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Active (not recruiting) Phase 3 NCT07220642

Weight Loss in People Living With Overweight or Obesity Following Treatment With Cagrilintide

Phase 3 – large-scale trial before approval
Conditions: Obesity Overweight

Sponsor: Novo Nordisk A/S

trial.available_in: БГ
Overview
This study will look at how much cagrilintide helps people with overweight or obesity lower their body weight. Cagrilintide is a new investigational medicine. Doctors may not yet prescribe cagrilintide. Participants will either get cagrilintide or placebo. Which treatment participants get is decided by chance. Participants are two times more likely to get cagrilintide than placebo. Like all medicines, the study medicine may have side effects. Possible side effects will be followed carefully during the study. For each participant, the study will last for about 1 year and 6 months.
Who can participate
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 * Female or male (sex at birth) * Age 18 years or above at the time of signing the informed consent * History of at least one self-reported unsuccessful dietary effort to lose body weight (a\*) * Body mass index (BMI) greater than or equal to \>= 30.0 kilogram per square meter (kg/m\^2), or BMI greater than or equal to \>= 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 (a\*) Exclusion criteria: * History of type 1 or type 2 diabetes (a\*) * Treatment, or intention to initiate treatment, with any medication prescribed for the indication of weight management within 180 days before screening (a\*) * Previous dosing of marketed or non-marketed amylin-based compounds (a\*) (a\*) - As declared by the participant, reported in the medical records or at the investigator's discretion.
Locations 10
Argentina (1)
CIPREC Pueyrredon
Buenos Aires
Australia (1)
Sydney Cardiometabolic Centre
Liverpool , New South Wales
Canada (1)
G.A. Research Associates Ltd.
Moncton , New Brunswick
France (1)
Centre Hospitalier Universitaire de Nantes-Hopital Nord Laennec
Saint-Herblain
Germany (1)
InnoDiab Forschung GmbH
Essen
Italy (1)
Fondazione Policlinico Universitario Agostino Gemelli IRCS
Rome , RM
Norway (1)
Haukeland Universitetssykehus
Bergen
Poland (1)
Osteo-Medic s.c. A. Racewicz, J. Supronik
Bialystok
United Kingdom (1)
Oak Tree Surgery
Liskeard , Cornwall
United States (1)
Diablo Clinical Research, Inc.
Walnut Creek , California
Technical details
Status
Active (not recruiting)
Phase
Phase 3
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
05.11.2025
Completion date
29.06.2027
Registry ID
NCT07220642
Source
anzctr
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Information is automatically extracted from ClinicalTrials.gov. Consult your doctor before taking action.