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Completed

NCT Number: NCT00280696

A Double-blind Confirmatory Trial of Levetiracetam in Epilepsy Patients With Partial Onset Seizures

A double-blind, randomized, multicenter, placebo controlled 5 parallel groups, confirmatory trial to evaluated the efficacy and safety of levetiracetam used as adjunctive treatment in patients from 16 to 65 years with epilepsy suffering from partial onset seizures.

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Key information

Age range

16 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Aichi-gun, Aichi-ken, Japan

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Epileptic patients who fulfill the following criteria are eligible for inclusion in the study:

  • Subjects aged from 16 to 65 years at the acquisition of informed consent to the trial participation
  • Seizure type: subjects with epileptic seizures which were diagnosed as partial seizures more than 2 years ago according to "Clinical and electroencephalographic classification of epileptic seizures (1981)" defined by the International League Against Epilepsy (ILAE) and confirmed with an EEG that has been performed within 1 year before Screening or at the Screening Visit
  • Subjects whose previous therapy before screening involved at least two standard anti-epileptic drugs (AEDs) for partial seizures, and in whom it can be confirmed that the doses met the daily dose specified for the treatment of epilepsy in the package insert and that the therapy has been continued for at least 3 months
  • Frequency of epileptic seizures: subjects experiencing partial seizures at least 12 times in 12 weeks during the Baseline Period (Week -12 to Week 0) and at least twice in every 4 weeks

Exclusion criteria

The following patients are not eligible for inclusion into the study:

  • Subjects who were diagnosed with status epilepticus within 3 months before screening
  • Subjects with no partial seizures of which frequency was measured during the Baseline Period
  • Subjects who underwent surgery for epilepsy within 2 years before Screening or who were scheduled to undergo brain surgery during the study period and within 4 weeks after the completion of this study
  • Subjects with a history of oral treatment with Levetiracetam (LEV)

Treatment and study plan

Levetiracetam 250 mg

Drug
  • Active Substance: Levetiracetam
  • Pharmaceutical Form: Film-coated tablet
  • Concentration: 250 mg
  • Route of Administration: Oral Use

Other names: Keppra

Levetiracetam 500 mg

Drug
  • Active Substance: Levetiracetam
  • Pharmaceutical Form: Film-coated tablet
  • Concentration: 500 mg
  • Route of Administration: Oral Use

Other names: Keppra

Placebo

Other
  • Active Substance: Placebo
  • Pharmaceutical Form: Film-coated tablet
  • Concentration: 250 mg and 500 mg
  • Route of Administration: Oral Use

Primary outcomes

  1. Percent reduction from Baseline in partial (Type I) seizure frequency per week over the Evaluation Period

    Time frame: From Baseline to the 12-week Evaluation Period

Secondary outcomes

  1. Partial (Type I) seizure frequency per week over the Evaluation Period

    Time frame: 12-week Evaluation Period

  2. Partial (Type I) seizure responder rates (50 %, 75 %) over the Evaluation Period

    Time frame: From Baseline to the 12-week Evaluation Period

  3. Seizure freedom over the Evaluation Period

    Time frame: 12-week Evaluation Period

  4. Categorized percentage reduction from Baseline in partial (Type I) seizure frequency per week over the Evaluation Period

    Time frame: From Baseline to the 12-week Evaluation Period

  5. Percentage reduction from Baseline in seizure frequency per week by seizure subtype (IA, IB, IC, IA + IB, other) over the Evaluation Period

    Time frame: From Baseline to the 12-week Evaluation Period

Sponsors and collaborators

Lead sponsor

UCB Japan Co. Ltd.

Industry

Registry information

Official study title

A Double-blind, Randomized, Placebo-controlled 5 Parallel Groups, Confirmatory Trial on the Efficacy and Safety of Levetiracetam Used as add-on Therapy at Doses of 0.5 to 3 g/Day in Patients From 16 to 65 Years With Epilepsy With Partial Onset Seizures Under Treatment With 1 to 3 Anti-epileptic Drug(s)

Important dates

Study start
2005
Primary completion
2007
Study completion
2007
First posted
Jan 23, 2006
Registry last updated
Feb 11, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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