Protocol Details

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

This study is currently recruiting participants.

Summary | Eligibility | Citations | Contacts

Summary

Number

000906-I

Sponsoring Institute

National Institute of Allergy and Infectious Diseases (NIAID)

Recruitment Detail

Type: Participants currently recruited/enrolled
Gender: Male & Female
Min Age: 18 Years
Max Age: 55 Years

Referral Letter Required

No

Population Exclusion(s)

Children;
Adults who are or may become unable to consent;
Pregnant Women

Keywords

Metabolism;
HIV;
Integrase Strand Transfer Inhibitors

Recruitment Keyword(s)

None

Condition(s)

Healthy Volunteer;
Weight Gain;
Metabolic Effects;
Integrase Strand Transfer Inhibitors

Investigational Drug(s)

None

Investigational Device(s)

None

Intervention(s)

Drug: Dolutegravir (DTG) AND Tenofovir alafenamide (TAF)
Drug: Tenofovir Disoproxil Fumarate
Drug: Dolutegravir
Drug: Tenofovir alafenamide

Supporting Site

National Institute of Allergy and Infectious Diseases

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

INCLUSION CRITERIA:

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.

EXCLUSION CRITERIA:

An individual who meets any of the following criteria will be excluded from participation in this study:

-Current infection with HIV or hepatitis A, B, or C.

-Body mass index (BMI) <18.5 kg/m^2 or >30.0 kg/m^2.

-Weight change >5% in the past 6 months.

-History of or current cardiovascular disease such as congestive heart failure, heart block, or clinically relevant abnormal ECG as determined by investigators.

-History of or current liver disease or alanine transaminase serum level >2x upper limit of normal.

-History of or current kidney disease or renal insufficiency, or estimated creatinine clearance <=80 mL/min (Modification of Diet in Renal Disease equation).

-Current cancer or history of cancer within 5 years of screening, with the exception of squamous cell carcinoma or basal cell carcinoma that is localized and does not require systemic therapy.

-History of bariatric surgery.

-Diabetes mellitus as defined by a prior diagnosis or a hemoglobin A1c of >6.4 percent on screening labs.

-Fasting serum glucose >126 mg/dL.

-History of or current hypo- or hyper-thyroid or abnormal TSH, except minor deviations deemed to be of no clinical significance by the investigator.

-History of or current asthma or chronic obstructive pulmonary disease.

-Psychological conditions by self-report, such as (but not limited to) clinical depression, bipolar disorders, which would be incompatible with safe and successful participation in this study.

-Pregnancy or within 1 year post-partum.

-Breastfeeding.

-Blood pressure >140/90 mm Hg or current antihypertensive therapy.

-Hemoglobin that is either 10 percent below the lower limit or 10 percent above the upper limit of the normal range for the Clinical Center Laboratory (acceptable ranges: females 10.08-17.27 g/dL, males 12.33-19.25 g/dL).

-History of illicit drug, opioid, or alcohol abuse within the last 5 years; current use of illicit drugs or opioids (by history) or excessive alcohol (CAGE assessment score >=2).

-Current use of the following prescription or over-the-counter medications and supplements:

--Carbamazepine

--Oxcarbazepine

--Phenobarbital

--Phenytoin

--Primidone

--Rifabutin

--Rifampin

--Rifapentine

--St. John's wort (Hypericum perforatum)

--Cation-containing antacids or laxatives

--Sucralfate

--Buffered medications

--Oral calcium, iron, magnesium, or zinc supplements, including multivitamins containing these polyvalent cations

--Dalfampridine

--Metformin

--Dofetilide

--Thyroid medications

--Corticosteroids

--Weight loss medications, including prescription drugs (eg, semaglutide and tirzepatide) and over-the-counter diet pills

-Use of TAF, TDF, and/or FTC for the purpose of HIV PrEP or in a research study within the past 6 months.

