Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 4:14 AM
Ignite Modification Date:
2025-12-25 @ 4:14 AM
NCT ID:
NCT02591420
Eligibility Criteria:
Inclusion Criteria:
* Able and willing to complete the informed consent process
* Passes Test of Understanding
* 18 to 50 years of age
* Experiencing early acute HIV-1 infection as defined by blood samples on at least two separate days positive by nucleic acid testing within 21 days of a negative nucleic acid HIV-1 test OR by a positive nucleic acid test or a positive 4th generation enzyme immunoassay (EIA) in the context of a negative 2nd or negative 3rd generation HIV EIA test
* No history of antiretroviral therapy for any indication in the last 30 days.
* In general good health
* Willing to have blood samples collected and stored
* Able to participate for 25 weeks for study visits
* Willing to have photo or fingerprint taken for identification purposes
Female-Specific Criteria:
* Agrees not to become pregnant from the time of study enrollment until the last study visit. If a woman has no history of hysterectomy, tubal ligation or menopause, she must agree to use an effective birth control method: abstinence; male or female condoms; diaphragm or cervical cap with spermicide; intrauterine device; contraceptive hormones delivered by pills, patch, injections, or vaginally; and hormonal implants under the skin; or a male partner who has previously undergone a vasectomy.
* Negative beta-human chorionic gonadotropin (HCG) pregnancy test (urine or serum) on day of enrollment for any woman unless she is post-menopause for 24 consecutive months or has undergone a surgical procedure that precludes pregnancy
Exclusion Criteria:
* Weight less than 46 kg or greater than 115 kg
* Previous receipt of humanized or human monoclonal antibody whether licensed or investigational
* Ongoing AIDS-related opportunistic infection (including oral thrush or active tuberculosis)
* Severe acute retroviral syndrome (as defined in Appendix I of the protocol) or clinical condition (other than HIV infection) constituting an indication for immediate antiretroviral therapy per local country guidelines
* Active injection drug use within previous 12 months
* History of a severe allergic reaction with generalized urticaria, angioedema, or anaphylaxis in the 2 years prior to enrollment
* History of chronic urticaria
* Physical finding on examination considered indicative of significant disease such as murmur (other than functional), hepatosplenomegaly, focal neurological deficit
* Hypertension that is not well controlled by medication
* Positive hepatitis B surface antigen at any time in the past
* History of hepatitis C infection
* Untreated syphilis infection
* Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) greater than 2 times the upper limit of normal (ULN).
* Absolute neutrophil count (ANC) less than 740 cells/mm\^3
* Estimated glomerular filtration rate (GFR) less than 50 ml/min within the past 90 days
* Breastfeeding
* Pregnancy
* Receipt of licensed vaccine or other investigational study agent within 28 days prior to enrollment or past participation in an investigational HIV vaccine study with receipt of active product
* Current or planned participation in another interventional clinical trial during the study period
* Chronic or recurrent use of medications that modify host immune response, e.g., oral or parenteral steroids, cancer chemotherapy
* Any other chronic or clinically significant medical condition that in the opinion of investigator would jeopardize the safety or rights of the volunteer. Including, but not limited to: diabetes mellitus type I, chronic hepatitis, renal failure; OR clinically significant forms of: drug or alcohol abuse, mental illness, severe asthma, autoimmune disease, psychiatric disorders, heart disease, or cancer.
* Study site employee
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
50 Years
Study:
NCT02591420
Study Brief:
Protocol Section:
NCT02591420