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Completed Phase 3 Interventional Results available

Efficacy and Safety of Adalimumab in Patients With Active Rheumatoid Arthritis Treated Concomitantly With Methotrexate.

ClinicalTrials.gov ID: NCT00195702

Public ClinicalTrials.gov record NCT00195702. 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, 5:20 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 Multicenter, Randomized, Double-Blind, Placebo-Controlled Study of the Human Anti-TNF Monoclonal Antibody Adalimumab in Rheumatoid Arthritis Patients Currently Receiving Treatment With Methotrexate

Brief summary

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

The purpose of the study was to assess the safety, immunogenicity, and clinical efficacy of adalimumab compared with placebo (during double-blind phase) and to to evaluate the long-term safety and maintenance of efficacy following repeated administration of adalimumab (during open-label extension phase) in patients with persistently active rheumatoid arthritis who were receiving concurrent methotrexate therapy.

Study identification

NCT ID
NCT00195702
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Abbott
Industry
Enrollment
619 participants

Conditions and interventions

Interventions

Biological · Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Jan 31, 2000
Primary completion
Aug 31, 2002
Completion
Jul 31, 2010
Last update posted
Aug 25, 2011

2000 – 2010

United States locations

U.S. sites
76
U.S. states
30
U.S. cities
67
Facility City State ZIP Site status
Site Ref # / Investigator 424 Huntsville Alabama 35801
Site Ref # / Investigator 2510 Mobile Alabama 36608
Site Ref # / Investigator 60729 Phoenix Arizona 85012
Site Ref # / Investigator 725 Scottsdale Arizona 85260
Site Ref # / Investigator 60736 Anaheim California 92801
Site Ref # / Investigator 360 Escondido California 92025
Site Ref # / Investigator 714 La Jolla California 92037-0943
Site Ref # / Investigator 469 La Jolla California 92037
Site Ref # / Investigator 419 Palm Desert California 92260
Site Ref # / Investigator 492 San Jose California 95126
Site Ref # / Investigator 60734 San Louis Obispo California 93405
Site Ref # / Investigator 60739 Van Nuys California 91405
Site Ref # / Investigator 712 Danbury Connecticut 06810
Site Ref # / Investigator 710 Aventura Florida 33180
Site Ref # / Investigator 498 Dunedin Florida 34698
Site Ref # / Investigator 499 Orlando Florida 32806
Site Ref # / Investigator 729 Tampa Florida 33614
Site Ref # / Investigator 463 Zephyrhills Florida 33542
Site Ref # / Investigator 2436 Boise Idaho 83704
Site Ref # / Investigator 485 Idaho Falls Idaho 83404
Site Ref # / Investigator 60732 Chicago Illinois 60611
Site Ref # / Investigator 726 Springfield Illinois 62704
Site Ref # / Investigator 2506 Indianapolis Indiana 46260
Site Ref # / Investigator 732 South Bend Indiana 46601
Site Ref # / Investigator 60730 Shawnee Mission Kansas 66216
Site Ref # / Investigator 467 Wichita Kansas 67203
Site Ref # / Investigator 494 Wichita Kansas 67208
Site Ref # / Investigator 491 Lexington Kentucky 40509
Site Ref # / Investigator 2508 Portland Maine 04102
Site Ref # / Investigator 392 Baltimore Maryland 21239
Site Ref # / Investigator 354 Cumberland Maryland 21502
Site Ref # / Investigator 730 Wheaton Maryland 20902
Site Ref # / Investigator 465 Burlington Massachusetts 01805
Site Ref # / Investigator 2512 Worcester Massachusetts 01610
Site Ref # / Investigator 471 Grand Rapids Michigan 49506
Site Ref # / Investigator 473 Kalamazoo Michigan 49009
Site Ref # / Investigator 731 Kansas City Missouri 64114
Site Ref # / Investigator 502 St Louis Missouri 63110
Site Ref # / Investigator 482 St Louis Missouri 63128
Site Ref # / Investigator 371 St Louis Missouri 63141
Site Ref # / Investigator 487 Omaha Nebraska 68114
Site Ref # / Investigator 353 Concord New Hampshire 03301
Site Ref # / Investigator 364 Dover New Hampshire 03820
Site Ref # / Investigator 60726 Mercerville New Jersey 08619
Site Ref # / Investigator 358 Voorhees Township New Jersey 08043
Site Ref # / Investigator 483 Rochester New York 14609
Site Ref # / Investigator 512 Durham North Carolina 27704
Site Ref # / Investigator 340 Greensboro North Carolina 27408
Site Ref # / Investigator 461 Raleigh North Carolina 27609
Site Ref # / Investigator 500 Raleigh North Carolina 27609
Site Ref # / Investigator 60731 Raleigh North Carolina 27612
Site Ref # / Investigator 60737 Salisbury North Carolina 28144
Site Ref # / Investigator 456 Mayfield Village Ohio 44143
Site Ref # / Investigator 470 Oklahoma City Oklahoma 73112
Site Ref # / Investigator 60723 Oklahoma City Oklahoma 73112
Site Ref # / Investigator 422 Eugene Oregon 97401
Site Ref # / Investigator 60735 Colmar Pennsylvania 18915-9671
Site Ref # / Investigator 2507 Duncansville Pennsylvania 16635
Site Ref # / Investigator 717 East Norriton Pennsylvania 19401
Site Ref # / Investigator 352 Mechanicsburg Pennsylvania 17055
Site Ref # / Investigator 480 Wexford Pennsylvania 15090
Site Ref # / Investigator 2511 Wyomissing Pennsylvania 19610
Site Ref # / Investigator 60724 Wyomissing Pennsylvania 19610
Site Ref # / Investigator 718 Charleston South Carolina 29406
Site Ref # / Investigator 460 Memphis Tennessee 38119
Site Ref # / Investigator 462 Nashville Tennessee 37205
Site Ref # / Investigator 716 Austin Texas 78705
Site Ref # / Investigator 60728 Galveston Texas 77555-0759
Site Ref # / Investigator 2509 Houston Texas 77074
Site Ref # / Investigator 510 Houston Texas 77074
Site Ref # / Investigator 60725 Falls Church Virginia 22044
Site Ref # / Investigator 711 Richmond Virginia 23219
Site Ref # / Investigator 509 Seattle Washington 98166-2967
Site Ref # / Investigator 356 Spokane Washington 99204
Site Ref # / Investigator 464 Tacoma Washington 98405
Site Ref # / Investigator 60738 Kenosha Wisconsin 53142

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 11 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00195702, 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 25, 2011 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00195702 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →