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NCT00233675 · ClinicalTrials.gov registry record · Phase 3

Evaluate the Safety of GABITRIL in Adults With Generalized Anxiety Disorder

A Phase 3 study of General Anxiety Disorder, sponsored by Cephalon.

Completed
Registry status
Phase 3
Development phase
20
Study locations

NCT00233675 is a Phase 3 study of General Anxiety Disorder that has completed, run by Cephalon. The trial reports 20 study locations across 11 states.

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The verdict

NCT00233675, a Phase 3 study of General Anxiety Disorder, has completed, sponsored by Cephalon.

COMPLETED
Registry status
Phase 3
Development phase
20
Study locations

Study Summary

To assess the long-term safety and tolerability of tiagabine treatment in patients with generalized anxiety disorder (GAD).

Conditions Studied

Interventions

  • DRUG GABITRIL (tiagabine hydrochloride; CEP-6671)

Study Locations (20)

California

  • Southwestern Research - Beverly Hills
  • Pharmacology Research Institut - Newport Beach
  • Pharmacology Research Institut - Northridge
  • Pacific Clinical Research Medi - Orange
  • Radiant Research San Diego - San Diego
  • Affiliated Research Institute - San Diego

New York

  • Social Psychiatry Research Ins - Brooklyn
  • Fieve Clinical Services, Inc. - New York
  • Medical and Behavioral - New York
  • Medical Research Network - New York

Florida

  • Clinical Neuroscience Solution - Jacksonville
  • Clinical Neuroscience Solution - West Palm Beach

Arizona

  • Pivotal Research Center - Mesa

Colorado

  • Radiant Research Denver - Denver

Connecticut

  • University of Connecticut - Farmington

Georgia

  • Carman Research - Smyrna

Illinois

  • Cunningham Clinical Research - Edwardsville

Trial Details

FieldValue
Start Date 2003-08
Phase Phase 3

Sponsor

Cephalon

64 total trials

What the Registry Record Tells You About NCT00233675

The ClinicalTrials.gov registry entry for NCT00233675 describes a study currently listed as completed, categorized as Phase 3. An enrollment target was not published in the registry record, which is common for early-stage or observational entries. The listed sponsor is Cephalon, which has 64 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with General Anxiety Disorder appearing as the primary indexed condition, and to 1 intervention - of which GABITRIL (tiagabine hydrochloride; CEP-6671) is the first listed.

NCT00233675 reports 20 study locations spanning 11 distinct geographic areas - top geographies include California, New York, Florida.

Frequently Asked Questions

What is clinical trial NCT00233675 about?

NCT00233675 is a clinical study titled "Evaluate the Safety of GABITRIL in Adults With Generalized Anxiety Disorder". To assess the long-term safety and tolerability of tiagabine treatment in patients with generalized anxiety disorder (GAD).

What is the current status of trial NCT00233675?

This trial is currently completed. It is a Phase 3 study. The study started on 2003-08.

What conditions does trial NCT00233675 study?

This clinical trial studies the following conditions: General Anxiety Disorder.

What interventions are being tested in trial NCT00233675?

The interventions under investigation include: GABITRIL (tiagabine hydrochloride; CEP-6671) (DRUG).

Who is sponsoring clinical trial NCT00233675?

This trial is sponsored by Cephalon, which has 64 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00233675 being conducted?

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

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.