| 
  HIV 
and AIDS Articles | 
| Therapies 
for Treatment-Experienced Patients
 | 
|  | Genotypic 
Testing Predicts Response to Maraviroc (Selzentry) 
as well as Viral Tropism Testing | 
|  | Once-daily 
 Lopinavir/ritonavir (Kaletra) Works as Well 
as Twice-daily dosing in Treatment-naive HIV Patients | 
|  | Once 
Daily Darunavir/ritonavir: Experience in a 
Single Centre | 
|  | FOTO 
Study Finds 5 Days On, 2 Days Off Treatment Strategy Maintains HIV 
Suppression while Reducing Cost | 
|  | 
| First-Line 
Therapy for Treatment-Naive Patients | 
|  | Treatment-naive 
Patients with Confirmed CCR5-tropic HIV Continue to Respond Well to Maraviroc 
(Selzentry) at 96 Weeks in the MERIT Study | 
|  | Nevirapine 
(Viramune) Has Equal Efficacy but a More Favorable Lipid Profile Compared 
with Boosted Atazanavir (Reyataz) | 
|  | Once 
Daily Darunavir/ritonavir: Experience in a 
Single Centre | 
|  | Integrase 
Inhibitor Raltegravir (Isentress) Compares 
Favorably to Efavirenz (Sustiva) at 144 Weeks 
in Treatment-naive Patients | 
|  | 
| Experimental 
HIV Therapies | 
|  | Potent 
Next-generation Experimental Integrase Inhibitor S/GSK134957 
Debuts at IAS 2009 | 
|  | 
| Adverse 
Events | 
|  | Lipid 
and Glucose Changes Related 
to Boosted Darunavir (Prezista) in Children and Adolescents with HIV: DELPHI Study | 
|  | HIV 
Positive People without Viral Hepatitis or Other Risk 
Factors Have a Fibrosis Distribution Similar to the General Population | 
|  | Liver 
Toxicity Related to Raltegravir (Isentress) Is Uncommon among HIV Patients, 
including those with HIV-HCV Coinfection | 
|  | Impact 
of Adverse Events on Survival of African HIV 
Patients in the DART Trial | 
|  | Confounding 
Factors May Explain Elevated Cardiovascular Risk 
in Patients Taking Abacavir | 
|  | Intensive 
 Cardiovascular Intervention Lowers Blood 
Lipids in HIV Patients on Antiretroviral Therapy | 
|  | 
| HIV 
Transmission and Prevention | 
|  | Daily 
Acyclovir (Zovirax) Delays HIV Disease Progression 
in People Coinfected with HIV and Herpes Simplex Virus Type 2 | 
|  | 
| Related 
Conditions | 
|  | Presence 
of Human Papillomavirus (HPV) Increases Risk 
of HIV Infection | 
|  | HIV 
Positive People without Viral Hepatitis or Other Risk 
Factors Have a Fibrosis Distribution Similar to the General Population | 
|  | Daily 
Acyclovir (Zovirax) Delays HIV Disease Progression in People Coinfected with HIV 
and Herpes Simplex Virus Type 2 | 
|  | Longer 
Duration of HIV Infection and Detectable Viral Load Linked to Higher Risk of Non-AIDS-defining 
Cancers | 
|  | Intensive 
 Cardiovascular Intervention Lowers Blood 
Lipids in HIV Patients on Antiretroviral Therapy | 
|  | IAS 
2009 Opening Session Emphasizes Need for Expanded Treatment of HIV 
and Tuberculosis in Developing Countries | 
|  | Research 
Offers Guidance on Scaling Up HIV and Tuberculosis Treatment 
Programs in Resource-limited Countries | 
|  | Widespread 
Use of Antiretroviral Therapy Associated with a Large Decrease in Tuberculosis 
Prevalence in South Africa | 
|  | HIV 
Latency Is a Myth: New HIV Paradigm May Focus on Inflammation | 
|  | 
| Developing 
Countries | 
|  | Can 
People in Low-income Countries Benefit from 
Antiretroviral Therapy without Routine Laboratory 
Monitoring? | 
|  | Impact 
of Adverse Events on Survival of African HIV Patients 
in the DART Trial | 
|  | IAS 
2009 Opening Session Emphasizes Need for Expanded Treatment of HIV and Tuberculosis 
