drugset / Trial / NCT04489420

Natural Killer Cell (CYNK-001) IV Infusion or IT Administration in Adults With Recurrent GBM

NCT04489420 ↗

Phase 1 Terminated 3 enrolled Celularity Incorporated
Non-randomizedSequentialOpen-labelTreatment

Summary

This study will find the maximum safe dose (MSD) or maximum tolerated dose (MTD) of CYNK-001 which are NK cells derived from human placental CD34+ cells and culture-expanded. CYNK-001 cells will be given after lymphodepleting chemotherapy for the systemic cohort (IV) (intravenous). The intratumoral cohort (IT) will not be giving lymphodepletion. The safety of this treatment will be evaluated, and researchers want to learn if NK cells will help in treating recurrent glioblastoma multiforme.

Timeline

Start
2020-10-01
Primary completion
2021-08-10
Completion
2021-08-10

Outcome

Outcome not reported

Stopped (Business): “Business decision.”

Drugs

EvaluationDrugModalityDoseRoute
Subject CYNK001-IT Cell therapy 2e+08 cells Other
Subject CYNK001-IV Cell therapy 6e+08 cells Intravenous
Subject CYNK001-IV Cell therapy 1.2e+09 cells Intravenous