RecruitingPhase 1NCT07597018

A Research Study to Compare Blood Levels of Cagrilintide After Multiple Doses of Different Versions of Cagrilintide in Adults With Overweight or Obesity

Bioequivalence Study of Cagrilintide B + Placebo Semaglutide I and Cagrilintide D Once Weekly in Participants With Overweight or Obesity


Sponsor

Novo Nordisk A/S

Enrollment

234 participants

Start Date

May 18, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This clinical study is testing two versions of the study medicine cagrilintide. The purpose of the study is to compare these two versions to understand their effects in participants with overweight or obesity. Participants will receive either cagrilintide version D or cagrilintide version B, and which treatment participants receive is decided by chance. Participants will be in this clinical study for about 6 months.


Eligibility

Min Age: 18 YearsMax Age: 64 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Cagrilintide B and placebo semaglutide I and a drug called Cagrilintide D for people with obesity and overweight. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 64 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGCagrilintide D

Cagrilintide D will be administered subcutaneously.

DRUGCagrilintide B and placebo semaglutide I

Cagrilintide B and placebo semaglutide I will be administered subcutaneously


Locations(1)

Parexel International GmbH

Berlin, Germany

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NCT07597018


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