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Safety and Efficacy of Long‐Term Deutetrabenazine Use in Children and Adolescents with Tics Associated with Tourette Syndrome: An Open‐Label Extension Study

BACKGROUND: Tourette syndrome (TS) is a neurodevelopmental disorder characterized by motor and phonic tics. OBJECTIVE: To assess the safety and efficacy of deutetrabenazine (Teva Neuroscience, Inc, Parsippany, NJ), a vesicular monoamine transporter 2 inhibitor, in children and adolescents with TS. M...

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Autores principales: Jankovic, Joseph, Coffey, Barbara, Claassen, Daniel O., Jimenez‐Shahed, Joohi, Gertz, Barry J., Garofalo, Elizabeth A., Stamler, David A., Wieman, Maria, Savola, Juha‐Matti, Harary, Eran, Alexander, Jessica, Barkay, Hadas, Gordon, Mark Forrest
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10525047/
https://www.ncbi.nlm.nih.gov/pubmed/37772282
http://dx.doi.org/10.1002/mdc3.13849
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author Jankovic, Joseph
Coffey, Barbara
Claassen, Daniel O.
Jimenez‐Shahed, Joohi
Gertz, Barry J.
Garofalo, Elizabeth A.
Stamler, David A.
Wieman, Maria
Savola, Juha‐Matti
Harary, Eran
Alexander, Jessica
Barkay, Hadas
Gordon, Mark Forrest
author_facet Jankovic, Joseph
Coffey, Barbara
Claassen, Daniel O.
Jimenez‐Shahed, Joohi
Gertz, Barry J.
Garofalo, Elizabeth A.
Stamler, David A.
Wieman, Maria
Savola, Juha‐Matti
Harary, Eran
Alexander, Jessica
Barkay, Hadas
Gordon, Mark Forrest
author_sort Jankovic, Joseph
collection PubMed
description BACKGROUND: Tourette syndrome (TS) is a neurodevelopmental disorder characterized by motor and phonic tics. OBJECTIVE: To assess the safety and efficacy of deutetrabenazine (Teva Neuroscience, Inc, Parsippany, NJ), a vesicular monoamine transporter 2 inhibitor, in children and adolescents with TS. METHODS: Alternatives for Reducing Tics in TS (ARTISTS) open‐label extension (OLE) (NCT03567291) was a 54‐week, global, phase 3, open‐label extension study of deutetrabenazine (6–48 mg daily) conducted May 28, 2018 to April 3, 2020 with a 2‐week randomized withdrawal period. Participants (6–16 years of age) had TS and active tics causing distress or impairment. Safety (primary outcome) was assessed by treatment‐emergent adverse events (TEAEs) and clinical laboratory testing. Efficacy was measured by the Yale Global Tic Severity Scale‐Total Tic Score (YGTSS‐TTS). RESULTS: The intent‐to‐treat population (228 participants; mean age, 12.0 years; 79.8% male; 86.4% white) had a median (range) duration of exposure of 28.4 (0.3–52.9) weeks. Of 227 participants in the safety analysis, 161 (70.9%) reported ≥1 TEAE (exposure‐adjusted incidence rate, 2.77/patient‐year), of which 95 (41.9%) were treatment related. The most frequently reported TEAEs were headaches, somnolence, nasopharyngitis, weight increases, and anxiety. No additional safety signals were observed. Worsening of YGTSS‐TTS after the 2‐week randomized withdrawal was not statistically significant (least squares mean difference, −0.4; P = 0.78). Several exploratory measures showed sustained improvement throughout the treatment periods. CONCLUSIONS: In this long‐term, open‐label trial, deutetrabenazine was well tolerated with low frequency of TEAEs. There was no significant difference in tics between treatment arms during the 2‐week randomized withdrawal period, however, descriptive statistics and comparison with baseline showed a numeric improvement in tics, quality of life, and other measures.
