drugset / Trial / NCT00357994

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

NCT00357994

Phase 3 Completed 36 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
2009-01
Primary completion
2011-10
Completion
2011-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator Carbidopa Unknown 5 mg/ml Other
Comparator Carbidopa Unknown 25 mg Other
Comparator Carbidopa Unknown 25 mg Oral
Comparator Levodopa Small molecule 20 mg/ml Other
Comparator Levodopa Small molecule 100 mg Other
Comparator Levodopa Small molecule 100 mg Oral

Indications