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Effect on Dyskinesia of the Early Combination of Amantadine to Levodopa-Therapy in Parkinson's Disease: A Randomized, Placebo-Controlled Study (PREMANDYSK)

Title: Effect on Dyskinesia of the Early Combination of Amantadine to Levodopa-Therapy in Parkinson's Disease: A Randomized, Placebo-Controlled Study (PREMANDYSK)
Authors: Rascol O; Ory-Magne F; Meissner WG; Maltete D; Defebvre L; Azulay J-P; Thobois S; Houeto J-L; Thalamas C; Sommet A; Geny C; Damier P; Anheim M; Marques A; Viallet F; Giroud M; Lefaucheur R; Costentin G; Spampinato U; Mariani L-L; Eusebio A; Prange S; Benatru I; Charif M; Brefel-Courbon C; Fabbri M; Galitzky M; Rousseau V; Ferreira JJ; Burn DJ; Corvol J-C; Samier-Foubert A; Boraud T; Tison F; Durif F; Debilly B; Bernard S; Carriere N; Mutez E; Torny F; Couratier P; Colin O; Gaudin T; Boutet P; Broussolle E; Caire C; Merle H; Nouira M; Derkinderen P; Faighel M; Talmant V; LeDily S; Lacomblez L; Bonnet A-M; Ansquer S; Rabois E; Fradet A; Vernon L; Tranchant C; Lagha-Boukbiza O; Wirth T; Catala H; Galiztky M; Saubion A; Ainaoui N; Dellapina E; Salis A; Eyvrard F; Jurado C; Boulloche N; Rey-Zermati J; Boulesteix JJ
Source: Movement Disorders, 2025
Publisher Information: John Wiley and Sons Inc
Publication Year: 2025
Collection: Newcastle University Library ePrints Service
Description: © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.Objective: Investigate the efficacy of immediate-release (IR) amantadine in reducing the risk of peak-dose dyskinesia in early Parkinson's disease (PD) as add-on to levodopa. Background: While the use of amantadine to manage dyskinesia in PD is well supported by controlled clinical trials, data on its efficacy in patients without motor complications remain limited. Methods: This 22-month, multicenter, randomized, placebo-controlled trial (NCT01538329) enrolled early PD patients on stable levodopa (≥150 mg/day for ≤1 year) without motor complications. The study included three double-blind phases: an 18-month treatment phase with adjunct amantadine-IR (200 mg/day) or placebo (Period 1), a 3-month delayed-start phase where all participants received amantadine-IR (Period 2), and a 1-month washout with placebo (Period 3). The primary outcome was dyskinesia incidence at month 18; secondary outcomes included dyskinesia rates at the end of Periods 2 and 3 to assess potential long-lasting mechanisms of the drug. Exploratory outcomes investigated the potential effects of amantadine-IR on motor and non-motor symptoms and quality of life. Results: A total of 207 patients were randomized to amantadine-IR (N = 99) or placebo (N = 108). Significantly fewer patients in the amantadine-IR group developed dyskinesia versus placebo during Period 1 (11% vs. 22%, P = 0.025), while the mean daily dose of levodopa (95% CI) increased by 70 (21–119) mg less (P = 0.005). The proportion of patients with dyskinesia was less in the amantadine-IR group versus placebo at the end of Periods 2 and 3, but the difference was not statistically significant (12% vs. 20%, P = 0.13 and 16% vs. 22%, P = 0.23, respectively). Mild but significant positive effects on freezing of gait, fatigue, and quality of life were observed during Period 1. The safety profile of amantadine-IR was in line with previous reports. ...
Document Type: article in journal/newspaper
File Description: application/pdf
Language: unknown
Relation: https://eprints.ncl.ac.uk/309588; https://eprints.ncl.ac.uk/fulltext.aspx?url=309588/1F3B4008-9113-417B-8A3C-3ECB97D1D942.pdf&pub_id=309588
Availability: https://eprints.ncl.ac.uk/309588
Rights: https://creativecommons.org/licenses/by-nc-nd/4.0/
Accession Number: edsbas.2FE7B29B
Database: BASE