High-Dose Nevirapine: Safety, Pharmacokinetics, And Antiviral Effect In Patients With Human Immunodeficiency Virus Infection

Nevirapine, a potent nonnucleoside reverse transcriptase inhibitor, produces a transient antiviral effect at ⩽200 mg/day due to the selection of resistant virus. To examine if higher levels of nevirapine could produce sustained antiviral activity, its safety, pharmacokinetics, and antiviral activity...

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Bibliographic Details
Published in:The Journal of infectious diseases Vol. 171; no. 3; pp. 537 - 545
Main Authors: Havlir, Diane, Cheeseman, Sarah H., Mclaughlin, Margaret, Murphy, Robert, Erice, Alejo, Spector, Stephen A., Greenough, Thomas C., Sullivan, John L., Hall, David, Myers, Maureen, Lamson, Michael, Richman, Douglas D.
Format: Journal Article
Language:English
Published: United States The University of Chicago Press 01-03-1995
University of Chicago Press
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Summary:Nevirapine, a potent nonnucleoside reverse transcriptase inhibitor, produces a transient antiviral effect at ⩽200 mg/day due to the selection of resistant virus. To examine if higher levels of nevirapine could produce sustained antiviral activity, its safety, pharmacokinetics, and antiviral activity at 400 mg/day were studied in 21 patients. There was a rapid reduction in immune complex-dissociated p24 antigen and serum human immunodeficiency virus RNA concentration in all patients, and 8 of 10 patients had > 50% reduction at 8 weeks. Nevirapine-resistant virus was isolated from all subjects tested at 12 weeks: The mean plasma trough level (4.0 µg/mL [l5.8µg/M]) exceeded the mean IC50 of resistant virus. Rash developed in 48% of patients and was a dose-limiting toxicity factor in 6. These data suggest that clinical testing of potent antiviral compounds that select for drug-resistant virus is justified to determine if serum levels of drug sufficient to overcome resistant virus can be attained.
Bibliography:Reprints or correspondence: Dr. Diane Havlir, UCSD Treatment Center, 2760 Fifth Ave., Suite 300. San Diego, CA 92103.
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ISSN:0022-1899
1537-6613
DOI:10.1093/infdis/171.3.537