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Study of Human Anti-TNF Monoclonal Antibody D2E7 in Subjects With Active Rheumatoid Arthritis

Phase 3
Completed
Conditions
Rheumatoid Arthritis
Registration Number
NCT00049751
Lead Sponsor
Abbott
Brief Summary

The purpose of the study is to evaluate safety by collecting serious adverse events in subjects with moderately to severely active rheumatoid arthritis who are unable to obtain etanercept and who have failed one or more prior disease-modifying antirheumatic drugs (DMARDs).

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
3000
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Change in disease activity score at visit week 12 as compared to baseline
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (53)

Thomas McGee, MD

πŸ‡ΊπŸ‡Έ

Mobile, Alabama, United States

Desert Valley Medical

πŸ‡ΊπŸ‡Έ

Apple Valley, California, United States

Kenneth Hsu, MD, Inc.

πŸ‡ΊπŸ‡Έ

Bakersfield, California, United States

Rheumatology Clinic

πŸ‡ΊπŸ‡Έ

Los Angeles, California, United States

Michael Harrington, MD

πŸ‡ΊπŸ‡Έ

Napa, California, United States

Midori Jane Nishio, MD

πŸ‡ΊπŸ‡Έ

Walnut Creek, California, United States

Naveen Raja, MD

πŸ‡ΊπŸ‡Έ

Whittier,, California, United States

Mountain Rheumatology

πŸ‡ΊπŸ‡Έ

Denver, Colorado, United States

Division of Rheumatic Diseases/University of CT Health Center

πŸ‡ΊπŸ‡Έ

Farmington,, Connecticut, United States

New Haven Medical Group, PC

πŸ‡ΊπŸ‡Έ

New Haven, Connecticut, United States

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Thomas McGee, MD
πŸ‡ΊπŸ‡ΈMobile, Alabama, United States

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