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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Published in: | The Journal of infectious diseases Vol. 171; no. 3; pp. 537 - 545 |
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Main Authors: | , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
The University of Chicago Press
01-03-1995
University of Chicago Press |
Subjects: | |
Online Access: | Get full text |
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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. |
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Bibliography: | Reprints or correspondence: Dr. Diane Havlir, UCSD Treatment Center, 2760 Fifth Ave., Suite 300. San Diego, CA 92103. istex:D1395BCDD3968F82F6A841640555A19D98F2CA16 ark:/67375/HXZ-5VSF56NB-G ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0022-1899 1537-6613 |
DOI: | 10.1093/infdis/171.3.537 |