Treatment Of Primary Generalized Tonic-Clonic Seizures With An Investigational New Drug

This study has been completed.
Sponsor:
Information provided by:
GlaxoSmithKline
ClinicalTrials.gov Identifier:
NCT00043901
First received: August 14, 2002
Last updated: January 26, 2012
Last verified: January 2012
  Purpose

The purpose of this study is to evaluate the effectiveness and safety of an investigational new drug for supplemental therapy in subjects with primary generalized tonic-clonic (PGTC) seizures.


Condition Intervention Phase
Epilepsy, Tonic-Clonic
Drug: lamotrigine
Phase 4

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Treatment
Official Title: A Multi-Center, Double-Blind, Randomized, Placebo-Controlled, Parallel-Group Evaluation of Lamotrigine Adjunctive Therapy in Subjects Wtih Primary Generalized Tonic-Clonic Seizures

Resource links provided by NLM:


Further study details as provided by GlaxoSmithKline:

Primary Outcome Measures:
  • % change from Baseline in average monthly PGTC seizure frequency

Secondary Outcome Measures:
  • Proportion of subjects with >/= 25%, 50%, 75% or 100% reduction in PGTC seizures %change from Baseline in average monthly seizure frequency.

Enrollment: 141
Study Start Date: December 2000
Study Completion Date: November 2003
Primary Completion Date: November 2003 (Final data collection date for primary outcome measure)
Intervention Details:
    Drug: lamotrigine
    Other Name: lamotrigine
  Eligibility

Ages Eligible for Study:   2 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

INCLUSION CRITERIA:

  • Weigh at least 13kg.
  • Have a confident diagnosis of epilepsy with primary generalized tonic-clonic (PGTC) seizures with or without other generalized seizure types.
  • Currently being treated with an antiepileptic drug(s) (AED).
  • Benzodiazepines are allowed with some frequency restrictions.
  • Vagus nerve stimulation is allowed if in place for at least 6 months prior to starting the study with no changes to the settings having occured during the month immediately prior to starting the study, and if no changes will occur during all phases of the study.
  • History of primary generalized tonic-clonic seizures with no focal onset.
  • Have at least 1 primary generalized tonic-clonic (PGTC) seizure during the 8 consecutive weeks prior to the baseline period of the study.
  • Have at least 3 PGTC seizures occur anytime during the 8-week baseline phase of the study.
  • Females must agree to acceptable form of birth control.

EXCLUSION CRITERIA:

  • A history of partial seizures or interictal expression of partial seizures as evidenced by electroencephalogram.
  • Have Lennox-Gastaut syndrome.
  • Currently using or has previously used the drug being studied.
  • Is abusing alcohol and/or other substance(s).
  • Has taken an investigational drug during the 30 days prior to the study or plans to take an investigational drug anytime during the study.
  • Is receiving chronic (long-term) treatment with any medication that could influence seizure control.
  • Follows the ketogenic diet.
  • Is planning surgery to control seizures during the study.
  • Is suffering from acute or progressive neurological disease, severe psychiatric disease, or severe mental abnormality.
  • Has any clinically significant heart, kidney, or liver condition, or a condition that affects how drugs are absorbed, distributed, metabolized, or removed from the body.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00043901

