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Enrolling By Invitation
NCT07906041
Tirzepatide and Organ-specific Biological Aging
Conditions: Longevity, Preventive Medicine, Biological Ageing
Sex: All
Ages: 50 Years – 75 Years
Healthy volunteers: Yes
Phase: PHASE2
Enrollment: 22
Sponsor: Atria Research and Global Health Institute (ARGHI)
Location: Atria Research and Global Health Institute New York New York
Summary
The purpose of this study is to evaluate blood-based measures of organ-specific biological age, with a particular focus on the brain, and to investigate their relationship with established clinical indicators of health and their response to treatment with tirzepatide.
Eligibility Criteria
Inclusion Criteria:
* Stable medical status (neurological, cardiovascular, and immuno inflammatory)
* Adults age 50-75 years
* Eligible and waitlisted for brain health program onboarding
* Willingness to undergo serial blood sampling, wearable monitoring, and MRI
* Willingness to be assigned to the interventional trial or non-interventional trial
* Willingness to accept tirzepatide treatment (interventional arm)
Exclusion Criteria:
* Major neurodegenerative disease (e.g., dementia)
* Clinical and correlative imaging history of ischemic or hemorrhagic stroke
* History of myocardial infarction (ACS) or heart failure
* Significant inflammatory, autoimmune, or infectious disease or current treatments/interventions likely to distort proteomic aging measures
* Contraindications to MRI
* Currently taking tirzepatide
* Pre-existing indications for tirzepatide (e.g., Type 2 diabetes, obesity, or obstructive sleep apnea)
* BMI less than 20.0
* Known contraindication to tirzepatide, including a personal or family history of medullary thyroid carcinoma, Multiple Endocrine Neoplasia syndrome type 2, or known serious hypersensitivity to tirzepatide
* Active pancreatitis or history of recurrent pancreatitis
* Severe gastroparesis
* Clinically significant renal, hepatic, glycemic, or other laboratory abnormality that could increase the risk associated with tirzepatide treatment
* Current use of insulin or insulin secretagogues (e.g., sulfonylureas)
* Use of another incretin-based therapy unless discontinued for at least 35 days prior to enrollment
* History of clinically significant intolerance to tirzepatide or another incretin-based therapy
* Any other condition, illness, or medication that, in the judgment of the clinical investigative team, would make the individual an unsuitable candidate for tirzepatide or participation in this trial
* Contraindication to a wearable ring
* Pregnancy or lactation
* Prisoners
Source: ClinicalTrials.gov (NCT07906041). StuddyBuddy aggregates publicly available trial information.