drugset / Trial / NCT00165789

A Study to Explore the Safety And Tolerability of Doses of E2007 Up to a Maximum of 8 mg In Patients With Parkinson's Disease Who Experience End-of-Dose Wearing Off Motor Fluctuations

NCT00165789

Phase 2 Completed 75 enrolled Eisai Inc.
RandomizedParallel-groupDouble-blind

Summary

This is a randomized, double-blind, two treatment, two group, parallel group study. Subjects will be randomized to one of two treatment groups (E2007 or Placebo) in a 3 to 1 ratio and receive treatment for a total of ten weeks (Days 1 to 70).

Timeline

Start
2005-09
Primary completion
2006-02
Completion
2006-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Perampanel Small molecule 8 mg

Indications