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Completed Phase 2 Interventional

Pediatric Epilepsy Study in Subjects 1-24 Months

ClinicalTrials.gov ID: NCT00044278

Public ClinicalTrials.gov record NCT00044278. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 28, 2026, 4:40 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-Label, Uncontrolled, Long-Term Study to Assess the Safety of LAMICTAL in Pediatric Subjects Previously Enrolled in Protocol LAM20006 and In LAMICTAL-naive Subjects (1-24 Months of Age)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will evaluate the long-term safety of LAMICTAL(lamotrigine)in subjects with partial seizures previously enrolled in protocol LAM20006 and in subjects 1-24 months of age who have never received LAMICTAL(LAMICTAL-naive). For LAMICTAL-naive subjects, LAMICTAL will be added to the subject's current epilepsy medications.

Study identification

NCT ID
NCT00044278
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
197 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
1 Month to 24 Months
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 2000 (Type not available)
Primary completion
Jun 2006 (Actual)
Completion
Jun 2006 (Actual)
Last update posted
Jan 18, 2017

2000 – 2006

United States locations

U.S. sites
41
U.S. states
21
U.S. cities
39
Facility City State ZIP Site status
GSK Investigational Site Mobile Alabama 36693 —
GSK Investigational Site Tucson Arizona 85712 —
GSK Investigational Site Jonesboro Arkansas 72401 —
GSK Investigational Site Little Rock Arkansas 72202 —
GSK Investigational Site Los Angeles California 90027 —
GSK Investigational Site Los Angeles California 90095 —
GSK Investigational Site Stanford California 94305-5235 —
GSK Investigational Site Denver Colorado 80218 —
GSK Investigational Site Washington D.C. District of Columbia 20010 —
GSK Investigational Site Jacksonville Florida 32207 —
GSK Investigational Site Miami Florida 33155-3009 —
GSK Investigational Site Orlando Florida 32835 —
GSK Investigational Site Tallahassee Florida 32308 —
GSK Investigational Site Tampa Florida 33609 —
GSK Investigational Site Atlanta Georgia 30342 —
GSK Investigational Site Augusta Georgia 30912 —
GSK Investigational Site Lexington Kentucky 40536-0284 —
GSK Investigational Site Saint Paul Minnesota 55102-2383 —
GSK Investigational Site Columbia Missouri 65211 —
GSK Investigational Site Kansas City Missouri 64108 —
GSK Investigational Site Cherry Hill New Jersey 8034 —
GSK Investigational Site Buffalo New York 14222 —
GSK Investigational Site Mineola New York 11501 —
GSK Investigational Site Syracuse New York 13210 —
GSK Investigational Site Chapel Hill North Carolina 27599 —
GSK Investigational Site Raleigh North Carolina 27607 —
GSK Investigational Site Akron Ohio 44308-1062 —
GSK Investigational Site Cleveland Ohio 44106 —
GSK Investigational Site Columbus Ohio 43205 —
GSK Investigational Site Portland Oregon 97201-2884 —
GSK Investigational Site Portland Oregon 97201-2984 —
GSK Investigational Site Pittsburgh Pennsylvania 15213-2583 —
GSK Investigational Site Morristown Tennessee 37813 —
GSK Investigational Site Nashville Tennessee 37212 —
GSK Investigational Site Dallas Texas 75230 —
GSK Investigational Site Fort Worth Texas 76104 —
GSK Investigational Site Houston Texas 77030 —
GSK Investigational Site Salt Lake City Utah 84113 —
GSK Investigational Site Charlottesville Virginia 22908 —
GSK Investigational Site Norfolk Virginia 23507 —
GSK Investigational Site Richmond Virginia 23298 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 29 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00044278, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 18, 2017 · Synced Oct 28, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00044278 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →