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Open Label Safety and Efficacy Study of Levetiracetam in Korean Patients With Epilepsy
This study has been completed.
Sponsored by: UCB
Information provided by: UCB
ClinicalTrials.gov Identifier: NCT00160628
  Purpose

A Korean open-label, community-based trial assessing the efficacy and safety of levetiracetam as adjunctive therapy in partial epilepsy.

Similarity with a similar study conducted in Caucasian epileptic subjects will be assessed.


Condition Intervention Phase
Epilepsy, Partial
Drug: Levetiracetam
Phase III

Genetics Home Reference related topics: autosomal dominant partial epilepsy with auditory features pyridoxal 5'-phosphate-dependent epilepsy pyridoxine-dependent epilepsy
MedlinePlus related topics: Epilepsy Seizures
Drug Information available for: Levetiracetam
U.S. FDA Resources
Study Type: Interventional
Study Design: Non-Randomized, Open Label, Uncontrolled, Single Group Assignment
Official Title: A Korean Open-Label, Multi-Center, Community-Based Trial Assessing the Efficacy and Safety of Levetiracetam as Adjunctive Therapy in Adult Subjects With Uncontrolled Partial Epilepsy for Bridging Purpose With a Similar Study on Caucasian Epileptic Subjects

Further study details as provided by UCB:

Primary Outcome Measures:
  • To evaluate efficacy of levetiracetam in community based practice (seizure frequency per week over 16 weeks).

Secondary Outcome Measures:
  • To assess safety of levetiracetam

Estimated Enrollment: 100
Study Start Date: March 2004
Study Completion Date: October 2004
Primary Completion Date: October 2004 (Final data collection date for primary outcome measure)
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Criteria

Inclusion Criteria:

  • Subjects with epilepsy experiencing partial seizures, whether or not secondarily generalized.
  • Subjects must present between 3 and 42 partial seizures over the three months prior to protocol Visit 1.
  • Use of one (1), but no more than two (2) concomitant marketed AEDs at the time of trial entry.

Exclusion Criteria:

  • Subjects on felbamate with less than 18 months exposure.
  • Subjects on vigabatrin, whose visual field has not been assessed as per recommendation of the manufacturer, i.e. every 6 months.
  • Presence of known pseudoseizures within the last year.
  • Presence of progressive cerebral disease, any other progressively degenerative neurological disease, or any cerebral tumors.
  • Uncountable seizures (clusters) or history of convulsive status epilepticus within the last five years.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00160628

Sponsors and Collaborators
UCB
Investigators
Study Director: Beh Kevin, MD UCB
  More Information

Study ID Numbers: N01099
Study First Received: September 8, 2005
Last Updated: March 7, 2008
ClinicalTrials.gov Identifier: NCT00160628  
Health Authority: Korea: Food and Drug Administration

Keywords provided by UCB:
Epilepsy
Partial Onset Seizures
Keppra
Levetiracetam

Study placed in the following topic categories:
Epilepsies, Partial
Epilepsy
Seizures
Piracetam
Central Nervous System Diseases
Etiracetam
Brain Diseases

Additional relevant MeSH terms:
Nootropic Agents
Therapeutic Uses
Physiological Effects of Drugs
Nervous System Diseases
Protective Agents
Neuroprotective Agents
Central Nervous System Agents
Pharmacologic Actions
Anticonvulsants

ClinicalTrials.gov processed this record on January 16, 2009