Semaglutide Treatment, Appetite, and Eating Behavior: Long-term Effects

PHASE4CompletedINTERVENTIONAL
Enrollment

120

Participants

Timeline

Start Date

July 26, 2022

Primary Completion Date

May 12, 2025

Study Completion Date

May 12, 2025

Conditions
Obesity
Interventions
BEHAVIORAL

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.

DRUG

Placebo

An inactive saline solution administered via subcutaneous injection

DRUG

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

Trial Locations (1)

19104

University of Pennsylvania Center for Weight and Eating Disorders, Philadelphia

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Novo Nordisk A/S

INDUSTRY

lead

University of Pennsylvania

OTHER