drugset / Trial / NCT01058291

Placebo-Controlled Double-Blind Crossover Comparative Study of KW-6500

NCT01058291

Phase 3 Completed 31 enrolled Kyowa Kirin, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a placebo-controlled double-blind crossover comparative study of KW-6500 in Parkinson's disease patients with motor response complications on levodopa therapy. The efficacy of KW-6500 is evaluated using the change of UPDRS part III score at double blind period after 12 weeks subcutaneous self-injections.

Timeline

Start
2010-01
Primary completion
2010-10
Completion
2010-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Apomorphine Unknown 1 mg Subcutaneous
Subject Apomorphine Unknown 6 mg Subcutaneous

Indications