A Phase 2 interventional study of Multiple therapeutic interventions in HIV - Human Immunodeficiency Virus, sponsored by Federal University of São Paulo. Recruiting at 1 site in Brazil. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2026-10-29.
Sponsored by Federal University of São Paulo · Phase 2, Interventional, and Basic science
Contemporary ART fails to eradicate the HIV-1 virus from PWH, resulting in a rebound in viremia within days to weeks after cessation of ART. Evidence indicates that disparities in biological and sociocultural characteristics between resource-limited and resource-privileged settings affect treatment outcomes. Consequently, resource-constrained settings must possess the capability to comprehend the mechanisms and drivers of HIV persistence, as well as to devise and evaluate therapies for HIV cure or prolonged remission within local populations. The investigators will employ genomic, metabolomics, and transcriptomics to analyze samples from a successful therapeutic trial we conducted in Brazil, a resource-constrained country, to identify and investigate mechanisms of HIV persistence and we will employ novel latency-reversal agents and advanced in vivo cell therapy.
The clinical trial the investigators will conduct will employ a multifaceted intervention strategy to achieve HIV remission through intensified ART to reduce residual HIV replication, a novel combination of latency reversal agents (LRA), and cell therapy utilizing autologous dendritic cells infused with autologous HIV peptides.
The development of effective, convenient, and well-tolerated antiretroviral therapy (ART) that leads to virologic suppression has transformed the natural history of a fatal disease into a chronic condition, allowing an almost normal life expectancy for people with HIV. Nevertheless, contemporary ART fails to eradicate the virus, resulting in a rebound in viremia within days to weeks after cessation of ART. Evidence indicates that disparities in biological and sociocultural characteristics between resource-limited and resource-privileged settings affect treatment outcomes. Consequently, resource-constrained settings must possess the capability to comprehend the mechanisms and drivers of HIV persistence, as well as to devise and evaluate therapies for HIV cure or prolonged remission within local populations. The investigators will employ genomic, metabolomics, and transcriptomics to analyze samples from a successful therapeutic trial the investigators conducted in Brazil, a resource-constrained country, to identify and investigate mechanisms of HIV persistence and we will employ novel latency-reversal agents and advanced in vivo cell therapy. The clinical trial to be conducted will employ a multifaceted intervention strategy to achieve HIV remission through intensified ART to reduce residual HIV replication, a novel combination of latency reversal agents (LRA), and cell therapy utilizing autologous dendritic cells infused with autologous HIV peptides.
Aging PWH increasingly experience HIV as a chronic condition characterized by multimorbidity, including cardiovascular disease, diabetes mellitus, non-AIDS-defining malignancies, and neurocognitive disorders; persistent immune activation and inflammation associated with HIV infection are hypothesized to contribute to accelerated biological aging.
Generalized immune activation and chronic inflammation constitute central hallmarks of HIV pathogenesis. Key drivers of HIV-associated immune activation include persistent viral replication, microbial translocation from the gastrointestinal (GI) tract, and co-infections.
Even under effective (ART), low-level viral replication in anatomical reservoirs such as the GI tract continues to contribute to systemic immune activation and disease burden.7 HIV-associated dysregulation of CD4⁺ T regulatory (Treg) cells further exacerbates this process, resulting in sustained immune activation due to impaired immunomodulatory control.8 The cumulative burden of viral gene products and microbial antigens promotes broad activation of both T and B lymphocytes, accompanied by increased production of pro-inflammatory cytokines, including tumor necrosis factor-alpha (TNF-α), interleukin-1 (IL-1), and interleukin-6 (IL-6), which drive bystander lymphocyte activation and contribute to immunosenescence.
HIV-1 replication per se is a major determinant of immune activation, with higher plasma viral loads directly correlating with increased levels of systemic inflammation.9 Notably, defective HIV proviruses, overwhelming prevalent in individuals receiving long-term suppressive ART, can still produce viral proteins capable of sustaining immune activation despite the absence of replication-competent viruses.10 This persistent inflammatory state is implicated in multiple downstream pathological processes, including accelerated CD4⁺ T-cell depletion, lymphoid tissue fibrosis, and increased risk of end-organ diseases such as chronic kidney disease, liver dysfunction, atherosclerosis, cardiovascular disease, and HIV-associated neurocognitive disorders.
Immunophenotypic and soluble biomarkers provide quantitative measures of in vivo T-cell activation and systemic inflammation. Emerging evidence indicates that the latent reservoir of individuals on suppressive ART is predominantly composed of defective proviruses containing large genomic deletions, which may nevertheless retain transcriptional and translational activity sufficient to drive immune activation. However, it remains uncertain whether curative strategies aimed at reducing reservoir size will effectively attenuate immune activation and inflammation, and thereby mitigate the downstream sequelae of HIV pathogenesis.
