A listing of clinical trials and observational studies related to the research effort to cure HIV infection, mainly derived from the clinicaltrials.gov online registry. Click the trial registry identifier numbers for a link to the full entry containing detailed information on the trial design, enrollment criteria, principal investigators and location(s). It’s important to appreciate that at the current time, none of these studies is expected to produce a cure for HIV infection—they represent research working toward that goal.
Entries shaded in light grey include analytical treatment interruptions (ATIs); in some cases the ATIs are only initiated if certain outcomes are achieved. Table 3 contains completed studies, with links to published or presented results where available. Changes from the previous update are highlighted in yellow. Starting in 2023, explanatory background on each monthly update will be posted to the TAG BSVC Project blog. Additional information on current approaches in HIV cure research can be found in TAG’s annual pipeline report. Please send updates, corrections, or suggestions to Richard Jefferys at richard.jefferys@treatmentactiongroup.org.
For more detailed background, see: A Brief Guide to TAG’s Listing of Research Toward an HIV Cure Clinical Trials and Observational Studies.
10/20/22: Based on this listing, Treatment Action Group has created a resource on the demographics of participation in HIV cure-related clinical research. The resource includes a detailed Excel file and summary PDF table of reported demographics in cure-related studies for which results have been presented or published from the beginning of 2018 to date.
Treatment Action Group gratefully acknowledges the support of the Foundation for AIDS & Immune Research (FAIR) for our HIV cure-related information and advocacy resources.
November 20, 2024
Table 1. Current Clinical Trials
Trial |
Trial Registry Identifier(s) |
Country location(s) |
Sponsor(s) |
Phase |
Estimated End Date/Interim |
ADOPTIVE IMMUNOTHERAPY |
|||||
AutoRESIST: HIV antigen-specific T-cells targeting conserved epitopes for treatment of HIV-associated lymphoma |
NCT04975698 |
United States |
Catherine Bollard, Children’s |
Phase II |
June 2026 |
AlloRESIST: Evaluate the safety, immunologic, and virologic responses of donor derived |
United States |
Catherine Bollard, Children’s |
Phase I |
April 2025 |
|
HST-NEETs: HIV-1 specific T-cells for HIV+ individuals |
NCT03485963 |
United States |
Children’s Research Institute |
Phase I |
December 2024 |
ANALYTICAL TREATMENT INTERRUPTION |
|||||
Assessment of HIV remission in |
France |
ANRS |
N/A |
July 2025 |
|
SCOPE-ATI |
United States |
UCSF |
N/A |
June 2026 |
|
Imaging and biopsy of people with |
United States |
National Cancer Institute (NCI) |
Phase II |
August 2026 |
|
ANTI-α4β7 INTEGRIN ANTIBODIES |
|||||
vedolizumab (anti-α₄β₇ integrin |
Canada |
Ottawa Hospital Research |
Phase II |
December 2023 |
|
ANTI-CMV THERAPY |
|||||
letermovir (Prevymis) |
NCT06626555 |
United Kingdom |
University College, London |
Phase II |
March 2026 |
ANTI-INFLAMMATORY |
|||||
Fecal Microbiota Transplantation (FMT) |
Canada |
Jean-Pierre Routy, McGill University Health |
Phase II |
September 2025 |
|
ANTIRETROVIRAL THERAPY |
|||||
Administration of high doses of antiretrovirals |
NCT06640192 |
Spain |
Fundacion para la |
Phase II |
January 2027 |
Codivir in addition to standard antiretroviral treatment |
Brazil |
Code Pharma |
Phase II |
December 2024 |
|
BCL-2 ANTAGONISTS |
|||||
venetoclax |
Australia, Denmark |
University of Aarhus |
Phase I/IIb |
March 2026 |
|
BISPECIFIC T-CELL ENGAGERS |
|||||
GS-8588 |
No clinicaltrials.gov entry, listed on UPenn |
United States |
Gilead Sciences |
Phase I |
N/A |
BROADLY NEUTRALIZING ANTIBODIES |
|||||
VRC01 (analytical |
NCT04860323 |
Botswana, Malawi, South Africa, |
HIV Vaccine Trials Network |
N/A |
February 2025 |
10-1074-LS + |
United Kingdom |
Imperial College London |
Phase II |
July 2027 |
|
3BNC117-LS + |
NCT06205602 |
Botswana, Malawi, South Africa, Zimbabwe |
AIDS Clinical Trials Group |
Phase II |
February 2029 |
3BNC117-LS + |
France |
French National Agency for |
Phase II |
December 2028 |
|
VRC07-523LS + |
Brazil, Peru, United States |
NIAID |
Phase II |
September 2028 |
|
Tatelo Plus: PGDM1400LS, |
NCT06508749 |
Botswana |
NIAID |
Phase I/II |
February 2028 |
3BNC117-LS-J + |
Botswana, Malawi, South Africa |
ACTG |
Phase I |
June 2026 |
|
3BNC117-LS + 10-1074-LS |
United States |
NIAID |
Phase I |
December 2025 |
|
AAV8-VRC07 (broadly neutralizing antibody |
NCT03374202 |
United States |
NIAID
|
Phase I |
August 2026 CROI 2022, Abstract 498 |
CAP256V2LS + |
South Africa |
Centre for the AIDS Programme of |
Phase I |
October 2025 |
|
VH4527079 bispecific |
United States |
ViiV Healthcare |
Phase I |
June 2026 |
|
CD4 ATTACHMENT INHIBITORS |
|||||
UB-421 (antibody inhibitor of HIV binding to |
NCT04404049 |
China |
UBP Greater China (Shanghai) Co., Ltd |
Phase II |
June 2025 |
COMBINATIONS |
|||||
VRC07-523LS, |
NCT05281510 |
South Africa |
Gilead Sciences |
Phase IIa |
March 2025 |
budigalimab (anti-PD-1 |
Belgium, Brazil, Canada, France, |
AbbVie |
Phase II |
March 2027 |
|
UB-421 + |
NCT04985890 |
Taiwan |
UBP Greater China (Shanghai) Co., |
Phase II |
December 2027 |
Ad26.Mos4.HIV, MVA-BN-HIV, |
NCT04983030 |
