The purpose of this study is to evaluate the safety and efficacy of KW-6500 when administered as long-term subcutaneous self-injections in Parkinson's disease patients with motor response complications on levodopa therapy.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
58
Subcutaneous injection of 1to 6 mg of KW-6500 for the OFF state
Unnamed facility
Tokyo, Japan
The incidence of adverse events after administration of KW-6500
Time frame: From first administration of study drug through Study Week 52
Time to expression of the ON state, continuous time of the ON state, raw score change and percent score change in Unified Parkinson's Disease Rating Scale (UPDRS) part III, response ratio, and UPDRS part II score
Time frame: From first administration of study drug through Study Week 52
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