Camu Camu in ART-treated People Living with HIV

3.2 Inclusion Criteria

Participants will be eligible for the study if they meet the following criteria:

• Male or female adults ≥18 years of age.
• Documented HIV-1 infection by Western Blot, Enzyme Immuno Assay (EIA) or viral load assay.
• On any ART for at least 2 years, with viremia less than 50 copies/ml during the last two years (occasional blips allowed).
• On a stable ART regimen (same prescription) for at least 3 months.
• CD4 count >200 and a CD4/CD8 ratio <1 suggesting an increase in inflammation and risk for non-AIDS events.
• Able to communicate adequately in either French or English.
• Able and willing to provide written informed consent prior to screening.
• Women of childbearing potential must have a negative serum pregnancy test.
• Women of childbearing potential must agree to use one of the following approved methods of birth control while in the study and until 2 weeks after completion:

• Complete abstinence from penile-vaginal intercourse from the screening period until two weeks after the study completion.
• Double barrier methods (acceptable barrier methods include diaphragm, coil, contraceptive foam, sponge with spermicide, condom); or
• Oral, injectable or implant contraceptives plus one barrier method;
• Intrauterine device (IUD) plus one barrier method; or
• Male partner sterilization confirmed prior to the female participant's entry into the study; this male is the sole partner for that participant.
• Approved hormonal contraception, started at least 30 days before screening.
• Another method approved by the trial physician with published data showing that the expected failure rate is <1% per year preferably with condom.

Any contraception method must be used consistently, in accordance with the approved product label, and for the duration of the study until two weeks after study completion.

• Women of non-child-bearing potential as defined as either post-menopausal (12 months of spontaneous amenorrhea and ≥ 45 years of age) or physically incapable of becoming pregnant with documented tubal ligation, hysterectomy or bilateral oophorectomy.
• Sexually active men with a female partner of childbearing potential must agree to one of the following methods of birth control:

• The use at least one barrier method of contraception (e.g. condom) with a female partner using a second approved method of contraception (IUD, hormonal contraceptive pill, diaphragm, spermicide etc.) during the study and until two weeks after study completion.
• Be confirmed sterile.
• Have had a successful vasectomy.

Exclusion criteria

Participants are not eligible to participate in the study if they meet any of the following conditions:

• Known allergy/hypersensitivity to Camu Camu.
• Current AIDS-related event or serious health condition including systemic infections in the last 3 months.
• Severe systemic diseases (e.g. uncontrolled hypertension, chronic renal failure), or active uncontrolled infections.
• Co-infection with active Hepatitis B or C Virus.
• Current use or have used in the past 3 months: immune-modulatory agents/chemotherapeutics, prophylactic antibiotics35/antibiotics, proton pump inhibitors, phosphate binders, Metformin or Morphine as these drugs can interact with vitamin C or modulate gut microbiota.
• Diagnosis of diabetes mellitus (HbA1c≥6.5%) as defined by the Canadian Clinical Practice Guidelines for the Prevention and Management of Diabetes42.
• Frequent use of polyphenol-rich prebiotics (e.g. cranberry and CC powders and/or capsules) in the last 12 months.
• Statin or other anti-cholesterol treatment use in the last 3 months.
• Recent changes in dietary habits, intermittent fasting, chronic constipation or laxative use as these can affect gut microbiota.
• Psychiatric or cognitive disturbance or any illness that could preclude compliance with the study.
• Current participation in an experimental therapy study or receipt of experimental therapy within the last 6 months.
• Women who are pregnant, planning to become pregnant, or breast-feeding.
• A score of higher than 8 on a Full AUDIT questionnaire (See Appendix 1) at the screening visit, suggesting an alcohol abuse problem.