Atlas Trials

A Randomized, Double-blind, Placebo-controlled, Five Parallel Groups Efficacy and Safety Study of NS 2330 (Tesofensine) (0.125 mg, 0.25 mg, 0.5 mg and 1.0 mg) Administered Orally Once Daily Over 14 Weeks in Levodopa Treated Parkinson Patients With Motor Fluctuations

Clinical trial NCT00148512 · COMPLETED

Trial details

NCT number
NCT00148512
Sponsor
Boehringer Ingelheim
Status
COMPLETED
Phase
Phase 2
Study type
INTERVENTIONAL
Parkinson Disease
Start date
2003-03-01
Primary completion
2005-02-01
Enrollment
254

View on ClinicalTrials.gov

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