Efficacy and Safety of Adjunctive Zonisamide in Paediatric Partial Onset Seizures (CATZ Study)
Status and phase
Conditions
Treatments
Details and patient eligibility
About
The purpose of this study is to compare the safety and efficacy of zonisamide with placebo.
Full description
This will be a double-blind, randomised, study comparing zonisamide with placebo: each arm will consist of 102 subjects. Zonisamide/placebo dosing will commence with a dose of 1 mg/kg. Further dose increases will occur at weekly intervals until a dose of 8 mg/kg is reached at the end of Week 8. In the event of dose limiting adverse events (AEs), during the eight week Titration Period, one down titration to a lower dose is permitted, this can happen at any point in the Titration Period. Subjects who require further down titration steps will be withdrawn from the study. During the Maintenance Period the dose of study medication must remain unchanged.
Changes in concomitant AEDs are not permitted during the Screening, Titration or Maintenance Periods.
This trial consists of the following periods:
- Screening Period (duration four weeks): once the Screening Visit has been performed, a seizure diary will be maintained to document the baseline seizure frequency in the eight weeks between the Screening Visit and the Randomisation Visit.
- Titration Period (duration four weeks): during this period, zonisamide/placebo dosing will commence with a dose of 1 mg/kg. Further dose increases will occur at one week intervals until a dose of 8 mg/kg is reached at Visit 6 (Week 8). In the event of dose limiting AEs during the Titration Period, one down titration step to the previous dose will be permitted.
- Maintenance Period (duration 12 weeks): during this period, randomised subjects will be treated with the dose of zonisamide/placebo which they were receiving at Visit 6 (Week 8). No changes to the dose are allowed during this phase.
Following the Maintenance Period subjects will have the opportunity to enter an open label extension study. This open label extension study will be the subject of a separate protocol and will not be discussed further at this time.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
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Subject is male or female aged 6-17 years inclusive.
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Parent/guardian is willing to sign an approved informed consent form, and accompany the subject on all study visits.
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Subject is willing to give informed (written or verbal) assent and if appropriate written informed consent.
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Subject has a clinical diagnosis of epilepsy with partial-onset seizures with or without secondary generalized seizures according to the International League Against Epilepsy's Classification of Epileptic Seizures (1981).
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Diagnosis has been established by clinical history, electroencephalogram (EEG) and computed tomography/ magnetic resonance imaging (CT/MRI) of the brain consistent with localization related epilepsy.
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Subject has > four (simple or complex) partial seizures (with or without secondary generalization) per month over the eight week Screening Period with at least one seizure in each four week period and with no 21 day period being seizure free.
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Subject is taking a stable regimen of one or two other AEDs for at least one month prior to Visit 1 (start of the Screening Period).
NOTE: If using a vagal nerve stimulator (VNS), it must have been implanted for at least five months and stimulator parameters must remain unchanged for at least one month prior to Visit 1 (start of the Screening Period), and throughout the entire study period. VNS will be considered as one AED for the purposes of this study.
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Subject is in general good health as determined by medical history, physical exam and screening laboratory results.
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Parent/guardian is willing and able to complete a seizure diary for the duration of the study.
Exclusion criteria
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Subject of body weight < 20 kg at the Screening Visit.
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Subject is unable to swallow capsules.
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Subject has progressive neurological disease (determined by diagnosis or a pre-existing brain image such as a CT scan or MRI).
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Subject has a history of idiopathic generalized epilepsy as defined by the International League Against Epilepsy (ILAE).
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Subjects with Lennox-Gastaut syndrome, absence, myoclonic, clonic and/or tonic (other than secondary generalized) and atonic seizures.
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Subject has psychogenic seizures
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Subject has a history of status epilepticus within a year of the Screening Visit whilst taking AEDs.
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Subject has seizures that only occur in clustered patterns, or has seizures that are too close together to count accurately.
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Subject has a history of renal calculi or renal insufficiency (creatinine levels >194 µmol/l (1.5 mg1/dl).
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Subject had a predisposing condition that might interfere with absorption, distribution, or excretion of zonisamide.
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Subject has a history of psychiatric illness.
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Subject has a history of suicide attempt.
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Female subject who is pregnant or lactating.
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Subject has a history of demonstrated non-compliance with treatment or, the subject, parent or legal guardian can be reasonably expected not to be compliant with study procedures or to complete the study.
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Female subject of 10 years of age or greater or of child bearing potential (i.e., started menses) and is not taking or prepared to take a medically acceptable form of contraception (i.e., oral contraceptive pill, surgical sterilization, an implant or an injected form of contraception, or intrauterine device), or who is not prepared to abstain from sexual activity for the duration of the study and one month after last administration of study medication.
NOTE: Should a female subject become of childbearing potential during the study, they must be reconsented in order to give consent to undergo pregnancy testing and either confirm abstinence or receive medically appropriate form of contraception.
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Subject has clinically significant abnormal laboratory values at the Screening Visit.
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Subject has received previous treatment with zonisamide.
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Subject is treated with a ketogenic diet or is likely to have surgery for epilepsy in the trial period.
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Subject requires frequent rescue benzodiazepines (> than once per week).
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Concomitant use of felbamate or use of felbamate within 2 months prior to Visit 1.
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Subject has elevations of liver enzymes, alanine aminotransferase (ALT), and aspartate aminotransferase (AST) > 2 times the upper limit of normal (ULN).
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Subject has evidence of significant active and unstable haematological disease; i.e., white blood cell (WBC) count < 2500/µL or an absolute neutrophil count < 1000/µL
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Subject with clinically significant active hepatic disease, cardiovascular, metabolic, respiratory, renal, endocrinological and gastrointestinal diseases or any other clinically significant organic disease, within 30 days prior to the Screening Visit.
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Subjects with known or suspected history of alcoholism or drug abuse within the previous two years, or a positive finding on urinary drug screening of any drugs other than prescribed medications.
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Subjects with any other condition that would make them, in the opinion of the Investigator unsuitable for this study.
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Subjects who have participated in a clinical trial involving administration of an investigational compound (including zonisamide) within three months of the Screening Visit.
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Subjects with a known or suspected hypersensitivity to zonisamide, or sulphonamides.
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Subjects taking acetazolamide, any carbonic anhydrase inhibitors e.g. topiramate, and any drugs with anticholinergic activity.
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Subjects who do not have a complete seizure diary during the Screening Period.
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Subjects with active and/or insufficiently treated neurocysticerosis or intercraniel tubiculosis. Note: subjects who have completed a curative antihelminthic or antituberculous treatment course more than 3 months before screening and who are free of signs and symptoms of active infection (including on a post treatment CT/MRI scan), may be enrolled in the study.
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Subjects taking antipsychotics, monoamine oxidase inhibitors (MAOIs), tricyclic antidepressants (TCAs) and benzodiazepines with barbiturates and amphetamines for disease other than epilepsy within 3 months of screening.
Trial design
Primary purpose
Allocation
Interventional model
Masking
207 participants in 2 patient groups, including a placebo group
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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