in Developing Countries | 
|  | Research 
Offers Guidance on Scaling Up HIV and Tuberculosis Treatment Programs in Resource-limited 
Countries | 
|  | Widespread 
Use of Antiretroviral Therapy Associated with a Large Decrease in Tuberculosis 
Prevalence in South Africa | 
|  | 
| Women 
and Children | 
|  | Large 
Numbers of Women and People of Color Can Be Successfully Enrolled in HIV 
Studies in U.S. | 
|  | Antiretroviral 
Therapy for Mothers Improves Pregnancy Outcomes and Reduces Risk of 
HIV Transmission via Breast-feeding | 
| 
  HIV-HCV 
and HIV-HBV Coinfection Articles | 
|  | HIV-HCV 
Coinfected Patients Treated with NRTI-Sparing Antiretroviral Regimens 
Respond Better to Pegylated Interferon plus Ribavirin | 
|  | Poor 
Outcomes with Ribavirin Pre-treatment and Double-dose Pegylated Interferon in 
 HIV-HCV Coinfected Patients | 
|  | Liver 
Toxicity Related to Raltegravir (Isentress) 
Is Uncommon among HIV Patients, including those with HIV-HCV Coinfection | 
|  | Hepatitis 
C Treatment and Normal Glucose Metabolism Promote Improved Fibrosis in HIV-HBV 
Coinfected People | 
|  | Antiretroviral 
Regimens with Lamivudine (Epivir) Produce 
Good CD4 Cell Recovery and HIV Suppression with Fewer Liver Flares in HIV-HBV 
Coinfected Patients | 
|  | Liver 
Fibrosis May Regress in HIV-HCV Coinfected Patients 
with Sustained Response to Pegylated Interferon plus 
Ribavirin | 
|  | 
| 
  Library 
of Slides and Posters | 
|  Therapies 
for Treatment-Experienced Patients
 | 
|  | Lopinavir/ritonavir 
(LPV/r) tablets administered once- (DQ) or twice-daily (BID) with NRTIs 
in antiretroviral-experienced HIV-1 infected subjects: Results of a 48-week randomized 
trial (Study M06-802) R Zajdenverg and others. IAS 
2009.
 | 
|  | Clinical 
endpoints reduced through etravirine use in 
treatment-experienced, HIV-1-infected patients: pooled 96-week results from the 
Phase III DUET trials J Eron and others. IAS 2009.
 | 
|  | Etravirine 
demonstrates durable efficacy in treatment-experienced patients in the DUET trials: 
pooled 96-week results A Mills and others. IAS 2009.
 | 
|  | Long-term 
safety profile of etravirine in treatment-experienced, 
HIV-1-infected patients: pooled 96-week results from the Phase III DUET trials T 
Campbell and others. IAS 2009.
 | 
|  | Recovery 
of Functional Immunity over 48 Weeks with Darunavir-based 
Therapy in the GRACE Immunology Substudy C Tsoukas 
and others. IAS 2009.
 | 
|  | GRACE 
(Gender, Race And Clinical Experience): 48-Week Results of Darunavir/r-based 
Therapy in the Largest Trial in North America to Focus on Treatment-experienced 
Women K Squires and others. IAS 2009.
 | 
|  | Integrase 
Inhibitor with Activity Against Integrase Inhibitor-Resistant Clinical 
Isolates from Patients Experiencing Virologic Failure while on Raltegravir 
Therapy M Underwood and others. IAS 2009. Copyright 
GlaxoSmithKline. Used with permission, 2009.
 | 
|  | 
| First-Line 
Therapy for Treatment-Naive Patients | 
|  | Efficacy 
and Safety of Atazanavir/RTV vs. Lopinavir/RTV 
in Treatment-Naïve Patients with Advanced Disease: CASTLE Study 96-Week Results J Uy and others. IAS 2009.
 | 
|  | Comparable 
Safety and Efficacy With Once-daily (QD) Versus Twice-daily (BID) Dosing of Lopinavir/ritonavir 
(LPV/r) Tablets With Emtricitabine (FTC) + 
Tenofovir DF (TDF) in Antiretroviral (ARV)-naïve, HIV-1-infected Subjects: 
96-Week Results of the Randomized Trial M05-730 J 
Gonzalez and others. IAS 2009.
