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Tirzepatide's Role in Postmenopausal HR+ Breast Cancer Survivors
Sponsor: Weill Medical College of Cornell University
Summary
This study will explore whether tirzepatide is a practical and acceptable treatment for postmenopausal women with a history of hormone receptor-positive breast cancer and obesity. The investigators aim to understand whether participants are willing and able to take this medication once weekly for 6 months and whether it may help improve weight and overall health. There will be monthly check-ins to monitor progress and safety. At the beginning and end of the study, participants will undergo body composition assessments, blood tests and a stool sample will be collected, and surveys will be completed.
Key Details
Gender
FEMALE
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
30
Start Date
2026-04-06
Completion Date
2027-12-30
Last Updated
2026-03-13
Healthy Volunteers
No
Conditions
Interventions
Tirzepatide
Participants will take tirzepatide weekly for 24 weeks. The dose will be adjusted on a monthly basis as clinically indicated.
Locations (1)
Weill Cornell Medicine
New York, New York, United States