Safety and Efficacy of 333369 in the Treatment of Partial Epilepsy
NCT00228969 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL
Last updated 2012-08-02
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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