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A
WEEK-IN-REVIEW FEATURED REPORT
POSTER
A
pilot study: lopinavir/ritonavir (LPV/r) plus lamivudine (3TC) as dual agents in
antiretroviral (ARV) naïve HIV-infected subjects
(the LOREDA study)
R. Andrade, E. Villarreal-Williams M. Mall
Poster
Abstract
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POSTER
Protease
genotypes in children and adolescents failing protease inhibitor (PI) -based
antiretroviral therapy (ART) at the
Botswana-Baylor Children's Clinical Centre of Excellence in Gaborone, Botswana
A. Gomila, B. Kirk, M. Tolle. et
al
Poster
Abstract
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POSTER
Switching
antiretroviral therapy to a reverse transcriptase inhibitor sparing combination
of lopinavir/ritonavir and raltegravir in virologically
suppressed HIV-infected patients is safe and well tolerated (the KITE study)
I. Ofotokun, A.N. Sheth, K.A. Easley.
Poster
Abstract
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POSTER
Lopinavir/ritonavir-based HAART in HIV-1 naïve children: rare protease inhibitor
resistance mutations but high 3TC/FTC resistance at the time of virologic
failure
P. Frange, S.
Blanche, N. Briand, et al
Poster
Abstract
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POSTER
HAART simplification with lopinavir/ritonavir monotherapy in HIV/HCV coinfected
patients starting anti-HCV treatment: final results of a
randomised, proof-of- principle clinical trial (KAMON 2 Study)
H. Hasson, L. Galli, G. Gallotta
Poster
Abstract
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POSTER
No effect of HCV infection on virological response 96 weeks after simplification
to lopinavir/ritonavir (LPV/r) monotherapy (MT) in the OK04 trial
F. Pulido, J. Arribas, OK04 Study Group
Poster
Abstract
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POSTER
Minimal food effect
on steady-state pharmacokinetics of lopinavir when administered as a tablet
formulation in Ugandan HIV- positive patients
M. Lamorde, P. Byakika-Kibwika, L. Nabukeera, et al
Poster
Abstract
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Long term efficacy of
lopinavir/r-based second-line antiretroviral treatment after 24 months of follow
up at ESTHER/Calmette Hospital in
Phnom Penh, Cambodia
L.
Ferradini, V. Ouk, O. Segeral, et al
Abstract
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Effects of steady-state
lopinavir/ritonavir on the pharmacokinetics of pitavastatin in healthy adult
volunteers
R. Morgan, S. Campbell, K. Suehira, et al
Abstract
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Bone mineral density (BMD)
analysis in antiretroviral (ART)-naïve subjects taking lopinavir/ritonavir
(LPV/r) combined with raltegravir (RAL) or tenofovir/emtricitabine (TDF/FTC) for
96 weeks in the PROGRESS study
R. Qaqish, R. Trinh, M. Tian, et al
Abstract
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Changes in bone mineral
density after 96 weeks of treatment with tenofovir DF/emtricitabine plus
atazanavir/ritonavir or lopinavir/ritonavir in HIV-1 infected treatment naïve
subjects: the CASTLE body composition sub-study
G. Moyle, D. Ward, A. Farajallah. et al
Abstract
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A comparative analysis
of risk factors associated with efavirenz, darunavir/ritonavir,
lopinavir/ritonavir, atazanavir/ritonavir and renal impairment
N. Rockwood, M. Nelson, S. Mandalia, B. Gazzard
Abstract
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Transplacental passage
of nevirapine, nelfinavir and lopinavir
S. van Hoog, K. Boer, J. Nellen
Abstract
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