| Criteria: |
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Inclusion Criteria
- Healthy males and females, as assessed by a medical history, physical exam, and
laboratory tests
- Willing to comply with the protocol and follow up for the planned duration of the
study (screening plus 18 months)
- In the opinion of the PI or designee, has understood the information provided.
Written informed consent needs to be given before any study-related procedures are
performed
- Amenable to HIV risk reduction counseling, committed to maintaining behavior
consistent with low risk of HIV exposure through the last required visit, and willing
to continue 5 yrs of annual follow-up contact
- Demonstrates understanding (assessment of understanding will be performed) of the
risk for harm observed in the STEP Study results
- Assessed by the clinic staff as being at "low risk" for HIV infection on the basis of
sexual behaviors within the 12 months prior to enrolment defined as follows:
- Sexually abstinent OR
- Had two or fewer mutually monogamous relationships with partners believed to be
HIV-uninfected and who did not use illicit drugs ( methamphetamines (crystal meth),
heroin, cocaine, including crack cocaine or chronic marijuana abuse) OR
- Had two or fewer partners believed to be HIV-uninfected and who did not use illicit
drugs (methamphetamines (crystal meth), heroin, cocaine, including crack cocaine or
chronic marijuana abuse), and with whom he/she regularly used condoms for vaginal and
anal intercourse
- Willing to undergo HIV Testing, HIV counseling and receive HIV Test results
- If sexually active female, using an effective method of contraception (hormonal
contraceptive; diaphragm; Intra Uterine Device (IUD); condoms; anatomical sterility
in self or partner) from screening until at least 4 months after last vaccination.
All female volunteers must be willing to undergo urine pregnancy tests at time points
as indicated in the Schedule of Procedures
- If sexually active male, willing to use an effective method of contraception (such as
condoms, anatomical sterility) from screening until 4 months after the last
vaccination
Exclusion Criteria
- Confirmed HIV-1 or HIV-2 infection
- Detection of Ad35-specific serum neutralizing antibody
- Reported high-risk behavior for HIV infection defined as:
- Within 12 months before vaccination, the volunteer has:
- Had unprotected vaginal or anal sex with a known HIV infected person or a casual
partner (i.e. no continuing established relationship)
- Engaged in sex work for money or drugs.
- Excessive daily alcohol use or frequent binge drinking or chronic marijuana use
or use of other illicit drugs.
- Recently acquired a sexually transmitted disease (STD) including syphilis,
gonorrhoea, non-gonococcal urethritis, Trichomonas vaginalis, symptomatic Herpes
genitalis (HSV-2), chlamydia, pelvic inflammatory disease (PID), mucopurulent
cervicitis, epididymitis, proctitis, lymphogranuloma venereum, chancroid, or
hepatitis B).
- Has a high-risk partner either currently or had such a partner within the
previous 12 months.
- Any clinically significant abnormality on history or examination, including history
of immunodeficiency or autoimmune disease; use of systemic corticosteroids (the use
of topical steroids and inhaled steroids for sinus decongestion are permitted),
immunosuppressive, antiviral, anticancer, anti-tuberculosis, or other medications
considered significant by the investigator within the previous 6 months;
- Any clinically significant acute or chronic medical condition that is considered
progressive or, in the opinion of the investigator, would make the volunteer
unsuitable for the study.
Any of the following abnormal laboratory parameters
- Hemoglobin <11.0 g/dL for women and <12.5 g/dL for men
- Absolute Neutrophil Count (ANL): ≤ 999/mm3
- Absolute Lymphocyte Count (ALC): ≤ 500/mm3
- Platelets: ≤ 90,000 ≥ 550,000/mm3
- Creatinine: >1.1 ULN
- AST: >1.25 x ULN
- ALT: >1.25 x ULN
- Urinalysis 2+ by urine dipstick
- Blood (not due to menses);
- Protein
- Leucocytes
- Confirmed diagnosis of hepatitis B (surface antigen HbsAg), hepatitis C (HCV
antibodies), or active syphilis
- If female, pregnant or planning a pregnancy within 4 months after last vaccination;
or lactating
- Receipt of live attenuated vaccine within the previous 60 days (live attenuated flu
vaccine within 14 days) or planned receipt within 60 days after vaccination with
Investigational Product or receipt of other vaccine within the previous 14 days or
planned receipt within 14 days after vaccination with Investigational Product
- Receipt of blood transfusion or blood products within the previous 6 months
- Participation in another clinical study of an investigational product currently,
within the previous 3 months or expected participation during this study
- Receipt of another investigational HIV vaccine candidate at any time
- History of severe or very severe local or systemic reactogenicity to vaccines or
history of severe allergic reactions
- Major psychiatric illness, including any history of schizophrenia or severe
psychosis, bipolar disorder requiring therapy, suicidal attempt or ideation in the
previous 3 yrs
- Unwilling to forgo donations of blood, sperm, eggs, bone marrow or organs during the
study
- Asplenia: any condition resulting in the absence of a spleen |