drugset / Trial / NCT06541444

Safety and Efficacy of NK520 to Treat Relapsed/Refractory Acute Myeloid Leukemia

NCT06541444 ↗

Non-randomizedSequentialOpen-labelTreatment

Summary

This study will evaluate the safety and efficacy of NK520 in the treatment of relapsed/refractory acute myeloid leukemia. NK520 will be administered by intravenous injection. The safety and efficacy of this treatment will be evaluated.

Timeline

Start
2024-07-01
Primary completion
2026-06-01
Completion
2026-06-01

Drugs

EvaluationDrugModalityDoseRoute
Subject NK520 Unknown 3e+07 cells/kg Intravenous
Subject NK520 Unknown 6e+07 cells/kg Intravenous
Subject NK520 Unknown 9e+07 cells/kg Intravenous