Cargando…

Randomized, Controlled Study of Opicapone in Japanese Parkinson's Patients with Motor Fluctuations

OBJECTIVES: This placebo‐controlled, randomized study evaluated the efficacy and safety of opicapone 25‐mg and 50‐mg tablets in Japanese levodopa‐treated patients with Parkinson's disease and motor fluctuations. METHODS: Japanese adults (n = 437, age 39–83 years) with Parkinson's disease (...

Descripción completa

Detalles Bibliográficos
Autores principales: Takeda, Atsushi, Takahashi, Ryosuke, Tsuboi, Yoshio, Nomoto, Masahiro, Maeda, Tetsuya, Nishimura, Akihisa, Yoshida, Kazuo, Hattori, Nobutaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7983910/
https://www.ncbi.nlm.nih.gov/pubmed/33073879
http://dx.doi.org/10.1002/mds.28322
_version_ 1783667962232700928
author Takeda, Atsushi
Takahashi, Ryosuke
Tsuboi, Yoshio
Nomoto, Masahiro
Maeda, Tetsuya
Nishimura, Akihisa
Yoshida, Kazuo
Hattori, Nobutaka
author_facet Takeda, Atsushi
Takahashi, Ryosuke
Tsuboi, Yoshio
Nomoto, Masahiro
Maeda, Tetsuya
Nishimura, Akihisa
Yoshida, Kazuo
Hattori, Nobutaka
author_sort Takeda, Atsushi
collection PubMed
description OBJECTIVES: This placebo‐controlled, randomized study evaluated the efficacy and safety of opicapone 25‐mg and 50‐mg tablets in Japanese levodopa‐treated patients with Parkinson's disease and motor fluctuations. METHODS: Japanese adults (n = 437, age 39–83 years) with Parkinson's disease (United Kingdom Parkinson's Disease Society criteria) received opicapone 25‐mg (n = 145), opicapone 50‐mg (n = 145), or placebo (n = 147) tablets over the double‐blind treatment period (14–15 weeks). The primary efficacy assessment was change in OFF‐time; secondary efficacy assessments included OFF/ON‐time responders (≥1 hour change from baseline), total ON‐time, ON‐time with and without troublesome dyskinesia, and Unified Parkinson's Disease Rating Scale. RESULTS: The least squares mean (standard error) change in OFF‐time from baseline to the last visit was −0.42 (0.21) hour for the placebo group, −1.16 (0.22) hour for the opicapone 25 mg group, and −1.04 (0.21) hour for the opicapone 50 mg group. The percentage of ON‐time responders, changes in total ON‐time/ON‐time without troublesome dyskinesia, and Unified Parkinson's Disease Rating Scale II (at OFF) all showed statistically significant improvements versus placebo for both opicapone tablet doses (P < 0.05). Unified Parkinson's Disease Rating Scale III (at ON) was improved versus placebo in patients who received opicapone 50 mg (P < 0.05). Adverse events were more common in patients treated with opicapone 25 mg (60.0%) or opicapone 50 mg (54.5%) versus placebo (48.3%). The most commonly reported adverse event was dyskinesia (placebo, 2.7%; opicapone 25 mg, 9.0%; opicapone 50 mg, 12.4%). CONCLUSIONS: In Japanese patients, both opicapone 25 and 50 mg were significantly more effective than placebo with no dose‐dependent difference in efficacy, and both doses were well tolerated. © 2020 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
format Online
Article
Text
id pubmed-7983910
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher John Wiley & Sons, Inc.
record_format MEDLINE/PubMed
spelling pubmed-79839102021-03-24 Randomized, Controlled Study of Opicapone in Japanese Parkinson's Patients with Motor Fluctuations Takeda, Atsushi Takahashi, Ryosuke Tsuboi, Yoshio Nomoto, Masahiro Maeda, Tetsuya Nishimura, Akihisa Yoshida, Kazuo Hattori, Nobutaka Mov Disord Regular Issue Articles OBJECTIVES: This placebo‐controlled, randomized study evaluated the efficacy and safety of opicapone 25‐mg and 50‐mg tablets in Japanese levodopa‐treated patients with Parkinson's disease and motor fluctuations. METHODS: Japanese adults (n = 437, age 39–83 years) with