ClinicalTrials.gg
CompletedNCT00150774Updated Sep 17, 2013

Levetiracetam as add-on Treatment of Myoclonic Jerks in Adolescents + Adults

A Phase 3 interventional study of Levetiracetam in Generalized Convulsive Epilepsy, sponsored by UCB Pharma. Completed. Open to participants aged 12 Years to 65 Years. Per ClinicalTrials.gov, last updated 2013-09-17.

Primary conditionEpilepsy, Idiopathic GeneralizedRegistry: Epilepsy, GeneralizedReclassifiedWhy we changed it
Registry
Epilepsy, Generalized — the first condition term the registry derived for this study.
ClinicalTrials.gg
Epilepsy, Idiopathic Generalized
Why
  1. The study's title name Epilepsy, Idiopathic Generalized, a narrower term within Epilepsy, Generalized.
Confidence
High: the new condition is named in the study's own title. Of 46 hand-checked studies reclassified this way, 72% were exactly right and 89% in the right disease family; the registry's first term was right for 4% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by UCB Pharma (part of UCB S.A.) · Phase 3, Interventional, and Treatment

Phase
Phase 3
Study type
Interventional
Enrollment
116
Allocation
Randomized
Ages
12 Years to 65 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • Generalized Convulsive Epilepsy

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Keywords

  • Idiopathic Generalized Epilepsy, Myoclonic seizures
  • Keppra - Levetiracetam
03

In context

Epilepsy, Idiopathic Generalized Reclassified

35 studies on the registry are indexed under Epilepsy, Idiopathic Generalized; 4 are open to participants now.

This study's enrollment of 116 is above the median of 71 across 26 interventional studies indexed under Epilepsy, Idiopathic Generalized.

Browse Epilepsy, Idiopathic Generalized studies →

Lead sponsor

UCB Pharma is the lead sponsor of 242 studies on the registry; none are open to participants now.

Compared within Epilepsy, Idiopathic Generalized, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Epilepsy, Generalized. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
12 Years to 65 Years
Sexes eligible
All

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

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.
05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double
Enrollment
116 participants

Interventions

06

What researchers measure

Primary outcomes

  1. Responder rate in myoclonic (type IIB) seizures days over 16 weeks

Secondary outcomes

  1. Safety and tolerability of levetiracetam by means of AE, laboratory assessments, plasma concentration

07

Study locations

No study locations are listed for this record.

08

References and documents

Publications

  • Rosenfeld WE, Benbadis S, Edrich P, Tassinari CA, Hirsch E. Levetiracetam as add-on therapy for idiopathic generalized epilepsy syndromes with onset during adolescence: analysis of two randomized, double-blind, placebo-controlled studies. Epilepsy Res. 2009 Jul;85(1):72-80. doi: 10.1016/j.eplepsyres.2009.02.016. Epub 2009 Mar 26. PubMed 19327967 ↗
  • Noachtar S, Andermann E, Meyvisch P, Andermann F, Gough WB, Schiemann-Delgado J; N166 Levetiracetam Study Group. Levetiracetam for the treatment of idiopathic generalized epilepsy with myoclonic seizures. Neurology. 2008 Feb 19;70(8):607-16. doi: 10.1212/01.wnl.0000297512.18364.40. PubMed 18285535 ↗
09

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Nov 2001, a primary completion of Dec 2004 and a completion of Dec 2004. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 6, 2005
First posted
Sep 8, 2005
Start
Nov 2001
Primary completionActual
Dec 2004
CompletionActual
Dec 2004
Last update
Sep 17, 2013
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 17, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00150774
Lead sponsor
UCB Pharma
First posted
Sep 8, 2005
Start date
Nov 2001
Primary completion
Dec 2004
Completion
Dec 2004
Last update
Sep 17, 2013

Study contacts

UCB Clinical Trial Call Center
study director · UCB Pharma
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2010. You cannot join it, but the record below documents what was studied.

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Studies of the drug tested here: Levetiracetam

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