NCT05360238

A Phase 1/2, Open Label, Multicenter Study to Assess the Safety, Tolerability and Efficacy of MB-106 in Patients With Relapsed or Refractory CD20+ B-Cell Non-Hodgkin Lymphoma or Chronic Lymphocytic Leukemia

Study Summary

Study to Assess the Safety, Tolerability and Efficacy of MB-106 in Patients with Relapsed or Refractory B-Cell NHL or CLL

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Interventions

MB-106BIOLOGICAL
T-cells derived from autologous leukapheresis that are genetically modified.

Study Locations

FacilityCityStateCountry
UC Irvine Health - Chao Family Comprehensive Cancer CenterOrangeCaliforniaUnited States
Massachusetts General Hospital (MGH)BostonMassachusettsUnited States
Memorial Sloan Kettering Cancer CenterNew YorkNew YorkUnited States
University of Rochester Medical CenterRochesterNew YorkUnited States
Cleveland ClinicClevelandOhioUnited States
Fred Hutchinson Cancer Research CenterSeattleWashingtonUnited States

Official Trial Information

View on ClinicalTrials.gov

Data sourced from ClinicalTrials.gov. Last updated: April 14, 2026