Parkinson's disease (United Kingdom Parkinson's Disease Society criteria) received opicapone 25‐mg (n = 145), opicapone 50‐mg (n = 145), or placebo (n = 147) tablets over the double‐blind treatment period (14–15 weeks). The primary efficacy assessment was change in OFF‐time; secondary efficacy assessments included OFF/ON‐time responders (≥1 hour change from baseline), total ON‐time, ON‐time with and without troublesome dyskinesia, and Unified Parkinson's Disease Rating Scale. RESULTS: The least squares mean (standard error) change in OFF‐time from baseline to the last visit was −0.42 (0.21) hour for the placebo group, −1.16 (0.22) hour for the opicapone 25 mg group, and −1.04 (0.21) hour for the opicapone 50 mg group. The percentage of ON‐time responders, changes in total ON‐time/ON‐time without troublesome dyskinesia, and Unified Parkinson's Disease Rating Scale II (at OFF) all showed statistically significant improvements versus placebo for both opicapone tablet doses (P < 0.05). Unified Parkinson's Disease Rating Scale III (at ON) was improved versus placebo in patients who received opicapone 50 mg (P < 0.05). Adverse events were more common in patients treated with opicapone 25 mg (60.0%) or opicapone 50 mg (54.5%) versus placebo (48.3%). The most commonly reported adverse event was dyskinesia (placebo, 2.7%; opicapone 25 mg, 9.0%; opicapone 50 mg, 12.4%). CONCLUSIONS: In Japanese patients, both opicapone 25 and 50 mg were significantly more effective than placebo with no dose‐dependent difference in efficacy, and both doses were well tolerated. © 2020 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society. John Wiley & Sons, Inc. 2020-10-19 2021-02 /pmc/articles/PMC7983910/ /pubmed/33073879 http://dx.doi.org/10.1002/mds.28322 Text en © 2020 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Regular Issue Articles
Takeda, Atsushi
Takahashi, Ryosuke
Tsuboi, Yoshio
Nomoto, Masahiro
Maeda, Tetsuya
Nishimura, Akihisa
Yoshida, Kazuo
Hattori, Nobutaka
Randomized, Controlled Study of Opicapone in Japanese Parkinson's Patients with Motor Fluctuations
title Randomized, Controlled Study of Opicapone in Japanese Parkinson's Patients with Motor Fluctuations
title_full Randomized, Controlled Study of Opicapone in Japanese Parkinson's Patients with Motor Fluctuations
title_fullStr Randomized, Controlled Study of Opicapone in Japanese Parkinson's Patients with Motor Fluctuations
title_full_unstemmed Randomized, Controlled Study of Opicapone in Japanese Parkinson's Patients with Motor Fluctuations
title_short Randomized, Controlled Study of Opicapone in Japanese Parkinson's Patients with Motor Fluctuations
title_sort randomized, controlled study of opicapone in japanese parkinson's patients with motor fluctuations
topic Regular Issue Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7983910/
https://www.ncbi.nlm.nih.gov/pubmed/33073879
http://dx.doi.org/10.1002/mds.28322
work_keys_str_mv AT takedaatsushi randomizedcontrolledstudyofopicaponeinjapaneseparkinsonspatientswithmotorfluctuations
AT takahashiryosuke randomizedcontrolledstudyofopicaponeinjapaneseparkinsonspatientswithmotorfluctuations
AT tsuboiyoshio randomizedcontrolledstudyofopicaponeinjapaneseparkinsonspatientswithmotorfluctuations
AT nomotomasahiro randomizedcontrolledstudyofopicaponeinjapaneseparkinsonspatientswithmotorfluctuations
AT maedatetsuya randomizedcontrolledstudyofopicaponeinjapaneseparkinsonspatientswithmotorfluctuations
AT nishimuraakihisa randomizedcontrolledstudyofopicaponeinjapaneseparkinsonspatientswithmotorfluctuations
AT yoshidakazuo randomizedcontrolledstudyofopicaponeinjapaneseparkinsonspatientswithmotorfluctuations
AT hattorinobutaka randomizedcontrolledstudyofopicaponeinjapaneseparkinsonspatientswithmotorfluctuations