United States |
Boris Juelg, MD PhD |
Phase I/IIa |
April 2026 |
ChAdOx1.tHIVconsv1, |
Brazil, United States |
NIAID |
Phase I/IIa |
April 2026 |
|
IMPAACT P1115 v2.0: Very |
Argentina, Brazil, Haiti, Kenya, |
IMPAACT |
Phase I/II |
December 2031 |
|
Therapeutic conserved element DNA |
NCT04357821 |
United States |
UCSF |
Phase I/II |
December 2025 |
HVRRICANE: HIVIS |
NCT04301154 |
South Africa |
PENTA Foundation |
Phase I |
February 2025 |
N-803 |
United States |
NIAID |
Phase I |
April 2026 |
|
N-803, |
NCT05245292 |
United States |
Rockefeller University |
Phase I |
December 2025 |
VRC07-523LS, |
NCT06484335 |
Thailand |
Henry M. Jackson Foundation for |
Phase I |
August 2027 |
CYTOKINES |
|||||
N-803 in acute |
Thailand |
Thai Red Cross AIDS Research Centre |
Phase II |
June 2025 |
|
GENE THERAPIES |
|||||
EBT-101 (CRISPR/Cas9 |
NCT05144386 |
United States |
Excision BioTherapeutics |
Phase I/IIa |
May 2025 |
LVgp120duoCAR-T cells |
United States |
Steven Deeks, UCSF |
Phase I/IIa |
December 2028 |
|
Cal-1: Dual anti-HIV gene transfer construct |
NCT02390297 |
United States |
Calimmune |
Phase I/II |
October 2031 |
An ATI study to evaluate the |
NCT05540964 |
United States |
American Gene Technologies |
Phase I |
July 2025 |
CD4 CAR + SB-728mR modified |
NCT03617198 |
United States |
University of Pennsylvania |
Phase I |
December 2027 |
Chimeric Antigen Receptor (CAR)-T |
China |
Guangzhou 8th People’s Hospital |
Phase I |
December 2030 |
|
CMV-specific HIV-CAR T Cells |
United States |
City of Hope Medical Center |
Phase I |
December 2026 |
|
EBT-101 (long-term follow-up study) |
NCT05143307 |
United States |
Excision BioTherapeutics |
Phase I |
April 2037 |
Long-term follow-up of study participants |
NCT05529342 |
United States |
American Gene Technologies International Inc. |
Phase I |
September 2038 |
SB-728mR-HSPC (autologous |
NCT02500849 |
United States |
City of Hope Medical Center |
Phase I |
December 2024 |
GENE THERAPIES FOR HIV-POSITIVE PEOPLE WITH CANCERS |
|||||
Stem cells gene-modified with CCR5 |
NCT02797470 |
United States |
AIDS Malignancy Consortium |
Phase I/II |
June 2025 |
Stem cells gene-modified to |
NCT02337985 |
United States |
City of Hope Medical Center |
Phase I |
December 2024 |
Stem cells gene-modified to |
NCT01961063 |
United States |
City of Hope Medical Center |
Phase I |
December 2024 |
IMAGING STUDIES |
|||||
Imaging immune activation in HIV by PET-MR |
United States |
University of California, San Francisco |
Phase I |
November 2025 |
|
Radiolabeled VRC01 |
United States |
University of California, San Francisco |
Phase I |
January 2025 |
|
IMMUNE CHECKPOINT INHIBITORS |
|||||
ASC22 (anti-PD-L1 antibody) |
China |
Ascletis Pharmaceuticals Co., Ltd. |
Phase II |
December 2023 |
|
NIVO-LD: Low dose nivolumab in |
Australia, Singapore |
University of Melbourne |
Phase I/II |
January 2026 |
|
IMMUNOMODULATORS |
|||||
lenalidomide, adenosylmethionine |
China |
First Affiliated Hospital of |
Phase IV |
November 2024 |
|
PEACH: Pomalidomide as an immune-enhancing agent for the |
NCT06660498 |
Australia, |
University of |
Phase I/IIb |
March 2026 |
JANUS KINASE INHIBITORS |
|||||
baricitinib |
United States |
Emory University |
Phase II |
January 2028 |
|
LATENCY-REVERSING AGENTS |
|||||
lauric acid |
Spain |
Hospital Universitari Vall d’Hebron Research |
N/A |
December 2025 |
|
panobinostat, lenalidomide + pyrimethamine |
NCT06240520 |
Netherlands |
Erasmus Medical Center |
Phase I/II |
October 2025 |
topiramate |
NCT06282783 |
Netherlands |
Erasmus Medical Center |
Phase I/II |
August 2025 |
arsenic trioxide |
China |
Guangzhou 8th People’s Hospital |
Phase I |
December 2025 |
|
decitabine, romidepsin |
France |
ANRS |
Phase I |
April 2026 |
|
STEM CELL TRANSPLANTATION |
|||||
Analytical treatment interruption |
NCT06582797 |
United States |
University of Kansas Medical |
N/A |
September 2034 |
T-CELL RECEPTOR-BASED BISPECIFICS |
|||||
IMC-M113V in |
Belgium, Spain, United Kingdom |
Immunocore |
Phase I/II |
N/A |
|
THERAPEUTIC VACCINES |
|||||
BELIEVE: BCG |
NCT05004038 |
Switzerland |
University of Zurich |
Phase IIa |
January 2024 |
HB-502/HB-501 (arenavírus |
United States |
Hookipa Biotech GmbH |
Phase Ib |
November 2025 |
|
GS-1966/GS-1144 HIV |
No clinicaltrials.gov entry, #7 on Midway Research |
United States |
Gilead Sciences |
Phase Ib |
N/A |
GRAdHIVNE1 (Gorilla |
NCT06617091 |
South Africa, Zimbabwe |
IAVI
|
Phase I |
December 2026 |
HIV Env mosaic |
NCT06449196 |
Uganda, Zimbabwe |
IAVI
|
Phase I |
December 2025 |
426c.Mod.Core-C4b, |
United States |
NIAID, HIV Vaccine Trials Network
|
Phase I |
December 2025 |
|
ChAdOx1.HIVconsv62–MVA.tHIVconsv4 |
United States |
University of North Carolina, Chapel Hill |
Phase I |
February 2025 |
|
DC-HIV04: a1DC + inactivated |
NCT03758625 |
United States |
Sharon Riddler, University of Pittsburgh |
Phase I |
March 2025 |
ICVAX: |
NCT06253533 |
China |
Shenzhen Immuno Cure Biomedical Company |
Phase I |
January 2025 |
NETI: |
United States |
NIAID |
Phase I |
November 2025 |
|
Therapeutic vaccine based |
NCT05786937 |
Brazil |
University of Sao Paulo General |
Phase I |
December 2023 |
TREATMENT INTENSIFICATION/EARLY TREATMENT |
|||||
DGVTAF: Immediate initiation of antiretroviral |
NCT02656511 |
United States |
UCSF |
Phase IV |
May 2028 |
AAHIV: Antiretroviral |
Thailand |
