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Completed Phase 3 Interventional Results available

A 1-year Study in Adolescents to Assess the Long-term Safety of Almotriptan Malate When Treating Their Migraine Headaches

ClinicalTrials.gov ID: NCT00257010

Public ClinicalTrials.gov record NCT00257010. 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 Jun 26, 2026, 9:46 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

Long-Term, Open-Label Safety Study of Oral Almotriptan Malate 12.5 mg in the Treatment of Migraine in Adolescents

Study identification

NCT ID
NCT00257010
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Janssen-Ortho LLC
Industry
Enrollment
447 participants

Conditions and interventions

Conditions

Interventions

  • Almotriptan Malate Drug

Drug

Eligibility (public fields only)

Age range
12 Years to 17 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
Nov 30, 2005
Primary completion
Nov 30, 2007
Completion
Nov 30, 2007
Last update posted
Feb 20, 2014

2005 – 2007

United States locations

U.S. sites
49
U.S. states
23
U.S. cities
49
Facility City State ZIP Site status
Not listed Mobile Alabama
Not listed Montgomery Alabama
Not listed Oxford Alabama
Not listed Mesa Arizona
Not listed Phoenix Arizona
Not listed Jonesboro Arkansas
Not listed Little Rock Arkansas
Not listed Santa Monica California
Not listed Centennial Colorado
Not listed Denver Colorado
Not listed Loxahatchee Groves Florida
Not listed Miami Florida
Not listed Orlando Florida
Not listed Tampa Florida
Not listed West Palm Beach Florida
Not listed Atlanta Georgia
Not listed Snellville Georgia
Not listed Idaho Falls Idaho
Not listed Chicago Illinois
Not listed Des Moines Iowa
Not listed Topeka Kansas
Not listed Witchita Kansas
Not listed Louisville Kentucky
Not listed Ann Arbor Michigan
Not listed Columbia Missouri
Not listed Springfield Missouri
Not listed St Louis Missouri
Not listed Endwell New York
Not listed Mineola New York
Not listed Mount Vernon New York
Not listed Plainview New York
Not listed Raleigh North Carolina
Not listed Cincinnati Ohio
Not listed Columbus Ohio
Not listed Oklahoma City Oklahoma
Not listed Philadelphia Pennsylvania
Not listed Pittsburgh Pennsylvania
Not listed Alcoa Tennessee
Not listed Bristol Tennessee
Not listed Germantown Tennessee
Not listed Morristown Tennessee
Not listed Nashville Tennessee
Not listed Dallas Texas
Not listed Fort Worth Texas
Not listed Houston Texas
Not listed San Antonio Texas
Not listed San Marcos Texas
Not listed Salt Lake City Utah
Not listed Madison 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 NCT00257010, 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 Feb 20, 2014 · Synced Jun 26, 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 protocol, eligibility criteria, and contact information for NCT00257010 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →