Efficacy and Safety of Eslicarbazepine Acetate as Monotherapy for Patients With Newly Diagnosed Partial-onset Seizures

NCT01162460 | Completed Phase 3

• 1 other identifier: BIA-2093-311
• Study Type: interventional
• Target: 815
• Locations: 1 country
• Sites: 1

Brief Summary

The purpose of this study is to investigate the efficacy and safety of eslicarbazepine acetate (BIA 2-093) as monotherapy for patients with newly diagnosed partial-onset seizures.

Conditions

Epilepsy

Outcome Measures

Primary Outcomes (1)

• The primary efficacy variable will be the proportion of subjects in the PP set who are seizure free for the entire 26-week Evaluation Period at the last received dose level.

  26 weeks

Secondary Outcomes (9)

• Proportion of subjects in the ITT set without a seizure during the 26-week Evaluation Period at the last evaluated dose.

  26 weeks

• Proportion of subjects without a seizure during the 26-week Evaluation Period at the last evaluated dose.

  26 weeks

• Proportion of seizure-free subjects during 1 year of treatment at the last evaluated dose, where the end of the 1-year period is defined as the same start date as for the 26-week evaluation +365 days.

  52 weeks

• Time to first seizure at the last evaluated dose set.

  up to 183 weeks

• QOLIE-31 and Bond-Lader VAS

  26 weeks; up to 183 weeks

Study Arms (2)

Carbamazepine controlled release

ACTIVE COMPARATOR

Drug: Eslicarbazepine acetate (BIA 2-093)

Eslicarbazepine acetate

EXPERIMENTAL

Drug: Eslicarbazepine acetate (BIA 2-093)

Interventions

Eslicarbazepine acetate (BIA 2-093) DRUG

Week 1 and 2 either 400mg/day Eslicarbazepine acetate (ESL) or 200mg/day Carbamazepine controlled release(CBZ-CR); Week 3 onwards either 800mg/day Eslicarbazepine acetate or 400mg/day CBZ-CR; this dose then to be maintained unless a subject has a seizure. Subjects experiencing a seizure will have their assigned treatment dose increased to ESL 1200mg/day or CBZ 800mg/day. Should a subject have another seizure, their assigned treatment is to be increased to ESL 1600mg/day or CBZ 1200mg/day. Subjects who remain seizure free for 26 weeks at any dose in an Evaluation Period will continue to receive the allocated treatment under double-blind conditions.

Carbamazepine controlled release; Eslicarbazepine acetate

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

For inclusion in the study, subjects must fulfill all of the following at the time points indicated: Visit 1 (Days -1 to -7; Screening) * Have signed an informed consent before undergoing any study-related activities. Subjects of Asian ancestry (subjects with a direct ancestor of Asian origin, irrespective of the generational difference) are required to give written informed consent for genotyping. * Male or female ≥18 years of age. * Newly diagnosed epilepsy with at least 2 well documented, unprovoked, clinically evaluated and classified partial seizures (with or without secondary generalization) with clear focal origin, documented clinically OR by electroencephalogram (EEG) OR by imaging studies, within 12 months of Visit 1. In this context, seizures that occur within a period of 48 hours are counted as one seizure. * At least 1 seizure during the previous 3 months. * Demonstrated cooperation and willingness to complete all aspects of the study. * Female subjects without childbearing potential (2 years postmenopausal, bilateral oophorectomy or tubal ligation, or complete hysterectomy) are eligible. Female subjects with childbearing potential must not be pregnant as confirmed by a negative serum ß-human chorionic gonadotropin (hCG) test and sexually active females must be using a medically acceptable effective non-hormonal method of contraception for the duration of the study and until the Post-study visit (PSV). Visit A1 (Day 1; Randomization and start of double-blind treatment period) * Have satisfactorily completed the electronic subject diary (eDiary). * Female subjects with childbearing potential must not be pregnant as confirmed by a negative urine pregnancy test and sexually active females must be using a medically acceptable effective non-hormonal method of contraception for the duration of the study and until the PSV. Subjects having any of the following at the time points indicated are to be excluded from the study: Visit 1 (Days -1 to -7) * History of pseudo-seizures * Seizures occurring only in clusters. * History of absence, myoclonic, clonic, tonic, or atonic seizures. * Documented EEG within 12 months of Visit 1 suggestive of primarily generalized epilepsy. * History of status epilepticus within the 3 months prior to Visit 1. * Known progressive neurologic disorder (progressive brain disease, epilepsy secondary to progressive cerebral lesion) as assessed by magnetic resonance imaging or computer tomography. * Former or current use of any anti-epileptic drug (AED), except for the use of a single AED for a maximum duration of 2 weeks before Visit 1. * Previous use of ESL or carbamazepine (CBZ). * Using mono-amine oxidase inhibitors (MAOIs), tricyclic antidepressants, nefazodone, isoniazid, or protease inhibitors or any other anti-retroviral agents (e.g. efavirez) that may raise the levels of CBZ-CR. * Known hypersensitivity to carboxamide derivatives or tricyclic antidepressants. * History of uncontrolled psychiatric illness or mood disorder requiring electro-convulsive or drug therapy within the previous 6 months, a history of suicide attempt, schizophrenia, chronic treatment with benzodiazepines (except short-acting benzodiazepines) or barbiturates. * Judged clinically to have a suicidal risk in the opinion of the investigator based upon a clinical interview and the Columbia Suicide-Severity Rating Scale (C-SSRS). * History of alcohol, drug, or medication abuse within the last 2 years. * Uncontrolled cardiac (including atrioventricular block and other clinically significant electrocardiographic abnormalities), renal, hepatic, endocrine, gastrointestinal, metabolic, hematological, or oncology disorder. * History of bone marrow depression. * History of hepatic porphyrias (e.g. acute intermittent porphyria, variegate porphyria, porphyria cutanea tarda). * Relevant clinical laboratory abnormalities (e.g. sodium \<130 mmol/L, alanine or aspartate transaminases \>2 x the upper limit of normal, white blood cell count \<3000 cells/mm3) (measured at Visit 1). * Estimated glomerular filtration rate (eGFR) \<60 mL/min/1.73 m2 (measured at Visit 1). * Subjects of Asian ancestry who test positive for the presence of the HLA-B\*1502 allele. * Pregnancy or lactating. * Participation in other drug clinical trial within the last 2 months or having received an investigational medicinal product (IMP) within 5 half-lives of that IMP, whichever is longer. * Any other condition or circumstance that, in the opinion of the investigator, could compromise the subject's ability to comply with the study protocol. Visit A1 (Day 1) * Former or current use of any AED, except for the use of a single AED for a maximum duration of 2 weeks before Visit 1 and with a drug-free period of at least 5 days before Visit A1. Benzodiazepines are allowed, no more than twice a week, for an epileptic indication and as rescue medication during the ≥5-day drug-free period. * Using prohibited medication. * Pregnancy. * Any other condition or circumstance that, in the opinion of the investigator, could compromise the subject's ability to comply with the study protocol.

Contact the study team to discuss eligibility requirements. They can help determine if this study is right for you.

Sponsors & Collaborators

• Bial - Portela C S.A.: lead

Study Sites (1)

BIAL - Portela & Cª, S.A.

S. Mamede Do Coronado, S. Mamede Do Coronado, 4045-457, Portugal

Location

MeSH Terms

Conditions

Epilepsy

Interventions

eslicarbazepine acetate

Condition Hierarchy (Ancestors)

Brain Diseases; Central Nervous System Diseases; Nervous System Diseases

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: July 13, 2010
• First Posted: July 14, 2010
• Study Start: December 1, 2010
• Primary Completion: September 1, 2016
• Study Completion: September 1, 2016
• Last Updated: September 29, 2016

Record last verified: 2016-09

Locations

PT (1)