Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional

Study Of Treximet, Formerly Known as Trexima, In The Acute Treatment Of Multiple Migraine Attacks

ClinicalTrials.gov ID: NCT00240617

Public ClinicalTrials.gov record NCT00240617. 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 19, 2026, 3:16 AM 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 (*Treximet)

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 (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
NCT00240617
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
623 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
Oct 2005 (Type not available)
Primary completion
Jun 2006 (Actual)
Completion
Jun 2006 (Actual)
Last update posted
Oct 26, 2016

2005 – 2006

United States locations

U.S. sites
52
U.S. states
27
U.S. cities
51
Facility City State ZIP Site status
GSK Investigational Site Anniston Alabama 36207 —
GSK Investigational Site Tuscaloosa Alabama 35406 —
GSK Investigational Site Mesa Arizona 85201 —
GSK Investigational Site Phoenix Arizona 85032 —
GSK Investigational Site Hot Springs Arkansas 71913 —
GSK Investigational Site Irvine California 92618 —
GSK Investigational Site Oceanside California 92056 —
GSK Investigational Site San Diego California 92108 —
GSK Investigational Site San Diego California 92128 —
GSK Investigational Site Boulder Colorado 80304 —
GSK Investigational Site Avon Connecticut 06001 —
GSK Investigational Site Miami Florida 33173 —
GSK Investigational Site Pembroke Pines Florida 33024 —
GSK Investigational Site South Daytona Florida 32119 —
GSK Investigational Site Stuart Florida 34996 —
GSK Investigational Site Atlanta Georgia 30342 —
GSK Investigational Site Decatur Georgia 30033 —
GSK Investigational Site Rome Georgia 30165 —
GSK Investigational Site Chicago Illinois 60607 —
GSK Investigational Site Evansville Indiana 47712 —
GSK Investigational Site Baton Rouge Louisiana 70808 —
GSK Investigational Site Ann Arbor Michigan 48104 —
GSK Investigational Site Saint Louis Park Minnesota 55426 —
GSK Investigational Site St Louis Missouri 63141 —
GSK Investigational Site Moorestown New Jersey 08057 —
GSK Investigational Site Albuquerque New Mexico 87108 —
GSK Investigational Site Albany New York 12206 —
GSK Investigational Site New York New York 10021 —
GSK Investigational Site Plainview New York 11803 —
GSK Investigational Site Rochester New York 14609 —
GSK Investigational Site The Bronx New York 10467 —
GSK Investigational Site Valley Stream New York 11580 —
GSK Investigational Site Chapel Hill North Carolina 27599 —
GSK Investigational Site Greensboro North Carolina 27401 —
GSK Investigational Site Raleigh North Carolina 27609 —
GSK Investigational Site Concinnati Ohio 45219 —
GSK Investigational Site West Chester Ohio 45069 —
GSK Investigational Site Westerville Ohio 43081 —
GSK Investigational Site Oklahoma City Oklahoma 73104 —
GSK Investigational Site Eugene Oregon 97401 —
GSK Investigational Site Salem Oregon 97301 —
GSK Investigational Site Philadelphia Pennsylvania 19114 —
GSK Investigational Site Anderson South Carolina 29621 —
GSK Investigational Site Bristol Tennessee 37620 —
GSK Investigational Site Clarksville Tennessee 37043 —
GSK Investigational Site Memphis Tennessee 38105 —
GSK Investigational Site Fort Worth Texas 76135 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Salt Lake City Utah 84121 —
GSK Investigational Site Seattle Washington 98195 —
GSK Investigational Site Tacoma Washington 98405 —
GSK Investigational Site Wenatchee Washington 98801 —

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 NCT00240617, 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 Oct 26, 2016 · Synced Oct 19, 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 NCT00240617 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →