Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 2 Interventional

A Study of the Efficacy of RWJ-333369 in the Prevention of Migraine

ClinicalTrials.gov ID: NCT00109083

Public ClinicalTrials.gov record NCT00109083. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 3:12 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Dose-Ranging, Multicenter Study of the Efficacy of RWJ-333369 in the Prophylaxis of Migraine

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate whether RWJ-333369 is a safe and effective treatment in reducing the number of migraine headaches when added to a person's usual medications for acute migraine headache relief.

Study identification

NCT ID
NCT00109083
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
SK Life Science, Inc.
Industry
Enrollment
300 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 2002 (Type not available)
Primary completion
Feb 2006 (Actual)
Completion
Feb 2006 (Actual)
Last update posted
Aug 2, 2012

2002 – 2006

United States locations

U.S. sites
25
U.S. states
19
U.S. cities
25
Facility City State ZIP Site status
Not listed Northport Alabama — —
Not listed Phoenix Arizona — —
Not listed Little Rock Arkansas — —
Not listed Berkeley California — —
Not listed Golden Colorado — —
Not listed Miami Florida — —
Not listed St. Petersburg Florida — —
Not listed Chicago Illinois — —
Not listed Baton Rouge Louisiana — —
Not listed Brockton Massachusetts — —
Not listed Springfield Massachusetts — —
Not listed Chaska Minnesota — —
Not listed Springfield Missouri — —
Not listed Greensboro North Carolina — —
Not listed Bismarck North Dakota — —
Not listed Cincinnati Ohio — —
Not listed Mogadore Ohio — —
Not listed Nashville Tennessee — —
Not listed Austin Texas — —
Not listed Houston Texas — —
Not listed Lake Jackson Texas — —
Not listed Richardson Texas — —
Not listed Alexandria Virginia — —
Not listed Olympia Washington — —
Not listed Middleton Wisconsin — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00109083, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 2, 2012 · Synced Oct 20, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00109083 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →