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Tirzepatide

Mounjaro, Zepbound, LY3298176

Quick Stats
Studies 183
Trials 100
Recruiting PHASE2 INTERVENTIONAL NCT06935838

Effects of Tirzepatide on Weight Loss and Chronic Inflammation in People With HIV

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

This is a prospective cohort study of 12 overweight (with one or more weight-related condition) or obese adults with well controlled HIV-1 on antiretroviral therapy (ART). An initial dose of tirzepatide (TZP) 2.5 mg subcutaneous (SQ) once weekly will be given, escalated by 2.5 mg at 4-week intervals to a final dose of 7.5mg. The investigators will collect the following information via review of the medical record: age, race/ethnicity, sex, medical conditions, medications, most recent standard of care HIV labs (including T-cell panel and HIV-1 viral load). The primary outcome will be the change in baseline body weight at 12 weeks. Secondary outcomes will be changes in body composition, liver fat content and liver stiffness, inflammatory markers, cardiometabolic markers (lipids and HbA1c), and monocytes at 12 weeks. There will be a 4-week safety follow up off TZP.

Interventions

Name: Tirzepatide
Type: DRUG
Description: Tirzepatide is approved by the Food and Drug Administration (FDA) for the treatment of type 2 diabetes, obesity and overweight with at least one weight-related medical condition, and moderate to severe obstructive sleep apnea. An initial dose of TZP 2.5 mg subcutaneous (SQ) once weekly will be given, escalated by 2.5 mg at 4-week intervals to a final dose of 7.5mg.

Primary Outcomes

Measure: Change in Baseline Body Weight
TimeFrame: 12 weeks
Description: The primary outcome will be the change in baseline body weight (measured in lbs) at 12 weeks.

Trial Information

NCT ID

NCT06935838

Status

Recruiting

Study Type

INTERVENTIONAL

Phases

PHASE2

Sponsor

University of Hawaii

Last Updated

December 15, 2025