Early ART to Limit Infection and Establishment of Reservoir

Completed · Phase 2

Conditions studied: HIV-1 Infection

In brief

The study was done to: * Start antiretroviral therapy (ART) early in those recently or acutely infected with HIV-1 * See how starting ART as soon as the infection is found affects the amount of HIV-1 in blood and how well the body fights the HIV-1 infection * Look at the amount of HIV-1 DNA (genetic material for HIV-1) seen in CD4+ T-cells (infection-fighting cells in blood) after 48 weeks of ART * See how early treatment for HIV affects the numbers of HIV-1 infection fighting cells (CD4+ and CD8+ T-cells) in blood

Key facts

Study ID

NCT02859558

Run by

Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections

People needed

195

Starts

2017-01-24

Expected to finish

2025-04-16

Last updated by the study team

2025-08-29

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Appropriate documentation from medical records of diagnosis of acute HIV-1 infection (AHI) within 7 days prior to enrollment, that includes one of the following:
• A detectable HIV-1 RNA within 28 days prior to study entry AND a non-reactive HIV-1 antibody within 7 days prior to entry OR
• A detectable HIV-1 RNA or a reactive HIV-1 antibody within 28 days prior to study entry AND a negative/indeterminate WB or negative/indeterminate Geenius HIV-1/HIV-2 Supplemental Assay within 7 days prior to entry OR
• A documented non-reactive HIV-1 antibody or negative HIV-1 RNA within 90 days prior to study entry AND a documented reactive HIV-1 antibody or positive WB that is negative for p31 band or a positive Geenius HIV-1/HIV-2 Supplemental Assay that is negative for p31 band within 7 days prior to entry OR
• ARCHITECT or GSCOMBO S/CO ≥10 within 7 days prior to entry AND a non-reactive HIV-1 antibody within 7 days prior to entry OR
• ARCHITECT or GSCOMBO S/CO ≥1 within 7 days prior to entry AND a non-reactive HIV-1 antibody within 7 days prior to entry AND a known prior S/CO <0.5 within 90 days prior to entry OR
• ARCHITECT or GSCOMBO S/CO >0.5 but <10 within 7 days prior to entry AND a non-reactive HIV-1 antibody within 7 days prior to entry AND detectable HIV-1 RNA within 7 days prior to entry
• Note A: HIV-1 RNA result must be reported from an FDA-approved or CE-marked assay.
• Note B: Since characterization of Fiebig stage using samples at the time of ART initiation was performed with results known within 12 weeks based on standardized, centralized testing, an estimated Fiebig group at enrollment based on inclusion criteria as shown in the table above will provide additional real-time monitoring for accruals into each study group.
• Ability and willingness of candidate to provide written informed consent.
• Ability and willingness to initiate ART at enrollment.
• Ability and willingness to participate in scheduled study visits for up to 72 weeks.
• Female candidates of reproductive potential who are not pregnant at the time of enrollment and who will receive the study-provided EVG/COBI/FTC/TAF and must agree not to participate in the conception process (ie, active attempt to become pregnant, in vitro fertilization), and if participating in sexual activity that could lead to pregnancy, the female candidate must agree to use at least one reliable form of contraceptive while receiving study-provided treatment.
• Female candidates are considered to be of reproductive potential if any of the following conditions apply:
• Candidate has experienced menarche.
• Candidate has not undergone bilateral tubal ligation, bilateral oophorectomy, or hysterectomy.
• Candidate has not experienced menopause, defined as lack of menstruation within the preceding 12 months.
• Acceptable contraceptive methods include:
• Condoms (male or female) with or without a spermicidal agent
• Diaphragm or cervical cap with spermicide
• Intrauterine device
• Hormonal contraceptive
• Female candidates who are not of reproductive potential or whose male partner(s) has documented azoospermia are not required to use contraceptives. Any statement of self-reported sterility or that of her partner must be entered in the source documents.
• NOTE: Acceptable documentation of lack of reproductive potential is oral or written documentation from the individual.
• Female candidates who are prescribed a non-study-provided ARV regimen should discuss the safety of that regimen during conception and pregnancy with the prescribing physician. Such individuals should follow medical guidance regarding any potential need for contraception while using the non-study-provided ARV regimen.

You may not qualify if…

• Positive HIV-1 antibody test ≥90 days prior to study entry.
• Active drug or alcohol use or dependence that, in the opinion of the site investigator, would interfere with adherence to study requirements.
• Any acute, chronic, or recent and clinically significant medical condition that, in the opinion of the site investigator, would interfere with adherence to study requirements or jeopardize the safety or rights of the participant.
• Receipt of an investigational study agent within 28 days prior to enrollment
• Chronic or recurrent use of medications that modify host immune response, eg, oral or parenteral steroids, cancer chemotherapy.
• AHI diagnosis within 60 days after receiving any investigational ARV or HIV-1 vaccine or immune prophylaxis for HIV-1 infection.
• Use of ARVs for pre- or post-exposure prophylaxis within 60 days prior to the diagnosis of AHI.

Where it is running

• 31788 Alabama CRS — Birmingham, Alabama, United States
• Ucsd, Avrc Crs (701) — San Diego, California, United States
• Harbor-UCLA Med. Ctr. CRS (603) — Torrance, California, United States
• Whitman Walker Health CRS (31791) — Washington D.C., District of Columbia, United States
• The Ponce de Leon Center CRS (5802) — Atlanta, Georgia, United States
• Northwestern University CRS (2701) — Chicago, Illinois, United States
• Rush Univ. Med. Ctr. ACTG CRS (2702) — Chicago, Illinois, United States
• Massachusetts General Hospital ACTG CRS (101) — Boston, Massachusetts, United States
• Brigham and Women's Hosp. ACTG CRS (107) — Boston, Massachusetts, United States
• Washington University CRS (2101) — St Louis, Missouri, United States
• 31786 New Jersey Medical School Clinical Research Center CRS — Newark, New Jersey, United States
• 7804 Weill Cornell Chelsea CRS — New York, New York, United States
• Columbia Physicians and Surgeons CRS (30329) — New York, New York, United States
• 3201 Chapel Hill CRS — Chapel Hill, North Carolina, United States
• Greensboro CRS (3203) — Greensboro, North Carolina, United States
• Univ. of Cincinnati CRS (2401) — Cincinnati, Ohio, United States
• The Ohio State Univ. AIDS CRS (2301) — Columbus, Ohio, United States
• 6201 Penn Therapeutics CRS — Philadelphia, Pennsylvania, United States
• Pittsburgh CRS (1001) — Pittsburgh, Pennsylvania, United States
• The Miriam Hosp. ACTG CRS (2951) — Providence, Rhode Island, United States
• 31443 Trinity Health and Wellness Center CRS — Dallas, Texas, United States
• 31473 Houston AIDS Research Team (HART) CRS — Houston, Texas, United States
• University of Washington AIDS CRS (1401) — Seattle, Washington, United States
• Hospital Nossa Senhora da Conceicao CRS (12201) — Porto Alegre, Rio Grande do Sul, Brazil
• Instituto de Pesquisa Clinica Evandro Chagas (12101) — Rio de Janeiro, Brazil

Full record on ClinicalTrials.gov

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