120
Participants
Start Date
July 26, 2022
Primary Completion Date
May 12, 2025
Study Completion Date
May 12, 2025
Behavioral Treatment
All participants, regardless of medication assignment, will receive the same 60-week behavioral weight loss program. Brief (15-minute), individual lifestyle counseling sessions will be delivered by a psychologist, behavioral health counselor, or registered dietitian (or other trained health care provider) at weeks 0 (i.e., baseline/randomization), 2, 4 and every fourth week from week 4 to week 60 (17 sessions) of Study 1. Subjects will be instructed to consume a self-selected diet of 1200-1500 kcal/day (for those who weigh \< 250 lb) or 1500-1800 kcal/day (for those who weigh ≥250 lb). They will be instructed to engage in low-to-moderate intensity physical activity (e.g., walking), gradually building to a goal of ≥150 minutes per week (spread across 5 days) by week 40. They will be instructed to use calorie counting and self-monitoring to meet their goals.
Placebo
An inactive saline solution administered via subcutaneous injection
Semaglutide 2.4 MG/0.75 ML Subcutaneous Solution [WEGOVY]
Semaglutide 2.4 mg is a once weekly subcutaneous glucagon-like peptide-1 (GLP-1) receptor agonist that has been FDA approved for weight loss
University of Pennsylvania Center for Weight and Eating Disorders, Philadelphia
Collaborators (1)
Novo Nordisk A/S
INDUSTRY
University of Pennsylvania
OTHER