Demonstration Project of PrEP Among Female Sex Workers in Dakar, Senegal

STUDY DESIGN This is a two-phase study, consisting of the following:

PHASE I - The feasibility evaluation for this study will take several forms.

• Observations - Field-based assessment of service delivery at each of the five sites;
• In-depth interviews - With policymakers, program managers, and service providers, as well as other community members and leaders; and
• Focus groups with registered and unregistered female sex workers (FSW). PHASE II - This will be a prospective demonstration study of oral pre-exposure prophylaxis (PrEP) with Emtricitabine/Tenofovir Disoproxil Fumarate (FTC/TDF) for FSW with 12 months of follow up and a 3-month accrual period. A total of 267 FSW will be enrolled.

OBJECTIVES

Primary Objectives:

• Build a sustainable HIV PrEP program for FSW in Dakar, Senegal.
• Demonstrate the feasibility of providing daily oral PrEP with FTC/TDF for 12 months to FSW at Ministry of Health (MoH)-run clinics in Pikine, Mbao, Rufisque and Diamniadio Health Centers) in Dakar.

POPULATION & SAMPLE SIZE

PHASE I:

• 10 Key Informants: Policymakers, program managers, and service providers, as well as other community members and leaders.
• Focus Group Participants: 8 Registered and 8 Unregistered HIV-negative FSW age 18 or older.

PHASE II:

• 267 HIV-negative FSW age 18 or older recruited from four public health centers in Dakar: Pikine, Mbao, Rufisque and Diamniadio Health Centers.

PROTOCOL EVALUATIONS

• PHASE I: Qualitative data from observations, key informant interviews, and focus groups will be collected, analyzed and used to inform the implementation of Phase II.
• PHASE II: Quantitative data will be collected using behavioral measures and clinical and laboratory evaluations. Data from electronic monitoring will also be collected.

STUDY DURATION 24 months

REGIMEN Daily oral PrEP with FTC/TDF for 12 months

Inclusion criteria

• • Completion of the written informed consent process prior to undergoing any screening evaluations

• ≥ 18 years and older
• Active sex work (Paid sex within the past six months)
• In general good health, confirmed by medical history and physical examination
• Has laboratory evidence of absence of HIV infection, defined as a negative 4th generation HIV ELISA test prior to enrollment
• Serum creatinine less than or equal to the upper limit of normal (ULN) and calculated creatinine clearance of at least 70 mL/minute by Cockcroft-Gault formula
• Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) less than 2.5 times ULN
• Hemoglobin greater than 8.5 g/dL
• Does not report intention to relocate out of the study area during the course of the study
• If able to become pregnant, self-reported use of an effective method of contraception at enrollment, and intending to use an effective method during the follow-up period
• Without signs or symptoms of acute HIV infection (acute retroviral syndrome)

Exclusion criteria

• • HIV-1 and HIV-2 screening tests are reactive

• Is enrolled in any other clinical product trial
• Serious and active medical condition
• Proteinuria 2+ or greater at screening
• Glucosuria 2+ or greater at screening
• Use of disallowed medications (*See note below)
• Presence of active serious psychiatric symptoms (e.g., active hallucinations, suicidal, homicidal, or exhibiting violent behavior) at the time of consent
• Intoxicated or under the influence of alcohol or other drugs at the time of screening
• Pregnant females and females who are breast-feeding
• Any other reason or condition that in the opinion of the investigator would interfere with participation, complicate interpretation of study outcome data, or otherwise interfere with achieving the study objectives