drugset / Trial / NCT00660387

Study of Efficacy, Safety and Tolerability of Levodopa-Carbidopa Intestinal Gel in Levodopa-Responsive Parkinson's Subjects

NCT00660387

Phase 3 Completed 35 enrolled AbbVie Quintiles, Inc. · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of this study was to demonstrate the superiority of levodopa - carbidopa intestinal gel over treatment with optimized oral levodopa/carbidopa during 12 weeks.

Timeline

Start
2009-12
Primary completion
2011-10
Completion
2011-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator Levodopa Small molecule Oral
Subject Levodopa-carbidopa intestinal gel Unknown

Indications