


Study Acronymn
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Full Study Name
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Brief description
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Anaemia Study
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A Pilot Study on the use of Low Dose Erythropoietin in the Management of HIV Associated Anaemia
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This was a four-week randomized clinical trial conducted among HIV positive patients with grade 1 to 2 anaemia to determine the effect of low dose erythropoietin on the patients' hemoglobin and their quality of life.
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HPTN 027
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This was a multi site phase I HIV vaccine trial in new born children to mothers infected with HIV. The aim of the trial was to evaluate the safety and tolerance and the immunogenicity of the ALVAC- HIV vCP1521 in new born infants to HIV positive mothers.
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ARROW PK Study
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Pharmacokinetics and acceptability of once- versus twice-daily lamivudine and abacavir in HIV-infected Ugandan children
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This was conducted as a Pharmacokinetic sub-study within the ARROW trial. Results were published and can be accessed here.
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ATRIPLA Food study
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ATRIPLA Food study
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This was a pharmacokinetic study investigating the effect of food on the bioavailability of the active components of the fixed drug combination of TDF/FTC/EFV.
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JTV Study
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Safety and Immunogenicity of LFn-P24C in HIV infected Adult Ugandan Volunteers who undergo monitored treatment interruption
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This was a phase I therapeutic vaccine clinical trial, aiming at describing the safety of a boosted dose of LFn-p24C administered to HIV-1 infected subjects who have received at least 3 doses of LFn-p24C and who had plasma HIV-1 RNA levels < 400 copies/ml on ART; and to measure the effects of LFn-p24C on plasma RNA and HIV-specific immune response after a closely monitored 4 weeks of treatment interruption.
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CD8 Study
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CD8 Study
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This was a cross-sectional, observational study lab-based to evaluate the prevalence of positive response to selected CD8 antigens. Plasma and PBMC were obtained from blood. PBMC were then used for ELISPOT
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Chemokine / Cytokine studies
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This encompassed a number of lab-based studies which included: Pleural- CT4, CT 12, CT14 and CT16 studies. Studies CT12, CT14 and CT16 have been completed.
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DART study
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Developing an Antiretroviral therapy for Africa
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This study investigated the monitoring strategy for adults initiating ART in Africa: whether it is safe and cost effective to deliver ART without the use of routine laboratory blood tests. The Study findings have been published, and can be accessed here.
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Pleural study (CT4)
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This was a cross sectional study, aiming at investigating the role of different mechanisms of activation of HIV-1 at the sites of MTB infection in patients with HIV and pleural TB. A total number of 141 patients were enrolled.
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SARA Study
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This was a follow on study from the DART study, which evaluated the ART switch strategy for patients starting second line ART.
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Pleural Study (CD4)
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This was a cross sectional study, aiming at investigating the role of different mechanisms of activation of HIV-1 at the sites of MTB infection in patients with HIV and pleural TB. A total number of 141 patients were enrolled.
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TU Study
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This was a cross sectional study aimed at characterizing T-cell responses to mycobacterium Tuberculosis antigens in children 10 years or below with localized or disseminated TB. A total of 388 children were enrolled. Plasma and PBMC were obtained from blood. PBMC were then used for ELISPOT
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