BENITIONSClinical Trial Intelligence

The Women TAF-FTC Benchmark Study

2/3상 완료 NCT05140954

대상 질환HIV Infections
임상 단계2/3상
스폰서University of Washington
상태완료
참여자 수54 명
중재(약물)co-formulated 25mg TAF/ 200mg FTC
시작일2023년 4월 10일
완료일2023년 12월 19일
결과 공개일2025년 10월 27일

요약

The study seeks to assess the safety of and define blood and tissue benchmark concentrations of tenofovir diphosphate (TFV-DP) and emtricitabine triphosphate (FTC-TP) in cisgender women using directly observed oral pre-exposure prophylaxis (PrEP) therapy with tenofovir alafenamide-emtricitabine (TAF-FTC). Cisgender women will be randomly assigned to receive varying frequencies of weekly PrEP doses and followed for up to 18 weeks.These data will help accurate interpretation of efficacy results obtained in HIV prevention trials and programs in cisgender women.

Frequency of Adverse Events

Assessed through the 10 week DOT dosing period · Number of adverse events

Poor Adherence69 Number of adverse events
Moderate Adherence60 Number of adverse events
Perfect Adherence62 Number of adverse events
Poor Adherence1 Number of adverse events
Moderate Adherence1 Number of adverse events
Perfect Adherence0 Number of adverse events

Concentrations of Tenofovir Disphosphate (TFV-DP) and Emtricitabine Triphosphate (FTC-TP) Measured at Ten Weeks in Dried Blood Spots (DBS)

Assessed at week 10 · fmol/punches

Poor Adherence432 fmol/punches
Moderate Adherence1214 fmol/punches
Perfect Adherence2345 fmol/punches
Poor Adherence261 fmol/punches
Moderate Adherence976 fmol/punches
Perfect Adherence4031 fmol/punches

Concentrations of Tenofovir Disphosphate (TFV-DP) and Emtricitabine Triphosphate (FTC-TP) Measured at Four Weeks in Peripheral Blood Mononuclear Cells (PBMCs)

Assessed at week 4 · fmol/10^6 cells

Poor Adherence70 fmol/10^6 cells
Moderate Adherence229 fmol/10^6 cells
Perfect Adherence680 fmol/10^6 cells
Poor Adherence407 fmol/10^6 cells
Moderate Adherence1859 fmol/10^6 cells
Perfect Adherence6402 fmol/10^6 cells

BENITIONS에서 보기 ClinicalTrials.gov 원문 보기

전체 임상

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