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spelling pubmed-105250472023-09-28 Safety and Efficacy of Long‐Term Deutetrabenazine Use in Children and Adolescents with Tics Associated with Tourette Syndrome: An Open‐Label Extension Study Jankovic, Joseph Coffey, Barbara Claassen, Daniel O. Jimenez‐Shahed, Joohi Gertz, Barry J. Garofalo, Elizabeth A. Stamler, David A. Wieman, Maria Savola, Juha‐Matti Harary, Eran Alexander, Jessica Barkay, Hadas Gordon, Mark Forrest Mov Disord Clin Pract Research Articles BACKGROUND: Tourette syndrome (TS) is a neurodevelopmental disorder characterized by motor and phonic tics. OBJECTIVE: To assess the safety and efficacy of deutetrabenazine (Teva Neuroscience, Inc, Parsippany, NJ), a vesicular monoamine transporter 2 inhibitor, in children and adolescents with TS. METHODS: Alternatives for Reducing Tics in TS (ARTISTS) open‐label extension (OLE) (NCT03567291) was a 54‐week, global, phase 3, open‐label extension study of deutetrabenazine (6–48 mg daily) conducted May 28, 2018 to April 3, 2020 with a 2‐week randomized withdrawal period. Participants (6–16 years of age) had TS and active tics causing distress or impairment. Safety (primary outcome) was assessed by treatment‐emergent adverse events (TEAEs) and clinical laboratory testing. Efficacy was measured by the Yale Global Tic Severity Scale‐Total Tic Score (YGTSS‐TTS). RESULTS: The intent‐to‐treat population (228 participants; mean age, 12.0 years; 79.8% male; 86.4% white) had a median (range) duration of exposure of 28.4 (0.3–52.9) weeks. Of 227 participants in the safety analysis, 161 (70.9%) reported ≥1 TEAE (exposure‐adjusted incidence rate, 2.77/patient‐year), of which 95 (41.9%) were treatment related. The most frequently reported TEAEs were headaches, somnolence, nasopharyngitis, weight increases, and anxiety. No additional safety signals were observed. Worsening of YGTSS‐TTS after the 2‐week randomized withdrawal was not statistically significant (least squares mean difference, −0.4; P = 0.78). Several exploratory measures showed sustained improvement throughout the treatment periods. CONCLUSIONS: In this long‐term, open‐label trial, deutetrabenazine was well tolerated with low frequency of TEAEs. There was no significant difference in tics between treatment arms during the 2‐week randomized withdrawal period, however, descriptive statistics and comparison with baseline showed a numeric improvement in tics, quality of life, and other measures. John Wiley & Sons, Inc. 2023-08-24 /pmc/articles/PMC10525047/ /pubmed/37772282 http://dx.doi.org/10.1002/mdc3.13849 Text en © 2023 The Authors. Movement Disorders Clinical Practice published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Jankovic, Joseph
Coffey, Barbara
Claassen, Daniel O.
Jimenez‐Shahed, Joohi
Gertz, Barry J.
Garofalo, Elizabeth A.
Stamler, David A.
Wieman, Maria
Savola, Juha‐Matti
Harary, Eran
Alexander, Jessica
Barkay, Hadas
Gordon, Mark Forrest
Safety and Efficacy of Long‐Term Deutetrabenazine Use in Children and Adolescents with Tics Associated with Tourette Syndrome: An Open‐Label Extension Study
title Safety and Efficacy of Long‐Term Deutetrabenazine Use in Children and Adolescents with Tics Associated with Tourette Syndrome: An Open‐Label Extension Study
title_full Safety and Efficacy of Long‐Term Deutetrabenazine Use in Children and Adolescents with Tics Associated with Tourette Syndrome: An Open‐Label Extension Study
title_fullStr Safety and Efficacy of Long‐Term Deutetrabenazine Use in Children and Adolescents with Tics Associated with Tourette Syndrome: An Open‐Label Extension Study
title_full_unstemmed Safety and Efficacy of Long‐Term Deutetrabenazine Use in Children and Adolescents with Tics Associated with Tourette Syndrome: An Open‐Label Extension Study
title_short Safety and Efficacy of Long‐Term Deutetrabenazine Use in Children and Adolescents with Tics Associated with Tourette Syndrome: An Open‐Label Extension Study
title_sort safety and efficacy of long‐term deutetrabenazine use in children and adolescents with tics associated with tourette syndrome: an open‐label extension study
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10525047/
https://www.ncbi.nlm.nih.gov/pubmed/37772282
http://dx.doi.org/10.1002/mdc3.13849
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