RecruitingPhase 2NCT05652478

Early Metabolic Effects of Antiretroviral Drugs in Healthy volUnteers: a Phase 2 Randomized Study

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


Sponsor

National Institute of Allergy and Infectious Diseases (NIAID)

Enrollment

120 participants

Start Date

Jun 2, 2026

Study Type

INTERVENTIONAL

Conditions

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

Min Age: 18 YearsMax Age: 55 Years

Plain Language Summary

Simplified for easier understanding

This study measures how two common HIV medications — dolutegravir and tenofovir alafenamide — affect metabolism (how the body uses energy, fat, and sugar) in healthy volunteers within weeks of starting them. This could explain why some people gain weight on HIV treatment. **You may be eligible if...** - You are between 18 and 55 years old and in good health - You do not have HIV but are willing to take HIV medications temporarily for research purposes - You are able to stay in a clinical research facility for two separate 11-day periods **You may NOT be eligible if...** - You have significant metabolic conditions (e.g., diabetes, thyroid disease) - You take medications that affect metabolism - You are pregnant or planning to become pregnant Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGDolutegravir (DTG) AND Tenofovir alafenamide (TAF)

50mg dolutegravir (DTG) one tablet AND 25mg tenofovir alafenamide (TAF) one tablet together, orally once daily for 4 wks (Day 14 to Day 42)

DRUGTenofovir Disoproxil Fumarate

300mg tenofovir disoproxil fumarate (TDF) one tablet orally once daily for 4 wks (Day 14 to Day 42)

DRUGDolutegravir

50mg dolutegravir (DTG) one tablet orally once daily for 4 wks (Day 14 to Day 42)

DRUGTenofovir alafenamide

25mg tenofovir alafenamide (TAF) one tablet orally once a day for 4 wks (Day 14 to Day 42)


Locations(1)

National Institutes of Health Clinical Center

Bethesda, Maryland, United States

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NCT05652478


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