INSIGHT protocol 004

This nonrandomized multicenter protocol is designed to obtain and store high-quality genomic DNA from persons who…

Effectiveness and tolerability of hepatitis C treatment in HIV-coinfected patients in routine care services in Asia: A pilot model of care project

This is an open-label study of standard HCV therapy with Pegylated-interferon and Ribavirin in HCV-HIV co-infected…

A prospective single arm, open-label, international, multicenter study to evaluate the safety, efficacy and pharmacokinetics of Atazanavir (ATV) powder boosted with Ritonavir (RTV) liquid with an optimized NRTI background therapy, in HIV infected pediatric patients greater than or equal to 3 months to less than 6 years; pediatric Atazanavir international clinical evaluation: The PRINCE I study

This study will evaluate the pharmacokinetic and efficacy data of atazanavir/r in HIV-infected children.

ICAMP

This study will prospectively validate the adherence monitoring tool among HIV-infected children and adolescents at 3…

A phase 2, dose-escalation, schedule comparison study to evaluate the safety, pharmacokinetics, and viral kinetics of ABX464 in untreated patients with HIV infection

The present study is intended to assess the safety, the tolerability, and pharmacokinetic parameters and to…

A phase 2b/3 double-blind safety and efficacy study of injectable Cabotegravir compared to daily oral Tenofovir Disoproxil Fumarate/Emtricitabine (TDF/FTC), for pre-exposure prophylaxis in HIV-uninfected cisgender men and transgender women who have sex with men

This is a Phase IIb/III, randomized, multi-site, two-arm, study of CAB LA compared to daily oral…

A cross-sectional study of socioeconomic factors effect on cognition, adaptive function and school status in the PREDICT cohort

This is across-sectional study of socioeconomic factors effect on cognition, adaptive function and school status in…

Prevalence of bacterial vaginosis in HIV-positive copper intrauterine device users

This is a cross-sectional study that will assess and compare the prevalence of BV and intermediate…

Optimization of reproductive health care for female adolescents living with HIV

This is a prospective cohort study that will be used to create a model of reproductive…

Pharmaceutical Equivalence Drugs Assessment-I (PEDA-I): Assess the pharmaceutical equivalence of generic antiretrovirals distributed in Thailand

This study will assess the pharmaceutical equivalence of generic antiretroviral drugs (i.e., TDF, EFV and LPV/r)…

Nonalcoholic Fatty Liver Disease (NAFLD) and long-term metabolic complications among perinatal HIV-infected children and adolescents receiving antiretroviral therapy

This is an age-matched case-control study that will evaluate the burden and associated risk factors of…

The Thai pediatric HIV disease progression: An observational database

The objective of this cohort is to describe the multicenter cohort of HIV-infected children in Thailand

Intervention to promote sexual health of adolescents and young adults with HIV in Thailand

This is a qualitative study assessing the efficacy of a proposed model to promote sexual health…

Trial to evaluate neurocognitive functions, neuropsychiatric changes and activities of daily living among HIV infected patients in the cohort HIV-NAT 006 study

This is a cross-sectional study to assess the long-term neurocognitive functions.

A phase 3b, randomized, open-label clinical study to demonstrate non-inferiority in virologic response rates of HIV-1 RNA suppression < 400 copies/mL of TDF/FTC/RPV versus TDF/FTC/EFV in first-line antiretroviral NNRTI-based suppressed patients

This randomized study will show that the efficacy of tenofovir disoproxil fumarate/emtricitabine/rilpivirine (TDF/FTC/RPV) is equivalent to…