South East Asia Research Collaboration with |
Phase III |
June 2033 |
|
EIT: Early infant HIV treatment in Botswana |
NCT02369406 |
Botswana |
Harvard School of Public Health |
Phase II/III |
June 2029 |
EARLIER: Early ART to limit infection and |
NCT02859558 |
Brazil, Malawi, Peru, South Africa, Thailand, |
AIDS Clinical Trials Group |
Phase II |
April 2025 |
TYROSINE KINASE INHIBITORS |
|||||
dasatinib |
Spain |
Eva Bonfill, Institut d’Investigacions |
Phase II |
June 2026 |
|
dasatinib |
Spain |
Fundació Institut Germans Trias i Pujol |
Phase II |
March 2025 |
Table 2. Current Observational Studies
Trial |
Trial Registry Identifier(s) |
Country location(s) |
Manufacturer/ |
Phase |
Estimated End Date/Interim |
Accurate staging of immuno-virological |
Belgium |
University Hospital, Ghent |
N/A |
January 2028 |
|
Analytic treatment interruption |
NCT02437526 |
United States |
Mayo Clinic |
N/A |
|
ANRS CO24 OncoVIHAC: Immune checkpoint |
France |
Inserm-ANRS |
N/A |
June 2022 |
|
APRIL: Analysis of the persistence, reservoir and |
France |
University Hospital, Strasbourg, France |
N/A |
February 2027 |
|
ARCH: Analysis of the reservoir in individuals |
NCT06016114 |
Belgium |
Sponsor University Hospital, Ghent |
N/A |
October 2028 |
ATGALIG-HIV: Study of autophagy and the effects |
France |
Centre Hospitalier Régional d’Orléans |
N/A |
November 2039 |
|
BICTEVOIR: A study to determine the cartography |
|
France |
ANRS
|
N/A |
March 2024 |
Characterization of acute and |
Switzerland |
University of Zurich |
N/A |
January 2025 |
|
CHRONO: A prospective cohort for ex vivo cure |
NCT04888754 |
Netherlands |
Erasmus Medical Center |
N/A |
January 2034 |
CODEX (the “Extreme” cohort, ANRS CO21) |
France |
Inserm-ANRS |
N/A |
September 2023 |
|
Comparing immune activation and HIV reservoir |
NCT05584397 |
United States |
University of Washington |
N/A |
February 2025 |
Developing a functional cure for HIV disease: |
NCT03215004 |
United States |
American Gene Technologies International Inc. |
N/A |
February 2021 |
Establish and characterize an acute HIV |
Thailand |
Southeast Asia Research Collaboration with |
N/A |
July 2033 |
|
Evaluation of the role of HIV-1 Tat protein |
NCT04263207 |
Italy |
Barbara Ensoli, MD, PhD, Istituto Superiore |
N/A |
June 2025 |
Extended follow-up of the ISS T-003 trial |
South Africa |
Istituto Superiore di Sanità |
N/A |
June 2024 |
|
EX VIVO: Ex vivo characterization and |
Netherlands |
Erasmus Medical Center |
N/A |
December 2030 |
|
FRESH (Females rising through education, support, |
Ragon Institute |
South Africa |
Ragon Institute of MGH, MIT and Harvard |
N/A
|
|
HI-ART: Optimising cohorts for HIV cure |
Australia |
Bayside Health |
N/A
|
December 2025 |
|
HIV-Mercuri: HIV study on measuring the reservoir |
Belgium |
University Hospital, Ghent |
N/A |
December 2025 |
|
HUSH restriction in HIV+ patients |
France |
Inserm-ANRS |
N/A |
September 2023 |
|
iCHIP: Effect of immune checkpoint inhibitors on |
hivcure.com.au (no registry entry) |
Australia |
University of Melbourne |
N/A |
N/A |
IciStem: |
IciStem website (no clinicaltrials.gov |
International |
amfAR |
N/A |
N/A CROI 2020, Abstract 339, Abstract 348LB |
Identification and quantification of HIV CNS |
Australia |
St Vincent’s Hospital, Sydney
|
N/A |
December 2020 |
|
Immuno-virological evaluation of persons |
NCT05973825 |
Belgium |
University Hospital, Ghent |
N/A |
July 2029 |
Investigation of the impact of inducible, |
Kenya |
Kenya Medical Research Institute |
N/A |
April 2022 |
|
LAMIVIH: Evolution of HIV reservoir, |
France |
Hôpital Européen Marseille |
N/A |
March 2024 |
|
Long-term clinical, immunologic, and virologic |
Botswana, Brazil, Haiti, Kenya, Malawi, South |
IMPAACT |
N/A |
November 2027 |
|
NOVA: Netherlands cohort study on acute HIV |
Netherlands |
Prof. Jan Prins |
N/A |
August 2028 |
|
Observational post-intervention controller |
International |
AIDS Clinical Trials Group |
N/A |
September 2029 |
|
PediacamNEG: Negative serology in children with |
Cameroon |
Inserm-ANRS |
N/A |
August 2025 |
|
Post analytic treatment interruption study |
Thailand |
South East Asia Research Collaboration with |
N/A |
March 2031 |
|
PRIMO (ANRS CO6): Primary infection cohort |
France |
Inserm-ANRS |
N/A |
September 2025 |
|
Quantification of antisense HIV RNA |
France |
Institut National de la Santé Et de la |
N/A |
December 2024 |
|
RESERVIH32: Bioclinical evaluation of two |
France |
Centre Hospitalier Universitaire de Nīmes |
N/A |
September 2026 |
|
Saturne-HIV: Sequential analysis before and after |
Belgium |
University Hospital, Ghent |
N/A |
January 2027 |
|
TatLat: Development of a new family of HIV |
NCT06441123 |
France |
University Hospital, Montpellier |
N/A |
December 2025 |
The Gemini Study: Safety and survival of |
NCT04799483 |
United States |
NIAID |
N/A |
January 2030 |
The Last Gift Study (for people with HIV and |
United States |
University of California, San Diego (UCSD) |
N/A |
N/A |
|
The role of the gastrointestinal-associated |
NCT05652088 |
United States |
Icahn School of Medicine at Mount Sinai |
N/A |
June 2025 |
The use of leukapheresis to support HIV pathogenesis |
United States |
University of California, San Francisco |
N/A |
July 2033 |
|
Thinking and memory problems in people with |
United States |
National Institute of Neurological Disorders |
N/A |
