Tissue Biopsy Clinical Trials

Clinical trials related to Tissue Biopsy Procedure

Early Metabolic Effects of Antiretroviral Drugs in Healthy Volunteers: A Phase 2 Randomized Study

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Background: People with HIV take drugs to keep the amount of virus in their body low. One type of these drugs, called integrase strand transfer inhibitors (INSTIs), can cause weight gain over time. Weight gain can cause diabetes, heart disease, and other serious issues. Researchers want to understand how INSTIs cause weight changes.

Objective: To characterize the change in plasma metabolite profile that 4 weeks of each treatment may induce in the absence of HIV infection

Eligibility: Healthy people aged 18 to 55.

Design: Participants will be screened in the outpatient clinic. They will have a physical exam and blood tests. They will have a nutritional assessment and tests of their heart function. Participants will be randomized to one of four oral treatments: Tenofovir Disoproxil Fumarate TDF/Viread, Tenovovir Alafenamide TAF/Vemlidy, Dolutegravir DTG/Tivicay, or both TAF and DTG taken together for 4 weeks. Participants will have a Day 0 visit for the Lead-In Baseline visit for an exam and blood tests and continuous glucose monitor placement. Participants will return in 2wks or Day 14/Wk 2 for a DEXA (dual-energy X-ray absorptiometry). DEXA is a kind of X-ray that measures body fat and bone density. Optional adiopse (fat) tissue biopsy in the abdomen, and optional microbiome specimen collections. Continuous glucose monitor changed. Oral once a day dose medication will be started with education. Participants will return in 2wks or Day 28/Wk 4 for exam, labs, and continuous glucose monitor changed. Participants will return in 2wks or Day 42/Wk 6 for final exam, labs, repeat DEXA scan, repeat adipose tissue biopsy, and microbiome specimen collections.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 55
Healthy Volunteers: t
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⁃ In order to be eligible to participate in this study, an individual must meet all of the following criteria:

• Aged 18 to 55 years.

• Able to provide informed consent.

• Willing to allow samples and data to be stored and shared for future research.

• Agrees to use a barrier method of contraception or abstain from sexual activity starting at screening though the end of study participation.

Locations
United States
Maryland
National Institutes of Health Clinical Center
RECRUITING
Bethesda
Contact Information
Primary
Mary E McLaughlin, R.N.
mmclaughli@niaid.nih.gov
(301) 435-8001
Backup
Brian P Epling, M.D.
brian.epling@nih.gov
(240) 460-9309
Time Frame
Start Date: 2026-06-23
Estimated Completion Date: 2030-01-31
Participants
Target number of participants: 120
Treatments
Active_comparator: Dolutegravir
50mg one tablet orally once a day for 4 weeks, Day 14 to Day 42
Active_comparator: Dolutegravir AND Tenofovir alafenamide
50mg one tablet orally AND 25mg one tablet orally together once a day for 4 weeks, Day 14 to Day 42
Active_comparator: Tenofovir alafenamide
25mg one tablet orally once a day for 4 weeks, Day 14 to Day 42
Active_comparator: Tenofovir Disoproxil Fumarate
300mg one tablet orally once daily for 4 weeks, Day 14 to Day 42
Related Therapeutic Areas
Sponsors
Leads: National Institute of Allergy and Infectious Diseases (NIAID)

This content was sourced from clinicaltrials.gov