Research Study on How Well Oral Semaglutide Works for Weight Loss in Adults With Excess Body Weight
Novo Nordisk A/S · NCT07770841
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 3
- Target enrollment
- 450
- US sites recruiting
- 15
- Study start
- August 12, 2026
- Record last updated
- September 9, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The purpose of this study is to see how oral semaglutide, when taken in lower doses help lowering of body weight in participants with excess body weight when compared to 'dummy' tablets (placebo). Results from this study will help select the most optimal lower dose of oral semaglutide that can be used for treating participants living with overweight or obesity.
Being studied: Semaglutide; Placebo
Conditions: Overweight; Obesity
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Informed consent obtained before any study-related activities. Study-related activities are any procedures that are carried out as part of the study, including activities to determine suitability for the study.
- Female or male (sex at birth).
- Age 18 years or above at the time of signing the informed consent.
- Body mass index (BMI) of
- ≥ 27.0 kilogram per square meter (kg/m\^2) with the presence of at least one weight-related comorbidity including, but not limited to, hypertension, dyslipidaemia, obstructive sleep apnoea or CV disease.
OR
- ≥ 30.0 kg/m\^2.
- History of at least one self-reported unsuccessful dietary effort to lose body weight.
Exclusion Criteria
- A self-reported change in body weight greater than (>) 5% within 90 days before screening irrespective of medical records.
- HbA1c ≥ 6.5% (48 millimoles per mole [mmol/mol]) as measured by the central laboratory at screening.
- Consistent use of glucagon like peptide-1 (GLP-1) receptor agonists, including medication with glucagon like peptide-1 receptor agonist (GLP-1 RA) activity like dual GLP-1/gastric inhibitory peptide RAs, or amylin analogues before screening. Consistent use is defined as treatment.
Recruiting US locations
Uni of Alabama at Birmingham
Birmingham, AL 35296
Headlands Research California, LLC
Escondido, CA 92025
National Research Institute - Huntington Park
Huntington Park, CA 90255
Los Angeles Institute for Metabolic Research
Los Angeles, CA 90015
ERG Holding Company, LLC / Evolution Research Group, LLC
Delray Beach, FL 33445
ERG Holding Company, LLC / Evolution Research Group, LLC
Fort Myers, FL 33192
Jedidiah Clinical Research
Tampa, FL 33619
East West Med Res Inst
Honolulu, HI 96814
L-MARC Research Center
Louisville, KY 40213
StudyMetrix Research LLC
City of Saint Peters, MO 63303
Jubilee Clinical Research, Inc.
Las Vegas, NV 89106
Corvallis Clinic PC Clinical Research Department
Corvallis, OR 97330-3737
Spartanburg Medical Research
Spartanburg, SC 29303
Cedar Health Research
Dallas, TX 75251
Selma Medical Associates
Winchester, VA 22601-3834
Study contacts (from the official record)
- Novo Nordisk · (+1) 866-867-7178 · clinicaltrials@novonordisk.com
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