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Taking peoplePhase 3

CagriSema versus semaglutide for weight loss in obesity, with or without type 2 diabetes

Compares CagriSema with semaglutide for weight loss in adults with obesity.

Plain-language title generated from the registry record
Registry title: A Research Study to Look at How Two Different Doses of CagriSema and One Dose of Semaglutide Help People Living With Obesity With or Without Type 2 Diabetes Lose Weight

Key facts

Where
Alken, Kluisbergen, La Louviere, Mechelen, Roeselare, and Sint-Lambrechts-Woluwe, BelgiumSee the 6 sites
Phase
Phase 3

Where in Belgium

  • AnimaAlken, BelgiumNo longer taking part
  • KormontKluisbergen, BelgiumNo longer taking part
  • Centre hospitalier universitaire de Tivoli Institut medical des Mutualites socialistesLa Louviere, BelgiumNo longer taking part
  • MeclinasMechelen, BelgiumNo longer taking part
  • Algemeen Ziekenhuis DeltaRoeselare, BelgiumNo longer taking part
  • Cliniques Universitaires Saint-LucSint-Lambrechts-Woluwe, BelgiumNo longer taking part

Questions to ask the study team

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  2. Are travel costs paid?
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  4. What happens if I want to stop?
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Trial details

Who runs it
Novo Nordisk A/S
Trial code
NCT07564414EU 2025-522488-14-00
Record updated
30 September 2026
Original description
This clinical study is testing how the study medicine CagriSema helps people living with obesity, with or without type 2 diabetes (T2D), lose weight. The purpose of the study is to find out how safe and effective CagriSema is for body weight loss in these participants. Participants will receive either CagriSema or semaglutide, and which treatment participants receive is decided by chance. CagriSema is a new study medicine being tested, while semaglutide is a medicine that doctors can already prescribe. The study will last for about 83 weeksRead full original descriptionShow less

A Clinical Study to Compare Efficacy and Safety of Two Different Doses of CagriSema and Semaglutide in Participants With Obesity With or Without Type 2 Diabetes

This clinical study is testing how the study medicine CagriSema helps people living with obesity, with or without type 2 diabetes (T2D), lose weight. The purpose of the study is to find out how safe and effective CagriSema is for body weight loss in these participants. Participants will receive either CagriSema or semaglutide, and which treatment participants receive is decided by chance. CagriSema is a new study medicine being tested, while semaglutide is a medicine that doctors can already prescribe. The study will last for about 83 weeks

Inclusion: 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; BMI≥ 35.0 kg/m\^2; Participants without T2D: No history of T2D and HbA1c < 6.5% (48 millimoles per mole (mmol/mol)) Participants with T2D: A history of T2D and HbA1c < 10% (< 86 mmol/mol). If a participant without a history of diabetes during the screening period receives an HbA1c result of 6.5% (48 mmol/mol) or higher, the investigator or the participant's healthcare provider must confirm the diagnosis of type 2 diabetes before the participant is randomised.

Exclusion: A self-reported change in body weight > 5% within 90 days before screening, irrespective of medical records; Use of any glucagon-like-peptide-1 receptor agonist (GLP-1 RA), including medication with GLP-1 RA activity, or amylin analogues, including medication with amylin activity, within 6 months before screening.

ClinicalTrials.gov NCT07564414 · EU CTIS 2025-522488-14-00