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Efficacy of pramipexole, a novel dopamine agonist, as monotherapy in mild to
moderate Parkinson's disease. The Pramipexole Study Group.
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A total of 335 patients with early Parkinson's disease (PD) were enrolled
in a multicenter, randomized, double-blind trial designed to assess the
efficacy and safety of pramipexole.

Entry was restricted to patients with idiopathic PD who were not receiving
levodopa. Pramipexole was administered according to an ascending dose
schedule up to 4.5 mg/d.

During the 7-week dose-escalation phase, each subject was titrated to his
or her maximally tolerated dose of study medication.

This was followed by a 24-week period of maintenance therapy.

The mean daily dose during the maintenance period was 3.8 mg. Pramipexole
significantly reduced the severity of PD symptoms and signs compared with
placebo, as measured by decreases in parts II (Activities of Daily Living)
and III (Motor Examination) of the Unified Parkinson's Disease Rating Scale
at week 24 compared with baseline (p < or = 0.0001).

Differences between the active drug and placebo groups emerged at week 3
(1.5 mg/d) in the ascending-dose interval and persisted throughout the
maintenance phase (p < or = 0.0001).

The majority of patients completed the study (pramipexole 83%, placebo 80%).

In the assessment of adverse events, nausea, insomnia, constipation,
somnolence, and visual hallucinations occurred more frequently in the
pramipexole treatment group compared with placebo patients.

No clinically significant changes were noted in blood pressure or pulse rate.

Overall, these results indicate that pramipexole is safe and effective in
the treatment of early PD.


Neurology 1997 Sep;49(3):724-728
Shannon KM, Bennett JP Jr, Friedman JH
Department of Neurological Sciences, Rush Medical College,
Rush-Presbyterian-St. Luke's Medical Center, Chicago, IL 60612, USA.
PMID: 9305331, MUID: 97450343
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