Individuals who naturally control HIV in the absence of ART, the so-called elite controllers, might provide insights for HIV cure research. Mechanisms involved include T cells, autologous antibodies targeting archived viruses, interferon sensitivity, and natural killer (NK) cells. More recently, the focus has moved towards the so-called "exceptional controllers, individuals who might be considered as true natural cures. Insights also come from "post-treatment controllers", those who can control viral replication after ART is interrupted. It is necessary to better understand viral dynamics associated with control of HIV replication in the absence of ART and to identify biomarkers that predict it to design more effective strategic ART interruptions.
HIV DNA remains detectable in peripheral blood mononuclear cells (PBMCs) in nearly all PWH on suppressive ART, with the majority of these proviral genomes being replication-defective. However, the precise cellular and anatomical sources of viral rebound following ART interruption remain incompletely characterized. Consequently, a detailed understanding of HIV integration site distribution during long-term ART, as well as the inducibility of proviruses relative to their chromosomal context, is essential. In parallel, identifying robust biomarkers to predict viral rebound in analytical treatment-interruption studies is a critical research priority. Furthermore, defining biomarkers associated with reservoir persistence and developing methodologies to quantify the impact of reservoir-reducing interventions accurately will be instrumental in advancing HIV cure strategies. Importantly, the selective elimination of defective proviruses that remain transcriptionally active and contribute to chronic low-grade inflammation may be necessary to optimize long-term clinical outcomes.
A primary mechanism underlying HIV persistence is the clonal proliferation of infected cells, which can occur independently of ongoing viral replication and leads to substantial expansion of infected cell populations. Therapeutic strategies aimed at limiting cellular proliferation, and thereby reducing HIV clonal expansion, may be required to attenuate chronic inflammation, decrease the risk of malignancies and other comorbidities, and move PWH on ART closer to a functional or sterilizing cure. Emerging evidence suggests that combinatorial approaches targeting multiple aspects of viral persistence are likely to be the most effective. Additionally, the development of sensitive and reproducible assays to quantify HIV reservoirs during suppressive ART and in the context of curative interventions will be essential to accelerate progress in HIV cure research.
3,035 studies on the registry are indexed under Acquired Immunodeficiency Syndrome; 306 are open to participants now.
This study's planned enrollment of 70 is below the median of 96 across 2,251 interventional studies indexed under Acquired Immunodeficiency Syndrome.
Browse Acquired Immunodeficiency Syndrome studies →Federal University of São Paulo is the lead sponsor of 439 studies on the registry; 23 are open to participants now.
Compared within Acquired Immunodeficiency Syndrome, the registry's first condition term, which may not be this study's main condition. Counted across the registry records on this site, refreshed daily. How we classify →
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
> 18 years old Documented -1 infection. Has voluntarily signed ICF. On HAART ≥ 2 years, without changes in the 24 weeks immediately prior to screening.
HIV viral load \<50 copies/mL, and never > 50 copies/mL on 2 consecutive occasions in the last 2 years. nadir.
> 350 cells/ mm3 Current CD4 count > 500 cells/ mm3. R5 HIV-1 at Screening as defined by proviral DNA genotropism.
Exclusion Criteria:
A subject will NOT be eligible for study participation if he/she meets ANY of the following criteria:
Any evidence of an active AIDS-defining condition. Any significant acute medical illness in the past 8 weeks. Women who are pregnant or breastfeeding. Use of any of the following within 90 days prior to entry: systemic cytotoxic chemotherapy; agents; immunomodulators (colony-stimulating factors, growth factors, systemic , vaccines, immune globulin, interleukins, interferons); coumadin, warfarin, or other Coumadin derivative anticoagulants. Use of an agent definitely or possibly associated with effects on : amiodarone, arsenic trioxide, astemizole, bepridil, chloroquine, chlorpromazine, cisapride, clarithromycin, disopyramide, dofetilide, domperidone, droperidol, erythromycin, halofantrine, haloperidol, ibutilide, levomethadyl, mesoridazine, methadone, pentamidine, pimozide, probucol, procainamide, quinidine, sotalol, sparfloxacin, terfenadine, thioridazine.
Receipt of compounds with HDAC inhibitor-like activity, such as valproic acid or nicotinamide within the last 30 days. Potential participants may enroll after a 30-day .
Known to the components of gold salt, nicotinamide or its analogs.
(HBsAg +) or (HCV RNA +) infection. Known renal insufficiency defined as calculated (Cockcroft Gault formula) \<60 mL/min.
Subjects with a laboratory abnormality grade 3 or 4 with the following exceptions: pancreatic amylase, cholesterol, triglyceride, gamma glutamyl transpeptidase, .
Any condition which, in the investigators opinion, could compromise the subject's safety or adherence to the trial protocol.
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
The human immunodeficiency virus, which weakens the immune system.
Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.
The number of CD4 cells, a type of white blood cell, in a given amount of blood. It is used to follow how well the immune system is doing in HIV.
A drug or device being studied in a clinical trial.
It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.
Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.
Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.