February 2037 |
|
TRESAX: T follicular helper reservoir in axillary |
hivcure.com.au (no registry entry) |
Australia |
Kirby Institute |
N/A |
N/A |
Table 3. Completed Studies
Trial |
Trial Registry Identifier(s) |
Manufacturer/ |
Phase |
Published/Presented Data |
ADOPTIVE IMMUNOTHERAPY |
||||
Early ART in combination with |
Yongtao Sun, MD, PhD, Tangdu |
Phase III |
N/A |
|
Reconstitution of HIV-specific |
Guangzhou 8th People’s Hospital |
Phase I/II |
N/A |
|
HIV-specific memory CD8 T cells |
Beijing You’an Hospital, Capital |
Phase I |
||
HXTC: HIV 1 |
University of North Carolina, |
Phase I |
||
ANALYTICAL TREATMENT INTERRUPTION |
||||
TESOVIR: |
Centre Hospitalier Régional |
N/A |
Terminated (no interesting |
|
ANTIBODIES |
||||
CHERUB 001: IVIG in |
No clinicaltrials.gov entry |
CHERUB |
N/A |
|
VRC01 (analytical |
HIV Vaccine Trials Network |
N/A |
HIVR4P 2024, Abstract OA0605 |
|
GSK3810109A (broadly neutralizing |
ViiV Healthcare |
Phase IIa |
EACS 2023, Abstracts PS8.O5 & eP.A.099 |
|
3BNC117 (broadly |
Rockefeller University |
Phase II |
||
3BNC117 |
Rockefeller University |
Phase II |
||
UB-421 (antibody inhibitor of HIV binding to |
United BioPharma |
Phase II |
N/A |
|
UB-421 |
United BioPharma |
Phase II |
||
vedolizumab (anti-α₄β₇ integrin |
Hospitales Universitarios Virgen |
Phase II |
JCI Insight. e182312. |
|
VRC01 (broadly |
National Institute of Allergy and |
Phase II |
Clin Infect Dis. |
|
PGT121 + |
International AIDS Vaccine |
Phase I/IIa |
Nat Med. 2024 Sep 12. |
|
VRC01 (broadly neutralizing antibody) in |
NIAID |
Phase I/II |
AIDS 2022, Abstract OALBB0102 |
|
VRC01LS + 10-1074 (broadly |
NIAID |
Phase I/II |
Sci Transl Med. 2023 |
|
ABBV-382 (anti-α₄β₇ integrin antibody) |
AbbVie |
Phase Ib |
N/A |
|
10-1074 (broadly neutralizing monoclonal |
Rockefeller University |
Phase I |
||
10-1074-LS + 3BNC117-LS (long-acting broadly neutralizing |
Rockefeller University |
Phase I |
N/A |
|
3BNC117 |
Rockefeller University |
Phase I |
||
3BNC117 + 10-1074 |
NIAID |
Phase I |
||
3BNC117 + 10-1074 |
Rockefeller University |
Phase I |
Nat Med. 2020 |
|
3BNC117 + 10-1074 |
Rockefeller University |
Phase I |
Nature. 2022 Apr 13 |
|
3BNC117-LS + 10-1074-LS in viremic HIV+ |
Rockefeller University |
Phase I |
CROI 2022, Abstract 140 |
|
3BNC117-LS |
Rockefeller University |
Phase I |
N/A |
|
elipovimab (formerly GS-9722; PGT121-derived |
GS-US-420-3902 Adisinsight entry |
Gilead Sciences |
Phase I |
CROI 2022, Abstract 349 |
PGDM1400 +/– PGT121 +/– VRC07-523LS (broadly |
International AIDS Vaccine Initiative |
Phase I |
Nat Med. 2022 May 12. |
|
PGT121 |
International AIDS Vaccine Initiative |
Phase I |
Nat Med. 2021 Oct 7. |
|
SAR441236 (tri-specific broadly neutralizing |
NIAID |
Phase I |
CROI 2024, Abstract 118 |
|
vedolizumab |
NIAID |
Phase I |
Sci Transl Med. |
|
VRC01 + 10-1074 |
NIAID |
Phase I |
Terminated: unable to recruit due |
|
VRC01 in acute HIV infection |
NIAID |
Phase I |
CROI 2023, Abstract 430 |
|
VRC01 |
NIAID |
Phase I |
||
VRC01 |
NIAID |
Phase I |
||
VRC01 |
NIAID |
Phase I |
CROI 2023, Abstract 390 |
|
VRC01 |
NIAID |
Phase I |
||
VRC01LS, VRC07-523LS (long-acting broadly neutralizing |
NIAID |
Phase I |
IAS 2019, Abstract WEAA0305LB (video, at 45:36) |
|
ANTI-CMV THERAPY |
||||
letermovir (Prevymis) |
NIAID |
Phase II |
CROI 2024, Abstract 354 |
|
ANTI-FIBROTIC |
||||
ACE inhibitors |
UCSF/amfAR |
Phase IV |
||
losartan |
University of Minnesota |
Phase II |
CROI 2020, Abstract 277 |
|
telmisartan |
AIDS Clinical Trials Group |
Phase II |
CROI 2019, Abstract 395 |
|
telmisartan |
Yale University |
Phase I |
CROI 2019, Abstract 300 |
|
ANTI-INFLAMMATORY |
||||
canakinumab (IL-1β inhibitor) |
University of California, San Francisco |
Phase II |
J Am Coll Cardiol. |
|
CD24Fc (human CD24 extracellular domain and human |
OncoImmune, Inc. |
Phase II |
“Terminated (Business Reasons)” |
|
High dose vitamin D supplementation |
University of Melbourne |
Phase II |
J Virus Erad. 2023 |
|
Camu Camu (Myrciaria dubia) |
McGill University Health Centre |
Phase I |
N/A |
|
CC-11050 (phosphodiesterase-4 inhibitor) |
NIAID |
Phase I |
OFID. 6(6):ofz246. |
|
ANTI-PROLIFERATIVE |
||||
mycophenolate mofetil (MMF) |
Fred Hutchinson Cancer Research Ctr |
Phase I |
OFID 2022, ofac620 |
|
ANTIRETROVIRAL THERAPY |
||||
dolutegravir in reservoirs |
Emory University |
Phase IV |
||
HIV reservoir dynamics after switching to |
Hospital Universitari Vall d’Hebron Research |
Phase IV |
N/A |
|
raltegravir or efavirenz + tenofovir + emtricitibine |
University of Alabama at Birmingham |
Phase IV |
N/A |
|
doravirine concentrations and antiviral |
Fundacio Lluita Contra la SIDA |
Phase III |
||
IDOLTIB: Impact of dolutegravir + lamivudine |
University of Liege |
Phase III |
N/A |
|
ABX464 |
Abivax S.A. |
Phase II |
||
ABX464 |
Abivax S.A. |
Phase I/II
|
J Infect Dis. |
|
ANTIRETROVIRAL THERAPY IN HIV CONTROLLERS |
||||
emtricitabine + rilpivirine |
AIDS Clinical Trials Group/NIAID |
Phase IV |
J Infect Dis. jiaa294 |
|
raltegravir + tenofovir + emtricitabine |
University of California, San Francisco |
Phase IV |
||
ASSEMBLY INHIBITORS |
||||
BIT225 |
Biotron Limited |
Phase II |
J Infect Dis. 2021 |
|
BIT225 |
Biotron Limited |
Phase I |
||
CANNABINOIDS |
||||
GALIG-CBD: Effects of cannabidiol on the |
Centre Hospitalier Régional d’Orléans |
Phase II |
||
