|  |  Library 
            of Slides and Posters | 
         
          |  | Analysis 
            of clinical outcomes in African American HIV-1 positive patients receiving 
             lopinavir/ritonavir in a large 
            urban AIDS clinic P Kadlecik and others. AIDS 2010.
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          |  | Limited 
            future regimen options for those starting 
            on NNRTI-based triple combinations due to antiretroviral 
            drug resistance mutations K Chan and others. AIDS 2010.
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          |  | Clinical 
            outcomes, immmunologic function and virologic suppression among HIV 
            infected children receiving Lopinavir/ritonavir-based 
            second line antiretroviral therapy at National Pediatric 
            Hospital, Phnom Penh, Cambodia S Sophan and others. AIDS 2010.
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          |  | Comparison 
            of total and unbound lopinavir (LPV) 
            pharmacokinetics (PK) in HIV-infected pregnant women receiving lopinavir/ritonavir 
            (LPV/r) soft-gel capsules (SGC) or tablets G Taylor and others. AIDS 2010.
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          |  | Single 
            boosted protease inhibitor versus double boosted protease inhibitors 
            for the salvage therapy in HIV-infected patients W Manosuthi and others. AIDS 2010.
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          |  | Antiretroviral 
            monotherapy with ritonavir-boosted lopinavir 
            or fosamprenavir in HIV-cirrhotic patients is a safe, effective 
            and costs-saving strategy A Moreno-Zamora and others. AIDS 2010.
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          |  | Lopinavir/ritonavir 
            combined with raltegravir demonstrated similar antiviral 
            efficacy and safety as lopinavir/ritonavir 
            combined with tenofovir disoproxil fumarate/emtricitabine 
            in treatment-naïve HIV-1 infected subjects J Reynes and others. AIDS 2010.
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          |  | Baseline 
            HIV-1 RNA does not affect virologic response to lopinavir/ritonavir-based 
            regimens in antiretroviral-naive subjects: results of a 
            96-week meta-analysis of >2400 subjects J van Wyk and others. AIDS 2010
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          |  | Market 
            shift towards heat-stable lopinavir/ritonavir 
            demonstrates the need for improved formulations for second 
            line treatment of HIV/AIDS in low- and middle-income countries B Waning and others. AIDS 2010.
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          |  | The 
            effect of lopinavir/r monotherapy 
            on viral load and on the selection of resistance-associated mutations 
            in seminal plasma E Nunes and others. AIDS 2010.
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          |  | Incidence 
            of emtricitabine, tenofovir, raltegravir, 
            and lopinavir resistance following twice-daily (BID) lopinavir/ritonavir 
            (LPV/r) in combination with once-daily (QD) emtricitabine/tenofovir 
            (FTC/TDF) or twice daily raltegravir 
            (RAL) in antiretroviral-naïve, HIV-1 infected subjects: 
            48-week results of a 96-week randomized trial (study M10-336) A Lawal and others. AIDS 2010.
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          |  | The 
            effect of lopinavir/ritonavir 
            on the pharmacokinetics of TMC207, an investigational antimycobacterial 
            agent R van Heeswijk and others. AIDS 2010.
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          |  | Real-life 
            safety and efficacy of lopinavir/ritonavir 
            (LPV/r) in drug-naive and antiretroviral (ARV) treatment-experienced 
            HIV patients: 96-week follow-up B Conway and others. AIDS 2010
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          |  | Drug-resistant 
            genotyping to guide selection of etravirine, 
            darunavir and raltegravir in salvage therapy for multi-drug-resistant 
            cases improves outcomes N Miyazaki and others. AIDS 2010.
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          |  | Duration 
            of antiretroviral regimens including Raltegravir, 
            Maraviroc, Darunavir and/or Etravirine in clinical practice I Castillo and others. AIDS 2010.
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          |  | Raltegravir 
            and enfuvirtide as a "bridge" antiretroviral 
            therapy in kidney-transplanted patients with HIV infection receiving 
            everolimus and low-dose cyclosporine: a case-control study S Cocchi and others. AIDS 2010.
