Tenofovir Pharmacology in Older HIV Infected Individuals
NCT02304263 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 45
Last updated 2016-09-26
Summary
Tenofovir continues to play a vital role in the treatment of the human immunodeficiency virus (HIV) and as the age of the HIV-infected population increases in the United States and worldwide, there is an urgent need to understand the extent to which older age influences the way this antiretroviral medication works in the body. The investigators study aims to characterize and compare the pharmacology of tenofovir in older versus younger HIV-infected adults and to assess kidney function over the course of approximately one year. The investigators will be analyzing tenofovir levels in different compartments of the blood and in hair samples, and will be assessing the relationship between tenofovir concentrations and changes in kidney function over time in the older and younger cohorts. Lastly, the investigators will be evaluating the relationship between tenofovir concentrations and functional status (including body composition, bone mineral density, and frailty) in study participants.
Conditions
- HIV
- Aging
Interventions
- DRUG
-
iohexol
5mL bolus of 300 mg/ml iohexol (Omnipaque) over 2 minutes
Sponsors & Collaborators
-
University of California, San Francisco
collaborator OTHER -
University of Colorado, Denver
lead OTHER
Principal Investigators
-
Sharon M Seifert, PharmD · University of Colorado, Denver
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-02-28
- Primary Completion
- 2016-09-30
- Completion
- 2016-09-30
More Related Trials
-
Comparison of Tenofovir Vaginal Gel and Film Formulations
NCT02280109 ·Status: COMPLETED ·Phase: EARLY_PHASE1
-
The Effectiveness of Three Drug Combinations in HIV-Infected Patients Who Have Taken Zidovudine for More Than 12 Weeks
NCT00001063 ·Status: COMPLETED ·Phase: PHASE2
-
GSK1349572 Drug Interaction With Tenofovir
NCT00726336 ·Status: COMPLETED ·Phase: PHASE1
-
Relative Mitochondrial Toxicity of Tenofovir Alafenamide (TAF) vs. Tenofovir Disoproxil Fumarate (TDF)
NCT03251144 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
A Compassionate Use Study of Tenofovir Disoproxil Fumarate as Treatment for HIV Infection
NCT00002453 ·Status: COMPLETED ·Phase: NA
-
Safety and Efficacy of Tenofovir DF in HIV-1 Infected Adolescents Failing Their Current Antiretroviral Therapy
NCT00352053 ·Status: COMPLETED ·Phase: PHASE3
-
The Safety of Tenofovir Disoproxil Fumarate Taken With Other Anti-HIV Drugs to Treat HIV-Infected Patients
NCT00007436 ·Status: UNKNOWN ·Phase: PHASE3
-
Once Daily 3TC, Efavirenz and ddI for HIV Infection
NCT00214435 ·Status: UNKNOWN ·Phase: PHASE4
-
Safety and Effectiveness of Tenofovir Disoproxil Fumarate (Tenofovir DF) Plus Other Anti-HIV Drugs in HIV-Infected Patients
NCT00002450 ·Status: COMPLETED ·Phase: PHASE3
-
Rectal Microbicide Safety and Acceptability Trial of Topically Applied Tenofovir Compared With Oral Tablet
NCT00984971 ·Status: COMPLETED ·Phase: PHASE1
-
Microbicide Safety and Acceptability in Young Men
NCT01283360 ·Status: COMPLETED ·Phase: PHASE1
-
A Safety and Efficacy Study of Amdoxovir in HIV-1 Treatment-experienced Subjects.
NCT01737359 ·Status: TERMINATED ·Phase: PHASE2
-
Influence of Reproductive Cycle and Menopause on HIV-1 Infection and TFV Gel Activity
NCT01810315 ·Status: COMPLETED ·Phase: PHASE1
-
Safety Study of a Tenofovir-containing Drug Regimen for the Prevention of Mother-to-child Transmission of HIV and HBV
NCT01125696 ·Status: COMPLETED ·Phase: PHASE2
-
Exploratory Pharmacodynamic Study of Tenofovir-Based Products
NCT02722343 ·Status: COMPLETED ·Phase: PHASE1
-
PrEP-Pod-IVR (TDF-FTC/Placebo IVR 28 Day Crossover Study)
NCT03255915 ·Status: ACTIVE_NOT_RECRUITING ·Phase: EARLY_PHASE1
-
Impact of Weekly Administration of Rifapentine and Isoniazid on Steady State Pharmacokinetics of Tenofovir Alafenamide in Healthy Volunteers (YODA)
NCT03510468 ·Status: COMPLETED ·Phase: PHASE1
-
Safety and Durability ofTenofovir and a Cell Cycle Agent for Viral Suppression
NCT00344981 ·Status: COMPLETED ·Phase: NA
-
A Study to Compare Anti-HIV Drugs Given Twice a Day or Once a Day, With or Without Direct Observation
NCT00036452 ·Status: COMPLETED ·Phase: PHASE2
-
Adherence and Acceptability to and Blood Levels of Tenofovir Gel and Tablets in HIV Uninfected Women
NCT00592124 ·Status: COMPLETED ·Phase: PHASE2
-
The Addition of Indinavir to Anti-HIV Treatment in HIV-Infected Patients
NCT00000861 ·Status: COMPLETED ·Phase: NA
-
Safety and Efficacy of a Switch to Doravirine, Tenofovir, Lamivudine (MK-1439A) in Human Immunodeficiency Virus (HIV-1)-Infected Participants Virologically Suppressed on an Anti-retroviral Regimen in Combination With Two Nucleoside Reverse Transcriptase Inhibitors (MK-1439A-024)
NCT02397096 ·Status: COMPLETED ·Phase: PHASE3
-
Study to Evaluate Switching From a Regimen Consisting of Efavirenz/Emtricitabine/Tenofovir Disoproxil Fumarate (EFV/FTC/TDF) Fixed Dose Combination (FDC) to Emtricitabine/Rilpivirine/Tenofovir Alafenamide (FTC/RPV/TAF) FDC in Virologically-Suppressed, HIV-1 Infected Adults
NCT02345226 ·Status: COMPLETED ·Phase: PHASE3
-
Pharmacokinetic Study of the Vaginal Microbicide Agent 1% Tenofovir Gel
NCT00561496 ·Status: COMPLETED ·Phase: PHASE1
-
A Phase I Study to Evaluate the Pharmacokinetics, Safety and Antiviral Effects of Concurrent Administration of Zidovudine (AZT) and 2'3'-Dideoxyinosine (ddI) in Patients With Human Immunodeficiency Virus (HIV)
NCT00002014 ·Status: COMPLETED ·Phase: PHASE1