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Brivaracetam as add-on Treatment of Unverricht-Lundborg Disease in Adolescents and Adults

Primary Purpose

Unverricht-Lundborg Disease

Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Brivaracetam 25 mg
Brivaracetam 50 mg
Placebo
Sponsored by
UCB Pharma SA
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Unverricht-Lundborg Disease focused on measuring Unverricht-Lundborg disease, Baltic myoclonus, progressive myoclonic epilepsies, myoclonus, brivaracetam

Eligibility Criteria

16 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Subjects with diagnosed Unverricht-Lundborg disease (ULD) ascertained by appropriate genetic testing for a homozygous or compound heterozygous mutation in the Cystatin B (CSTB) gene Subjects with moderate to severe myoclonus documented by an Action Myoclonus sum score of ≥ 30 (evaluation by investigator) Subjects currently being or having been treated with clonazepam up to the maximum recommended daily dose of 20 mg or up to their individual optimal dose as assessed by the investigator Subjects currently being or having been treated with valproate up to the maximum recommended daily dose 60 mg/kg or serum levels of 100 mcg/ml or up to their individual optimal dose as specified by the investigator Exclusion Criteria: Subjects currently on felbamate or having been on felbamate within less than 18 months prior to Visit 1 Subjects currently treated with phenytoin or having been on phenytoin in the last month prior to Visit 1 Subjects currently on vigabatrine. Subjects having been on vigabatrine if no visual fields examination report available including standard static (Humphrey or Octopus) or cinetic perimetry (Goldman) Subject taking any drug with possible central nervous system (CNS) effects Subjects taking any drug that may significantly influence the metabolism of BRV (CYP2C or CYP3A potent inducers/inhibitors) Known clinically significant acute or chronic illness or illness which may impair reliable participation in the trial, necessitate the use of medication not allowed by protocol or represent a safety risk in the Investigator's opinion Subjects with history of severe adverse hematological reaction to any drug Impaired hepatic function: ALAT/SGPT, ASAT/SGOT, alkaline phosphatase, GGT value of more than three times the upper limit of the reference range History of suicide attempt during the last 5 years Subject with suicidal ideations within the last year or at risk of suicide attempt unless cleared by written confirmation from a psychiatrist and approved by the UCB physician Ongoing psychiatric disorder other than mild controlled disorder

Sites / Locations

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Placebo Comparator

Experimental

Experimental

Arm Label

Placebo

Brivaracetam 50 mg/day

Brivaracetam 150 mg/day

Arm Description

BRV 50 mg/day

BRV 150 mg/day

Outcomes

Primary Outcome Measures

Percent reduction from baseline on the Action Myoclonus score (Unified Myoclonus Rating Scale (UMRS) Section 4) at the end of the Treatment Period

Secondary Outcome Measures

Percent reduction from baseline on the functional disability score (UMRS Section 5) at the end of the Treatment Period
Percent reduction from baseline on the stimulus sensitivity score (UMRS Section 3) at the end of the Treatment Period
Percent reduction from baseline on the myoclonus patient questionnaire (UMRS Section 1) at the end of the Treatment Period
Global Evaluation Scale by Investigator (I-GES) at the end of the Treatment Period

Full Information

First Posted
July 25, 2006
Last Updated
May 15, 2015
Sponsor
UCB Pharma SA
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1. Study Identification

Unique Protocol Identification Number
NCT00357669
Brief Title
Brivaracetam as add-on Treatment of Unverricht-Lundborg Disease in Adolescents and Adults
Official Title
A Multi-center, Randomized, Double-blind, Placebo-controlled, Parallel Study to Evaluate the Efficacy and Safety of Brivaracetam Used as Adjunctive Treatment for 12 Weeks in Adolescent and Adult Patients (≥16 Years) With Genetically Ascertained Unverricht-Lundborg Disease
Study Type
Interventional

2. Study Status

Record Verification Date
May 2015
Overall Recruitment Status
Completed
Study Start Date
November 2006 (undefined)
Primary Completion Date
October 2007 (Actual)
Study Completion Date
October 2007 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
UCB Pharma SA

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The study will compare the efficacy and safety of brivaracetam with placebo in patients with Unverricht-Lundborg disease.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Unverricht-Lundborg Disease
Keywords
Unverricht-Lundborg disease, Baltic myoclonus, progressive myoclonic epilepsies, myoclonus, brivaracetam

