Start Date
December 31, 2022
Primary Completion Date
May 31, 2026
Study Completion Date
May 31, 2039
FT596
Dosing to be initiated at a dose no higher than highest tolerable dose in study FT596-101, intravenously
Cyclophosphamide
750 mg/m\^2 intravenously
Doxorubicin
50 mg/m\^2 intravenously
Vincristine
1.4 mg/m\^2 (maximum dose 2 mg) intravenously
Prednisone
100 mg orally
Rituximab
375 mg/m\^2 intravenously
Bendamustine
90 mg/m\^2 IV infusion
Lead Sponsor
Fate Therapeutics
INDUSTRY