67
Participants
Start Date
November 28, 2022
Primary Completion Date
January 31, 2026
Study Completion Date
January 31, 2026
IMT-009
Participants will receive an IV infusion of IMT-009 on Day 1 during each 21-day cycle.
Fruquintinib
Fruquintinib will be administered according to the FDA-approved United States Prescribing Information (USPI).
Site 9112, Fairfax
Site 4100, Orlando
Site 4060, Sarasota
Site 3000, Nashville
Site 4500, Oklahoma City
Site 9384, Austin
Site 5000, Denver
Site 9618, Tucson
Site 9280, Portland
Lead Sponsor
Immunitas Therapeutics
INDUSTRY