Phase 1Recruiting

Rapalog Pharmacology (RAP PAC) Study

Safer mTOR Inhibition for Human Geroprotection

Sponsor
University of Wisconsin, Madison (Academic or other)
Enrolment
72 planned
Conditions
Aging
Interventions
Sirolimus; Everolimus
Ages
adults, older adults
Registry
NCT05949658

From the registry

The objective of RAP PAC is to identify safe and effective weekly dose(s) for the mTOR inhibitors sirolimus and everolimus that intervene on the underlying fundamental biology of aging. Participants who are 55-89 years old that are free of overt chronic diseases will be assigned to either 6 weeks of sirolimus or everolimus (5 mg, 10 mg, or 15 mg once per week). The investigators will complete the everolimus arm first and then subsequently complete the sirolimus arm of the study. Total time on study would be up to 17 weeks to complete baseline and follow up visits.

Primary outcomes

  • Dose Limited Toxicities (DLTs)
Full record on ClinicalTrials.gov