to 39.9 (95% CI, 36.2-43.6), for a treatment benefit of 4.3 (95% CI, 0.4 to 8.3) (P = .03). There was no difference between groups (mean difference of 1.0 unit; 95% CI, -0.3 to 2.3; P = .14), for improvement in the Berg Balance Test, which improved by 2.2 units (95% CI, 1.3-3.1) in the deutetrabenazine group and by 1.3 units (95% CI, 0.4-2.2) in the placebo group. Adverse event rates were similar for deutetrabenazine and placebo, including depression, anxiety, and akathisia. CONCLUSIONS AND RELEVANCE: Among patients with chorea associated with Huntington disease, the use of deutetrabenazine compared with placebo resulted in improved motor signs at 12 weeks. Further research is needed to assess the clinical importance of the effect size and to determine longer-term efficacy and safety. TRIAL REGISTRATION: clinicaltrials.gov Identifier: NCT01795859.

Medical Subject Headings

Adrenergic Uptake Inhibitors (therapeutic use); Chorea (drug therapy); Cytochrome P-450 CYP2D6 (metabolism); Double-Blind Method; Drug Administration Schedule; Female; Humans; Huntington Disease (drug therapy); Maintenance Chemotherapy (methods); Male; Middle Aged; Tetrabenazine (analogs & derivatives, therapeutic use); Treatment Outcome

Publication Date

7-5-2016

Publication Title

JAMA

E-ISSN

1538-3598

Volume

316

Issue

1

First Page

40

Last Page

50

PubMed ID

27380342

Digital Object Identifier (DOI)

10.1001/jama.2016.8655

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