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Completed Phase 3 Interventional Results available

Phase IIIB Switching From Intravenous to Subcutaneous Study

ClinicalTrials.gov ID: NCT00663702

Public ClinicalTrials.gov record NCT00663702. 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 12, 2026, 7:09 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 Phase 3B Multi-center Open-Label Study to Evaluate the Safety of Abatacept in Subjects Who Switch From Intravenous to Subcutaneous Abatacept Therapy

Brief summary

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

The purpose of this study is to determine whether switching to subcutaneous administration of abatacept will be safe in participants with rheumatoid arthritis who previously received long-term therapy with intravenous abatacept

Study identification

NCT ID
NCT00663702
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
123 participants

Conditions and interventions

Interventions

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
Apr 30, 2008
Primary completion
Nov 30, 2009
Completion
Dec 31, 2011
Last update posted
Mar 8, 2015

2008 – 2012

United States locations

U.S. sites
18
U.S. states
13
U.S. cities
18
Facility City State ZIP Site status
Rheumatology Associates Of N. Al, P.C. Huntsville Alabama 35801
Allergy & Rheumatology Medical Clinic, Inc. La Jolla California 92037
Valerius Medical Group &Research Ctr. Of Greater Long Beach Long Beach California 90806
Desert Medical Advances Palm Desert California 92260
Inland Rheumatology Clinical Trials Inc. Upland California 91786
Arthritis & Rheumatic Disease Specialties Aventura Florida 33180
Diagnostic Rheumatology And Research,Pc Indianapolis Indiana 46227
Graves Gilbert Clinic Bowling Green Kentucky 42101
Physician Research Collaboration, Llc Lincoln Nebraska 68516
Innovative Health Research Las Vegas Nevada 89128
The Center For Rheumatology, Llp Albany New York 12206
The Arthritis Clinic & Carolina Bone & Joint Charlotte North Carolina 28210
Unifour Medical Research Hickory North Carolina 28601
Cincinnati Rheumatic Disease Study Group Cincinnati Ohio 45219
Portland Rheumatology Clinic Lake Oswego Oregon 97035
Rheumatic Disease Associates, Ltd. Willow Grove Pennsylvania 19090
Walter F. Chase, Md Austin Texas 78705
Arthritis Centers Of Texas Dallas Texas 75246

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 12 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00663702, 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 Mar 8, 2015 · Synced Sep 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00663702 live on ClinicalTrials.gov.

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