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Completed Phase 4 Interventional Results available

A Safety Study of VIMOVO in Adolescents With Juvenile Idiopathic Arthritis (JIA)

ClinicalTrials.gov ID: NCT01544114

Public ClinicalTrials.gov record NCT01544114. 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 Jul 23, 2026, 11:26 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 6-month, Multicenter, Open-label, Safety Study of VIMOVO (250 mg/20 mg, 375 mg/20 mg, and 500 mg/20 mg Naproxen/Esomeprazole) in Adolescents Aged 12 to 16 Years, Inclusive, With Juvenile Idiopathic Arthritis (JIA)

Study identification

NCT ID
NCT01544114
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Amgen
Industry
Enrollment
46 participants

Conditions and interventions

Interventions

  • VIMOVO 250/20 Drug
  • VIMOVO 375/20 Drug
  • VIMOVO 500/20 Drug

Drug

Eligibility (public fields only)

Age range
12 Years to 16 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 31, 2012
Primary completion
Jan 31, 2015
Completion
Jan 31, 2015
Last update posted
Dec 16, 2024

2012 – 2015

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
Research Site Little Rock Arkansas 72202
Research Site San Francisco California 94143
Research Site Aurora Colorado 80045
Research Site Washington D.C. District of Columbia 20010
Research Site West Palm Beach Florida 33407
Research Site Augusta Georgia 30912
Research Site Chicago Illinois 60637
Research Site Omaha Nebraska 68114
Research Site Brooklyn New York 11203
Research Site New Hyde Park New York 11040
Research Site New York New York 10021
Research Site Cincinnati Ohio 45229
Research Site Cleveland Ohio 44195
Research Site Toledo Ohio 43623
Research Site Philadelphia Pennsylvania 19134
Research Site Memphis Tennessee 38119
Research Site Fairfax Virginia 22030

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 NCT01544114, 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 Dec 16, 2024 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01544114 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →