A Phase 1 interventional study of VRC07-523LS and PGDM1400LS in HIV Infections, PLWH and ART, sponsored by Henry M. Jackson Foundation for the Advancement of Military Medicine. Recruiting at 1 site in Thailand. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2026-09-04.
Sponsored by Henry M. Jackson Foundation for the Advancement of Military Medicine · Phase 1, Interventional, and Treatment
This is a phase I, randomized, double-blind, placebo-controlled clinical trial to investigate the safety of VRC07-523LS and PGDM1400LS in combination with ChAdOx1.tHIVconsv1, ChAdOx1.HIVconsv62 prime, MVA.tHIVconsv4 and A244d11gp120/ALFQ vaccination, and the impact on viral load setpoint during analytic treatment interruption (ATI) in people living with human immunodeficiency virus-1 (HIV-1, PLWH) who have initiated or will initiate antiretroviral therapy (ART) during acute HIV-1 infection (AHI).
This is a phase I, randomized, double-blinded, placebo-controlled clinical trial to investigate the safety of VRC07-523LS and PGDM1400LS in combination with ChAdOx1.tHIVconsv1, ChAdOx1.tHIVconsv62, MVA.tHIVconsv4 and A244d11 gp120/ALFQ vaccination, and the impact on viral load setpoint during ATI in PLWH who initiated ART during AHI.
To evaluate the primary objectives, the study will enroll up to 40 adults already enrolled in the RV 254/WRAIR #1494 study who initiated ART during Fiebig I-V acute HIV-1 infection, with plasma HIV-1 RNA \< 50 copies/mL for ≥ 48 weeks, CD4 T-cell counts ≥ 400 cells/mm3, viruses susceptible to VRC07-523LS and/or PGDM1400LS, and the absence of known protective HLA allele (Groups 1 and 2).
Participants currently on ART who meet study entry criteria will be randomized (Section 6.2) in a 1:1 allocation to the Active (Group 1) or Comparator (Group 2) Arms prior to entering Step 1.
To evaluate exploratory objectives, the study will also enroll up to 8 adults who are newly enrolled in the RV 254/WRAIR #1494 study, diagnosed during Fiebig I-V AHI, and have not yet initiated ART (Group 3).
Inclusion/Exclusion Step 1 Inclusion Criteria (Groups 1 and 2 only)
Participants are eligible to be included in the protocol Step 1 only if all of the following criteria are met:
Currently on integrase inhibitor-based ART regimen (excluding long-acting injectable regimens) and no recent (≤8 weeks prior to screening) changes to ART regimen.
a. There must be at least one documented plasma HIV-1 RNA \<50 cps/mL after the last ART change prior to complete study screening
Must be medically stable as confirmed by medical history, physical examination, vital signs, and clinical laboratory tests performed at screening, and as per the Investigator's discretion.
a. If the results of the screening laboratory panel are outside the normal reference ranges, the participant may be included only if the Investigator judges the abnormalities or deviations from normal to be not clinically significant or to be appropriate and reasonable for the population under study after discussion with the Sponsor's Representative.
The following laboratory values at screening:
HIV-1 RNA \<50 copies/ml for ≥48 weeks at screening.
Participants who meet any of the following criteria will be excluded from the study:
Presence of HLA B*57:01 allele associated with viral control.
a) Note: test results derived from RV 254 data
Step 2 Inclusion Criteria (Group 3 only)
Group 3 will enter the study in Step 2. Participants are eligible to be included in the Group 3 protocol Step 2 only if all of the following criteria are met:
The following laboratory values at screening:
Experiencing early acute HIV-1 infection as defined by
Step 2 Exclusion Criteria (Group 3 only)
Participants who meet any of the following criteria will be excluded from the study for Group 3:
Presence of HLA B*57:01 allele associated with viral control.
a) Note: test result derived from RV 254 data
Step 3 (ATI) Inclusion Criteria (All Groups) Step 3 will begin after the third and final vaccine (or placebo) administration (end of Step 2). Participant clinical status or laboratory tests may potentially change during Steps 1 and 2. To ensure that participants continue to meet safety criteria for proceeding to ATI, they will be screened (to include all required screening laboratory tests) for Step 3 inclusion criteria at the visit for the third and final vaccine/placebo dose (Last Step 2 visit): Step 2, Week 20 for Groups 1 and 2; Step 2, Week 28 for Group 3.