On an ECG, the QT interval is the time the heart’s lower chambers take to activate electrically and recover in each beat. QTc is that time adjusted for heart rate (QTcF by Fridericia’s formula, QTcB by Bazett’s). Some medicines lengthen it, and a long QTc can raise the risk of a dangerous heart rhythm.
The study may name a correction formula and a limit in milliseconds, often around 450–480.
A planned gap after a treatment, so that its effects can lessen before the study treatment or a study assessment. Ask the study team and the doctor who prescribed it before changing any medicine.
An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.
Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.
Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.
Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.
After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.
How quickly the kidneys clear creatinine, a waste product, from the blood. A study may estimate it from a blood test with age, weight and sex (often by the Cockcroft–Gault formula), or measure it using blood and urine collected over a set time. Given in mL/min; higher is better.
A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.
Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.
HIV
The human immunodeficiency virus, which weakens the immune system.
Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
CD4 count
The number of CD4 cells, a type of white blood cell, in a given amount of blood. It is used to follow how well the immune system is doing in HIV.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Investigational drug or device
A drug or device being studied in a clinical trial.
It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Corticosteroids (steroids)
Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.
Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
QT and QTc
On an ECG, the QT interval is the time the heart’s lower chambers take to activate electrically and recover in each beat. QTc is that time adjusted for heart rate (QTcF by Fridericia’s formula, QTcB by Bazett’s). Some medicines lengthen it, and a long QTc can raise the risk of a dangerous heart rhythm.
The study may name a correction formula and a limit in milliseconds, often around 450–480.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Washout period
A planned gap after a treatment, so that its effects can lessen before the study treatment or a study assessment. Ask the study team and the doctor who prescribed it before changing any medicine.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Hypersensitivity
An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Hepatitis B tests
Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.
Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Hepatitis C tests
Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.
After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Creatinine clearance (CrCl)
How quickly the kidneys clear creatinine, a waste product, from the blood. A study may estimate it from a blood test with age, weight and sex (often by the Cockcroft–Gault formula), or measure it using blood and urine collected over a set time. Given in mL/min; higher is better.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Bilirubin
A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.
Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Drug: Multiple therapeutic interventions
intensified antiretroviral treatment using 2 NRTIs, dolutegravir, boosted darunavir/r, and maraviroc or Leronlimab, (ii) use of the HDACi nicotinamide Riboside or nicotinamide, and dendritic cell therapy using peptides of autologous HIV. After the intervention, participants will undergo analytical treatment interruption of antiretrovirals (ATI) and will be closely followed to monitor rebound of HIV viremia.
Evolution of viral load of HIV RNA over the time frame of the study by ultrasensitive RT-qPCR
Time frame: baseline, weeks 12, 24, 36 and 48 and every 3 weeks after the antiretroviral ATI up to 36 months after antiretroviral ATI
Evolution of cell-associated HIV RNA in PBMCs by qPCR. over the study time frame
Time frame: baseline, weeks 12, 24, 36 and 48 and every 3 weeks after the antiretroviral ATI up to 36 months after antiretroviral ATI
Evolution of total DNA and episomal HIV DNA in lymphoid tissue (rectal biopsy)
Quantification by in-house virological assay
Time frame: baseline, week 48, after resurgence of viremia in the analytical interruption of antiretrovirals, or after 24 and 96 weeks after analytical interruption of antiretrovirals.
Evolution of percentages of CD38 and HLA DR in CD4 + and CD8 + T lymphocytes
Measurement by flow cytometry of cell activation of CD4+ and CD8+ T lymphocytes as a means of assessing immune and inflammatory responses
Time frame: baseline, weeks 12, 24, 36 and 48 and every 3 weeks after the antiretroviral ATI up to 36 months after antiretroviral ATI
Evolution of the HIV RNA sequence of the V3 region of gp 120, protease, reverse transcriptase and integrase regions of the pol gene, and of the gag gene
NGS sequencing of the V3 region of gp120, the protease, reverse transcriptase, and integrase regions of the pol gene, and of the gag gene of HIV RNA
Time frame: baseline, week 24, week 48, after resurgence of viremia after ATI and before reintroduction of ART
Evolution of plasma cytokines IL-2, IL-4, IL-6, IL-10, IL-17, TNF and IFN-γ
Measurement by ELISA Assay of plasma cytokines IL-2, IL-4, IL-6, IL-10, IL-17, TNF and IFN-γ as a means of assessing immune and inflammatory responses
Time frame: baseline, week 24, week 48, after resurgence of viremia after ATI and before reintroduction of ART
Started Aug 2026 (actual). Primary completion is estimated for Jul 2027, 11 months after the start.
Of 57 non-industry phase 2 interventional studies under Acquired Immunodeficiency Syndrome, half reached primary completion within 47 months of starting (the median), counting those still running; a quarter within 22 and three quarters within 65. This study's planned 11 months is below that.
Counting every sponsor, half of 86 studies reached it within 36 months; a quarter within 18 and three quarters within 71.
How these figures are worked out, and which studies are left out of them.
From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗
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