 | 
|  | Prospective 
randomised comparison of Nevirapine and Atazanavir/ritonavir 
both combined with  Tenofovir DF/Emtricitabine 
in treatment-naïve HIV-1 infected patients: ARTEN Study week 48 results V 
Soriano and others. IAS 2009.
 | 
|  | ARTEMIS:Week 
96 safety and efficacy of darunavir/r by gender, 
age and race J Fourie and others. IAS 2009.
 | 
|  | Effects 
of once-daily darunavir/ritonavir versus lopinavir/ritonavir 
on lipid parameters and anthropometrics in treatment-naïve, HIV-1-infected ARTEMIS 
patients at Week 96 E Baraldi and others. IAS 2009.
 | 
|  | Differences 
in Virologic Response Among African-Americans and Females Regardless of Therapy 
in the HEAT Study K 
Smith and others. IAS 2009. Copyright GlaxoSmithKline. Used with permission, 2009.
 | 
|  | Similar 
Declines in HIV-1 RNA (Viral load, VL) from Baseline (BL) to 96 Weeks Observed 
in Subjects Randomized to ABC/3TC or TDF/FTC 
each with Lopinavir/Ritonavir (LPV/r) in the 
HEAT Trial (EPZ104057) L Yau and others. IAS 2009. 
Copyright GlaxoSmithKline. Used with permission, 2009.
 | 
|  | Similar 
Efficacy and Tolerability of Atazanavir Compared 
to Atazanavir/Ritonavir, each with ABC/3TC 
after Initial Suppression with ABC/3TC + ATV/r K 
Squires and others. IAS 2009. Copyright GlaxoSmithKline. Used with permission, 
2009.
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|  | 
| Experimental 
HIV Therapies | 
|  | Potent 
Antiviral Activity of S/GSK1349572, A Next 
Generation Integrase Inhibitor (INI), in INI-Naïve 
HIV-1-Infected Patients: ING111521 Protocol J Lalezari 
and others. IAS 2009. Copyright GlaxoSmithKline. Used with permission, 2009.
 | 
|  | Pharmacokinetic 
(PK) and Pharmacodynamic (PD) Relationship of S/GSK1349572, 
a Next Generation Integrase Inhibitor (INI), in HIV-1 Infected Patients I 
Song and others. IAS 2009. Copyright GlaxoSmithKline. Used with permission, 2009.
 | 
|  | S/GSK1349572 
is a Potent Next Generation HIV Integrase Inhibitor A 
Soto and others. IAS 2009. Copyright GlaxoSmithKline. Used with permission, 2009.
 | 
|  | Pharmacokinetics 
(PK) and Safety in Healthy Subjects of S/GSK1349572, 
a Next Generation, Once-Daily HIV Integrase Inhibitor (INI) S 
Min and others. IAS 2009. Copyright GlaxoSmithKline. Used with permission, 2009.
 | 
|  | 
| Developing 
Countries | 
|  | The 
Development of AntiRetroviral Therapy in Africa(DART) 
trial P Mugyenyi and others. IAS 2009.
 | 
|  | 
| Special 
Populations | 
|  | 48 
week lipid- and glucose-related safety profile of darunavir/ritonavir
in treatment-experienced,paediatric patients in DELPHI T 
Meyers and others. IAS 2009.
 | 
|  | The 
Safety, Efficacy, and Steady State Pharmacokinetics of Atazanavir/Ritonavir 
(ATV/r) Once Daily During Pregnancy: Results of Study AI424182 F 
Conradie and others. IAS 2009.
 | 
|  | Bioavailability 
of Efavirenz Capsule Contents (Sprinkles) 
Mixed with a Small Amount of Food Compared with Intact Capsules in Healthy Adults S 
Kaul and others. IAS 2009.
 | 
|  | 
| Treatment 
Strategies | 
|  | The 
MONET trial: darunavir/ritonavir monotherapy 
shows non-inferior efficacy to standard HAART, for patients with HIV RNA <50 copies/mL 
at baseline J Arribas and others. IAS 2009.
 | 
|  | The 
FOTO Sudy- 48 week Results to assess durability of the strategy of 
taking Efavirenz, Tenofovir and Emtricitabine 
Five-days-On, Two-days-Off each week in virologically suppressed patients C 
Cohen and others. IAS 2009.
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