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Spots Global Cancer Trial Database for Phase III Study of BMS-188667 (CTLA4Ig) in Patients With Rheumatoid Arthritis Who Are Currently Failing Anti-TNF Therapy or Who Have Failed Anti-TNF Therapy in the Past.

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Trial Identification

Brief Title: Phase III Study of BMS-188667 (CTLA4Ig) in Patients With Rheumatoid Arthritis Who Are Currently Failing Anti-TNF Therapy or Who Have Failed Anti-TNF Therapy in the Past.

Official Title: A Phase III, Multi-Center, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of BMS-188667 in Subjects With Active Rheumatoid Arthritis on Background Disease Modifying Anti-Rheumatic Drugs (DMARDS) Who Have Failed Anti-Tumor Necrosis Factor (TNF) Therapy

Study ID: NCT00048581

Study Description

Brief Summary: The purpose of this clinical research study is to determine whether abatacept treatment on a background of Disease Modifying Antirheumatic Drugs (DMARDs) will relieve the symptoms of rheumatoid arthritis (RA) in participants who are currently receiving anti-tumor necrosis factor (TNF) therapy for at least 3 months and are not responding or have taken anti-TNF therapy in the last 3 months and did not respond. The safety of treatment with abatacept will also be evaluated. This study also has a 4.5-year long-term extension beginning 6 months after the start of the study.

Detailed Description:

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Local Institution, Birmingham, Alabama, United States

Local Institution, Mobile, Alabama, United States

Local Institution, Paradise Valley, Arizona, United States

Local Institution, La Jolla, California, United States

Local Institution, Long Beach, California, United States

Local Institution, Palo Alto, California, United States

Local Institution, Rancho Mirage, California, United States

Local Institution, Denver, Colorado, United States

Local Institution, Englewood, Colorado, United States

Local Institution, Bridgeport, Connecticut, United States

Local Institution, Hamden, Connecticut, United States

Local Institution, Clearwater, Florida, United States

Local Institution, Fort Lauderdale, Florida, United States

Local Institution, Largo, Florida, United States

Local Institution, Palm Harbor, Florida, United States

Local Institution, Tampa, Florida, United States

Local Institution, Rome, Georgia, United States

Local Institution, Indianapolis, Indiana, United States

Local Institution, Wichita, Kansas, United States

Local Institution, New Orleans, Louisiana, United States

Local Institution, Boston, Massachusetts, United States

Local Institution, Springfield, Massachusetts, United States

Local Institution, Lincoln, Nebraska, United States

Local Institution, New Brunswick, New Jersey, United States

Local Institution, Albany, New York, United States

Local Institution, Syracuse, New York, United States

Local Institution, Charlotte, North Carolina, United States

Local Institution, Hickory, North Carolina, United States

Local Institution, Bismarck, North Dakota, United States

Local Institution, Cincinnati, Ohio, United States

Local Institution, Oklahoma City, Oklahoma, United States

Local Institution, Eugene, Oregon, United States

Local Institution, Portland, Oregon, United States

Local Institution, Duncansville, Pennsylvania, United States

Local Institution, Norristown, Pennsylvania, United States

Local Institution, Sellersville, Pennsylvania, United States

Local Institution, Willow Grove, Pennsylvania, United States

Local Institution, Charleston, South Carolina, United States

Local Institution, Austin, Texas, United States

Local Institution, Dallas, Texas, United States

Local Institution, Vancouver, Washington, United States

Local Institution, Milwaukee, Wisconsin, United States

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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