Overview

Semaglutide Effects on Heart Disease and Stroke in Patients With Overweight or Obesity

Status:
Recruiting
Trial end date:
2023-09-28
Target enrollment:
0
Participant gender:
All
Summary
The researchers are doing the study to see if semaglutide may reduce the risk of having cardiovascular events in patients with overweight or obesity and with prior cardiovascular disease. The participant will either get semaglutide (active medicine) or placebo ("dummy" medicine). Which treatment the participants get is decided by chance. The participant's chance of getting semaglutide or placebo is the same. The participant will get the study medicine in a pen. The participants will need to use the pen to inject the study medicine in a skinfold once a week. The study will last for about 2.5 to 5 years. Participants will have up to 25 clinic visits with the study doctor.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Novo Nordisk A/S
Criteria
Inclusion Criteria:

- Male or female, age greater than or equal to 45 years at the time of signing informed
consent

- Body mass index (BMI) greater than or equal to 27 kg/m^2

- Have established cardiovascular (CV) disease as evidenced by at least one of the
following: prior myocardial infarction; prior stroke (ischemic or haemorrhagic
stroke); or symptomatic peripheral arterial disease (PAD), as evidenced by
intermittent claudication with ankle-brachial index (ABI) less than 0.85 (at rest), or
peripheral arterial revascularization procedure, or amputation due to atherosclerotic
disease

Exclusion Criteria:

- Any of the following: myocardial infarction, stroke, hospitalisation for unstable
angina pectoris or transient ischaemic attack within the past 60 days prior to the day
of screening

- HbA1c greater than or equal to 48 mmol/mol (6.5 %) as measured by the central
laboratory at screening

- History of type 1 or type 2 diabetes (history of gestational diabetes is allowed)