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Title
Brivaracetam 50 mg/day
Arm Type
Experimental
Arm Description
BRV 50 mg/day
Arm Title
Brivaracetam 150 mg/day
Arm Type
Experimental
Arm Description
BRV 150 mg/day
Intervention Type
Drug
Intervention Name(s)
Brivaracetam 25 mg
Other Intervention Name(s)
ucb34714
Intervention Description
Active Substance: Brivaracetam Pharmaceutical Form: Tablet Concentration: 25 mg Route of Administration: Oral use
Intervention Type
Drug
Intervention Name(s)
Brivaracetam 50 mg
Other Intervention Name(s)
ucb34714
Intervention Description
Active Substance: Brivaracetam Pharmaceutical Form: Tablet Concentration: 50 mg Route of Administration: Oral use
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Active Substance: Placebo Pharmaceutical Form: Tablet Concentration: 25 mg and 50 mg Route of Administration: Oral use
Primary Outcome Measure Information:
Title
Percent reduction from baseline on the Action Myoclonus score (Unified Myoclonus Rating Scale (UMRS) Section 4) at the end of the Treatment Period
Time Frame
End of treatment period (Week 14 or early discontinuation visit)
Secondary Outcome Measure Information:
Title
Percent reduction from baseline on the functional disability score (UMRS Section 5) at the end of the Treatment Period
Time Frame
End of treatment period (week 14 or early discontinuation visit)
Title
Percent reduction from baseline on the stimulus sensitivity score (UMRS Section 3) at the end of the Treatment Period
Time Frame
End of treatment period (week 14 or early discontinuation visit)
Title
Percent reduction from baseline on the myoclonus patient questionnaire (UMRS Section 1) at the end of the Treatment Period
Time Frame
End of treatment period (week 14 or early discontinuation visit)
Title
Global Evaluation Scale by Investigator (I-GES) at the end of the Treatment Period
Time Frame
End of treatment period (week 14 or early discontinuation visit)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subjects with diagnosed Unverricht-Lundborg disease (ULD) ascertained by appropriate genetic testing for a homozygous or compound heterozygous mutation in the Cystatin B (CSTB) gene Subjects with moderate to severe myoclonus documented by an Action Myoclonus sum score of ≥ 30 (evaluation by investigator) Subjects currently being or having been treated with clonazepam up to the maximum recommended daily dose of 20 mg or up to their individual optimal dose as assessed by the investigator Subjects currently being or having been treated with valproate up to the maximum recommended daily dose 60 mg/kg or serum levels of 100 mcg/ml or up to their individual optimal dose as specified by the investigator Exclusion Criteria: Subjects currently on felbamate or having been on felbamate within less than 18 months prior to Visit 1 Subjects currently treated with phenytoin or having been on phenytoin in the last month prior to Visit 1 Subjects currently on vigabatrine. Subjects having been on vigabatrine if no visual fields examination report available including standard static (Humphrey or Octopus) or cinetic perimetry (Goldman) Subject taking any drug with possible central nervous system (CNS) effects Subjects taking any drug that may significantly influence the metabolism of BRV (CYP2C or CYP3A potent inducers/inhibitors) Known clinically significant acute or chronic illness or illness which may impair reliable participation in the trial, necessitate the use of medication not allowed by protocol or represent a safety risk in the Investigator's opinion Subjects with history of severe adverse hematological reaction to any drug Impaired hepatic function: ALAT/SGPT, ASAT/SGOT, alkaline phosphatase, GGT value of more than three times the upper limit of the reference range History of suicide attempt during the last 5 years Subject with suicidal ideations within the last year or at risk of suicide attempt unless cleared by written confirmation from a psychiatrist and approved by the UCB physician Ongoing psychiatric disorder other than mild controlled disorder
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
UCB Clinical Trial Call Center
Organizational Affiliation
+1 877 822 9493 (UCB)
Official's Role
Study Director
Facility Information:
City
Kuopio
Country
Finland
City
Tampere
Country
Finland
City
Marseille
Country
France
City
Montpellier Cedex 5
Country
France
City
Bologna
Country
Italy
City
Messina
Country
Italy
City
Milano
Country
Italy
City
Napoli
Country
Italy
City
Heemstede
Country
Netherlands
City
Heeze
Country
Netherlands
City
St Pierre Cedex
Country
Réunion
City
Goteborg
Country
Sweden
City
Tunis
Country
Tunisia

12. IPD Sharing Statement

Citations:
PubMed Identifier
33461041
Citation
Ben-Menachem E, Baulac M, Hong SB, Cleveland JM, Reichel C, Schulz AL, Wagener G, Brandt C. Safety, tolerability, and efficacy of brivaracetam as adjunctive therapy in patients with focal seizures, generalized onset seizures, or Unverricht-Lundborg disease: An open-label, long-term follow-up trial. Epilepsy Res. 2021 Feb;170:106526. doi: 10.1016/j.eplepsyres.2020.106526. Epub 2020 Dec 4.
Results Reference
derived
PubMed Identifier
26666500
Citation
Kalviainen R, Genton P, Andermann E, Andermann F, Magaudda A, Frucht SJ, Schlit AF, Gerard D, de la Loge C, von Rosenstiel P. Brivaracetam in Unverricht-Lundborg disease (EPM1): Results from two randomized, double-blind, placebo-controlled studies. Epilepsia. 2016 Feb;57(2):210-21. doi: 10.1111/epi.13275. Epub 2015 Dec 15.
Results Reference
derived

Learn more about this trial

Brivaracetam as add-on Treatment of Unverricht-Lundborg Disease in Adolescents and Adults

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