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          |  | Impact 
            of raltegravir on immune reconstitution 
            and thymopoiesis in HIV-1-infected patients with undetectable viremia 
            on HAART C Garrido and others. AIDS 2010.
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          |  | Impact 
            of the HIV-1 integrase flexibility on the alternative resistance pathways 
            to raltegravir S Abdel-Azeim and others. AIDS 2010.
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          |  | Immunological 
            benefit of raltegravir when used 
            as part of switch strategies C Garrido and others. AIDS 2010.
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          |  | Early 
            viral response in a cohort of heavily ARV-experienced patients receiving 
            a salvage regimen recommended 
            by a national advisory board in Mexico Y Vargas-Infante and others. AIDS 2010.
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          |  | Raltegravir-based-HAART 
            and lymphoma chemotherapy S Marcotte and others. AIDS 2010.
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          |  | Virological 
            response to atazanavir, ritonavir and tenofovir/emtricitabine: 
            relation to individual pharmacokinetic parameters and adherence measured 
            by medication events monitoring system (MEMS) in naïve HIV-infected 
            patients (ANRS134 trial) C Goujard and others. AIDS 2010.
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          |  | METABOLIK 
            (Metabolic Evaluation in Treatment-naïves Assessing the impact 
            of two BOosted protease inhibitors on LIpids and other marKers): comparison 
            of the metabolic effects of darunavir/ritonavir 
            versus atazanavir/ritonavir over 12 weeks J Aberg and others. AIDS 2010.
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          |  | Long-term 
            efficacy and safety of a switch to unboosted atazanavir 
            (ATV) in well controlled HIV-1 infected patients, results 
            of the NEAT Unboosted Atazanavir Cohort A Rachline and others. AIDS 2010.
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          |  | Safety 
            and efficacy of treatment simplification to atazanavir/ritonavir 
            plus lamivudine in patients on two NRTIs plus atazanavir/ritonavir 
            with optimal virologic control: 24 weeks results from a pilot study 
            (atazanavir and lamivudine simplification study, ATLAS) A De Luca and others. AIDS 2010.
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          |  | Risk 
            of Neutropenia, anemia and skin-rash among HIV exposed infants receiving 
             nevirapine and cotrimoxazole 
            compared to cotrimoxazole prophylaxis alone J Aizire and others. AIDS 2010.
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          |  | Randomized 
            trial comparing two nevirapine 
            starting doses after switching from efavirenz 
            due to side effects (the Venice/GESIDA-4905 study) E Ribera and others. AIDS 2010.
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          |  | Influence 
            of CYP2B6 haplotype on plasma 
            efavirenz and nevirapine levels when co-administered with rifampicin 
            in HIV/TB co-infected Thai adults S Uttayamakul and others. AIDS 2010.
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          |  | Treatment 
            outcomes of patients co-infected with HIV 
            and tuberculosis who received  nevirapine-based 
            antiretroviral regimen: a 4-year prospective study W Manosuthi and others. AIDS 2010
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          |  | Comparison 
            of 48 week efficacy and safety of 400 mg QD nevirapine extended release 
            formulation (Viramune XR) versus 
            200 mg BID nevirapine immediate release formulation (Viramune 
            IR) in combination with Truvada 
            in antiretroviral (ARV) naïve HIV-1 infected patients (VERxVE) J Gathe and others. AIDS 2010
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          |  | Both 
            Immune Activation and Viral Load are Reduced Within 28 Days by VS411, 
            the First AntiViral-HyperActivation Limiting Therapeutic (AV-HALT). 
            A Phase II Study E Katabira and others. AIDS 2010.
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          |  | DermaVir 
            for initial treatment of HIV-infected subjects demonstrates preliminary 
            safety, immunogenicity and HIV-RNA reduction versus placebo immunization J Lunzen and others. AIDS 2010.
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          |  | Pooled 
            Week 48 efficacy and safety results from ECHO and THRIVE, two double-blind, 
            randomised, Phase III trials comparing TMC278 
            versus efavirenz in treatment-naïve, HIV-1-infected patients C Cohen and others. AIDS 2010.