TN-TC11M2, TN-C200M2 oral capsules |
McGill University Health Center |
Phase II |
J Pers Med. 14(7):745. |
|
COMBINATIONS |
||||
maraviroc, dolutegravir, |
Federal University of São Paulo |
Not listed |
CROI 2023, Abstract 383 |
|
Perturbing of HIV reservoir with immune |
University of California, San Diego |
Not listed |
AIDS. 2024 Mar 25. |
|
ART +/- |
Juan A. Arnaiz |
Phase IV |
Lancet HIV. |
|
MVA.HTI + |
Aelix Therapeutics |
Phase IIa |
CROI 2023, Abstract 433 |
|
ROADMAP: romidepsin |
Rockefeller University |
Phase IIa |
Lancet Microbe. 2022 |
|
TITAN: |
University of Aarhus |
Phase IIa |
Nat Med. 2023 Sep 11 |
|
Adoptive transfer of haploidentical |
University of Minnesota – Clinical and |
Phase II |
||
Albuvirtide (fusion |
|
Frontier Biotechnologies Inc. |
Phase II |
N/A, unknown if study opened |
ASC22 (anti-PD-L1 antibody) + chidamide (HDAC inhibitor) |
Shanghai Public Health Clinical Center |
Phase II |
Signal Transduct |
|
eCLEAR: |
Aarhus University Hospital |
Phase II |
CROI 2024, Abstract 486 |
|
ERAMUNE-01 |
ORVACS/Cytheris SA/Merck Sharp & Dohme |
Phase II |
||
ERAMUNE-02 (DNA/Ad5 vaccine, ART intensification) |
|
Vical/GenVec/CHERUB/NIH Vaccine Research |
Phase II |
Lancet HIV. 2015 CROI 2014, Poster abstract 422 |
MVA HIV-B +/- vedolizumab |
ANRS |
Phase II |
Stopped due to logistical issues |
|
Research in Viral Eradication of HIV |
Imperial College London |
Phase II |
J Exp Med. 221(11):e20241091. |
|
UB-421 + |
United BioPharma |
Phase II |
N/A |
|
vorinostat +/- tamoxifen |
NIAID |
Phase II |
Clin Infect Dis. 2022 |
|
disulfiram + vorinostat |
NCT03198559 |
The Peter Doherty Institute for Infection and |
Phase I/II |
AIDS. 2021 Sep 29. |
GTU-MultiHIV B-clade + MVA HIV-B |
Inserm-ANRS |
Phase I/II |
Terminated due to bankruptcy of |
|
panobinostat + pegylated |
Massachusetts General Hospital |
Phase I/II |
Cell. |
|
Vacc-4x |
Bionor Immuno AS/Celgene |
Phase I/II
|
CROI 2023, Abstract 337 |
|
Vacc-4x |
Bionor Immuno AS |
Phase I/II |
||
vorinostat + hydroxychloroquine + |
NCT02475915 |
South East Asia Research |
Phase I/II |
Clin Infect Dis. |
elipovimab (formerly |
GS-US-420-3902 (#18 on list, no |
Gilead Sciences |
Phase Ib |
N/A, elipovimab discontinued (see Adis Insight) |
Adoptive transfer of haploidentical |
University of Minnesota – Clinical and |
Phase I |
||
AGS-004 + vorinostat |
NIAID |
Phase I |
Sci Rep. 10(1):5134. |
|
CD4-ZETA gene–modified T |
University of Pennsylvania |
Phase I |
CROI 2020, Abstract 337, Webcast |
|
chemotherapy + |
Fundacion para la Investigacion Biomedica del |
Phase I |
Terminated due to futility criteria |
|
Chidamide + CAR-T |
Guangzhou 8th People’s Hospital |
Phase I |
||
DCV3 |
Judit Pich Martínez, Fundació |
Phase I |
Front Immunol. 2021 |
|
MVA-B (viral |
Hospital Clinic of |
Phase I |
||
MVA.HIVconsv |
IrsiCaixa |
Phase I
|
EBioMedicine. |
|
peginterferon |
Wistar Institute |
Phase I |
CROI 2024, Abstracts 179, 511, 1091, 1106 |
|
vorinostat + HXTC: HIV 1 |
Julia Sung, MD, University of North Carolina, |
Phase I |
J Infect Dis. |
|
VRC07-523LS + vorinostat |
University of North Carolina, Chapel Hill |
Phase I |
J Infect Dis. |
|
CYTOKINES |
||||
interleukin-2 (IL-2) |
Case Western Reserve University |
Phase II |
HIV Persistence Workshop 2022, Abstract OP 8.2 (slides) |
|
Effect of N-803 on B cell |
University of Minnesota |
Phase I |
N/A |
|
N-803 |
University of Minnesota – Clinical and |
Phase I |
Nat Med. 2022 Jan 31. |
|
DUAL-AFFINITY RE-TARGETING (DART) MOLECULES |
||||
MGD020 +/- MGD014 |
MacroGenics |
Phase I |
N/A |
|
MGD014 |
MacroGenics |
Phase I |
AIDS 2022, Abstract OAA0403 |
|
GENE THERAPIES |
||||
OZ1 |
Janssen-Cilag Pty Ltd |
Phase II |
||
Cal-1: Dual anti-HIV gene transfer construct |
Calimmune |
Phase I/II |
||
SB-728mR-T (autologous CD4 T cells genetically |
Sangamo BioSciences |
Phase I/II |
N/A |
|
SB-728-T + |
Sangamo BioSciences |
Phase I/II
|
CROI 2023, Abstract 182 CROI 2015, Poster abstract 434 CROI 2014, Abstract 141, Webcast |
|
SB-728-T |
Sangamo BioSciences |
Phase I/II |
N/A |
|
SB-728-T |
Case Western Reserve University |
Phase I/II |
N/A |
|
VRX496 |
University of Pennsylvania |
Phase I/II |
||
AGT103-T (gene-modified HIV-specific CD4 T |
American Gene Technologies International Inc. |
Phase I |
||
C34-CXCR4 (autologous |
University of Pennsylvania
|
Phase I |
N/A |
|
HGTV43 |
No clinicaltrials.gov entry |
Enzo Biochem |
Phase I |
AIDS 2006, Abstract MOPDA06 |
Long-term follow-up of HIV+ participants |
Sangamo Therapeutics |
Phase I |
||
MazF-T |
Takara Bio/University of |
Phase I |
Mol Ther 2020 Nov 10 |
|
Redirected high affinity Gag-specific T cells |
University of Pennsylvania/Adaptimmune |
Phase I |
Study closed (safety): Mol Ther. 2015 Jul; |
|
SB-728mR-T + |
University of Pennsylvania |
Phase I |
J Clin Invest. 2021. |
|
SB-728-T |
Sangamo BioSciences |
Phase I |
CROI 2023, Abstract 182 |
|
SB-728-T
|
Sangamo Biosciences/University of |
Phase I |
||
shRNA-modified CD34+ cells |
Shanghai Public Health Clinical Center |
Phase I |
N/A |
|
TCTIWHI: Third-generation CAR-T-cell therapy |
Beijing 302 Hospital |
Phase I |
N/A |
|
GENE THERAPIES FOR HIV-POSITIVE PEOPLE WITH CANCERS |
||||
CRISPR CCR5 modified CD34+ cells |
307 Hospital of PLA (Affiliated |
Not listed |
||
Stem cells gene-modified with M87o vector |
Universitätsklinikum Hamburg-Eppendorf |
Phase I/II |
N/A |
|