Participants enrolled in all Groups of the study may proceed with Step 3 if they meet all the following inclusion criteria:
Step 3 (ATI) Exclusion Criteria (All Groups)
Enrolled participants who meet any of the following criteria will be excluded from moving to Step 3:
Active Arm (Group 1) will have 20 participants. For the primary objectives and endpoints, this study will enroll participants of the RV 254/WRAIR #1494 study, who are PLWH aged 18 - 60 years, initiated ART during Fiebig I-V AHI, are virologically suppressed (HIV-1 RNA \< 50 copies/mL for ≥ 48 weeks) on uninterrupted ART, and who meet study inclusion criteria into Groups 1 and 2. For Active Arm: Group 1 will receive: i. VRC07-523LS and PGDM1400LS at Step 2, Week 0 ii. ART starting at Step 2, Week 1 iii. ChAdOx1.tHIVconsv1 and ChAdOx1.HIVconsv62 vaccination at Step 2, Week 4 iv. MVA.tHIVconsv4 and A244d11 gp120/ALFQ vaccination at Step 2, Weeks 12 and 20
Biological: VRC07-523LS · Biological: PGDM1400LS · Biological: ChAdOx1.tHIVconsv1 · Biological: ChAdOx1.HIVconsv62 · Biological: MVA.tHIVconsv4 · Biological: A244d11 gp120 · Biological: ALFQ
Comparator Arm (Group 2) will have 20 participants. For the primary objectives and endpoints, this study will enroll participants of the RV 254/WRAIR #1494 study, who are PLWH aged 18 - 60 years, initiated ART during Fiebig I-V AHI, are virologically suppressed (HIV-1 RNA \< 50 copies/mL for ≥ 48 weeks) on uninterrupted ART, and who meet study inclusion criteria into Groups 1 and 2. For Comparator Arm - Group 2 will receive: i. VRC07-523LS and PGDM1400LS at Step 2, Week 0 ii. ART starting at Step 2, Week 1 iii. Placebo vaccination at Step 2, Weeks 4, 12 and 20
Biological: VRC07-523LS · Biological: PGDM1400LS · Other: Placebo
Exploratory Arm (Group 3) will have 8 participants. This study will also enroll an Exploratory arm of newly enrolled participants of the RV 254/ WRAIR #1494 study, who are PLWH aged 18 - 60 years, diagnosed during Fiebig I-V AHI, have not yet initiated ART, and meet all study inclusion criteria into Group 3. For the Exploratory Arm - Group 3 will receive: iv. VRC07-523LS and PGDM1400LS at Step 2, Week 0 v. ART starting at Step 2, Week 0 vi. ChAdOx1.tHIVconsv1 and ChAdOx1.HIVconsv62 vaccination at Step 2, Week 12 vii. MVA.tHIVconsv4 and A244d11 gp120/ALFQ vaccination at Step 2, Weeks 20 and 28
Biological: VRC07-523LS · Biological: PGDM1400LS · Biological: ChAdOx1.tHIVconsv1 · Biological: ChAdOx1.HIVconsv62 · Biological: MVA.tHIVconsv4 · Biological: A244d11 gp120 · Biological: ALFQ
VRC07-523LS (VRC-HIVMAB075-00-AB) is a recombinant human immunoglobulin G1 (IgG1) broadly neutralizing monoclonal antibody (bNAb) directed against the HIV-1 CD4 binding site
PGDM1400LS is a recombinant human IgG1 bNAb targeted against the HIV-1 V2 apex epitope region.
ChAdOx1.tHIVconsv1 is a replication-deficient virus expressing six conserved sub-protein regions of Gag and Pol (regions 1-6) of HIV-1 as one chimeric protein designated HIVconsv1.
ChAdOx1.HIVconsv62 is a replication-deficient virus expressing six conserved sub-protein regions of Gag and Pol (regions 1-6) of HIV-1 as one chimeric protein designated HIVconsv62.
MVA.tHIVconsv4 is a recombinant, non-replicating Modified Vaccinia Ankara (MVA) virus expressing six conserved sub-protein regions of Gag and Pol (regions 1-6) of HIV-1 as one chimeric protein designated tHIVconsv4.
A244d11 gp120, consists of the gp120 envelope glycoprotein HIV-1 subtype CRF\_01AE A244 derived from the CM244 CRF\_01AE strain, with an 11 amino N-terminal deletion. It is a modification of the A244 rgp120 immunogen from the AIDSVAX®B/E vaccine.
ALFQ (Army Liposome Formulation, ALF) is a liposomal adjuvant containing a synthetic
Normal saline (0.9% sodium chloride for injection) will be used as a placebo.
To evaluate the safety of VRC07-523LS and PGDM1400LS in combination with ChAdOx1.tHIVconsv1, ChAdOx1.HIVconsv62, MVA.tHIVconsv4 and A244d11 gp120/ALFQ vaccination in PLWH who initiated ART during AHI.
