Elsevier

The Lancet

Volume 338, Issue 8758, 6 July 1991, Pages 6-9
The Lancet

Comparison of ribavirin and placebo in CDC group III human immunodeficiency virus infection

https://doi.org/10.1016/0140-6736(91)90003-8Get rights and content

Abstract

To assess the efficacy and safety of ribavirin in patients with human immunodeficiency virus (HIV) infection a multicentre, placebo-controlled, prospectively randomised trial was conducted in CDC group III HIV-infected individuals between February, 1988, and October, 1989. Mean treatment time was 39 weeks (range 6-52); 152 individuals were enrolled, of whom 133 could be evaluated. The two treatment groups were similar at baseline and 66% of all subjects had intravenous drug abuse as the main risk factor for HIV infection. Ribavirin was given at a dose of 15 mg/kg daily by mouth (average daily dose 1000 mg). 9 of 67 patients in the placebo group (13·4%) progressed to CDC Groups IVA, C1, or D vs 6 of 66 (9%) in the ribavirin group. Progressions to group IVC2 were 7 (10·4%) and 9 (13·6%), respectively. These differences are not statistically significant. There were no clinically or statistically significant differences in CD4 cell counts, total lymphocytes, total white cells, or CD4/CD8 ratios between the two groups during treatment, and no clinically important side-effects were noted.

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    Correspondence to Dr José M Gatell, Infectious Diseases Unit, Hospital Clinic Villarroel, 170 08036 Barcelona, Spain.

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