Tesamorelin as an Adjunct to Exercise for Improving Physical Function in HIV

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Behavioral, Drug
Study Type: Interventional
Study Phase: Phase 2
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Maximum Age: 80
Healthy Volunteers: f
View:

• Men and women, 50-80 years old

• 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

• Sedentary lifestyle, defined as self-reported physical activity that breaks a sweat \<3 days/week with no regular resistance exercise in the past 3 months

• ≥1 Fried frailty criterion (weakness, slow gait speed, exhaustion, decreased physical activity, or unintentional weight loss as defined by specific thresholds)

• Waist circumference ≥102 cm in men and ≥88 cm in women

• Normal mammogram within 2 years (females ≤74 years old) or prostate specific antigen \<4 ng/mL (males ≤70 years old) per U.S. Preventive Services Task Force (USPSTF) age-appropriate cancer screening guidelines

• For females, postmenopausal defined as no menses for ≥12 months and anti-müllerian hormone (AMH) \<20 pg/mL or history of bilateral oophorectomy at least 3 months ago

• Provider approval to participate

Locations
United States
Colorado
University of Colorado - Anschutz Medical Campus
RECRUITING
Aurora
Massachusetts
Massachusetts General Hospital
RECRUITING
Boston
Contact Information
Primary
Lindsay T. Fourman, MD
lfourman@mgb.org
617-643-4590
Backup
Kristine M. Erlandson, MD
kristine.erlandson@cuanschutz.edu
303-724-4941
Time Frame
Start Date: 2025-07-07
Estimated Completion Date: 2028-06-30
Participants
Target number of participants: 100
Treatments
Active_comparator: Tesamorelin Plus Exercise
Tesamorelin WR 1.28 mg given subcutaneously daily plus home-based semi-supervised exercise intervention
Placebo_comparator: Placebo Plus Exercise
Identical placebo given subcutaneously daily plus home-based semi-supervised exercise intervention
Related Therapeutic Areas
Sponsors
Leads: Massachusetts General Hospital
Collaborators: University of Colorado, Denver

This content was sourced from clinicaltrials.gov