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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 (...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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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 |
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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 |
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