-Any history of exposure to cabotegravir or lenacapavir (eg, as HIV PrEP or as a participant in a research study for these drug).

-Current use of prescrtiption or nonprescriptive medications that may have interactions with study drugs or confound the study measurements as determined by the investigators.

-History of adverse or allergic reactions to the study drugs.

-Daily caffeine intake >500 mg (about 4 cups of coffee).

-Current smoker or user of tobacco products.

-A change in the participant s diet and/or exercise regimen in the past 3 months or during the timeframe of the study period that, in the opinion of the investigator, would compromise the integrity of the data.

-High-risk sexual activity as determined by the investigators, and/or inability or unwillingness to use barrier contraception during the protocol.

-Any other condition, medication, or dietary pattern that, in the opinion of the investigators, increases risk to the participant, prevents the participant from complying with study procedures, prevents the participant from completing the study, or interferes with the interpretation of study results.


Citations:

Squires K, Kityo C, Hodder S, Johnson M, Voronin E, Hagins D, Avihingsanon A, Koenig E, Jiang S, White K, Cheng A, Szwarcberg J, Cao H. Integrase inhibitor versus protease inhibitor based regimen for HIV-1 infected women (WAVES): a randomised, controlled, double-blind, phase 3 study. Lancet HIV. 2016 Sep;3(9):e410-e420. doi: 10.1016/S2352-3018(16)30016-9. Epub 2016 May 27. PMID: 27562742; PMCID: PMC5825001.

Molina JM, Clotet B, van Lunzen J, Lazzarin A, Cavassini M, Henry K, Kulagin V, Givens N, de Oliveira CF, Brennan C; FLAMINGO study team. Once-daily dolutegravir versus darunavir plus ritonavir for treatment-naive adults with HIV-1 infection (FLAMINGO): 96 week results from a randomised, open-label, phase 3b study. Lancet HIV. 2015 Apr;2(4):e127-36. doi: 10.1016/S2352-3018(15)00027-2. Epub 2015 Mar 10. Erratum in: Lancet HIV. 2015 Apr;2(4):e126. PMID: 26424673.

Lennox JL, Landovitz RJ, Ribaudo HJ, Ofotokun I, Na LH, Godfrey C, Kuritzkes DR, Sagar M, Brown TT, Cohn SE, McComsey GA, Aweeka F, Fichtenbaum CJ, Presti RM, Koletar SL, Haas DW, Patterson KB, Benson CA, Baugh BP, Leavitt RY, Rooney JF, Seekins D, Currier JS; ACTG A5257 Team. Efficacy and tolerability of 3 nonnucleoside reverse transcriptase inhibitor-sparing antiretroviral regimens for treatment-naive volunteers infected with HIV-1: a randomized, controlled equivalence trial. Ann Intern Med. 2014 Oct 7;161(7):461-71. doi: 10.7326/M14-1084. Erratum in: Ann Intern Med. 2014 Nov 4;161(9):680. PMID: 25285539; PMCID: PMC4412467.

Contacts:

Principal Investigator

Referral Contact

For more information:

Brian P. Epling, M.D.
National Institute of Allergy and Infectious Diseases (NIAID)
NIHBC 10 - CLINICAL CENTER BG RM 8C402
10 CENTER DR
BETHESDA MD 20892
(240) 460-9309
brian.epling@nih.gov
Mary E. McLaughlin, R.N.
National Institute of Allergy and Infectious Diseases (NIAID)
National Institutes of Health
Building 10
Room 8C404
10 Center Drive
Bethesda, Maryland 20892
(301) 435-8001
mmclaughli@niaid.nih.gov
Office of Patient Recruitment
National Institutes of Health Clinical Center (CC)
Building 61, 10 Cloister Court
Bethesda, Maryland 20892
Toll Free: 1-800-411-1222
Local Phone: 301-451-4383
TTY: TTY Users Dial 7-1-1
ccopr@nih.gov

Clinical Trials Number:

NCT05652478
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