Stem cells gene-modified with Cal-1 |
Assistance Publique – Hôpitaux de |
Phase I/II |
||
Stem cells gene-modified to encode multiple |
City of Hope Medical Center |
Phase I |
||
GONADOTROPIN-RELEASING HORMONE (GnRH) AGONISTS |
||||
triptorelin acetate depot |
Immune System Regulation AB |
Phase II |
N/A |
|
HORMONES |
||||
somatotropin (human growth |
McGill University Health Center |
Phase II |
CROI 2021, Abstract 298, Webcast |
|
IMAGING STUDIES |
||||
123I radiolabeled 3BNC117 |
University of Lausanne Hospitals |
Phase I |
N/A |
|
Radiolabeled 3BNC117 + Copper-64 radio |
Bayside Health |
Phase I |
EBioMedicine. 2021 |
|
IMMUNE CHECKPOINT INHIBITORS |
||||
durvalumab (anti-PD-L1 antibody) in solid |
Spanish Lung Cancer Group |
Phase II |
ESMO 2020, Abstract 1275P |
|
cemiplimab (anti-PD-1 antibody) |
NIAID |
Phase I/II |
OFID 11(3):ofad694. |
|
budigalimab (anti-PD-1 |
AbbVie |
Phase Ib |
CROI 2024, Abstract 106 |
|
BMS-936559 (anti-PD-L1 antibody) |
National Institute of Allergy and Infectious |
Phase I |
J Infect Dis. 2017 CROI 2016, Abstract 25, Webcast |
|
budigalimab (anti-PD-1 antibody) |
AbbVie |
Phase I |
EACS 2023, Abstract PS10.O3 |
|
ipilimumab (anti-CTLA-4 antibody) |
Medarex |
Phase I |
||
nivolumab (anti-PD-1 antibody) + |
NCT02408861 |
National Cancer Institute (NCI) |
Phase I |
AIDS 2024, Abstract OAA1308 |
pembrolizumab (anti-PD-1 antibody) |
National Cancer Institute (NCI) |
Phase I |
CROI 2023, Abstract 181 |
|
pembrolizumab (anti-PD-1 antibody) |
National Institute of Neurological Disorders |
Phase I |
HIV Persistence Workshop 2022, Abstract OP 1.10 (slides) |
|
IRON CHELATORS |
||||
deferiprone |
ApoPharma |
Phase I |
N/A |
|
JANUS KINASE INHIBITORS |
||||
ruxolitinib |
NIAID |
Phase II |
CROI 2024, Abstract 521 |
|
LATENCY-REVERSING AGENTS |
||||
disulfiram |
University of California, San Francisco/ |
Not specified |
||
Chidamide |
Tang-Du Hospital |
Phase II/III |
N/A |
|
vorinostat (HDAC inhibitor) |
Bayside Health/Merck |
Phase II |
||
valproic acid (HDAC inhibitor) |
McGill University |
Phase II |
||
valproic acid |
University of North Carolina at Chapel |
Phase II
|
||
Chidamide (HDAC inhibitor) |
Tang-Du Hospital |
Phase I/II |
HIV Med. 2020 |
|
disulfiram (acetaldehyde dehydrogenase |
University of California, San |
Phase I/II |
CROI 2015, Poster abstract 428LB |
|
panobinostat (HDAC |
University of Aarhus/ |
Phase I/II |
CROI 2015, Abstract 109, Webcast |
|
romidepsin (HDAC inhibitor) |
AIDS Clinical Trials Group/NIAID/Gilead |
Phase I/II
|
JID, jiaa777 |
|
valproic acid + pyrimethamine |
Erasmus Medical Center |
Phase I/II |
||
vorinostat |
University of North Carolina at Chapel |
Phase I/II |
J Clin Invest. 2017 Aug 1;127(8):3126-3135. |
|
bryostatin 1 (PKC agonist) |
Fundacion para la Investigacion Biomedica del |
Phase I |
||
Euphorbia kansui |
Shanghai Public Health Clinical Center |
Phase I |
N/A, unknown if study opened |
|
Kansui (traditional Chinese medicine with |
UCSF |
Phase I |
Study terminated |
|
mTOR INHIBITORS |
||||
Impact of Everolimus on HIV |
UCSF |
Phase IV |
||
metformin |
University of Hawaii |
Phase II/III |
ARHR 36(4):303-305. |
|
Sirolimus |
ACTG |
Phase I/II |
Cell Rep Med. 101745. |
|
metformin |
McGill University Health Center |
Phase I |
EBioMedicine |
|
OBSERVATIONAL STUDIES |
||||
2000HIV: 2000 HIV human functional genomics partnership |
Radboud University |
N/A |
CROI 2024, Abstracts 319, 442, 515 |
|
2000HIVTrained: 2000 HIV trained |
Radboud University |
N/A |
CROI 2024, Abstract 442 |
|
ACTG A5321: Decay of HIV-1 reservoirs in |
N/A |
AIDS Clinical Trials Group |
N/A
|
CROI 2023, Abstracts 392, 398 CROI 2018, Abstract 119, Webcast |
ANRS CO24 OncoVIHAC: Immune checkpoint |
|
Inserm-ANRS |
N/A |
Cells. 2022 Mar 17;11(6):1015. |
ANRS EP 44: Residual replication |
Inserm-ANRS |
N/A |
N/A |
|
ANRS EP63: A chronological study of the |
Inserm-ANRS |
N/A |
N/A |
|
APACHE: |
Ospedale San Raffaele |
N/A |
PLoS One. 2022 Mar J Antimicrob |
|
ATN 147 |
The Adolescent Medicine Trials Network for |
N/A |
CROI 2023, Abstract 457 |
|
AVIR: Characterization of HIV-1 reservoirs in |
Chantal Biya International Reference Centre |
N/A |
||
Biomarkers to predict time to |
AIDS Clinical Trials Group |
N/A |
JCI Insight. 9(3):e173864 |
|
CHERUB 003 (prospective HIV chemotherapy cohort |
Imperial College London/CHERUB |
N/A |
N/A |
|
CLEAC: Comparison of late versus early antiretroviral |
Inserm-ANRS |
N/A |
Front Immunol. 2021 |
|
DOLUVOIR: Cartography of virologic reservoir |
Inserm-ANRS |
N/A |
N/A |
|
EARTH: Early antiretroviral treatment in children |
PENTA Foundation |
N/A |
||
Effects of dolutegravir based regimen on |
University Hospital, Strasbourg, France |
N/A |
||
EPIC4: Early Pediatric Initiation: Canada Child |
Canadian Institutes of Health Research |
N/A
|
AIDS. 34(5):687-697 |
|
Expectation, motivation, and experience of |
ANRS |
N/A |
||
EURECA: Exploratory study of cellular reservoirs in |
Centre Hospitalier Universitaire de Besancon |
N/A |
||
FXReservoir: Study of the effects of farnesoid X |
Hospices Civils de Lyon |
N/A |
N/A |
|
Genotyping FcɣRs genes |
University Hospital, Strasbourg, France |
N/A |
||
HCURE: Impact of HCV DAAs on antiviral |
Assistance Publique Hopitaux De Marseille |
N/A |
N/A |
|
HEATHER: HIV reservoir targeting with early |
UK CPMS17589 |
University of Oxford/Medical Research |
N/A |
