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Completed Phase 3 Interventional Results available

Study of Human Anti-TNF Monoclonal Antibody Adalimumab in Children With Polyarticular Juvenile Idiopathic Arthritis (JIA)

ClinicalTrials.gov ID: NCT00048542

Public ClinicalTrials.gov record NCT00048542. 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 21, 2026, 6:06 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 Multicenter, Randomized, Double-Blind, Placebo-Controlled Study of the Safety, Efficacy, and Pharmacokinetics of the Human Anti-TNF Monoclonal Antibody Adalimumab in Children With Polyarticular Juvenile Idiopathic Arthritis

Study identification

NCT ID
NCT00048542
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Abbott
Industry
Enrollment
171 participants

Conditions and interventions

Interventions

  • Double-Blind Adalimumab/Placebo + MTX Biological
  • Double-Blind Adalimumab/Placebo Biological
  • OLE BSA Adalimumab +/- MTX Drug
  • OLE FD Adalimumab +/- MTX Drug

Biological · Drug

Eligibility (public fields only)

Age range
4 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
Aug 31, 2002
Primary completion
Dec 31, 2004
Completion
May 31, 2010
Last update posted
Aug 21, 2011

2002 – 2010

United States locations

U.S. sites
15
U.S. states
13
U.S. cities
15
Facility City State ZIP Site status
Site Ref # / Investigator 45524 Birmingham Alabama 35294-3300
Site Reference ID/Investigator# 2235 Los Angeles California 90027
Site Reference ID/Investigator# 642 Stanford California 94305
Site Reference ID/Investigator# 638 Delray Beach Florida 33406
Site Ref # / Investigator 45543 St. Petersburg Florida 33701
Site Reference ID/Investigator# 640 Chicago Illinois 60649
Site Reference ID/Investigator# 644 Kansas City Kansas 66160
Site Reference ID/Investigator# 641 Minneapolis Minnesota 55455
Site Reference ID/Investigator# 645 Omaha Nebraska 68131
Site Reference ID/Investigator# 2501 Livingston New Jersey 07039
Site Ref # / Investigator 45542 New Hyde Park New York 11040
Site Ref # / Investigator 45544 Chapel Hill North Carolina 27599-7220
Site Reference ID/Investigator# 386 Columbus Ohio 43205
Site Ref # / Investigator 45525 Salt Lake City Utah 84312-2206
Site Reference ID/Investigator# 406 Norfolk Virginia 23507

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 16 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00048542, 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 21, 2011 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00048542 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →