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Safety and Efficacy of 333369 in the Treatment of Partial Epilepsy

Primary Purpose

Refractory Epilepsy

Status
Completed
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
RWJ-333369
Sponsored by
SK Life Science, Inc.
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Refractory Epilepsy

Eligibility Criteria

18 Years - 79 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age 18-70 years old, Diagnosis of epilepsy for at least 1 year, Presenting, on average, at least 3 partial onset seizures per month, Currently treated with a stable dose (i.e., for at least 4 weeks) of no more than 3 anti-epileptic drugs (AEDs), Exclusion Criteria: Have experienced status epilepticus in the past 3 months, Have any serious diseases, History of major psychiatric disorders within the past 2 years. Have received an experimental drug/device within the past 30 days Are pregnant or breastfeeding.

Sites / Locations

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
June 30, 2005
Last Updated
August 1, 2012
Sponsor
SK Life Science, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT00228969
Brief Title
Safety and Efficacy of 333369 in the Treatment of Partial Epilepsy
Study Type
Interventional

2. Study Status

Record Verification Date
August 2012
Overall Recruitment Status
Completed
Study Start Date
February 2005 (undefined)
Primary Completion Date
May 2006 (Actual)
Study Completion Date
May 2006 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
SK Life Science, Inc.

4. Oversight

5. Study Description

Brief 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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Refractory Epilepsy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
RWJ-333369

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
79 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18-70 years old, Diagnosis of epilepsy for at least 1 year, Presenting, on average, at least 3 partial onset seizures per month, Currently treated with a stable dose (i.e., for at least 4 weeks) of no more than 3 anti-epileptic drugs (AEDs), Exclusion Criteria: Have experienced status epilepticus in the past 3 months, Have any serious diseases, History of major psychiatric disorders within the past 2 years. Have received an experimental drug/device within the past 30 days Are pregnant or breastfeeding.
Facility Information:
City
Birmingham
State/Province
Alabama
Country
United States
City
Huntsville
State/Province
Alabama
Country
United States
City
Mobile
State/Province
Alabama
Country
United States
City
Northport
State/Province
Alabama
Country
United States
City
Phoenix
State/Province
Arizona
Country
United States
City
Little Rock
State/Province
Arkansas
Country
United States
City
Irvine
State/Province
California
Country
United States
City
Northridge
State/Province
California
Country
United States
City
Sacramento
State/Province
California
Country
United States
City
Fort Collins
State/Province
Colorado
Country
United States
City
Wilmington
State/Province
Delaware
Country
United States
City
Decatur
State/Province
Georgia
Country
United States
City
Lexington
State/Province
Kentucky
Country
United States
City
Louisville
State/Province
Kentucky
Country
United States
City
Baton Rouge
State/Province
Louisiana
Country
United States
City
Golden Valley
State/Province
Minnesota
Country
United States
City
St. Paul
State/Province
Minnesota
Country
United States
City
Chesterfield
State/Province
Missouri
Country
United States
City
Cincinnati
State/Province
Ohio
Country
United States
City
Portland
State/Province
Oregon
Country
United States
City
Philadelphia
State/Province
Pennsylvania
Country
United States
City
Sellersville
State/Province
Pennsylvania
Country
United States
City
Nashville
State/Province
Tennessee
Country
United States
City
Dallas
State/Province
Texas
Country
United States
City
El Paso
State/Province
Texas
Country
United States
City
Bennington
State/Province
Vermont
Country
United States
City
Charlottesville
State/Province
Virginia
Country
United States
City
Roanoke
State/Province
Virginia
Country
United States
City
Madison
State/Province
Wisconsin
Country
United States
City
Ciudad de Buenos Aires
Country
Argentina
City
Ciudad de Cordoba
Country
Argentina
City
Salta
Country
Argentina
City
Budapest
Country
Hungary
City
Debrecen
Country
Hungary
City
Gyor
Country
Hungary
City
Pecs
Country
Hungary
City
Zalaegerszeg-Pozva
Country
Hungary
City
Breda
Country
Netherlands
City
Heemstede
Country
Netherlands
City
Heeze
Country
Netherlands
City
Rotterdam
Country
Netherlands
City
Gdansk
Country
Poland
City
Katowice
Country
Poland
City
Kielce
Country
Poland
City
Krakow
Country
Poland
City
Lublin
Country
Poland
City
Mosina
Country
Poland
City
Warszawa
Country
Poland
City
Zabrze
Country
Poland
City
Moscow
Country
Russian Federation
City
Saint-Petersburg
Country
Russian Federation
City
Samara
Country
Russian Federation
City
Barcelona
Country
Spain
City
Madrid
Country
Spain
City
Malaga
Country
Spain
City
Pamplona
Country
Spain
City
Glasgow
Country
United Kingdom
City
Middlesbrough
Country
United Kingdom
City
Northampton
Country
United Kingdom
City
Oxford
Country
United Kingdom
City
Reading
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
34870321
Citation
Lu C, Zheng J, Cao Y, Bresnahan R, Martin-McGill KJ. Carisbamate add-on therapy for drug-resistant focal epilepsy. Cochrane Database Syst Rev. 2021 Dec 6;12(12):CD012121. doi: 10.1002/14651858.CD012121.pub2.
Results Reference
derived

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Safety and Efficacy of 333369 in the Treatment of Partial Epilepsy

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