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HomeTrials › NCT07639021

Obesity & weight · Phase 2 · Opening soon

A Research Study Comparing Different Ways of Increasing the Dose of NNC0662-0419 in Participants With Obesity

NCT07639021 · Sponsor: Novo Nordisk A/S

What this trial means for you

This study is opening soon at 24 US sites. It's studying NNC0662-0419, Semaglutide, NNC0662-0419 Placebo, Semaglutide placebo for obesity.

Who can joinAll sexes, 18 Years and older
Healthy volunteersNo — diagnosis required
What you'd takeNNC0662-0419, Semaglutide, NNC0662-0419 Placebo, Semaglutide placebo
Study length~13 months overall
Planned participants230
TypeInterventional (you receive treatment)

What participants typically get: study medication (or placebo, if the trial uses one) and study-related medical care at no cost, plus close monitoring. Compensation for time and travel varies by study — ask the site. Note that in many trials you can't choose your treatment group, and some participants receive a placebo.

The study, in the sponsor's words

The purpose of the study is to find out if NNC0662-0419 is safe and effective for treating participants living with obesity.

Can you join? The exact criteria

Below is the verbatim eligibility text from the registry — bring it to your doctor; it's written for clinicians, and your own clinician is the right person to interpret it with you.

Full eligibility criteria (for you and your doctor)

Inclusion Criteria: * Male or female (sex assigned at birth, inclusive of all gender identities). * Age 18 years or above at the time of signing the informed consent. * Body mass index (BMI) greater than or equal to (≥) 30.0 kilogram per square meter (kg/m\^2) at screening. * Participant must have a desire and be committed to lose at least 25 percentage (%) of their body weight from randomisation. Exclusion Criteria: * Known or suspected hypersensitivity to study intervention(s) or related products. * Treatment with any medication prescribed for the indication of obesity or weight management (e.g. glucagon-like-peptide-1 (GLP-1) receptor agonists (RA), dual GLP-1/gastric inhibitory peptide (GIP) RAs (or any other GLP-1 based treatment) or amylin analogues)) within 90 days before screening. * Glycated haemoglobin (HbA1c) ≥ 6.5% (48 Millimoles per mole \[mmol/mol\]) as measured by the central laboratory at screening. * History of type 1 or type 2 diabetes mellitus.

Study sites by state

Alabama

  • Chambliss Clinical Trials, LLC — Montgomery

California

  • FDRC — Costa Mesa
  • Los Angeles Institute for Metabolic Research — Los Angeles

Florida

  • Encore Medical Research LLC — Hollywood
  • South Broward Research LLC — Miramar
  • West Orange Endocrinology — Ocoee

Illinois

  • Cedar-Crosse Research Center — Chicago
  • Great Lakes Clinical Trials — Chicago

Indiana

  • Midwest Inst For Clin Res — Indianapolis

Kentucky

  • L-MARC Research Center — Louisville

Maryland

  • Endo And Metab Cons — Rockville

Missouri

  • StudyMetrix Research LLC — City of Saint Peters

New York

  • Great Lakes Medical Research — Westfield

North Carolina

  • KDCILM, LLC & Accellacare US, Inc. — Wilmington

Ohio

  • Family Practice Center of Wadsworth Inc. — Wadsworth

Pennsylvania

  • UPA Ctr Weight and Eating Dis — Philadelphia

Rhode Island

  • Clinical Res Collaborative — Cumberland

Tennessee

  • Holston Medical Group_Bristol — Bristol
  • Holston Medical Group — Kingsport
  • Clinical Research Associates — Nashville

Texas

  • PlanIt Research, PLLC — Houston
  • Pinnacle Clinical Research — San Antonio

Virginia

  • National Clin Res Inc. — Richmond

Washington

  • Rainier Clin Res Ctr Inc — Renton

View the official record on ClinicalTrials.gov →

Verify before you act. Medical disclaimer: content on this site is for informational purposes only and is not medical advice. GLP-1 medications are prescription drugs; always consult a licensed healthcare provider about eligibility, risks, and benefits. Trial details and enrollment status change frequently — always verify on the official registry and talk to your own clinician before contacting a study site. This page was generated from registry data and is not affiliated with the study sponsor.

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