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Tesamorelin Plus Exercise for HIV (TRIUMPH Trial)

Phase 2
Waitlist Available
Led By Lindsay T. Fourman, MD
Research Sponsored by Massachusetts General Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
1. Men and women, 50-80 years old
2. Documented HIV infection on suppressive antiretroviral therapy for at least 1 year with HIV-1 RNA \<200 copies/mL and CD4+ T cell count \>200/µL 3
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline to week 24
Awards & highlights

Summary

People with HIV experience earlier impairments in physical function compared to people in the general population. They also exhibit an earlier presentation and more rapid development of frailty, a multisystemic syndrome of aging characterized by reduced activity, fatigue, slowness, weakness, and weight loss. While exercise can improve physical function in people with HIV, it is less effective in doing so than in the general population and is difficult to sustain in the long-term. The goal of this clinical trial is to learn whether the medication tesamorelin will improve physical function and muscle health in adults with HIV when combined with exercise. Tesamorelin is a growth hormone-releasing hormone analogue that is FDA-approved to treat abdominal fat accumulation in people with HIV. While tesamorelin has also been shown to increase muscle mass and improve measures of muscle health, its effects on physical performance and muscle strength have not yet been evaluated. During a 24-week intervention phase, half of participants will be randomly assigned to receive tesamorelin and half of participants will be randomly assigned to receive placebo (a look-alike substance that contains no drug). All participants also will engage in a home-based exercise intervention supervised by an exercise coach. During a subsequent 24-week extension phase, individuals will be monitored off study drug and supervised exercise, and be encouraged to continue to exercise independently. The investigators will investigate effects of tesamorelin on physical function, muscle mass and quality, quality of life, and exercise adherence and self-efficacy. They also will evaluate whether effects of tesamorelin are maintained following treatment cessation. This study may identify an important strategy to improve how individuals aging with HIV function and feel with potential applications to other patient populations.

Who is the study for?
Adults with HIV who are experiencing physical function impairments and signs of aging such as frailty or abdominal obesity may join this trial. The study aims to see if tesamorelin helps improve their muscle health and physical performance when combined with exercise.
What is being tested?
The trial is testing the effects of tesamorelin, a drug approved for reducing belly fat in people with HIV, on improving physical function when added to an exercise regimen. Participants will either receive tesamorelin or a placebo while following a supervised home-based exercise program.
What are the potential side effects?
Possible side effects from tesamorelin include joint pain, skin reactions at the injection site, swelling in legs and arms, muscle pain, numbness and tingling sensations. Exercise might cause typical discomfort like sore muscles.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline to week 24
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline to week 24 for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change in Repeated Chair Stand Time
Secondary study objectives
Change in 1-Repetition Maximum Leg Press
Change in 400-Meter Walk Time
Change in Appendicular Lean Tissue Mass
+8 more

Trial Design

2Treatment groups
Active Control
Placebo Group
Group I: Tesamorelin Plus ExerciseActive Control2 Interventions
Tesamorelin SV 1.4 mg given subcutaneously daily plus home-based semi-supervised exercise intervention
Group II: Placebo Plus ExercisePlacebo Group2 Interventions
Identical placebo given subcutaneously daily plus home-based semi-supervised exercise intervention

Find a Location

Who is running the clinical trial?

University of Colorado - Anschutz Medical CampusUNKNOWN
3 Previous Clinical Trials
538 Total Patients Enrolled
Massachusetts General HospitalLead Sponsor
2,979 Previous Clinical Trials
13,220,200 Total Patients Enrolled
Lindsay T. Fourman, MDPrincipal InvestigatorMassachusetts General Hospital
~67 spots leftby Mar 2028