drugset / Trial / NCT03126370

Effects of Ledipasvir/Sofosbuvir on the Pharmacokinetics and Renal Safety of Tenofovir Alafenamide (TAF)

NCT03126370

Phase 4 Completed 10 enrolled University of Colorado, Denver
NaSingle-groupOpen-labelOther

Summary

This study will evaluate the effect of ledipasvir/sofosbuvir (LDV/SOF) treatment on the pharmacokinetics (PK) and renal safety of tenofovir in the form of tenofovir alafenamide (TAF). Subjects living with human immunodeficiency virus (HIV) who are receiving tenofovir-based antiretroviral therapy (in the form of tenofovir disoproxil fumarate \[TDF\]), and are also taking a ritonavir- or cobicistat-boosted protease inhibitor will be invited to participate. The study will consist of five visits: a screening visit, three abbreviated 4-hour pharmacokinetic visits, and one end-of-study follow-up visit. Subjects will also be asked to use a Wisepill device, which will track medication adherence throughout the study.

Timeline

Start
2018-01-08
Primary completion
2019-07-12
Completion
2019-10-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ledipasvir Small molecule 90 mg
Subject Sofosbuvir Small molecule 400 mg
Subject tenofovir alafenamide Small molecule 25 mg
Background Tenofovir disoproxil fumarate Small molecule 300 mg
Background emtricitabine Other / unclassified 200 mg