MODERATO Study to Assess the Effect of Rasagiline on Patients With Parkinson Disease and Mild Cognitive Impairment

Summary

Parkinson disease (PD) with mild cognitive impairment (PD-MCI) is relatively common in nondemented PD patients, but currently there is no approved treatment. The phase 4 MODERATO is evaluating the effect of 24 weeks of treatment with rasagiline 1 mg/d as add-on therapy in adults with PD-MCI. The trial, which has enrolled 170 patients, is the largest to date to evaluate a treatment for PC-MCI.

  • MODERATO
  • NCT01723228
  • rasagiline
  • Parkinson disease
  • mild cognitive impairment
  • PD-MCI
  • neurology clinical trials
  • extrapyramidal & movement disorders

Parkinson disease with mild cognitive impairment (PD-MCI) is thought to affect as many as one-third of nondemented PD patients. However, it is rarely diagnosed, and currently there are no approved treatments. The MODERATO study [NCT01723228] is designed to evaluate the effect of rasagiline on cognitive function in adult PD patients with MCI. Daniel Weintraub, MD, University of Pennsylvania and the Parkinson’s Disease Center at the Philadelphia VA Medical Center, Philadelphia, Pennsylvania, USA, and one of the study investigators, presented the MODERATO study design and the baseline data for the enrolled patients.

Rasagiline is a selective irreversible MAO-B inhibitor indicated for the treatment of signs and symptoms of PD. Results of a small randomized, double-blind, placebo-controlled study indicated that it might exert beneficial effects on attention and executive abilities in PD patients with MCI [Hanagasi HA et al. Mov Disord. 2011].

MODERATO, the largest trial to date to evaluate a treatment for PD-MCI, is a 24-week, double-blind, placebo-controlled, phase 4 add-on study in men and women aged 45 through 80 years with idiopathic PD (based on the UK Parkinson’s Disease Society Brain Bank Clinical Diagnostic Criteria) and PD-MCI as defined by the Movement Disorder Society Task Force Diagnostic Criteria and a Montreal Cognitive Assessment (MoCA) rating scale score of 20 to 25. Patients were required to be Hoehn and Yahr stage ≥ 1 and ≤ 3 and on a stable dopaminergic medication regimen for ≥ 30 days before entering the study. Patients with dementia were excluded. Eligible participants were randomized to 24 weeks of treatment with rasagiline 1 mg/d or placebo in addition to their current medications.

The purpose of the study is to measure the effectiveness of rasagiline on cognition in PD-MCI individuals with mild cognitive impairment. The primary study outcome measure is the mean change from baseline to week 24 in the Scales for Outcomes in Parkinson’s Disease-Cognition summary score. Key secondary measures include the Unified Parkinson’s Disease Rating Scale motor and activities of daily living scores, MoCA scores, and Functional Independence Index. A total of 170 patients have been enrolled from 40 study centers.

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