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COMPLETED Phase 2

To Determine Tolerability and Efficacy of Long-term Oral Lacosamide in Patients With Partial Seizures

NCT00552305 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this trial is to determine whether lacosamide is safe and effective for long-term use in patients with partial-seizures from epilepsy.

Conditions Studied

Interventions

  • DRUG lacosamide

Study Locations (20)

Florida

  • — Gainesville
  • — Hollywood
  • — Miami
  • — Ponte Vedra Beach

Alabama

  • — Birmingham
  • — Huntsville

Arizona

  • — Phoenix
  • — Tucson

Illinois

  • — Chicago
  • — Springfield

Kentucky

  • — Crestview Hills
  • — Lexington

Maryland

  • — Baltimore
  • — Frederick

Arkansas

  • — Little Rock

California

  • — Los Angeles

Trial Details

FieldValue
Enrollment Target 370 participants
Start Date 2001-08
Est. Completion 2010-02
Phase Phase 2

Sponsor

UCB Pharma

20 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00552305

The ClinicalTrials.gov registry entry for NCT00552305 describes a study currently listed as completed. It is categorized as Phase 2, 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 370 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is UCB Pharma, which has 20 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 Epilepsies appearing as the primary indexed condition, and to 1 intervention — of which lacosamide 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: NCT00552305 reports 20 study locations spanning 12 distinct geographic areas — top geographies include Florida, Alabama, Arizona. 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 NCT00552305 about?

NCT00552305 is a clinical study titled "To Determine Tolerability and Efficacy of Long-term Oral Lacosamide in Patients With Partial Seizures". The purpose of this trial is to determine whether lacosamide is safe and effective for long-term use in patients with partial-seizures from epilepsy.

What is the current status of trial NCT00552305?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 370 participants. The study started on 2001-08. Estimated completion is 2010-02.

What conditions does trial NCT00552305 study?

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

What interventions are being tested in trial NCT00552305?

The interventions under investigation include: lacosamide (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00552305?

This trial is sponsored by UCB Pharma, which has 20 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00552305 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