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COMPLETED Phase 3

Efficacy and Safety of Eslicarbazepine Acetate (BIA 2-093) as Adjunctive Therapy for Refractory Partial Seizures

NCT00988429 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to determine whether Eslicarbazepine acetate (BIA 2-093) is an effective adjunct therapy in the treatment of refractory partial seizures

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG 800 mg QD Eslicarbazepine acetate
  • DRUG 1200 mg QD Eslicarbazepine acetate

Study Locations (20)

California

  • Kern County Neurological Medical Group, INC. — Bakersfield
  • Neuro-Pain Medical Center, Inc. — Fresno
  • Loma Linda University — Loma Linda
  • Collaborative Neuroscience Network, INC — Long Beach
  • Viking Clinical Research Center — Murrieta
  • Bright Minds Institute — San Francisco
  • Milestone Clinical Research — San Jose
  • Neurosearch II, Inc. — Ventura

Arizona

  • 21st Century Neurology - Division of Xenoscience, Inc. — Phoenix
  • Barrow Neurological Institute / St. Joseph's Hospital and Medical Center — Phoenix
  • Phoenix Neurological Associates/Clinical Research Advantage — Phoenix
  • ANI Research, PC — Sun City
  • University of Arizona Health Sciences Center — Tucson

Alabama

  • University of South Alabama Department of Neurology — Mobile
  • Neurology Clinic, P.C. — Northport

Arkansas

  • Arkansas Neurology — Conway
  • Clinical Trials Inc. — Little Rock

Colorado

  • University of Colorado Health Sciences — Aurora
  • Denver Health — Denver

Florida

  • Bradenton Research Center — Bradenton

Trial Details

FieldValue
Enrollment Target 653 participants
Start Date 2008-12-02
Est. Completion 2012-01-12
Phase Phase 3

Sponsor

Bial - Portela C S.A.

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00988429

The ClinicalTrials.gov registry entry for NCT00988429 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 653 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bial - Portela C S.A., which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Partial Epilepsy appearing as the primary indexed condition, and to 3 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00988429 reports 20 study locations spanning 6 distinct geographic areas — top geographies include California, Arizona, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00988429 about?

NCT00988429 is a clinical study titled "Efficacy and Safety of Eslicarbazepine Acetate (BIA 2-093) as Adjunctive Therapy for Refractory Partial Seizures". The purpose of this study is to determine whether Eslicarbazepine acetate (BIA 2-093) is an effective adjunct therapy in the treatment of refractory partial seizures

What is the current status of trial NCT00988429?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 653 participants. The study started on 2008-12-02. Estimated completion is 2012-01-12.

What conditions does trial NCT00988429 study?

This clinical trial studies the following conditions: Partial Epilepsy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00988429?

The interventions under investigation include: Placebo (DRUG), 800 mg QD Eslicarbazepine acetate (DRUG), 1200 mg QD Eslicarbazepine acetate (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00988429?

This trial is sponsored by Bial - Portela C S.A., which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00988429 being conducted?

This trial has 20 study locations across Alabama, Arizona, Arkansas, California, Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial