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A Study to Test the Effect of Survodutide (BI 456906) on Cardiovascular Safety in People With Overweight or Obesity (SYNCHRONIZE™ - CVOT)

Obesity

This study is open to adults who are at least 18 years old and have a body mass index (BMI)bof 27 kg/m2 or more. People can take part if they have cardiovascular or chronic kidney disease. People who have at least 2 health problems related to their weight or risks of cardiovascular disease can participate. Participants must have previously tried to lose weight by changing their diet.

The purpose of this study is to find out whether people with overweight or obesity who take a medicine called survodutide (BI 456906) are less or more likely to develop serious cardiovascular problems. It also aims to find out whether health parameters like blood pressure improve. Overweight and obesity are linked to cardiovascular disease. Survodutide is a medicine that is developed to help people with obesity or overweight to lose weight.

Participants are divided into 3 groups of almost equal size. 2 groups get different doses of survodutide and 1 group gets placebo. Placebo looks like survodutide but does not contain any medicine. Every participant has a 2 in 3 chance of getting survodutide. Participants inject survodutide or placebo under the skin once a week. All participants also receive counselling on diet and physical activity.

Participants are in the study for up to 2 years and 3 months. During this time, it is planned that participants visit the study site up to 21 times and attend remote visits by video calls. During these visits, the doctors check participants' cardiovascular and overall health. The results are compared between survodutide and placebo groups. The study staff also takes note of any unwanted effects.

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    18 and up

Participation Criteria

Inclusion Criteria:

1. Male or female, age ≥18 years at the time of signing informed consent, and at least the legal age of consent in countries where it is \>18 years.
2. Body mass index (BMI) ≥27 kg/m2 at screening with established cardiovascular disease (CVD) and/or at least 2 weight-related complications or risk factors for CVD OR BMI ≥30 kg/m2 at screening with established CVD or chronic kidney disease (CKD), and/or at least 2 weight-related complications or risk factors for CVD.

Further inclusion criteria apply.

Exclusion criteria:

1. Previous treatment with glucagon-like peptide-1 receptor (GLP-1R) agonists within 3 months before screening.
2. Type 1 diabetes.
3. Less than 3 months between the last dose of GLP-1R agonists and GLP-1R agonist/insulin/glucose-dependent insulinotropic polypeptide (GIP) combinations and screening.
4. Known clinically significant gastric emptying abnormality (e.g., severe diabetic gastroparesis or gastric outlet obstruction).

Further exclusion criteria apply.

Study Location

Surrey Memorial Hospital
Surrey Memorial Hospital
Surrey, British Columbia
Canada

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Centricity Research (Brampton)
Centricity Research (Brampton)
Brampton, Ontario
Canada

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Premier Clinical Trial Network
Premier Clinical Trial Network
Hamilton, Ontario
Canada

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Canadian Phase Onward Inc.
Canadian Phase Onward Inc.
Toronto, Ontario
Canada

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Ecogene-21
Ecogene-21
Chicoutimi, Quebec
Canada

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Centre de Medecine Metabolique de Lanaudiere
Centre de Medecine Metabolique de Lanaudiere
Terrebonne, Quebec
Canada

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CARe Clinic (Red Deer)
CARe Clinic (Red Deer)
Red Deer, Alberta
Canada

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QEII Health Sciences Centre
QEII Health Sciences Centre
Halifax, Nova Scotia
Canada

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Centricity Research (Etobicoke)
Centricity Research (Etobicoke)
Etobicoke, Ontario
Canada

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Bluewater Clinical Research
Bluewater Clinical Research
Sarnia, Ontario
Canada

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Clinical Research Solutions Inc. (Waterloo)
Clinical Research Solutions Inc. (Waterloo)
Waterloo, Ontario
Canada

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Recherche Clinique Sigma Inc.
Recherche Clinique Sigma Inc.
Québec, Quebec
Canada

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Richmond Road Diagnostic & Treatment Centre
Richmond Road Diagnostic & Treatment Centre
Calgary, Alberta
Canada

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Victoria Heart Institute Foundation
Victoria Heart Institute Foundation
Victoria, British Columbia
Canada

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Wharton Medical Clinic (Burlington)
Wharton Medical Clinic (Burlington)
Burlington, Ontario
Canada

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Western Centre for Public Health & Family Medicine (LHRI)
Western Centre for Public Health & Family Medicine (LHRI)
London, Ontario
Canada

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Centricity Research (Bayview)
Centricity Research (Bayview)
Toronto, Ontario
Canada

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Montreal Heart Institute
Montreal Heart Institute
Montreal, Quebec
Canada

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Diex Recherche (Trois-Rivieres)
Diex Recherche (Trois-Rivieres)
Trois-Rivieres, Quebec
Canada

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C-ENDO Diabetes & Endocrinology Clinic
C-ENDO Diabetes & Endocrinology Clinic
Calgary, Alberta
Canada

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Winnipeg Clinic
Winnipeg Clinic
Winnipeg, Manitoba
Canada

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Cambridge Cardiac Care Centre
Cambridge Cardiac Care Centre
Cambridge, Ontario
Canada

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Centricity Research (Oshawa)
Centricity Research (Oshawa)
Oshawa, Ontario
Canada

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Diabetes Heart Research Centre
Diabetes Heart Research Centre
Toronto, Ontario
Canada

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Montreal General Hospital - McGill University Health Centre
Montreal General Hospital - McGill University Health Centre
Montreal, Quebec
Canada

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Study Sponsored By
Boehringer Ingelheim
Participants Required
More Information
Study ID: NCT06077864