Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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EUCTR |
Last refreshed on:
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30 June 2019 |
Main ID: |
EUCTR2011-003100-21-ES |
Date of registration:
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08/05/2015 |
Prospective Registration:
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Yes |
Primary sponsor: |
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Public title:
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A study to assess the safety and efficacy of Lacosamide versus placebo (a pill without active medication) in patients with idiopathic generalised epilepsy who are already taking anti-epileptic medications
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Scientific title:
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A DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED, PARALLEL-GROUP, MULTICENTER STUDY TO EVALUATE THE EFFICACY AND SAFETY OF LACOSAMIDE AS ADJUNCTIVE THERAPY FOR UNCONTROLLED PRIMARY GENERALIZED TONIC-CLONIC SEIZURES IN SUBJECTS WITH IDIOPATHIC GENERALIZED EPILEPSY |
Date of first enrolment:
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26/06/2015 |
Target sample size:
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200 |
Recruitment status: |
Not Recruiting |
URL:
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https://www.clinicaltrialsregister.eu/ctr-search/search?query=eudract_number:2011-003100-21 |
Study type:
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Interventional clinical trial of medicinal product |
Study design:
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Controlled: yes Randomised: yes Open: no Single blind: no Double blind: yes Parallel group: yes Cross over: no Other: no If controlled, specify comparator, Other Medicinial Product: no Placebo: yes Other: no Number of treatment arms in the trial: 2
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Phase:
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Human pharmacology (Phase I): no
Therapeutic exploratory (Phase II): no
Therapeutic confirmatory - (Phase III): yes
Therapeutic use (Phase IV): no
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Countries of recruitment
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Australia
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Belgium
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Brazil
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Bulgaria
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Czech Republic
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France
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Germany
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Hungary
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Israel
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Italy
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Japan
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Korea, Republic of
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Mexico
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Poland
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Portugal
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Romania
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Russian Federation
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Slovakia
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Spain
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Taiwan
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Turkey
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United States
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Contacts
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Name:
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Clin Trial Reg & Results disclosure
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Address:
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Alfred-Nobel-Strasse 10
40789
Monheim
Germany |
Telephone:
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900 811 335 |
Email:
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clinicaltrials@ucb.com |
Affiliation:
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UCB BIOSCIENCES GmbH |
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Name:
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Clin Trial Reg & Results disclosure
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Address:
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Alfred-Nobel-Strasse 10
40789
Monheim
Germany |
Telephone:
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900 811 335 |
Email:
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clinicaltrials@ucb.com |
Affiliation:
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UCB BIOSCIENCES GmbH |
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Key inclusion & exclusion criteria
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Inclusion criteria: ? Subject with a confirmed diagnosis at least 24 weeks prior to Visit 1 and a disease onset prior to 30 years of age, consistent with idiopathic generalized epilepsy (IGE) experiencing primary generalized tonic-clonic (PGTC) seizures (Type IIE) that are classifiable according to the International League Against Epilepsy (ILAE) Classification of Epileptic Seizures (ILAE, 1981).
? Subject has >=3 PGTC seizures during the 16-week Combined Baseline (12-week Historical Baseline plus 4-week Prospective Baseline)
? If a brain magnetic resonance imaging (MRI)/computed tomography (CT) scan has been performed, there must be no evidence of any progressive abnormality or any lesion likely to be associated with partial-onset seizures.
? Subject has been maintained on a stable dose regimen of 1 to 2 non-benzodiazepine marketed Anti-epileptic drugs (AEDs) OR 1 to 3 AEDs (with at least 1 AED identified as a benzodiazepine) for at least 28 days prior to Visit 1 with or without additional concurrent stable Vagus nerve stimulation (VNS).
? Subjects are required to have had an electroencephalogram (EEG) report consistent with IGE (eg, generalized >= 3Hz epileptiform discharges and a normal EEG background) confirmed by a Central Reviewer. Are the trial subjects under 18? yes Number of subjects for this age range: 100 F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 90 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 10
Exclusion criteria: ? History of partial onset seizures or EEG findings indicating partial onset seizures
? Symptomatic generalized epilepsy, e.g. Lennox-Gastaut Syndrome
? Lifetime history of suicide attempt, or suicidal ideation in past 6 months
? Women of child bearing potential must practice contraception according to protocol requirements
? Regular use of neuroleptics, narcotics, monoamine oxidase (MOA) inhibitors, barbiturates (for indication other than epilepsy) within 28 days prior to Visit 1
? Use of Felbamate or Vigabatrin within last 6 months
? Subject is on a ketogenic diet
Age minimum:
Age maximum:
Gender:
Female: yes Male: yes
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Health Condition(s) or Problem(s) studied
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Therapeutic area: Diseases [C] - Nervous System Diseases [C10]
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Epilepsy
MedDRA version: 20.0
Level: LLT
Classification code 10071096
Term: Idiopathic generalized epilepsy
System Organ Class: 100000004852
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Intervention(s)
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Trade Name: Vimpat 50 mg film-coated tablets Product Name: Lacosamide Product Code: SPM927 Pharmaceutical Form: Film-coated tablet INN or Proposed INN: LACOSAMIDE Current Sponsor code: SPM 927 Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 50- Pharmaceutical form of the placebo: Coated tablet Route of administration of the placebo: Oral use
Trade Name: Vimpat 10mg/ml Oral Solution Product Name: Lacosamide Product Code: SPM927 Pharmaceutical Form: Oral solution INN or Proposed INN: LACOSAMIDE Current Sponsor code: SPM 927 Concentration unit: mg/ml milligram(s)/millilitre Concentration type: equal Concentration number: 10- Pharmaceutical form of the placebo: Oral solution Route of administration of the placebo: Oral use
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Primary Outcome(s)
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Timepoint(s) of evaluation of this end point: 24-week Treatment Period from Visit 2 (Week 0) to Visit 10 (Week 24)
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Main Objective: To demonstrate the efficacy of oral lacosamide (LCM) vs placebo as adjunctive therapy for uncontrolled primary generalized tonic-clonic (PGTC) seizures in subjects with idiopathic generalized epilepsy (IGE) currently taking 1 to 3 concomitant anti-epileptic drugs (AEDs) independent of the number of prior failed AEDs
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Primary end point(s): Time to the second primary generalized tonic clonic (PGTC) seizure
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Secondary Objective: To assess the safety and tolerability of lacosamide (LCM) in subjects with idiopathic generalized epilepsy (IGE) with uncontrolled primary generalized tonic-clonic (PGTC) seizures
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Secondary Outcome(s)
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Secondary end point(s): Seizure freedom for primary generalized tonic clonic (PGTC) seizures
The percent change in primary generalized tonic clonic (PGTC) seizure frequency per 28 days
Time to the first primary generalized tonic clonic (PGTC) seizure
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Timepoint(s) of evaluation of this end point: 24-week Treatment Period from Visit 2 (Week 0) to Visit 10 (Week 24)
From the Combined Baseline (combined 12-week Historical and 4-week Prospective Baseline) to the first 6 weeks of the Treatment Period
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Secondary ID(s)
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SP0982
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2011-003100-21-PT
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Source(s) of Monetary Support
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UCB BIOSCIENCES, Inc.
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Ethics review
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Status: Approved
Approval date:
Contact:
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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