Pre-exposure Prophylaxis (PrEP) Adherence Enhancement Guided by iTAB and Drug Levels for Women

Completed · Phase 4

Conditions studied: HIV Prevention

In brief

The purpose of this study is to test a program that uses drug level monitoring, text messaging ("iTAB") and personalized counseling with HIV prevention services, including PrEP (medicine that can help prevent HIV infection when taken daily).

Key facts

Study ID

NCT02584140

Run by

University of California, Los Angeles

People needed

136

Starts

2016-05-01

Expected to finish

2019-06-14

Last updated by the study team

2021-07-08

Who can join

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

You may qualify if…

• Female at birth and identifies as female gender
• Age 18 years or older
• Able to understand and provide consent in English or Spanish
• HIV negative by 4th generation test (Ag/Ab test) or combination of enzymeimmunoassay (EIA) and HIV RNA
• Creatinine clearance ≥ 60 ml/min (via Cockcroft-Gault formula)
• At-Risk Criteria (at least one):
• Condomless sex in the last 3 months with one or more male partners of unknown HIV status known to be at substantial risk of HIV infection (IDU, bisexual, sex for goods, recently incarcerated, from a country with HIV prevalence >1%, interpersonal Partner Violence);
• STI (rectal or vaginal gonorrhea or syphilis) diagnosis during the last 6 months.
• Previous post-exposure prophylaxis (PEP) use during the last 12 months.
• Has at least one HIV-infected sexual partner for ≥4 weeks.
• Sex for exchange of money, goods or services

You may not qualify if…

• Pregnancy at enrollment.
• Any condition, which in the opinion of the provider, will seriously compromise the participant's ability to comply with the protocol, including adherence to PrEP medication dosing, such as active, untreated or unstable major mental illness (i.e. untreated psychotic disorder).
• Use of prohibited medications, in particular, agents known to be nephrotoxic or drugs slow in renal excretion.
• Previous participation in an HIV vaccine trial. Participants that were documented to have received only placebo are not excluded.
• Signs or symptoms suspicious for Primary HIV Infection (PHI).

Where it is running

• APLA Health & Wellness' Gleicher / Chen Health Center — Los Angeles, California, United States
• Los Angeles Biomedical Research Institute at Harbor-UCLA — Los Angeles, California, United States
• USC 5P21 Rand Schrader Clinic — Los Angeles, California, United States
• T.H.E. at Ruth Temple — Los Angeles, California, United States
• UCSD Antiviral Research Center — San Diego, California, United States

Full record on ClinicalTrials.gov

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