  Hide Study Locations
Locations
United States, Alabama
GSK Investigational Site
Alabaster, Alabama, United States, 35007
GSK Investigational Site
Mobile, Alabama, United States, 36693
GSK Investigational Site
Northport, Alabama, United States, 35476
United States, Arkansas
GSK Investigational Site
Little Rock, Arkansas, United States, 72205
United States, California
GSK Investigational Site
Bakersfield, California, United States, 93309
GSK Investigational Site
Irvine, California, United States, 92618
GSK Investigational Site
Northridge, California, United States, 91325
GSK Investigational Site
Sacramento, California, United States, 95871
United States, Colorado
GSK Investigational Site
Denver, Colorado, United States, 80218
United States, Delaware
GSK Investigational Site
Newark, Delaware, United States, 19713
United States, District of Columbia
GSK Investigational Site
Washington, District of Columbia, United States, 20037
United States, Florida
GSK Investigational Site
Gainsville, Florida, United States, 32611
GSK Investigational Site
Miami, Florida, United States, 33125
GSK Investigational Site
Miami, Florida, United States, 33136
GSK Investigational Site
Orlando, Florida, United States, 32835
GSK Investigational Site
Panama City, Florida, United States, 32405
GSK Investigational Site
Tallahassee, Florida, United States, 32308
GSK Investigational Site
Tampa, Florida, United States, 33607-6350
GSK Investigational Site
West Palm Beach, Florida, United States, 33407
United States, Georgia
GSK Investigational Site
Atlanta, Georgia, United States, 30338
GSK Investigational Site
Atlanta, Georgia, United States, 30342
GSK Investigational Site
Atlanta, Georgia, United States, 30309
GSK Investigational Site
Augusta, Georgia, United States, 30912
United States, Idaho
GSK Investigational Site
Boise, Idaho, United States, 83712
GSK Investigational Site
Idaho Falls, Idaho, United States, 83404
United States, Illinois
GSK Investigational Site
Chicago, Illinois, United States, 60637-1470
GSK Investigational Site
Springfield, Illinois, United States, 62702
United States, Indiana
GSK Investigational Site
Indianapolis, Indiana, United States, 46202 - 5111
United States, Kansas
GSK Investigational Site
Wichita, Kansas, United States, 67214
United States, Kentucky
GSK Investigational Site
Lexington, Kentucky, United States, 40536-0284
GSK Investigational Site
Lexington, Kentucky, United States, 40503
United States, Maryland
GSK Investigational Site
Baltimore, Maryland, United States, 21201
United States, Massachusetts
GSK Investigational Site
Newton, Massachusetts, United States, 02459
GSK Investigational Site
Sharon, Massachusetts, United States, 02067
United States, Michigan
GSK Investigational Site
Detroit, Michigan, United States, 48202
GSK Investigational Site
Farmington Hills, Michigan, United States, 48334
United States, Minnesota
GSK Investigational Site
Minneapolis, Minnesota, United States, 55422
GSK Investigational Site
St. Cloud, Minnesota, United States, 56303
United States, Missouri
GSK Investigational Site
Kansas City, Missouri, United States, 64108
GSK Investigational Site
Springfield, Missouri, United States, 65807
GSK Investigational Site
St. Louis, Missouri, United States, 63110-1093
United States, Nevada
GSK Investigational Site
Las Vegas, Nevada, United States, 89102
United States, New Jersey
GSK Investigational Site
Cherry Hill, New Jersey, United States, 8034
GSK Investigational Site
Medford, New Jersey, United States, 08055
GSK Investigational Site
New Brunswick, New Jersey, United States, 8903
United States, New York
GSK Investigational Site
Albany, New York, United States, 12205
GSK Investigational Site
Mount Vernon, New York, United States, 10550
United States, North Carolina
GSK Investigational Site
Asheville, North Carolina, United States, 28801
GSK Investigational Site
Charlotte, North Carolina, United States, 28207
GSK Investigational Site
Greenville, North Carolina, United States, 27834
GSK Investigational Site
Raleigh, North Carolina, United States, 27607
GSK Investigational Site
Winston-Salem, North Carolina, United States, 27157
United States, Ohio
GSK Investigational Site
Canton, Ohio, United States, 44718
GSK Investigational Site
Cleveland, Ohio, United States, 44195
GSK Investigational Site
Cleveland, Ohio, United States, 44106
GSK Investigational Site
Toledo, Ohio, United States, 43614-5809
United States, Oklahoma
GSK Investigational Site
Oklahoma City, Oklahoma, United States, 73104
United States, Oregon
GSK Investigational Site
Medford, Oregon, United States, 97504-8456
GSK Investigational Site
Portland, Oregon, United States, 97201-2984
United States, Pennsylvania
GSK Investigational Site
Danville, Pennsylvania, United States, 17822-4201
GSK Investigational Site
Natrona Heights, Pennsylvania, United States, 15065
United States, South Carolina
GSK Investigational Site
Spartanburg, South Carolina, United States, 29303
United States, Tennessee
GSK Investigational Site
Germantown, Tennessee, United States, 38138
GSK Investigational Site
Memphis, Tennessee, United States, 38119
GSK Investigational Site
Nashville, Tennessee, United States, 37212
United States, Texas
GSK Investigational Site
Arlington, Texas, United States, 76015
GSK Investigational Site
Dallas, Texas, United States, 75235
GSK Investigational Site
Fort Worth, Texas, United States, 76104
GSK Investigational Site
Houston, Texas, United States, 77030
GSK Investigational Site
San Antonio, Texas, United States, 78229
United States, Utah
GSK Investigational Site
Salt Lake City, Utah, United States, 84102
GSK Investigational Site
Salt Lake City, Utah, United States, 84113
United States, Vermont
GSK Investigational Site
Bennington, Vermont, United States, 05201
United States, Virginia
GSK Investigational Site
Danville, Virginia, United States, 24541
GSK Investigational Site
Newport News, Virginia, United States, 23601
United States, Washington
GSK Investigational Site
Tacoma, Washington, United States, 98405
United States, Wisconsin
GSK Investigational Site
Madison, Wisconsin, United States, 53715
GSK Investigational Site
Marshfield, Wisconsin, United States, 54449
GSK Investigational Site
Milwaukee, Wisconsin, United States, 53226
Argentina
GSK Investigational Site
Buenos Aires, Argentina, C1428AQK
GSK Investigational Site
Capital Federal, Argentina
Chile
GSK Investigational Site
Santiago, Región Metro De Santiago, Chile
GSK Investigational Site
Valparaiso, Valparaíso, Chile, 2341131
Peru
GSK Investigational Site
San Isidro, Lima, Peru, Lima 27
Sponsors and Collaborators
GlaxoSmithKline
Investigators
Study Director: GSK Clinical Trials GlaxoSmithKline
  More Information

Publications:
Responsible Party: Cheri Hudson; Clinical Disclosure Advisor, GSK Clinical Disclosure
ClinicalTrials.gov Identifier: NCT00043901     History of Changes
Other Study ID Numbers: LAM40097
Study First Received: August 14, 2002
Last Updated: January 26, 2012
Health Authority: United States: Food and Drug Administration

Keywords provided by GlaxoSmithKline:
PGTC
Lamotrigine
epilepsy
seizures
primary generalized tonic-clonic

Additional relevant MeSH terms:
Epilepsy
Epilepsy, Tonic-Clonic
Seizures
Epilepsy, Generalized
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Neurologic Manifestations
Signs and Symptoms
Lamotrigine
Calcium Channel Blockers
Membrane Transport Modulators
Molecular Mechanisms of Pharmacological Action
Pharmacologic Actions
Cardiovascular Agents
Therapeutic Uses
Anticonvulsants
Central Nervous System Agents

ClinicalTrials.gov processed this record on June 17, 2013