Occurrence of ≥ grade 3 AE or SAE that are possibly, probably, or definitely related to the IPs during the study
Time frame: Measured from enrollment to a minimum of 50 weeks to a maximum of 100 weeks per participant
To evaluate the impact of VRC07-523LS and PGDM1400LS in combination with ChAdOx1.tHIVconsv1, ChAdOx1.HIVconsv62, MVA.tHIVconsv4 and A244d11 gp120/ALFQ vaccination on viral load setpoint after viral rebound during ATI.
Viral Load setpoint after 2 weeks post viral rebound during ATI.
Time frame: Measured for 50 weeks from entry into step 3 (treatment interruption and last mAb administration)
To evaluate the impact of VRC07-523LS and PGDM1400LS in combination with ChAdOx1.tHIVconsv1, ChAdOx1.HIVconsv62, MVA.tHIVconsv4 and A244d11 gp120/ALFQ vaccination on time to first documented HIV-1 RNA viral rebound of ≥50 copies/mL following ATI.
Time (days) from ATI to first documented HIV-1 RNA viral rebound of ≥50 copies/mL
Time frame: Measured for 50 weeks from entry into step 3 (treatment interruption and last mAb administration)
To evaluate the impact of VRC07-523LS and PGDM1400LS in combination with ChAdOx1.tHIVconsv1, ChAdOx1.HIVconsv62, MVA.tHIVconsv4 and A244d11 gp120/ALFQ vaccination on time to first documented HIV-1 RNA viral rebound of ≥1000 copies/mL following ATI.
Time (days) from ATI to first documented HIV-1 RNA viral rebound of ≥1000 copies/mL
Time frame: Measured for 50 weeks from entry into step 3 (treatment interruption and last mAb administration)
To evaluate the impact of VRC07-523LS and PGDM1400LS in combination with ChAdOx1.tHIVconsv1, ChAdOx1.HIVconsv62, MVA.tHIVconsv4 and A244d11 gp120/ALFQ vaccination on viral rebound dynamics during ATI.
Peak viral load, nadir viral load, and viral load area under the curve (AUC) during the first 8 weeks after viral rebound.
Time frame: Measured for 50 weeks from entry into step 3 (treatment interruption and last mAb administration)
To evaluate the impact of VRC07-523LS and PGDM1400LS in combination with ChAdOx1.tHIVconsv1, ChAdOx1.HIVconsv62, MVA.tHIVconsv4 and A244d11 gp120/ALFQ vaccination on the number of participants with plasma HIV-1 RNA < 1000 copies/mL at 12 and 24 weeks of
The number of participants with plasma HIV-1 RNA \< 1000 copies/mL at 12 and 24 weeks of ATI.
Time frame: Measured for 50 weeks from entry into step 3 (treatment interruption and last mAb administration)
To evaluate the impact of VRC07-523LS and PGDM1400LS in combination with ChAdOx1.tHIVconsv1, ChAdOx1.HIVconsv62, MVA.tHIVconsv4 and A244d11 gp120/ALFQ vaccination on time to ART resumption for an HIV-related (virologic, immunologic, or clinical) reason d
Time (days) from ATI to ART resumption during Step 3
Time frame: i. Measured for 50 weeks from entry into step 3 (treatment interruption and last mAb administration)
To measure the effects of VRC07-523LS and PGDM1400LS in combination with ChAdOx1.tHIVconsv1, ChAdOx1.HIVconsv62, MVA.tHIVconsv4 and A244d11 gp120/ALFQ vaccination on HIV-1 RNA levels while on ART.
HIV-1 RNA levels using single copy assay while on ART
Time frame: Measured for 50 weeks from entry into step 3 (treatment interruption and last mAb administration)
To assess the impact of VRC07-523LS and PGDM1400LS in combination with ChAdOx1.tHIVconsv1, ChAdOx1.HIVconsv62, MVA.tHIVconsv4 and A244d11 gp120/ALFQ vaccination on total HIV-1 DNA levels prior to ATI
Total HIV-1 DNA levels prior to ATI.
Time frame: Measured for 50 weeks from entry into step 3 (treatment interruption and last mAb administration)
To assess the effects of VRC07-523LS and PGDM1400LS in combination with ChAdOx1.tHIVconsv1, ChAdOx1.HIVconsv62, MVA.tHIVconsv4 and A244d11 gp120/ALFQ vaccination on HIV-1 specific cellular immune responses prior to ATI.
Magnitude, breadth, cytokine production, cytotoxicity, proliferation and related functions of HIV-1 specific CD4 and CD8 T-cells prior to ATI.
Time frame: Measure during step 2: from the initial administration of bNab therapy through week 22 in arms 1 and 2 and through week 30 in arm 3.
To assess the effects of VRC07-523LS andPGDM1400LSin combination withChAdOx1.tHIVconsv1, ChAdOx1.HIVconsv62,MVA.tHIVconsv4 and A244d11 gp120/ALFQvaccination on HIV-1 specific humoral immuneresponses.
