Frontiers in Neurology (Jun 2022)

A Randomized Clinical Trial to Evaluate the Effects of Safinamide on Apathetic Non-demented Patients With Parkinson's Disease

  • Jaime Kulisevsky,
  • Jaime Kulisevsky,
  • Jaime Kulisevsky,
  • Jaime Kulisevsky,
  • Jaime Kulisevsky,
  • Saul Martínez-Horta,
  • Saul Martínez-Horta,
  • Saul Martínez-Horta,
  • Saul Martínez-Horta,
  • Antonia Campolongo,
  • Antonia Campolongo,
  • Antonia Campolongo,
  • Antonia Campolongo,
  • Antonia Campolongo,
  • Berta Pascual-Sedano,
  • Berta Pascual-Sedano,
  • Berta Pascual-Sedano,
  • Berta Pascual-Sedano,
  • Berta Pascual-Sedano,
  • Juan Marín-Lahoz,
  • Helena Bejr-kasem,
  • Helena Bejr-kasem,
  • Helena Bejr-kasem,
  • Helena Bejr-kasem,
  • Ignacio Aracil-Bolaños,
  • Ignacio Aracil-Bolaños,
  • Ignacio Aracil-Bolaños,
  • Ignacio Aracil-Bolaños,
  • Andrea Horta-Barba,
  • Andrea Horta-Barba,
  • Andrea Horta-Barba,
  • Andrea Horta-Barba,
  • Arnau Puig-Davi,
  • Arnau Puig-Davi,
  • Arnau Puig-Davi,
  • Javier Pagonabarraga,
  • Javier Pagonabarraga,
  • Javier Pagonabarraga,
  • Javier Pagonabarraga

DOI
https://doi.org/10.3389/fneur.2022.866502
Journal volume & issue
Vol. 13

Abstract

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BackgroundApathy is highly prevalent and disabling in Parkinson's disease (PD). Pharmacological options for its management lack sufficient evidence.ObjectiveWe studied the effects of safinamide on apathy in PD.MethodsProspective, 24-week, two-site, randomized, double-blind, placebo-controlled, parallel-group exploratory study in non-demented PD on stable dopaminergic therapy randomized 1:1 to adjunct safinamide (50 mg/day for 2 weeks and 100 mg/day for 22 weeks) or placebo. The primary endpoint was the mean change from baseline to week 24 on the Apathy Scale (AS) total score. Secondary endpoints included changes in cognition, activities of daily living, motor scores, the impression of change, and safety and tolerability measures.ResultsIn total, 30 participants (active treatment = 15; placebo = 15; 80% showing clinically significant apathetic symptoms according to the AS) were enrolled, and included in the intention-to-treat analysis. Change in AS (ANOVA) showed a trend to significance [p = 0.059] mediated by a more marked decrease in AS score with safinamide (−7.5 ± 6.9) than with placebo (−2.8 ± 5.7). Post-hoc analysis (paired t-test) showed a significant positive change in the AS score between 12-week and 24-week [p = 0.001] only in the active group. No significant or trend changes were found for any of the secondary outcome variables. Adverse events were few and only mild in both treatment groups.ConclusionsSafinamide was safe and well-tolerated, but failed to provide evidence of improved apathy. The positive trend observed in the post-hoc analyses deserves to be studied in depth in larger studies.Trial RegistrationEudraCT 2017-003254-17.

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