Study of Olatorepatide in Adult Participants Living With Overweight or Obesity Without Diabetes
Regeneron Pharmaceuticals · NCT07685808
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 2
- Target enrollment
- 360
- US sites recruiting
- 21
- Study start
- July 28, 2026
- Record last updated
- October 26, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
This study will test an experimental drug called olatorepatide ("study drug") to determine how safe and effective this drug is compared to placebo and how easily the body can accept this drug at different doses and dosing schedules without causing side effects, as well as how the drug is processed in the body by participants with overweight or obesity but do not have diabetes.
The study is looking at
- What side effects the study drug might cause
- How much study drug is in the blood at different times
- How well the study drug works
- What effects the study drug may have on the body at different dosing schedules
- If the body makes antibodies to the study drug as this may cause the study drug to not work as well
Being studied: Olatorepatide; Placebo
Conditions: Overweight or Obesity
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Key Inclusion Criteria
- Body Mass Index (BMI) ≥30.0 kg/m\^2 to \<45.0 kg/m\^2 at screening OR
- BMI ≥27.0 kg/m\^2 at screening with at least 1 of the following weight-related co-morbidities: Hypertension, Dyslipidemia, Prediabetes, established Obstructive Sleep Apnea (OSA), established Coronary Artery Disease (CAD), Heart failure, established cerebrovascular disease as described in the protocol
Key Exclusion Criteria
- Previous or current diagnosis of Type 1 or Type 2 diabetes at screening
- Change in body weight >5 kg within approximately 3 months before screening as described in the protocol
- Bariatric surgery, including any procedures to revise, reverse, or remove any previous bariatric surgery interventions as described in the protocol
- History of acute or chronic pancreatitis, cholecystitis, or symptomatic gallbladder stones
- History or family history of medullary thyroid carcinoma or multiple endocrine neoplasia type 2
Note: Other Protocol Defined Inclusion/ Exclusion Criteria Apply
Recruiting US locations
AMR Clinical - Mobile
Mobile, AL 36608
Diablo Clinical Research - Flourish Research
Walnut Creek, CA 94598
Chase Medical Research
Waterbury, CT 06708
Alliance for Multispecialty Research (AMR) Clinical Miami
Doral, FL 33172
AMR Clinical - Fort Myers
Fort Myers, FL 33912
AGA Clinical Trials
Hialeah, FL 33012
Flourish Research, Nature Coast Clinical Research
Inverness, FL 34452
Flourish Research, Jacksonville Center for Clinical Research
Jacksonville, FL 32216
K2 Medical Research Maitland LLC, Main Office
Maitland, FL 32751
The IMA Group, IMA Clinical Research St. Petersburg
St. Petersburg, FL 33704
Charter Research LLC - The Villages
The Villages, FL 32162
Clinical Site Partners, LLC DBA Flourish Research
Winter Park, FL 32789
Charter Research LLC - Chicago
Chicago, IL 60618
Flourish Research, Ravenswood Rheumatology
Chicago, IL 60640
AMR Clinical - Chicago Oak Brook
Oak Brook, IL 60523
AMR Clinical Wichita
Wichita, KS 67226
AMR Clinical - Lexington
Lexington, KY 40509
Velocity Clinical Research - Omaha
Omaha, NE 68134
NYC Research Inc
New York, NY 10016
Rochester Clinical Research
Rochester, NY 14609
Tribe Clinical Research
Greenville, SC 29607
Study contacts (from the official record)
- Clinical Trials Administrator · 844-734-6643 · clinicaltrials@regeneron.com
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