Treatment Of Primary Generalized Tonic-Clonic Seizures With An Investigational New Drug
This study has been completed.
Sponsor:
GlaxoSmithKline
Information provided by:
GlaxoSmithKline
ClinicalTrials.gov Identifier:
NCT00043901
First received: August 14, 2002
Last updated: January 26, 2012
Last verified: January 2012
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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:
Genetics Home Reference related topics:
pyridoxal 5'-phosphate-dependent epilepsy
Drug Information available for:
Lamotrigine
U.S. FDA Resources
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
Show 84 Study Locations
Show 84 Study LocationsSponsors 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 May 23, 2013