Trial record 17 of 60 for:
"Epilepsy, Generalized"
Levetiracetam as add-on Treatment of Myoclonic Jerks in Adolescents + Adults
This study has been completed.
Sponsor:
UCB, Inc.
Information provided by:
UCB, Inc.
ClinicalTrials.gov Identifier:
NCT00150774
First received: September 6, 2005
Last updated: February 22, 2010
Last verified: February 2010
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Purpose
A double-blind, placebo-controlled study to assess the efficacy of adjunctive treatment with LEV 3000mg/day in reducing myoclonic seizures in adolescents and adults suffering from idiopathic generalised epilepsy and to evaluate the safety of LEV in the same population.
| Condition | Intervention | Phase |
|---|---|---|
|
Generalized Convulsive Epilepsy |
Drug: Levetiracetam |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Double-Blind Primary Purpose: Treatment |
| Official Title: | A Double-blind, Multicenter, Randomized, Placebo-controlled Study to Evaluate the Efficacy and Safety of Levetiracetam (LEV) (Oral Tablets of 500 mg b.i.d.) at a Dose of 3000 mg/Day as Adjunctive Treatment in Adolescents (≥ 12 Years) and Adults (≤ 65 Years) Suffering From Idiopathic Generalized Epilepsy With Myoclonic Seizures. |
Resource links provided by NLM:
Genetics Home Reference related topics:
pyridoxal 5'-phosphate-dependent epilepsy
Drug Information available for:
Levetiracetam
U.S. FDA Resources
Further study details as provided by UCB, Inc.:
Primary Outcome Measures:
- Responder rate in myoclonic (type IIB) seizures days over 16 weeks
Secondary Outcome Measures:
- Safety and tolerability of levetiracetam by means of AE, laboratory assessments, plasma concentration
| Estimated Enrollment: | 116 |
| Study Start Date: | November 2001 |
| Study Completion Date: | December 2004 |
| Primary Completion Date: | December 2004 (Final data collection date for primary outcome measure) |
Eligibility| Ages Eligible for Study: | 12 Years to 65 Years |
| Genders Eligible for Study: | Both |
Criteria
Inclusion Criteria:
- Subjects with a confirmed diagnosis consistent with idiopathic generalized epilepsy experiencing myoclonic seizures (IIB) that are classifiable according to the International Classification of Epileptic Seizures. To ensure an idiopathic generalized epilepsy population, only these subjects with the diagnosis of juvenile myoclonic epilepsy (JME), juvenile absence epilepsy (JAE) or epilepsy with generalized tonic- clonic seizures on awakening must be included.
- Presence of at least eight days with at least one myoclonic seizure (IIB) per day during the eight weeks of the Baseline period.
- Absence of brain lesion documented on a CT scan or MRI; if a CT scan or MRI has not been performed within the past five years before Visit 1, a CT scan (or MRI where legally required) should be performed during the Baseline period.
- Presence of EEG features consistent with idiopathic generalized epilepsy on an EEG recorded during the Baseline period or no more than one year before Visit 1.
- Male/female children ≥ 12 years of age or adult ≤ 65 years of age at Visit 1.
- Subject on a stable dose of one standard anti-epileptic treatment for at least four weeks before Visit 1.
Exclusion Criteria:
- Previous exposure to levetiracetam.
- History of partial seizures.
- History of convulsive or non-convulsive status epilepticus within 3 months prior to Visit 1.
- Subject taking vigabatrin or tiagabine, subject on felbamate with less than 18 months exposure, and subject under vagal nerve stimulation or ketogenic diet.
- Subject taking any drug (except the concomitant AEDs) with possible CNS effects.
Contacts and Locations
More Information
Publications:
| ClinicalTrials.gov Identifier: | NCT00150774 History of Changes |
| Other Study ID Numbers: | N166 |
| Study First Received: | September 6, 2005 |
| Last Updated: | February 22, 2010 |
| Health Authority: | Austria: Federal Ministry for Health and Women Australia: Department of Health and Ageing Therapeutic Goods Administration Belgium: Directorate general for the protection of Public health: Medicines Canada: Health Canada France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis) Germany: Paul-Ehrlich-Institut Ireland: Irish Medicines Board Italy: Ministry of Health Mexico: National Institute of Public Health, Health Secretariat New Zealand: Food Safety Authority Poland: Ministry of Health Spain: Ministry of Health and Consumption Switzerland: Swissmedic Netherlands: The Central Committee on Research Involving Human Subjects (CCMO) United Kingdom: Medicines and Healthcare Products Regulatory Agency United States: Food and Drug Administration |
Keywords provided by UCB, Inc.:
|
Idiopathic Generalized Epilepsy, Myoclonic seizures Keppra - Levetiracetam |
Additional relevant MeSH terms:
|
Epilepsy, Generalized Epilepsy Epilepsies, Myoclonic Myoclonus Brain Diseases Central Nervous System Diseases Nervous System Diseases Dyskinesias Neurologic Manifestations Signs and Symptoms |
Etiracetam Piracetam Anticonvulsants Central Nervous System Agents Therapeutic Uses Pharmacologic Actions Nootropic Agents Neuroprotective Agents Protective Agents Physiological Effects of Drugs |
ClinicalTrials.gov processed this record on May 22, 2013