FT596 With Rituximab as Relapse Prevention After Autologous HSCT for NHL

PHASE1CompletedINTERVENTIONAL
Enrollment

7

Participants

Timeline

Start Date

September 22, 2020

Primary Completion Date

February 8, 2023

Study Completion Date

November 30, 2023

Conditions
NHLNon Hodgkin LymphomaDiffuse Large B Cell LymphomaHigh-grade B-cell Lymphoma
Interventions
DRUG

FT596

FT596 is given 2-3 days after rituximab; however, it may be delayed for up to 7 days until all rituximab infusion related toxicities resolve to ≤Grade 1.

DRUG

Rituximab

Rituximab 375 mg/m\^2 is administered as an IV infusion per institutional standard of care and package insert on 2-3 days (48 to 72 hours) prior to the FT596 infusion

Trial Locations (2)

55401

University of Minnesota, Minneapolis

63110

Washington University School of Medicine - Siteman Cancer Center, St Louis

All Listed Sponsors
collaborator

National Cancer Institute (NCI)

NIH

lead

Masonic Cancer Center, University of Minnesota

OTHER

NCT04555811 - FT596 With Rituximab as Relapse Prevention After Autologous HSCT for NHL | Biotech Hunter | Biotech Hunter