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 —