Binding antibodies to HIV-1, ADCC, ADCP andother functional ab-mediated responses prior toATI.
Time frame: Measure at week 0 of Step 3 in all groups, just prior to ATI.
To assess the impact of VRC07-523LS andPGDM1400LS in combination withChAdOx1.tHIVconsv1, ChAdOx1.HIVconsv62,MVA.tHIVconsv4 and A244d11 gp120/ALFQvaccination on the HIV-1 reservoir prior to ATI
Measurements of HIV-1 reservoir using assaysbased on contemporary literature that may includebut are not limited to total and/or intact HIV-1DNA, quantitative infectious virus outgrowth(qVOA), cell- associated HIV-1 RNA, and relatedassays prior to ATI.
Time frame: Measure at week 0 of Step 3 in all groups, just prior to ATI.
To characterize the pharmacokinetics of VRC07-523LS and PGDM1400LS.
Levels of VRC07-523LS and PGDM1400LS
Time frame: Measure at week 0 of Step 3 in all groups, just prior to ATI.
To describe the neurological, neuroimaging andneuro-cognitive effects that occur after receiptof VRC07-523LS and PGDM1400LS incombination with ChAdOx1.tHIVconsv1,ChAdOx1.HIVconsv62, MVA.tHIVconsv4 andA244d11 gp120/ALFQ vaccination and ATI
Findings on CSF examination, MRI/MRS,neurological and neurocognitive testing before andafter receipt of study products and ATI
Time frame: Measure at week 0 of Step 3 in all groups, just prior to ATI.
To assess the effects of VRC07-523LS and PGDM1400LSin combination with ChAdOx1.tHIVconsv1, ChAdOx1.HIVconsv62, MVA.tHIVconsv4 and A244d11 gp120/ALFQ vaccination on HIV-1 specific humoral immune responses.
Measure Antibody Dependent Cellular Phagocytosis using clade AE protein coated target cells
Time frame: Measure at week 0 of Step 3 in all groups, just prior to ATI.
To assess the impact of VRC07-523LS and PGDM1400LS in combination with ChAdOx1.tHIVconsv1, ChAdOx1.HIVconsv62, MVA.tHIVconsv4 and A244d11 gp120/ALFQ vaccination on the HIV-1 reservoir prior to ATI
Total HIV intact DNA measured by the Intact Proviral DNA Assay
Time frame: Measure at week 0 of Step 3 in all groups, just prior to ATI.
To assess the impact of VRC07-523LS and PGDM1400LS in combination with ChAdOx1.tHIVconsv1, ChAdOx1.HIVconsv62, MVA.tHIVconsv4 and A244d11 gp120/ALFQ vaccination on the HIV-1 reservoir prior to ATI
Total HIV cell associate RNA measured by the quantitative RNA PCR
Time frame: Measure at week 0 of Step 3 in all groups, just prior to ATI.
To characterize the pharmacokinetics of VRC07-523LS and PGDM1400LS.
Concentration of PGDM1400LS during ATI by MSD
Time frame: Measured for 50 weeks from entry into step 3 (treatment interruption and last mAb administration)
To assess the impact of VRC07-523LS andPGDM1400LS in combination withChAdOx1.tHIVconsv1, ChAdOx1.HIVconsv62,MVA.tHIVconsv4 and A244d11 gp120/ALFQvaccination on the HIV reservoir when started at thetime of AHI and ART initiation
Measurements of HIV-1 reservoir using assaysbased on contemporary literature that may includebut are not limited to total and/or intact HIV-1DNA, quantitative infectious virus outgrowth(qVOA), cell- associated HIV-1 RNA, and relatedassays prior to and following ATI
Time frame: Measure at week 0 of Step 3 in all groups, just prior to ATI.
To assess the development of anti- drug antibody toVRC07-523LS and PGDM1400LS.
Levels of ADA to VRC07-523LS andPGDM1400LS.
Time frame: Measure at week 0 of Step 3 in all groups, just prior to ATI.
To evaluate baseline ChAdOx1 and ModifiedVaccinia Ankara (MVA) serostatus and its effects onimmune response and primary outcomes.
ChAdOx1 nAbs titer at baseline and Vaccinia-virus-specific nAbs titer at baseline.
Time frame: Measure at week 0 of Step 3 in all groups, just prior to ATI.
To characterize participant experiences in the trialand preferences about participation in HIV remissiontrials with treatment interruptions
Responses to study participation questionnaires and pilot discrete choice experiment survey
Time frame: Measured for 50 weeks from entry into step 3 (treatment interruption and last mAb administration)
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Henry M. Jackson Foundation for the Advancement of Military Medicine