Volume 48, Issue 4 pp. 927-934
Research Article

Anakinra, a recombinant human interleukin-1 receptor antagonist (r-metHuIL-1ra), in patients with rheumatoid arthritis: A large, international, multicenter, placebo-controlled trial

Roy M. Fleischmann

Corresponding Author

Roy M. Fleischmann

St. Paul University Hospital, Dallas, Texas

St. Paul University Hospital, Department of Rheumatology, 5939 Harry Hines Boulevard, Suite 400, Dallas, TX 75235Search for more papers by this author
Joy Schechtman

Joy Schechtman

Sun Valley Arthritis Center, Glendale, Arizona

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Ralph Bennett

Ralph Bennett

Arizona Arthritis and Rheumatism Associates, Mesa

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Malcolm L. Handel

Malcolm L. Handel

Prince of Wales Hospital, Sydney, Australia

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Gerd-Rudiger Burmester

Gerd-Rudiger Burmester

Charite Humboldt University, Berlin, Germany

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John Tesser

John Tesser

Phoenix Center for Clinical Research, Phoenix, Arizona

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Dennis Modafferi

Dennis Modafferi

Amgen Inc., Thousand Oaks, California

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Jennifer Poulakos

Jennifer Poulakos

Amgen Inc., Thousand Oaks, California

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Gordon Sun

Gordon Sun

Amgen Inc., Thousand Oaks, California

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First published: 03 April 2003
Citations: 285

Abstract

Objective

To evaluate the safety of anakinra (a recombinant human interleukin-1 receptor antagonist) in a large population of patients with rheumatoid arthritis (RA), typical of those seen in clinical practice.

Methods

A total of 1,414 patients were randomly assigned to treatment with 100 mg of anakinra or placebo, administered daily by subcutaneous injection. Background medications included disease-modifying antirheumatic drugs, corticosteroids, and nonsteroidal antiinflammatory drugs, alone or in combination. The primary end point was safety, which was evaluated by adverse events (including infections), discontinuation from study due to adverse events, and death.

Results

Safety was evaluated in 1,399 patients (1,116 in the anakinra group and 283 in the placebo group; 15 patients were randomized but did not receive any study drug) during the initial 6-month, double-blind, placebo-controlled phase of this long-term safety study. Baseline demographics, disease characteristics, and concomitant medications were similar between the 2 groups. The study group included patients with numerous comorbid conditions and a wide range of RA disease activity. Serious adverse events occurred at a similar rate in the anakinra group and the placebo group (7.7% and 7.8%, respectively). Serious infectious episodes were observed more frequently in the anakinra group (2.1% versus 0.4% in the placebo group). The rate of withdrawal due to adverse events was 13.4% in the anakinra group and 9.2% in the placebo group.

Conclusion

Results from this large, placebo-controlled safety study demonstrate that anakinra is safe and well tolerated in a diverse population of patients with RA, including those with comorbid conditions and those using multiple combinations of concomitant therapies. Although the frequency of serious infection was slightly higher in the anakinra group, no infection was attributed to opportunistic microorganisms or resulted in death.

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