Evaluation of Single Dosing With Two F/TAF Tablets Among Healthy Volunteers

Exclusion Criteria8

• History of oral PrEP (F/TDF or F/TAF) use in the preceding two months
• Persons who have a reactive or positive HIV result from screening visit.
• Positive hepatitis B surface antigen (HBsAg) test
• Participants with a history of having a gastrectomy, colostomy, ileostomy, or any other procedure altering the gastrointestinal tract or drug absorption
• History of any behaviors that place the participant at high-risk for HIV acquisition (e.g., needle sharing, unprotected sex with ≥1 partner in the prior 2 weeks)
• Taking concomitant medications that that are known inducers/inhibitors of P-gp that would effect TAF absorption
• Pregnancy or lactation
• Any other condition or prior therapy that, in the opinion of the investigator, would preclude informed consent, make study participation unsafe, make the individual unsuitable for the study or unable to comply with the study requirements. Such conditions may include, but are not limited to, current or recent history of severe, progressive, or uncontrolled substance abuse, or renal, hepatic, hematological, gastrointestinal, endocrine, pulmonary, neurological, or cerebral disease