The purpose of this double-blind, placebo controlled study is to evaluate the safety and effectiveness of an investigational Parkinson's disease drug in patients with advanced disease who are not well-controlled on their L-dopa medication.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
393
Mean change from baseline in awake time "off" at Week 24 LOCF (last observation carried forward).
Mean change from baseline in:
amount and percent of awake time spent "on"
percent awake time spent "off"
Unified Parkinson's Disease Rating Scale (UPDRS) total motor score
UPDRS Activities of Daily Living score
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
GSK Investigational Site
Birmingham, Alabama, United States
GSK Investigational Site
Northridge, California, United States
GSK Investigational Site
San Francisco, California, United States
GSK Investigational Site
Englewood, Colorado, United States
GSK Investigational Site
Boca Raton, Florida, United States
GSK Investigational Site
Panama City, Florida, United States
GSK Investigational Site
St. Petersburg, Florida, United States
GSK Investigational Site
Tampa, Florida, United States
GSK Investigational Site
Atlanta, Georgia, United States
GSK Investigational Site
Atlanta, Georgia, United States
...and 66 more locations