20
Participants
Start Date
May 31, 2025
Primary Completion Date
May 31, 2026
Study Completion Date
July 31, 2026
Tirzepatide
This intervention will consist of the FDA-approved dosing schedule. Participants will receive 2.5mg weekly injections for 4 weeks. IDS will extract tirzepatide and draw the doses into syringes.
Saline Placebo
Placebo syringes of saline and matching volume will be produced by IDS.
Brigham and Women's Hospital, Boston
Brigham and Women's Faulkner Hospital, Jamaica Plain
Brigham and Women's Hospital
OTHER