Phase
Condition
Weight Loss
Obesity
Diabetes Prevention
Treatment
Placebo
Semaglutide 2.4mg
Clinical Study ID
Ages 18-75 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Self-identify as being of Hispanic/Latino ethnicity
BMI >30
Age 18-75 years old
Able to provide informed consent before any trial related activities
Exclusion
Exclusion Criteria:
Current cancer treatment
Diabetes, Type 1 or Type 2
Eating disorders
Medication use targeting the GPL-1 system
In the last 30 days, attempted to lose weight by lifestyle modification alone orwith the use of anti-obesity medications resulting in more than 5 pounds of weightloss.
History of bariatric surgery
Use of obesogenic medications (including but not limited to steroids, haloperidol,clozapine, risperidone, olanzapine, amitriptyline, imipramine, paroxetine, andlithium) which cannot be substituted or stopped.
Pregnant or planning to become pregnant in the next 8 months
Genetic disorders and/or physical or mental handicaps that would limit participationin the study and/or the intensive lifestyle intervention.
Any contraindication to semaglutide 2.4 mg including personal or family history ofmedullary thyroid carcinoma or Multiple Endocrine Neoplasia Syndrome Type 2,hypersensitivity to semaglutide 2.4 mg or any product components.
Any known or suspected allergy to semaglutide 2.4 mg or related products
Previous participation in this trial, either initial screening or grouprandomization
Study Design
Connect with a study center
Loma Linda University Health
Loma Linda, California 92350
United StatesSite Not Available
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