120
Participants
Start Date
October 16, 2025
Primary Completion Date
December 31, 2025
Study Completion Date
December 31, 2025
Patient switched from IV vedolizumab to subcutaneous vedolizumab as part of normal patient care
This study does not include any subject enrollment or randomization. This is a retrospective cohort review of patients referred to start subcutaneous vedolizumab from a VUMC IBD provider.
Vanderbilt University Medical Center, Nashville
Takeda Pharmaceuticals U.S.A., Inc.
UNKNOWN
Vanderbilt University Medical Center
OTHER