Pharmacokinetic Interaction between Amprenavir and Rifabutin or Rifampin in Healthy Males

Author:

Polk Ronald E.1,Brophy Donald F.1,Israel Debra S.1,Patron Roberto1,Sadler Brian M.2,Chittick Gregory E.2,Symonds William T.2,Lou Yu2,Kristoff Debbie1,Stein D. S.2

Affiliation:

1. School of Pharmacy, Virginia Commonwealth University/Medical College of Virginia Campus, Richmond, Virginia,1 and

2. Glaxo Wellcome, Inc., Research Triangle Park, North Carolina2

Abstract

ABSTRACT The objective of this study was to determine if there is a pharmacokinetic interaction when amprenavir is given with rifabutin or rifampin and to determine the effects of these drugs on the erythromycin breath test (ERMBT). Twenty-four healthy male subjects were randomized to one of two cohorts. All subjects received amprenavir (1,200 mg twice a day) for 4 days, followed by a 7-day washout period, followed by either rifabutin (300 mg once a day [QD]) (cohort 1) or rifampin (600 mg QD) (cohort 2) for 14 days. Cohort 1 then received amprenavir plus rifabutin for 10 days, and cohort 2 received amprenavir plus rifampin for 4 days. Serial plasma and urine samples for measurement of amprenavir, rifabutin, and rifampin and their 25- O -desacetyl metabolites, were measured by high-performance liquid chromatography. Rifabutin did not significantly affect amprenavir's pharmacokinetics. Amprenavir significantly increased the area under the curve at steady state (AUC ss ) of rifabutin by 2.93-fold and the AUC ss of 25- O -desacetylrifabutin by 13.3-fold. Rifampin significantly decreased the AUC ss of amprenavir by 82%, but amprenavir had no effect on rifampin pharmacokinetics. Amprenavir decreased the results of the ERMBT by 83%. The results of the ERMBT after 2 weeks of rifabutin and rifampin therapy were increased 187 and 156%, respectively. Amprenavir plus rifampin was well tolerated. Amprenavir plus rifabutin was poorly tolerated, and 5 of 11 subjects discontinued therapy. Rifampin markedly increases the metabolic clearance of amprenavir, and coadministration is contraindicated. Amprenavir significantly decreases clearance of rifabutin and 25- O -desacetylrifabutin, and the combination is poorly tolerated. Amprenavir inhibits the ERMBT, and rifampin and rifabutin are equipotent inducers of the ERMBT.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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