Safety and Efficacy of 333369 in the Treatment of Partial Epilepsy

NCT00228969 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL

Last updated 2012-08-02

No results posted yet for this study

Summary

The primary objective of this study is to evaluate the efficacy, safety, and tolerability of 4 daily doses of RWJ-333369 as adjunctive treatment of refractory partial epilepsy in subjects who are between 18 and 70 years of age, inclusive

Conditions

  • Refractory Epilepsy

Interventions

DRUG

RWJ-333369

Sponsors & Collaborators

  • SK Life Science, Inc.

    lead INDUSTRY

Study Design

Purpose
TREATMENT

Eligibility

Min Age
18 Years
Max Age
79 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-02-28
Primary Completion
2006-05-31
Completion
2006-05-31

Countries

  • United States
  • Argentina
  • Hungary
  • Netherlands
  • Poland
  • Russia
  • Spain
  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00228969 on ClinicalTrials.gov