The study is a multicenter, randomized, open-label, active-controlled, Phase II clinical study. The aim of this trial is to evaluated the pharmacokinetics, pharmacodynamics,efficacy and assessed the safety of HRG2010 compared with a sustained-release cabridopa-levodopa formulation in Parkinson's Disease Patients With Motor Fluctuations.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
61
Beijing Hospital
Beijing, Beijing Municipality, China
Change from baseline in average percent "Off" time during waking hours at Day 33
Time frame: Last three days collected at the end of treatment period
"Off" and"On" time hours during in clinic observation
Time frame: Days 1 and 13
MDS-UPDRS Part III
Time frame: Days 1 and 33
Change from baseline in "Off" time at Day 33
Time frame: Last three days collected at the end of treatment period
Change from baseline in the Movement Disorders Society Version of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS) at Day 33
Time frame: Day 33
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