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COMPLETED Phase 3

Long Term Follow-up Study With Keppra XR (Levetiracetam XR) for Partial Seizures

NCT00419393 · View on ClinicalTrials.gov ↗

Study Summary

To provide continued treatment of Keppra XR (Levetiracetam XR) and to assess the long term safety of Keppra XR in subjects with partial onset seizures.

Conditions Studied

Interventions

  • DRUG Keppra XR (Levetiracetam XR)

Study Locations (20)

Other

  • — Aguascalientes
  • — Guadalajara
  • — Guadalajara Jalisco
  • — Mexico City

Alabama

  • — Dothan
  • — Northport

Georgia

  • — Atlanta
  • — Suwanee

New York

  • — Buffalo
  • — Cedarhurst

Arizona

  • — Phoenix

Arkansas

  • — Little Rock

California

  • — Bakersfield

Florida

  • — Loxahatchee Groves

Trial Details

FieldValue
Enrollment Target 190 participants
Start Date 2007-12
Est. Completion 2010-03
Phase Phase 3

Sponsor

UCB Pharma

20 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00419393

The ClinicalTrials.gov registry entry for NCT00419393 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 190 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 Epilepsy appearing as the primary indexed condition, and to 1 intervention — of which Keppra XR (Levetiracetam XR) 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: NCT00419393 reports 20 study locations spanning 14 distinct geographic areas — top geographies include Other, Alabama, Georgia. 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 NCT00419393 about?

NCT00419393 is a clinical study titled "Long Term Follow-up Study With Keppra XR (Levetiracetam XR) for Partial Seizures". To provide continued treatment of Keppra XR (Levetiracetam XR) and to assess the long term safety of Keppra XR in subjects with partial onset seizures.

What is the current status of trial NCT00419393?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 190 participants. The study started on 2007-12. Estimated completion is 2010-03.

What conditions does trial NCT00419393 study?

This clinical trial studies the following conditions: 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 NCT00419393?

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

Who is sponsoring clinical trial NCT00419393?

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 NCT00419393 being conducted?

This trial has 20 study locations across Alabama, Arizona, Arkansas, California, Florida. 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