Front Immunol. 2024 |
HIV-PRADA: HIV persistence in lymph node and |
University of Melbourne |
N/A |
Cell Rep Med. 2022 |
|
HIV resistance and treatment strategies |
NIAID |
N/A |
N/A |
|
HIV-STAR: HIV |
University Hospital, Ghent
|
N/A |
Cell Rep. |
|
Host & viral factors associated with HIV |
UK CPMS16146 |
University College London Hospitals NHS |
N/A |
N/A |
HSCT-HIV: Allogeneic hematopoietic stem cell |
Kirby Institute |
N/A |
Terminated by Protocol Steering Committee |
|
ImmunoCo27: Co-adaptation between HIV and CD8 |
Inserm-ANRS |
N/A |
N/A |
|
IMPAACT 2015: Evaluation of the |
IMPAACT |
N/A |
||
Impact of ART adherence on HIV persistence |
University of Colorado, Denver |
N/A |
N/A |
|
Impact of a short-term ATI and |
NIAID |
N/A |
||
In vitro autologous vaccine development to |
UK CPMS17532 (link currently broken) |
Imperial College London/amfAR |
N/A |
N/A |
ISALA: Analytical |
Institute of Tropical Medicine, |
N/A |
Strategies for an HIV |
|
Long-term effects of ART in acute HIV |
Key Laboratory of AIDS Immunology of National |
N/A |
N/A |
|
LoViReT: Low viral reservoir treated patients |
IrsiCaixa |
N/A |
HIV Persistence Workshop 2022, Abstract PP 3.13 |
|
Measurement for viral reservoir and immune |
National Taiwan University Hospital |
N/A |
||
MUCOVIR: Exploration of HIV reservoirs |
Objectif Recherche Vaccins SIDA |
N/A |
||
PembroHIV: Treatment with immunological |
IrsiCaixa |
N/A |
HIV Persistence Workshop 2019, Abstract PP |
|
PITCH: |
NHS Health Research |
University of Oxford |
N/A |
Eur J Immunol. 2024 |
Quantitative measurement and correlates of |
NIAID |
N/A |
EBioMedicine. 105040. |
|
Role of anti-Tat immunity on disease |
National HIV/AIDS Research Center |
N/A |
||
Role of anti-Tat immunity on disease |
CNAIDS, Istituto Superiore di Sanità, Rome, Italy |
N/A |
||
Role of the IL-33/amphiregulin pathway as a |
Inserm-ANRS |
N/A |
||
Seroprevalence of anti-Tat antibodies in |
CNAIDS, Istituto Superiore di Sanità, Rome, Italy |
N/A |
N/A |
|
Size of the HIV-1 reservoir and ongoing |
UK CPMS16004 (link currently broken) |
University College London/amfAR |
N/A |
N/A |
Specimen repository for HIV |
AIDS Healthcare Foundation |
N/A |
N/A |
|
Tissue drug levels of HIV medications |
University of Minnesota – Clinical and |
N/A |
||
ULTRASTOP (Towards |
Objectif Recherche VACcin Sida |
N/A |
||
VIRECT: Impact of pre-ART CD4 T cell level on the |
Centre Hospitalier Universitaire de Saint |
N/A |
N/A |
|
PROTEASOME INHIBITORS |
||||
ixazomib |
Mayo Clinic |
Phase I |
||
STEM CELL TRANSPLANTATION |
||||
HIVECT: HIV |
Puerta de Hierro University |
N/A |
N/A |
|
IMPAACT P1107: Cord |
International Maternal Pediatric |
N/A |
Cell. 2023 Mar |
|
Cord blood transplant with OTS for the |
Fred Hutchinson Cancer Research Center |
Phase II |
Study stopped due to end of |
|
BMT CTN 0903: Allogeneic transplant |
National Heart, Lung, & Blood |
Phase II |
Biol Blood Marrow |
|
HLA-mismatched unrelated donor bone marrow |
Center for International Blood and Marrow |
Phase II |
HRSA Advisory Council |
|
Immune response after stem cell transplant in |
Fred Hutchinson Cancer Research Center |
Phase II |
N/A |
|
Optimized antiretroviral therapy during |
Sidney Kimmel Comprehensive Cancer Center at |
Phase I |
JAIDS 2021 Nov 8. |
|
STIMULANTS |
||||
EMRLHD: Effect of methamphetamine on residual |
University of California, San Francisco |
Phase IV |
N/A |
|
T-CELL RECEPTOR-BASED BISPECIFICS |
||||
IMC-M113V in |
IMC-M113V-101 |
Immunocore |
Phase I/II |
CROI 2023, Abstract 436 |
THERAPEUTIC VACCINES |
||||
AGS-004 |
Argos Therapeutics |
Phase IIb |
||
AGS-004 |
Argos Therapeutics |
Phase IIb |
CROI 2014, Poster abstract 344 |
|
iHIVARNA-01 |
Rob Gruters, Erasmus Medical |
Phase IIa |
||
DermaVir (topically applied DNA vaccine) |
Genetic Immunity |
Phase II |
N/A |
|
DermaVir |
Genetic Immunity |
Phase II
|
N/A |
|
GSK Biologicals HIV Vaccine 732462 (p24-RT-Nef-p17 |
GlaxoSmithKline |
Phase II |
||
GTU-multiHIV + |
Inserm-ANRS |
Phase II
|
J Virol. 2021 May; |
|
Tat protein vaccine |
NCT01513135 |
CNAIDS, Istituto Superiore di Sanità, Rome, Italy |
Phase II |
|
Tat protein vaccine |
NCT00751595 |
Barbara Ensoli, MD, Istituto Superiore di |
Phase II |
Front. Immunol. |
Vacc-4x (peptide-based |
Bionor Immuno AS |
Phase II |
||
Vacc-4x |
Bionor Immuno AS |
Phase II |
||
VAC-3S |
InnaVirVax |
Phase II |
NPJ Vaccines (2019) |
|
VAC-3S |
InnaVirVax |
Phase I/IIa |
N/A |
|
VAC-3S (peptide-based |
InnaVirVax |
Phase I/IIa |
30 Years of HIV Science, 2013, Poster abstract 145 |
|
AGS-004 |
University of North Carolina at Chapel |
Phase I/II |
N/A |
|
Autologous |
Sharon Riddler, University of |
Phase I/II |
||
Dendritic cells |
University of Sao Paulo General Hospital |
Phase I/II |
||
Dendritic cell |
Massachusetts General Hospital |
Phase I/II |
||
Dendritic |
Hospital Clinic of Barcelona |
Phase I/II |
||
DermaVir |
AIDS Clinical Trials Group |
Phase I/II |
||
GTU®-MultiHIV B clade |
Imperial College London |
Phase I/II |
||
p24CE1/2 + p55^gag |
NIAID |
Phase I/II |
||
PENNVAX-GP or |
Steven Deeks, UCSF |
Phase I/II |
HIVR4P 2024, Abstract OA0302 |
|
Tat Oyi (protein-based |
Biosantech |
Phase I/II |
||
THV01 |
Theravectys S.A. |
Phase I/II |
N/A |
|
TUTI-16 (synthetic |
Thymon, LLC |
Phase I/II |
||
Vacc-C5 (peptide-based |
Bionor Immuno AS |
Phase I/II |
||
Ad26.Mos4.HIV + |
