drugset / Trial / NCT03081780

Open Label NK Cell Infusion (FATE-NK100) With Subq IL-2 in Adults With AML

NCT03081780

Phase 1 Completed 6 enrolled Masonic Cancer Center, University of Minnesota
NaSingle-groupOpen-labelTreatment

Summary

This is a Phase I open-label dose escalation study of a single infusion of FATE-NK100 and a short course of subcutaneous interleukin-2 (IL-2) administered after lymphodepleting chemotherapy (CY/FLU) in subjects with refractory or relapsed acute myelogenous leukemia (AML). FATE-NK100 is a natural killer (NK) cell product that is enriched for NK cells with an "adaptive", or human cytomegalovirus (CMV)-induced, phenotype. The NK cell product is comprised of peripheral blood (PB) leukocytes sourced from a related donor (HLA-haploidentical or better but not fully HLA-matched) that is seropositive for cytomegalovirus (CMV+), and enriched for adaptive NK cells by depletion of CD3+ (T-lymphocytes) and CD19+ (B-lymphocytes) cells followed by ex-vivo culture expansion.

Timeline

Start
2017-04-27
Primary completion
2020-08-01
Completion
2020-12-01

Drugs

EvaluationDrugModalityDoseRoute
Subject FATE-NK100 Cell therapy
Background Cyclophosphamide Other / unclassified 60 mg/kg
Background Fludarabine Small molecule 25 mg/m2
Background aldesleukin Protein / enzyme biologic 6e+06 iu Subcutaneous