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          |  | Pharmacokinetic 
            interaction study between TMC278, 
            a next-generation NNRTI, and methadone H Crauwels and others. AIDS 2010.
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          |  | Relative 
            bioavailability of a concept paediatric formulation of TMC278, 
            an investigational NNRTI H Crauwels and others. AIDS 2010.
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          |  | Darunavir/ritonavir 
            increases rosuvastatin concentrations but does not alter lipid lowering 
            effect in healthy volunteers C Fichtenbaum and others. AIDS 2010.
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          |  | Hepatic 
            laboratory parameters in the MONET Trial: association with Hepatitis 
            C co-infection M Nelson and others. AIDS 2010.
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          |  | The 
            MONET trial 96 week analysis: darunavir/r 
            monotherapy versus darunavir/r + 2NRTIs, for patients with 
            HIV RNA < 50 copies/mL at baseline A Rieger and others. AIDS 2010.
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          |  | Effect 
            of adherence on virological response to once-daily versus twice-daily 
            darunavir/ritonavir in treatment-experienced, 
            HIV-1-infected patients with no darunavir resistance-associated mutations: 
            ODIN 48-week data C Workman and others. AIDS 2010.
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          |  | Effects 
            of once-daily versus twice-daily darunavir/ritonavir 
            on lipid parameters at Week 48 in treatment-experienced, HIV-1-infected 
            patients with no darunavir resistance-associated mutations in the 
            ODIN study J Arribas and others. AIDS 2010.
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          |  | Subgroup 
            analysis and predictors of virological response in treatment-experienced, 
            HIV-1-infected patients in the ODIN trial P Cahn and others. AIDS 2010.
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          |  | METABOLIK 
            (Metabolic Evaluation in Treatment-naïves Assessing the impact 
            of two Boosted protease inhibitors on LIpids and other marKers): Comparison 
            of the Metabolic Effects of Darunavir/ritonavir 
            versus Atazanavir/ritonavir over 12Weeks J Aberg and others. AIDS 2010.
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          |  | The 
            SENSE Trial: Etravirine (ETR) 
            shows fewer Neuropsychiatric Adverse Events than Efavirenz 
            (EFV) in Treatment-naïve HIV-1 Infected Patients B Gazzard and others. AIDS 2010.
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          |  | Prevalence 
            of genotypic and phenotypic susceptibility to etravirine 
            in US samples received for routine resistance testing G Picchio and others. AIDS 2010.
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          |  | SWITCH-EE 
            Study: A Randomized Cross-over Study to Compare Etravirine 
            and Efavirenz treatment A Nguyen and others. AIDS 2010.
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          |  | Bioequivalence 
            of the Co-Formulation of Emtricitabine/Rilpivirine/Tenofovir 
            DF A Mathias and others. AIDS 2010.
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          |  | Switching 
            from Kivexa [ABC/3TC ]+Kaletra [LPV/r] to Truvada 
            [TDF/FTC]+Kaletra [LPV/r] Reduces High Cholesterol: Results of a 12 
            Week Randomized, Controlled Study (ROCKET II) G Behrens and others. AIDS 2010.
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          |  | Switching 
            to Atripla® (EFV/FTC/TDF) 
            from ABC/3TC FDC (Kivexa®/Epzicom®) 
            + Efavirenz (EFV) Improves Lipid 
            Levels Towards NCEP Recommendations: Primary Endpoint Results of a 
            24-week Randomised Study G Moyle and others. AIDS 2010.
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          |  | The 
            SPARTAN Study: A Pilot Study to Assess the Safety and Efficacy of 
            an Investigational NRTI- and RTV-Sparing 
            Regimen of Atazanavir 
            (ATV) Experimental Dose of 300mg BID plus Raltegravir 
            (RAL) 400mg BID (ATV+RAL) in Treatment-Naïve HIV-Infected Subjects. M Kozal and others. AIDS 2010.
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