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HomeTrials › NCT07745504

Obesity & weight · Phase 3 · Opening soon

A Research Study to Compare Two Different Versions of Injectable Cagrilintide and Placebo in People With Excess Body Weight

NCT07745504 · Sponsor: Novo Nordisk A/S

What this trial means for you

This study is opening soon at 11 US sites. It's studying Cagrilintide, Placebo cagrilintide, Placebo semaglutide for overweight, obesity.

Who can joinAll sexes, 18 Years and older
Healthy volunteersNo, diagnosis required
What you'd takeCagrilintide, Placebo cagrilintide, Placebo semaglutide
Study length~9 months overall
Planned participants285
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 this clinical study is to look at how well a study medicine called cagrilintide helps people living with excess body weight to lose weight. Participants will either get cagrilintide, the active study medicine being tested or placebo, a medicine that has no active medicine in it. Which treatment participants get is decided by chance. Cagrilintide is a new medicine under development that doctors cannot prescribe yet, but it has been tested in humans before. Participants will be in this clinical study for about 9 months.

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: * 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. * 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 kilograms per square meter (kg/m\^2), or BMI \>= 27.0 kg/m\^2 with the presence of at least one weight related comorbidity including, but not limited to, hypertension, dyslipidaemia, obstructive sleep apnoea or cardiovascular disease. Exclusion criteria: * History of Type 1 Diabetes (T1D) or Type 2 Diabetes (T2D). * Previous dosing of marketed or non-marketed amylin-based compounds. * Treatment, or intention to initiate treatment, with any medication prescribed for the indication of weight management within 180 days before screening.

Study sites by state

Georgia

  • Hope Clin Res & Wellness, Conyers

Hawaii

  • East West Med Res Inst, Honolulu

Illinois

  • Walgreens - Store 11760, Oak Park

Indiana

  • Midwest Inst For Clin Res, Indianapolis

Kentucky

  • The Alliance for Multispecialty Research LLC AMR, Lexington

North Carolina

  • PharmQuest, Greensboro
  • KDCILM, LLC & Accellacare US, Inc., Wilmington

South Carolina

  • Coastal Carolina Res Ctr, North Charleston

Virginia

  • Health Res of Hampton Roads, Newport News
  • National Clin Res Inc., Richmond
  • Selma Medical Associates, Winchester

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, so 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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