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A Study of the Effectiveness and Safety of Topiramate in the Treatment of Children With Epilepsy

Primary Purpose

Epilepsy, Epilepsies, Partial, Seizures

Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
topiramate
Sponsored by
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Epilepsy focused on measuring topiramate, epilepsy, partial epilepsies, partial epilepsy, seizures, epileptic seizures, partial seizure disorder, children, pediatric

Eligibility Criteria

1 Year - 16 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients must weigh at least 36 pounds (16 kilograms) patients must have partial onset seizures (with or without secondarily generalized seizures) being treated with at least one, but no more than two antiepileptic drugs (AEDs) patients must have at least 6 partial onset seizures during the 8-week baseline phase, with at least one seizure during each 4-week period an electroencephalogram (EEG) with features consistent with partial epilepsy performed prior to study initiation or during the baseline phase Exclusion Criteria: Females who are pregnant, nursing, or those not using adequate birth control if capable of having children patients with a treatable cause of seizures (for example, infections) patients with a progressive disorder of the nervous system patients with a clinical diagnosis of Lennox-Gastaut syndrome patients with a history of generalized status epilepticus (repeated or prolonged seizures) while on appropriate anti-epileptic therapy

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Percent reduction in the average monthly seizure rate from baseline to end of treatment

    Secondary Outcome Measures

    Percent of patients responding to treatment (>= 50% reduction in seizure rate from baseline to end of treatment); parent's or guardian's global assessments at beginning of treatment and end of study; incidence of adverse events throughout study

    Full Information

    First Posted
    October 7, 2005
    Last Updated
    June 6, 2011
    Sponsor
    Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00236743
    Brief Title
    A Study of the Effectiveness and Safety of Topiramate in the Treatment of Children With Epilepsy
    Official Title
    Topiramate (RWJ 17021-000) Clinical Trial In Children With Partial Onset Seizures
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2011
    Overall Recruitment Status
    Completed
    Study Start Date
    June 1994 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    October 2000 (Actual)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Johnson & Johnson Pharmaceutical Research & Development, L.L.C.

    4. Oversight

    5. Study Description

    Brief Summary
    The purpose of this study is to evaluate the safety and effectiveness of oral topiramate as add-on therapy in children with uncontrolled partial onset seizures who are taking one or two standard anti-epileptic drugs.
    Detailed Description
    Epilepsy is characterized by seizures, which are abnormal electrical discharges in the brain that temporarily disrupt normal brain function. Seizures are classified as "generalized," originating in both sides of the brain simultaneously, or "partial-onset," starting in one area of the brain. Antiepilepsy medications, such as topiramate, are selected based on seizure type. This is a double-blind, placebo-controlled study that includes a baseline phase and a treatment phase. During the baseline phase (8 weeks duration), patients receive a stable dose of one or two standard antiepileptic drugs (AEDs), and the parent or guardian records the occurrences of seizure in a diary. Patients who continue to have seizures during treatment with standard AEDs proceed into the double-blind treatment phase. Patients then receive topiramate or placebo once daily at a dosage of 25 milligrams[mg] or 50 mg based on body weight (to 6mg/kg per day), increasing gradually to twice daily dosing at a maximum of 125-400 mg (based on body weight) for 112 days (16 weeks total duration of the double-blind phase), while continuing on their standard AED regimen. Assessments of effectiveness include the percent reduction in the average monthly seizure rate, percent of patients responding to treatment (having equal to or greater than 50% reduction in seizure rate), and the parent's or guardian's global assessment of medication at end of study. Safety assessments include the incidence of adverse events throughout the study, clinical laboratory tests (hematology, chemistry, urinalysis), neurologic examinations, and vital sign measurements (blood pressure, pulse, body weight) at specific intervals during the treatment phase. The study hypothesis is that topiramate, taken as add-on therapy to treatment with AEDs, will significantly reduce seizure frequency, compared with placebo, in children with refractory partial epilepsy: that is, children who continue to have seizures despite treatment with first-line AEDs. In addition, it is hypothesized that topiramate is well-tolerated. Oral topiramate, daily for 112 days. Starting dose is 25 mg or 50mg, based on body weight. Maximum doses based on patient weight: 125 mg/day (36-54 pounds[lb]); 175 mg/day (55-74 lb); 225 mg/day (75-94 lb); and 400 mg/day (95 or more pounds). Matching placebo was used to maintain blinding.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Epilepsy, Epilepsies, Partial, Seizures
    Keywords
    topiramate, epilepsy, partial epilepsies, partial epilepsy, seizures, epileptic seizures, partial seizure disorder, children, pediatric

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    Double
    Allocation
    Randomized
    Enrollment
    90 (Actual)

    8. Arms, Groups, and Interventions

    Intervention Type
    Drug
    Intervention Name(s)
    topiramate
    Primary Outcome Measure Information:
    Title
    Percent reduction in the average monthly seizure rate from baseline to end of treatment
    Secondary Outcome Measure Information:
    Title
    Percent of patients responding to treatment (>= 50% reduction in seizure rate from baseline to end of treatment); parent's or guardian's global assessments at beginning of treatment and end of study; incidence of adverse events throughout study

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    1 Year
    Maximum Age & Unit of Time
    16 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients must weigh at least 36 pounds (16 kilograms) patients must have partial onset seizures (with or without secondarily generalized seizures) being treated with at least one, but no more than two antiepileptic drugs (AEDs) patients must have at least 6 partial onset seizures during the 8-week baseline phase, with at least one seizure during each 4-week period an electroencephalogram (EEG) with features consistent with partial epilepsy performed prior to study initiation or during the baseline phase Exclusion Criteria: Females who are pregnant, nursing, or those not using adequate birth control if capable of having children patients with a treatable cause of seizures (for example, infections) patients with a progressive disorder of the nervous system patients with a clinical diagnosis of Lennox-Gastaut syndrome patients with a history of generalized status epilepticus (repeated or prolonged seizures) while on appropriate anti-epileptic therapy
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Johnson & Johnson Pharmaceutical Research & Development, L.L. C. Clinical Trial
    Organizational Affiliation
    Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    10768307
    Citation
    Ritter F, Glauser TA, Elterman RD, Wyllie E. Effectiveness, tolerability, and safety of topiramate in children with partial-onset seizures. Topiramate YP Study Group. Epilepsia. 2000;41(S1):82-5. doi: 10.1111/j.1528-1157.2000.tb02178.x.
    Results Reference
    result
    Links:
    URL
    http://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_JNJ_6051&studyid=648&filename=CR005467_CSR.pdf
    Description
    A study of the effectiveness and safety of topiramate in the treatment of children with epilepsy

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    A Study of the Effectiveness and Safety of Topiramate in the Treatment of Children With Epilepsy

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