A Clinical Trial of Combination HIV-Specific Broadly Neutralizing Monoclonal Antibodies Combined With ART Initiation During Acute HIV Infection to Induce HIV Remission

Inclusion Criteria:

Step 1:

1. Appropriate documentation from medical records of diagnosis of AHI prior toenrollment that includes one of the following:

2. A detectable HIV-1 RNA within 28 days prior to study entry AND a non-reactiveHIV-1 antibody within 7 days prior to entry; OR

3. A detectable HIV-1 RNA or a reactive HIV-1 antibody within 28 days prior tostudy entry AND a negative/indeterminate Western Blot (WB) ornegative/indeterminate Geenius HIV-1/HIV-2 Supplemental Assay within 7 daysprior to entry; OR

4. A documented non-reactive HIV-1 antibody or negative HIV-1 RNA within 90 daysprior to study entry AND a documented reactive HIV-1 antibody or positive WBthat is negative for p31 band or a positive Geenius HIV-1/HIV-2 SupplementalAssay that is negative for p31 band within 7 days prior to entry; OR

5. ARCHITECT or GSCOMBO S/CO ≥10 within 7 days prior to entry AND a non-reactiveHIV-1 antibody within 7 days prior to entry; OR

6. ARCHITECT or GSCOMBO S/CO ≥1 within 7 days prior to entry AND a non-reactiveHIV-1 antibody within 7 days prior to entry AND a known prior S/CO <0.5 within 90 days prior to entry; OR

7. ARCHITECT or GSCOMBO S/CO >0.5 but <10 within 7 days prior to entry AND anon-reactive HIV-1 antibody within 7 days prior to entry AND detectable HIV-1RNA within 7 days prior to entry

8. The following laboratory values obtained within 21 days prior to entry:

• Absolute neutrophil count (ANC) ˃1,000/mm3

• Hemoglobin:

• >10 g/dL for cisgender men and transgender women

• >9 g/dL for cisgender women and transgender men

• Platelet count ˃100,000/mm3

• Estimated glomerular filtration rate (eGFR) ≥50 mL/min/1.73m2 using the ChronicKidney Disease Epidemiology Collaboration (CKD-Epi) equation, withconsideration for lower rates in special circumstances.

• ALT (SGPT) ≤2.5 x ULN

• AST (SGOT) ≤2.5 x ULN

• Total bilirubin <1.5 x ULN

3. For persons who are able to become pregnant, negative urine or serum pregnancy testwithin 24 hours prior to study entry.

4. Persons who are able to become pregnant must agree to use two methods ofcontraception throughout Step 1 if participating in sexual activity that could leadto pregnancy. One contraceptive method must be a highly effective method and thesecond method of contraception must be a barrier method.

5. Participants of reproductive potential who engage in sexual activity that could leadto their partner's becoming pregnant must agree to use a barrier method ofcontraception throughout Step 1.

6. Ability and willingness to use a barrier method or abstinence from sexualintercourse with all partners who are vulnerable to HIV or whose HIV serostatus isunknown in order to prevent HIV transmission during Step 2, Step 3, and until plasmaHIV-1 RNA is less than the limit of detection after ART restart in Step 4.

7. Age ≥18 and ≤70 years.

8. Ability and willingness to initiate ART at enrollment.

9. Ability and willingness to participate in scheduled study visits, including duringthe ATI, per Schedule of Evaluations (SOE).

10. Ability and willingness of participant to provide informed consent.

Step 2:

1. Documented negative hepatitis B virus (HBV) surface antigen (HBsAg) obtained within 16 weeks prior to Step 2 registration.

2. Documented negative hepatitis C virus (HCV) antibody (anti-HCV) or negative HCV RNAPCR obtained within 16 weeks prior to Step 2 registration.

3. Receipt of full doses of study infusions at enrollment (VRC07-523LS + PGT121.414.LSor placebo [Sodium Chloride for Injection USP, 0.9%]).

4. HIV-1 RNA <200 copies/mL obtained within 6 weeks prior to Step 2 registration.

5. CD4+ T-cell count ≥450 cells/mm3 obtained within 6 weeks prior to Step 2registration.

6. For participants who are able to become pregnant, negative serum or urine pregnancytest within 48 hours prior to Step 2 entry.

7. To avoid pregnancy, participants who are able to become pregnant must agree to usecontraception or practice abstinence from sexual activity that could lead topregnancy throughout Step 2.

8. Ability and willingness to use a barrier method or abstinence from sexualintercourse with partners who are vulnerable to HIV or whose HIV serostatus isunknown in order to prevent HIV transmission throughout Step 2.

9. Ability and willingness to interrupt ART.

10. Completion of Step 1.

Step 3:

1. Has not met ART restart criteria.

2. Completion of Step 2.

3. Willing to continue ATI.

4. To avoid pregnancy, participants who are able to become pregnant must agree to usecontraception or practice abstinence from sexual activity that could lead topregnancy throughout Step 3.

