🔎 Trials Near Me

Home › Overweight › NCT07685808

Study of Olatorepatide in Adult Participants Living With Overweight or Obesity Without Diabetes

RecruitingPhase 2

A Phase 2, Randomized, Placebo-Controlled Study to Assess the Safety, Tolerability, Pharmacokinetics, and Efficacy of Olatorepatide, a GLP-1/GIP Receptor Agonist, With Different Doses and Drug-Titration Algorithms in Participants Living With Overweight or Obesity

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Key Inclusion Criteria:

1. Body Mass Index (BMI) ≥30.0 kg/m\^2 to \<45.0 kg/m\^2 at screening OR
2. 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:

1. Previous or current diagnosis of Type 1 or Type 2 diabetes at screening
2. Change in body weight \>5 kg within approximately 3 months before screening as described in the protocol
3. Bariatric surgery, including any procedures to revise, reverse, or remove any previous bariatric surgery interventions as described in the protocol
4. History of acute or chronic pancreatitis, cholecystitis, or symptomatic gallbladder stones
5. History or family history of medullary thyroid carcinoma or multiple endocrine neoplasia type 2

Note: Other Protocol Defined Inclusion/ Exclusion Criteria Apply

About the study

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

What is being tested

Sponsor: Regeneron Pharmaceuticals · Participants: 360 · Started: Jul 28, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07685808

Locations in the U.S.

AlabamaAMR Clinical - Mobile, Mobile
CaliforniaDiablo Clinical Research - Flourish Research, Walnut Creek
FloridaAMR Clinical - Miami, Doral
AMR Clinical - Fort Myers, Fort Myers
AGA Clinical Trials, Hialeah
Flourish Research, Nature Coast Clinical Research, Inverness
Flourish Research, Jacksonville Center for Clinical Research, Jacksonville
K2 Medical Research Maitland LLC, Main Office, Maitland
IMA Clinical Research St. Petersburg, St. Petersburg
Charter Research LLC - The Villages, The Villages
Clinical Site Partners, LLC DBA Flourish Research, Winter Park
IllinoisCharter Research LLC - Chicago, Chicago
Flourish Research - Chicago, Chicago
AMR Clinical - Chicago Oak Brook, Oak Brook
KansasAMR Clinical - Wichita, Wichita
KentuckyAMR Clinical - Lexington, Lexington
New YorkRochester Clinical Research, Rochester
South CarolinaTribe Clinical Research, Greenville

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.