Phase 2Completed

Everolimus Aging Study (EVERLAST)

Clinical Evaluation of mTORC1 Inhibition for Geroprotection

Sponsor
University of Wisconsin, Madison (Academic or other)
Enrolment
106 enrolled
Conditions
Aging; Insulin Resistance
Interventions
Everolimus 0.5 MG once per day; Everolimus 5 MG once per week; Placebo once per day; Placebo once per week
Ages
adults, older adults
Registry
NCT05835999

From the registry

The objective of this project is to determine if mTORC1 inhibition by 24 weeks of daily (0.5 mg/day) or weekly (5 mg/week) everolimus can safely improve physiological and molecular hallmarks of aging in humans. Participants who are 55-80 years old and insulin resistant or prediabetic will be randomized to treatment and can expect to be on study for up to approximately 38 weeks. Participants aged 18-35 will not receive the intervention and can expect to be on study for up to approximately 8 weeks.

Primary outcomes

  • Metabolic Function: Change in peripheral insulin sensitivity
Full record on ClinicalTrials.gov