drugset / Trial / NCT00148486

A Fourteen-Week Placebo-Controlled Dose-Response Efficacy and Safety Study of NS 2330 in Early Parkinson's Disease Patients (Study for Proof of Concept in Early Parkinson's Disease of a Triple Reuptake Inhibitor, NS 2330 / SCEPTRE)

NCT00148486

Phase 2 Completed 261 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

To demonstrate efficacy and dose-response of NS 2330 versus placebo in patients with early Parkinson's Disease in 14 weeks of treatment, and to investigate the safety and tolerability of NS 2330 in these patients.

Timeline

Start
2003-06
Primary completion
2005-03
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Tesofensine Small molecule

Indications