The primary objectives of this study are to assess the efficacy of TB006 in improving motor function and to assess the safety of TB006 in participants with Parkinson's Disease (PD).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
62
Parkinson's Research Centers of America - Orange County
Aliso Viejo, California, United States
Parkinson's Research Centers of America - Palo Alto
Palo Alto, California, United States
Change from Baseline in Parkinson's Disease Rating Scale Score
Time frame: Baseline to 28 weeks
Number of Participants Experiencing Adverse Events
Time frame: 28 weeks
Number of Participants Experiencing Serious Adverse Events
Time frame: 28 weeks
Change from Baseline in Parkinson's Disease Rating Scale Sub-score
Time frame: Baseline to 28 weeks
Change from Baseline in Patient Perceived Severity of Disease
Time frame: Baseline to 28 weeks
Change from Baseline in Clinician Perceived Severity of Disease
Time frame: Baseline to 28 weeks
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CenExel Rocky Mountain Clinical Research
Englewood, Colorado, United States
Parkinson's Disease and Movement Disorders Center of Boca Raton
Boca Raton, Florida, United States
University of Miami
Miami, Florida, United States
University of South Florida Parkinson's and Movement Disorders Center
Tampa, Florida, United States
Consultants in Neurology, Ltd
Northbrook, Illinois, United States
Josephson Wallack Munshower Neurology - Southeast
Indianapolis, Indiana, United States
University of Kansas Medical Center
Kansas City, Kansas, United States
Quest Research Institute
Farmington Hills, Michigan, United States
...and 4 more locations