5. Ability and willingness to use a barrier method or abstinence from sexualintercourse with all partners who are vulnerable to HIV or whose HIV serostatus isunknown in order to prevent HIV transmission throughout Step 3.

Step 4:

1. Has met any of the ART restart criteria during Step 2 or Step 3. -OR- Has completedStep 3 and is not enrolling to ACTG A5385.

2. To avoid pregnancy, participants who are able to become pregnant must agree to usecontraception or practice abstinence from sexual activity that could lead topregnancy throughout Step 4.

3. Ability and willingness to use a barrier method or abstinence from sexualintercourse with all partners who are vulnerable to HIV or whose HIV serostatus isunknown in order to prevent HIV transmission until plasma HIV-1 RNA is less than thelimit of detection after ART restart.

Exclusion Criteria:

Step 1:

1. Previous receipt of immunoglobulin (IgG) therapy.

2. Previous receipt of humanized or human monoclonal antibody whether licensed orinvestigational (other than for the prevention and/or treatment ofSARS-CoV-2/COVID-19).

3. History of a severe allergic reaction with generalized urticaria, angioedema oranaphylaxis in the 2 years prior to enrollment.

4. History of chronic urticaria requiring daily treatment.

5. Receipt of investigational study agent within 28 days prior to enrollment.

6. Past participation in an investigational study of a candidate HIV vaccine or immuneprophylaxis for HIV-1 infection with receipt of active product or with receipt ofactive product or placebo and remains blinded to what they actually received.

7. Active or recent non-HIV-associated malignancy requiring systemic chemotherapy orsurgery in the preceding 36 months or for whom such therapies are expected in thesubsequent 12 months.

8. Use of any immunomodulatory medications within 6 months of study entry includingsystemic corticosteroids (long-term), immunosuppressants, anti-cancer, interleukins,systemic interferons, systemic chemotherapy, or other medications that the siteinvestigator feels could have an immune modulatory effect.

9. Use of ART for any reason, including pre- or post-exposure prophylaxis, within 60days prior to study entry.

10. Active drug or alcohol use or dependence that, in the opinion of the siteinvestigator, would interfere with adherence to study requirements.

11. Known history of active Hepatitis B or Hepatitis C infection.

12. Any acute, chronic, or recent and clinically significant medical condition that, inthe opinion of the site investigator, would interfere with adherence to studyrequirements or jeopardize the safety or rights of the participant.

13. History of or current clinical atherosclerotic cardiovascular disease (ASCVD) asdefined by 2013 American College of Cardiology (ACC)/American Heart Association (AHA) guidelines, including a previous diagnosis of any of the following:

• Acute myocardial infarction

• Acute coronary syndromes

• Stable or unstable angina

• Coronary or other arterial revascularization

• Stroke

• TIA

• Peripheral arterial disease presumed to be of atherosclerotic origin

14. Currently breastfeeding or pregnant.

15. Weight >115 kg.

16. Use of prohibited medications for bictegravir, emtricitabine, and tenofoviralafenamide (refer to protocol section 5.8) within 7 days prior to entry, or planneduse of prohibited medications during the period of study participation.

17. Absence of adequate venous access for the administration of infusion or forphlebotomy to assess for the primary study endpoint.

Step 2:

1. Viral failure, as defined in protocol section 6.2.4, after Step 1 week 24.

2. Failure to initiate ART in Step 1.

3. Receipt of any non-nucleoside reverse transcriptase inhibitor (NNRTI) or long-actingART (any therapy dosed at an interval less than daily), such as cabotegravir orrilpivirine injections, after Step 1 entry.

4. Receipt of any immunoglobulin therapy or immunomodulatory medications after Step 1entry including systemic corticosteroids (long-term), immunosuppressants,anti-cancer, interleukins, systemic interferons, systemic chemotherapy, or othermedications that the site investigator feels could have an immune modulatory effect.

5. Does not have HIV-1.

6. Participant was in Fiebig stage VI at the time of study entry.

7. Failure by the participant to attend three consecutive Step 1 study visits.

8. Intercurrent illness, new medical diagnosis, laboratory abnormality, sign, orsymptom that, in the opinion of the site investigator, would place participant athigher risk of morbidity during ATI.

9. Pregnancy or breastfeeding.

10. Active drug or alcohol use or dependence that, in the opinion of the siteinvestigator, would interfere with adherence to study requirements.

Step 3:

1. Transfer to A5385 (The Post-Intervention Cohort Study).

2. ART restart in Step 2.

3. Intercurrent illness, new medical diagnosis, laboratory abnormality, sign, orsymptom that, in the opinion of the site investigator, would place participant athigher risk of morbidity during analytic treatment interruption.

4. Active drug or alcohol use or dependence that, in the opinion of the siteinvestigator, would interfere with adherence to study requirements.

Step 4:

1. Unwillingness or inability to restart ART after meeting an ART restart criterion inStep 2 or Step 3.