drugset / Trial / NCT00462007

Study to Evaluate Initiation of Stalevo in Early Wearing-off

NCT00462007

Phase 4 Completed 115 enrolled Orion Corporation, Orion Pharma
Non-randomizedSingle-groupOpen-labelTreatment

Summary

An open, non-randomised, multinational, multicentre direct switch study in levodopa-treated Parkinson's disease patients suffering from early wearing-off in Parkinson's disease. The study will consist of 2 consecutive periods: screening period and study treatment period. Duration of the study will be up to 8 weeks for each subject. The study treatment dosage will be determined by the subject's current, separately administered standard levodopa/DDCI treatment (3-4 doses per day, maximum of total daily dose of 600 mg levodopa) which will be switched to an equivalent dose of Stalevo® without changing the number of doses per day. The levodopa daily dose during Stalevo® treatment may be adjusted according to the study subject's clinical response.

Timeline

Start
2006-09
Primary completion
2007-08
Completion
2007-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Stalevo Unknown Oral

Indications