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Antimicrobial Agents and Chemotherapy, June 1999, p. 1516-1519, Vol. 43, No. 6
Department of Pharmaceutics, University of
Washington, Seattle, Washington1;
Division of Infectious Diseases, Chicago Children's Memorial
Hospital, Chicago, Illinois2; University
of California at San Diego Medical Center, San Diego,
California3; St. Jude Children's
Research Hospital, Memphis, Tennessee4;
Boston Medical Center5 and
Statistical & Data Analysis Center, Harvard School of Public
Health,6 Boston, Massachusetts; and
Glaxo Wellcome, Inc., Research Triangle Park, North
Carolina7
Received 13 July 1998/Returned for modification 19 December
1998/Accepted 11 March 1999
To evaluate if atovaquone (ATQ) interacts pharmacokinetically with
azithromycin (AZ) in human immunodeficiency virus-infected children, 10 subjects (ages, 4 to 13 years) were randomized in a crossover study to
receive AZ (5 mg/kg/day) alone (ALONE) or AZ (5 mg/kg/day) and ATQ (30 mg/kg/day) simultaneously (SIM) prior to receiving AZ and ATQ staggered
by 12 h. Despite a lack of significant difference in the mean AZ
pharmacokinetic parameters, the steady-state values of AZ's area under
the concentration-time curve from 0 to 24 h and maximum
concentration in serum were consistently lower (n = 7 of 7) for the SIM regimen than they were for the ALONE regimen. A
larger study will be required to determine if ATQ affects AZ
pharmacokinetics and efficacy in a clinically significant manner.
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Pharmacokinetics of Azithromycin Administered Alone
and with Atovaquone in Human Immunodeficiency Virus-Infected
Children
for the Actg
254 Team
*
Corresponding author. Mailing address: Box 357610, H272
Health Sciences Building, Department of Pharmaceutics, School of
Pharmacy, University of Washington, Seattle, WA 98195. Phone: (206)
543-9434. Fax: (206) 543-3204. E-mail:
jash{at}u.washington.edu.
Other members of the ACTG 254 team are listed in the Appendix.
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