At a glance
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A Phase 3, 12-Week, Double-Blind, Double-Dummy, Placebo- and Active-Controlled Efficacy and Safety Study of Preladenant in Subjects With Moderate to Severe Parkinson's Disease (Phase 3;Protocol No. P04938)
In Brief
A Phase 3 clinical trial evaluating Preladenant 2 mg tablet, Preladenant 5 mg tablet, and 4 other interventions for Parkinson Disease. Completed, enrolled 778 participants.
Detailed Summary
When a patient with Parkinson's disease (PD) is initially treated with L-dopa or dopamine agonists, the symptoms of PD improve or disappear. After several years of taking L dopa or dopamine agonists, patients notice that their PD medications wear off sooner than when they first started taking them. This "wearing off" is characterized by the return of symptoms (i.e., tremor, slowness, and rigidity) and may occur over the course of a few minutes to an hour. When a patient's PD symptoms have returned, the patient is said to be in the "off" state. When the patient takes another dose of medication, and his/her PD symptoms improve or resolve, the patient is said to be in the "on" state. Antagonism of adenosine Type 2a receptors (A2a) may provide relief of PD symptoms. This trial will test the hypothesis that A2a receptor antagonism can lead to improvement in the function of PD participants taking a stable dose of L-dopa, as measured by a reduction in "off" time.
Study Details
Timeline
Interventions
one 2 mg tablet orally twice daily
one 5 mg tablet orally twice daily
one 10 mg tablet orally twice daily
one tablet orally twice daily
one 1 mg capsule orally in AM
one capsule orally in AM