Janssen Vaccines & Prevention B.V. |
Phase I |
||
Ad26.Mos.HIV |
Janssen Vaccines & Prevention |
Phase I |
Clin Infect Dis. |
|
AFO-18 (peptide-based |
Statens Serum Institut (SSI)/Ministry of the |
Phase I |
||
AFO-18 (peptide-based |
SSI/Rigshospitalet/Hvidovre University |
Phase I |
||
AT20-KLH |
MED-AT20-001 |
Medestea Research & Production SpA, Turin |
Phase I |
|
ChAdOx1.HTI, |
IrsiCaixa |
Phase I |
N/A |
|
ChAdV63.HIVconsv + MVA.HIVconsv |
IrsiCaixa/Fundació Lluita contra la |
Phase I |
EClinicalMedicine. |
|
Dendritic |
Baylor Research Institute/ANRS |
Phase I |
PLoS Pathog. 2019 |
|
DermaVir |
Genetic Immunity |
Phase I |
||
D-GPE DNA + M-GPE MVA (DNA + viral |
Centers for Disease Control and Prevention, |
Phase I |
N/A |
|
DNA.HTI + |
Fundacio Lluita Contra la SIDA |
Phase I |
N/A |
|
DNA.HTI + |
Aelix Therapeutics |
Phase I |
HIV Persistence Workshop 2022, Abstract OP 8.3 (slides) |
|
HIVAX |
GeneCure Biotechnologies |
Phase I |
Vaccine. |
|
HIV-v (peptide-based |
PepTcell Limited |
Phase I |
||
iHIVARNA-01 (TriMix |
Biomedical Research Institute August Pi i |
Phase I |
||
JS7 DNA + |
GeoVax, Inc. |
Phase I |
||
MAG pDNA vaccine +/- IL-12 |
NIAID |
Phase I |
||
MAG-pDNA + |
NIAID/Profectus Biosciences, Inc. |
Phase I |
J. Virology May 20, |
|
MVA.HIVconsv |
University of Oxford/Medical Research Council |
Phase I |
||
MVA.tHIVconsv3 |
University of North Carolina, Chapel Hill |
Phase I |
||
PENNVAX-B (Gag, Pol, |
Inovio Pharmaceuticals |
Phase I |
||
PENNVAX-B +/- |
University of Pennsylvania |
Phase I |
N/A |
|
Recombinant |
China CDC |
Phase I |
N/A |
|
rMVA-HIV + rFPV-HIV (viral vector |
NIAID |
Phase I |
||
Tat protein vaccine |
NCT00505401 NCT01024595 (extended follow-up |
CNAIDS, Istituto Superiore di Sanità, Rome, Italy |
Phase I
|
Rev Recent Clin Trials. 2009 Sep;4(3):195-204 Vaccine. 2009 May |
TOLL-LIKE RECEPTOR AGONISTS |
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MGN1703 toll-like |
University of Aarhus |
Phase Ib/IIa |
EBioMedicine. 2019 |
|
Poly-ICLC (TLR3 agonist) |
Nina Bhardwaj, MD/Campbell |
Phase I/II |
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vesatolimod (TLR7 |
Gilead Sciences |
Phase Ib |
Front Immunol. CROI 2020, Abstract 40, Webcast |
|
vesatolimod (formerly GS-9620) (TLR7 agonist) |
Gilead Sciences |
Phase Ib |
Eur J Immunol. |
|
vesatolimod |
Gilead Sciences |
Phase I |
Terminated: Sponsor decision to change the |
|
TRADITIONAL CHINESE MEDICINE |
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Triptolide wilfordii |
Peking Union Medical College |
Phase III |
N/A |
|
TREATMENT INTENSIFICATION/EARLY TREATMENT |
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enfuvirtide |
NIAID |
Not listed |
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enfuvirtide |
Canadian Immunodeficiency Research |
Not listed |
N/A |
|
New Era Study: Treatment with |
MUC Research GmbH |
Not listed |
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PLUS: Pilot |
University of California, San Francisco |
Not listed
|
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Anti-HIV medications |
NIAID |
Phase IV |
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Antiretroviral regime for viral eradication |
National Center for Women and Children’s |
Phase IV |
N/A |
|
DIORR: Dolutegravir impact on residual replication |
University of Melbourne |
Phase IV |
CROI 2018, Abstract 71, Webcast |
|
DRONE: Impact of starting a dolutegravir-based |
University Hospital, Strasbourg, France |
Phase IV |
N/A |
|
LEOPARD: Latency |
Columbia University |
Phase IV |
PLoS Pathog. CID, ciab586 |
|
P25-INACTION: |
Adriano Lazzarin, MD |
Phase IV |
IJAA. 64(2):107200. |
|
ANRS 147 OPTIPRIM: Optimization of |
Inserm-ANRS |
Phase III |
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maraviroc |
Germans Trias i Pujol Hospital |
Phase III |
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raltegravir + |
Centre Hospitalier Intercommunal de Toulon La |
Phase III |
N/A |
|
raltegravir |
Germans Trias i Pujol Hospital |
Phase III |
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tenofovir/emtricitabine + dolutegravir |
Inserm/ANRS |
Phase III |
N/A |
|
VIRECURE: Impact of extremely early ART to |
David Garcia Cinca, Hospital Clinic of |
Phase III |
EACS 2019, Abstract PE38/2 |
|
Intense acute infection study |
University of Toronto |
Phase II/III |
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EDIT: Effect of dolutegravir intensification on |
University of Liege |
Phase II |
CROI 2023, Abstract 429 |
|
maraviroc |
Fundación para la Investigación Biomédica del |
Phase II |
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peginterferon alfa-2a (Pegasys) |
Wistar Institute |
Phase II |
EBioMedicine. 2020 Aug 19;59:102945. |
|
peginterferon alfa-2b |
University of Pennsylvania/Wistar |
Phase II |
AIDS Res Hum |
|
peginterferon alfa-2b |
Wistar Institute |
Phase II |
HIV Persistence Workshop 2019, |
|
raltegravir |
Canadian Immunodeficiency Research |
Phase II |
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raltegravir |
Fundación para la Investigación Biomédica del Hospital |
Phase II |
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Viral suppression after analytic |
South East Asia Research |
Phase II |
Clin Infect Dis. |
|
alpha interferon intensification |
NIAID |
Phase I/II |
N/A |
|
indinavir + |
NIAID |
Phase I |
N/A |