Actively Recruiting
Tesamorelin as an Adjunct to Exercise for Improving Physical Function in HIV
Led by Massachusetts General Hospital · Updated on 2025-07-29
100
Participants Needed
2
Research Sites
155 weeks
Total Duration
On this page
Sponsors
M
Massachusetts General Hospital
Lead Sponsor
U
University of Colorado, Denver
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Tesamorelin as an Adjunct to Exercise for Improving Physical Function in HIV
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Men and women aged 50 to 80 years
- Documented HIV infection with viral load under 200 copies/mL and CD4+ T cell count over 200/µL for at least 1 year on antiretroviral therapy
- Sedentary lifestyle with physical activity causing sweat fewer than 3 days per week and no regular resistance exercise in past 3 months
- At least one frailty sign such as weakness, slow walking, exhaustion, low activity, or unintentional weight loss
- Waist circumference of 102 cm or more in men, 88 cm or more in women
- Normal mammogram within 2 years for women under 74 or prostate-specific antigen under 4 ng/mL for men under 70 per guidelines
- Postmenopausal women defined as no menstruation for 12 months and low anti-müllerian hormone or bilateral oophorectomy at least 3 months prior
- Approval from a healthcare provider to participate
You will not qualify if you...
- Use of tesamorelin or other growth hormone therapies within 6 months
- Insulin-like growth factor 1 (IGF-1) z-score above 2.0
- HbA1c greater than 8%
- Active or suspected cancer (except non-melanoma skin cancer) within 24 months
- High doses or recent changes in testosterone or corticosteroid treatments within 3 months
- Changes in glucose-lowering medications within 3 months
- Active or unstable heart disease, chest pain, or serious arrhythmia
- History of hypopituitarism, head irradiation, or other conditions affecting growth hormone axis
- Known allergy to tesamorelin or mannitol
- Any acute or chronic illness that makes participation unsafe as judged by the investigator
AI-Screening
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Trial Site Locations
Total: 2 locations
1
University of Colorado - Anschutz Medical Campus
Aurora, Colorado, United States, 80045
Actively Recruiting
2
Massachusetts General Hospital
Boston, Massachusetts, United States, 02114
Actively Recruiting
Research Team
L
Lindsay T. Fourman, MD
CONTACT
K
Kristine M. Erlandson, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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