Mechanisms of Semaglutide Therapy in Heart Failure Patients

PHASE1/PHASE2RecruitingINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

July 10, 2024

Primary Completion Date

July 10, 2025

Study Completion Date

September 1, 2025

Conditions
Heart FailureObesity
Interventions
DRUG

Semaglutide

"10 overweight patients with heart failure will be enrolled, including 5 patients with heart failure with preserved ejection fraction (HFpEF) and 5 patients with heart failure with reduced ejection fraction (HFrEF). The diagnosis of HFpEF and HFrEF will be based on the most recent European Society of Cardiology guidelines for the diagnosis and treatment of heart failure.~After their baseline blood sample collections, all participants will receive once-weekly subcutaneous semaglutide (Ozempyc, Novo Nordisk A/S Bagsvaerd, Denmark) at a dose of 0.25 mg for 2 weeks, 0.5 mg for 2 weeks, and then 1.0 mg for a period of 12 weeks. At the end of the 3-month and 4-month period, blood sample collections will be repeated. All blood samples will be sent to Stanford Cardiovascular Institute for further analyses. At baseline, and again at 4 months transthoracic echocardiography, 6-minute walk test, and body composition assessment will be performed."

Trial Locations (3)

1000

RECRUITING

University Medical Center Ljubljana, Ljubljana

94304

RECRUITING

Greenstone Biosciences, Palo Alto

94305

RECRUITING

Stanford Cardiovascular Institute, Stanford

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Stanford University

OTHER

collaborator

Greenstone Biosciences

UNKNOWN

lead

University Medical Centre Ljubljana

OTHER

NCT06541509 - Mechanisms of Semaglutide Therapy in Heart Failure Patients | Biotech Hunter | Biotech Hunter