Feasibility of Semaglutide in Advanced Lung Disease
Part of paid clinical trials in Philadelphia, Pennsylvania.
- Sponsor
- University of Pennsylvania
- Study ID
- NCT05746039
- Phase
- PHASE1/PHASE2
- Status
- Recruiting
Conditions
- Chronic Obstructive Pulmonary Disease
- Interstitial Lung Disease
- Obesity
- Pulmonary Hypertension
- Sarcoidosis, Pulmonary
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 80 Years
- Healthy Volunteers
- Not accepted
Interventions
- Semaglutide Pen Injector — DRUGOnce weekly subcutaneous injection
Study Details
The goal of this clinical trial is to learn whether semaglutide, an FDA-approved treatment for diabetes and obesity, is feasible and tolerable in patients with advanced lung disease. The main question\[s\] it aims to answer are: 1. Are patients with advanced lung disease able to tolerate semaglutide therapy? 2. Are we able to titrate semaglutide therapy to a target weight? Participants will be asked to perform pulmonary function, physical function and body composition testing, as well as a blood draw before and after 12-weeks of semaglutide therapy. While on therapy, subjects will be surveyed regarding any adverse events or side effects.
Key Dates
- Start date
- Jan 29, 2024
- Status verified
- Apr 2026
- Primary completion
- Dec 28, 2027
- Completion
- Dec 28, 2027
Study Design
- Enrollment
- 8 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Study Drug (semaglutide)Semaglutide Pen Injector 1.0 mg weekly Once weekly subcutaneous injection Other Name: Wegovy
Primary Outcome Measure
Tolerability [ Time Frame: 12 weeks ]
Central Contacts
- Michaela R Anderson, MD215-662-3202
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Pennsylvania Perelman School of Medicine | Philadelphia | Pennsylvania | 19104 | Apurva Raje |
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