Blocking Tumor Necrosis Factor in Ankylosing Spondylitis
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|ClinicalTrials.gov Identifier: NCT00000433|
Recruitment Status : Completed
First Posted : January 19, 2000
Last Update Posted : January 4, 2007
|Condition or disease||Intervention/treatment||Phase|
|Spondylitis, Ankylosing||Drug: Anti-Tumor Necrosis Factor||Phase 2|
In this Phase II clinical trial we will use tumor necrosis factor receptor p75 fusion protein (TNFR:Fc, or etanercept) to treat patients with ankylosing spondylitis (AS). TNFR:Fc is an antagonist of tumor necrosis factor (TNF), a cytokine that researchers have shown to play a possible role in disease pathogenesis of ankylosing spondylitis, rheumatoid arthritis, and vasculitis, as well as other inflammatory conditions.
TNFR:Fc consists of two molecules of the extracellular portion of the p75 receptor, each consisting of 235 amino acids. The two receptors are fused to the Fc portion of human IgG1, which consists of 232 amino acids. The gene fragments encoding the truncated TNFR and the Fc portion of human IgG1 are expressed in a Chinese hamster ovary cell line.
Recent observations from animal and human studies suggest that tumor necrosis factor-alpha (TNF-alpha) may play a role in disease activity in AS and other seronegative spondyloarthropathies. This study aims to test the efficacy of TNFR:Fc used in conjunction with standard medications in the treatment of AS. We will give patients either 25mg of TNFR:Fc or placebo subcutaneously twice a week for 4 months. Outcome measures will include measures of function, pain, morning stiffness, patient global assessment, and swollen joint count, as well as safety measures.
|Study Type :||Interventional (Clinical Trial)|
|Enrollment :||42 participants|
|Intervention Model:||Single Group Assignment|
|Official Title:||Anti-Tumor Necrosis Factor (TNFR:Fc) in Ankylosing Spondylitis|
|Study Start Date :||October 1999|
|Study Completion Date :||March 2002|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00000433
|United States, California|
|UCSF-Clinical Trials Center|
|San Francisco, California, United States, 94143-0792|
|Principal Investigator:||John C. Davis, MD, MPH||Division of Rheumatology, University of California - San Francisco Department of Medicine|