Status:
COMPLETED
Safety and Efficacy of Eslicarbazepine Acetate as Adjunctive Therapy for Partial Seizures in Elderly Patients
Lead Sponsor:
Bial - Portela C S.A.
Conditions:
Epilepsy
Eligibility:
All Genders
65+ years
Phase:
PHASE3
Brief Summary
This is an open Label study to investigate the safety and efficacy of eslicarbazepine acetate as adjunctive therapy for partial seizures in elderly patients.
Detailed Description
Multicenter study in approximately 100 elderly patients. The study will follow an open-label design and will consist of 8-week baseline period, followed by a 26-week treatment period and a 4-week foll...
Eligibility Criteria
Inclusion
- Written informed consent form;
- Of age 65 years or older;
- A documented diagnosis of epilepsy for at least 12 months,
- At least 2 partial-onset seizures (including subtypes of simple partial, complex partial and/or partial seizures evolving to secondarily generalised) in the 4 weeks prior to screening;
- Currently treated with 1 or 2 AEDs (any except oxcarbazepine) in a stable dosage regimen for at least 4 weeks prior to screening. Vagus nerve stimulation (VNS) is to be considered as an AED (i.e., only one concomitant AED is allowed in patients with VNS);
- Willing and able to comply with all trial requirements, in the judgment of the investigator;
- At least 2 partial-onset seizures (documented in the diary) per 4 weeks during the 8-week baseline period;
- Satisfactorily complied with the study requirements during the baseline period
Exclusion
- Only simple partial seizures with no motor symptomatology (classified as A2-4) according to the International Classification of Epileptic Seizures);
- Primarily generalised seizures;
- Known progressive neurological disorders (progressive brain disease, epilepsy secondary to progressive central nervous system lesion) and progressive dementia;
- Occurrence of seizures too close to count accurately;
- History of status epileptic or cluster seizures 8i.e. 3 or more seizures within 30 minutes) within the 3 months prior to screening;
- Seizures of non-epileptic origin;
- Major psychiatric disorders;
- History of suicide attempt;
- Currently treated with oxcarbazepine;
- Previous use of ESL or participation in a clinical study with ESL;
- Known hypersensitivity to other carboxamide derivatives (e.g. oxcarbazepine, carbamazepine) or to any of the excipients;
- Uncontrolled cardiac, renal, hepatic, endocrine, gastrointestinal, metabolic, haematological or oncology disorder, hypo - or hyper thyroidism of any type;
- Second or third-degree atrioventricular blockade or any clinically significant abnormality in the 12-lead electrocardiogram (ECG) as determined by the investigator;
- Relevant clinical laboratory abnormalities as determined by the investigator (e.g. plasma sodium \<130 mmol/L, alanine or aspartate aminotransferases \>2.0 times above the upper limit of the range, or white blood cell count \<3,000 cells/mm3;
- Calculated creatinine values \< 30 mL/min at screening;
- Any other condition or circumstance that, in the opinion of the investigator, may compromise the patient's ability to comply with the study protocol;
- Received an investigational drug (or a medical device) within 3 months of screening or is currently participating in another trial of an investigational drug (or medical device) trial.
Key Trial Info
Start Date :
April 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2013
Estimated Enrollment :
72 Patients enrolled
Trial Details
Trial ID
NCT01422720
Start Date
April 1 2010
End Date
September 1 2013
Last Update
August 7 2017
Active Locations (48)
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1
Universitätsklinik für Neurologie; Arbeitsgruppe Epileptologie
Innsbruck, Austria
2
Universitätsklinik für Neurologie; Christian-Doppler-Klinik
Salzburg, Austria
3
Medizinische Universitat Wien Klinik fur Neurologie
Vienna, Austria
4
4 MHAT Sofia
Sofia, Bulgaria