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Pharmacokinetics of plasma lopinavir/ritonavir following the administration of 400/100 mg, 200/150 mg and 200/50 mg twice daily in HIV-negative volunteers
Author(s) -
Akil Jackson,
A.D. Hill,
Rebekah Puls,
LJ Else,
Janaki Amin,
David Back,
Enmoore Lin,
Saye Khoo,
Sean Emery,
Roland Morley,
Brian Gazzard,
Marta Boffito
Publication year - 2010
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dkq468
Subject(s) - lopinavir , ritonavir , pharmacokinetics , lopinavir/ritonavir , regimen , medicine , tolerability , pharmacology , trough concentration , gastroenterology , adverse effect , human immunodeficiency virus (hiv) , viral load , antiretroviral therapy , immunology
Data suggest that some licensed antiretroviral doses could be reduced. We assessed the safety, tolerability and pharmacokinetics of lopinavir/ritonavir at doses of 400/100, 200/150 and 200/50 mg twice daily in HIV-negative volunteers (http://clinicaltrials.gov/ct2/show/NCT00985543).

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