Abstract
One hundred five patients were enrolled in a 12-week, randomized, prospective, double-blind, placebo-controlled trial of recombinant human gamma-interferon (rHu gamma-IFN) for the treatment of rheumatoid arthritis. Fifty-four patients received rHu gamma-IFN and 51 received placebo. Forty-two patients in each group completed the 12-week trial. Some clinical improvement occurred in both groups of patients. Although the improvement with rHu gamma-IFN was greater than that with placebo, the differences were generally not statistically significant.
Publication types
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Clinical Trial
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Comparative Study
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Randomized Controlled Trial
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
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Adult
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Aged
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Antigens, Surface / metabolism
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Arthritis, Rheumatoid / drug therapy*
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Arthritis, Rheumatoid / immunology
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Arthritis, Rheumatoid / metabolism
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Clinical Trials as Topic
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Double-Blind Method
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Drug Tolerance
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Female
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Humans
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Interferon-gamma / adverse effects
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Interferon-gamma / therapeutic use*
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Leukocytes / immunology
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Leukocytes / metabolism
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Male
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Membrane Proteins / metabolism
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Middle Aged
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Placebos / therapeutic use*
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Recombinant Proteins
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Time Factors
Substances
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Antigens, Surface
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Membrane Proteins
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Placebos
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Recombinant Proteins
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Interferon-gamma