Effects of Sofosbuvir/Ledipasvir Treatment on the Pharmacokinetics and Renal Safety of Tenofovir
Primary Purpose
Hepatitis C and HIV Coinfection
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Blood draws for tenofovir PK, renal function
Sponsored by
About this trial
This is an interventional other trial for Hepatitis C and HIV Coinfection
Eligibility Criteria
Inclusion Criteria:
- On tenofovir and a ritonavir-boosted PI for at least 30 days initiating HCV treatment with SOF/LDV
- HCV RNA <48 copies/mL at most recent clinic visit
Exclusion Criteria:
- eGFR < 60 ml/min
- history of renal disease
- Pregnant or planning pregnancy
- Any medical, social, or mental-health issue(s) that, in the opinion of the investigators, could interfere with study participation or the study outcomes
Sites / Locations
- University of Colorado Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Tenofovir PK before and after SOF/LDV
Arm Description
Outcomes
Primary Outcome Measures
Change in area under the plasma concentration (AUC) of tenofovir
Compare tenofovir AUC0-24 before and after administration of SOF/LDV
Secondary Outcome Measures
Change in Estimated Glomerular Filtration Rate (eGFR)
Compare eGFR calculated using Modification of Diet in Renal Disease (MDRD) equation before and after the addition of SOF/LDV.
Change in concentrations of tenofovir-diphosphate
Compare concentrations of tenofovir-diphosphate in peripheral blood mononuclear cells and red blood cells before and after the addition of SOF/LDV
Full Information
NCT ID
NCT02588287
First Posted
October 26, 2015
Last Updated
August 10, 2021
Sponsor
University of Colorado, Denver
1. Study Identification
Unique Protocol Identification Number
NCT02588287
Brief Title
Effects of Sofosbuvir/Ledipasvir Treatment on the Pharmacokinetics and Renal Safety of Tenofovir
Official Title
Effects of Sofosbuvir/Ledipasvir Treatment on the Pharmacokinetics and Renal Safety of Tenofovir
Study Type
Interventional
2. Study Status
Record Verification Date
August 2021
Overall Recruitment Status
Completed
Study Start Date
November 2015 (undefined)
Primary Completion Date
September 2016 (Actual)
Study Completion Date
September 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Colorado, Denver
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study evaluates the effect of sofosbuvir/ledipasvir (SOF/LDV) treatment on the pharmacokinetics (PK) and renal safety of tenofovir. Subjects receiving tenofovir-based antiretroviral therapy with human immunodeficiency virus (HIV) protease inhibitors (HIV PI/r) and initiating SOF/LDV treatment for Hepatitis C virus (HCV) will be invited to participate. The study consists of three visits: a screening visit and two abbreviated 4-hour pharmacokinetic visits (one before initiating SOF/LDV and a second approximately 4 weeks after initiating SOF/LDV).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis C and HIV Coinfection
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
14 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Tenofovir PK before and after SOF/LDV
Arm Type
Experimental
Intervention Type
Other
Intervention Name(s)
Blood draws for tenofovir PK, renal function
Primary Outcome Measure Information:
Title
Change in area under the plasma concentration (AUC) of tenofovir
Description
Compare tenofovir AUC0-24 before and after administration of SOF/LDV
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
Change in Estimated Glomerular Filtration Rate (eGFR)
Description
Compare eGFR calculated using Modification of Diet in Renal Disease (MDRD) equation before and after the addition of SOF/LDV.
Time Frame
14 weeks
Title
Change in concentrations of tenofovir-diphosphate
Description
Compare concentrations of tenofovir-diphosphate in peripheral blood mononuclear cells and red blood cells before and after the addition of SOF/LDV
Time Frame
4 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
On tenofovir and a ritonavir-boosted PI for at least 30 days initiating HCV treatment with SOF/LDV
HCV RNA <48 copies/mL at most recent clinic visit
Exclusion Criteria:
eGFR < 60 ml/min
history of renal disease
Pregnant or planning pregnancy
Any medical, social, or mental-health issue(s) that, in the opinion of the investigators, could interfere with study participation or the study outcomes
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jennifer Kiser, PharmD
Organizational Affiliation
University of Colorado, Denver
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Colorado Hospital
City
Aurora
State/Province
Colorado
ZIP/Postal Code
80045
Country
United States
12. IPD Sharing Statement
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Effects of Sofosbuvir/Ledipasvir Treatment on the Pharmacokinetics and Renal Safety of Tenofovir
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