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Completed Phase 3 Interventional

Treximet (Sumatriptan/Naproxen Sodium), Formerly Known as Trexima, In The Acute Treatment Of Multiple Migraine Attacks

ClinicalTrials.gov ID: NCT00240630

Public ClinicalTrials.gov record NCT00240630. 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 Sep 2, 2026, 4:59 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, Multi-center, Placebo-controlled, Cross-over Study to Determine the Consistency of Response for Trexima (Sumatriptan 85mg/Naproxen Sodium 500mg) Administered During the Mild Pain Phase for the Acute Treatment of Multiple Migraine Attacks

Brief summary

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

The purpose of this study is to determine the consistency of response for Treximet (sumatriptan/naproxen sodium), formerly known as Trexima, when treating four acute migraine attacks at the mild pain phase and within 1 hour of onset of head pain.

Study identification

NCT ID
NCT00240630
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
646 participants

Conditions and interventions

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
Sep 30, 2005
Primary completion
May 31, 2006
Completion
May 31, 2006
Last update posted
Apr 15, 2015

2005 – 2006

United States locations

U.S. sites
50
U.S. states
26
U.S. cities
48
Facility City State ZIP Site status
GSK Investigational Site Chandler Arizona 85224
GSK Investigational Site Phoenix Arizona 85013
GSK Investigational Site Little Rock Arkansas 72205
GSK Investigational Site Irvine California 92618
GSK Investigational Site Newport Beach California 92660
GSK Investigational Site San Francisco California 94109
GSK Investigational Site Santa Monica California 90404
GSK Investigational Site Walnut Creek California 94596
GSK Investigational Site Westlake Village California 91361
GSK Investigational Site Colorado Springs Colorado 80904
GSK Investigational Site Hartford Connecticut 06106
GSK Investigational Site Stamford Connecticut 06902
GSK Investigational Site Daytona Beach Florida 32114
GSK Investigational Site Hollywood Florida 33021
GSK Investigational Site Palm Beach Gardens Florida 33410
GSK Investigational Site West Palm Beach Florida 33407
GSK Investigational Site Atlanta Georgia 30308
GSK Investigational Site Austell Georgia 30106
GSK Investigational Site Chicago Illinois 60614
GSK Investigational Site Fort Wayne Indiana 46805
GSK Investigational Site Wichita Kansas 67207
GSK Investigational Site Braintree Massachusetts 02184
GSK Investigational Site Milford Massachusetts 01757
GSK Investigational Site Kalamazoo Michigan 49009
GSK Investigational Site Minneapolis Minnesota 55422
GSK Investigational Site Las Vegas Nevada 89146
GSK Investigational Site Endwell New York 13760
GSK Investigational Site Manhasset New York 11030
GSK Investigational Site Manlius New York 13104
GSK Investigational Site New York New York 10022
GSK Investigational Site Fargo North Dakota 58122
GSK Investigational Site Cleveland Ohio 44195
GSK Investigational Site Oklahoma City Oklahoma 73112
GSK Investigational Site Tulsa Oklahoma 74136
GSK Investigational Site Eugene Oregon 97401
GSK Investigational Site Medford Oregon 97504-8456
GSK Investigational Site Philadelphia Pennsylvania 19107-2568
GSK Investigational Site Pittsburgh Pennsylvania 15236
GSK Investigational Site Mt. Pleasant South Carolina 29464
GSK Investigational Site Germantown Tennessee 38138
GSK Investigational Site Nashville Tennessee 37203
GSK Investigational Site Austin Texas 78705
GSK Investigational Site Georgetown Texas 78626
GSK Investigational Site Houston Texas 77004
GSK Investigational Site Houston Texas 77030
GSK Investigational Site San Antonio Texas 78229
GSK Investigational Site San Antonio Texas 78258
GSK Investigational Site Salt Lake City Utah 84107
GSK Investigational Site Burlington Vermont 05405
GSK Investigational Site Seattle Washington 98122

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 NCT00240630, 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 Apr 15, 2015 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00240630 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →