This study is a Phase 1 dose-escalation and dose-confirmation study to evaluate the safety and antitumor activity of UB-VV111. The study will enroll patients with relapsed/refractory large B-cell lymphoma (LBCL) and chronic lymphocytic leukemia (CLL).
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
106
City of Hope
Duarte, California, United States
NOT_YET_RECRUITINGThe David and Etta Jonas Center for Cellular Therapy
Chicago, Illinois, United States
RECRUITINGWashington University School of Medicine/Siteman Cancer Center
Percentage of participants with common adverse events (AEs)
Percentage of participants with commonly reported AEs overall and by severity
Time frame: Up to 2 years after UB-VV111 administration
Overall response rate (ORR)
Percentage of participants with a best overall response (BOR) of complete response (CR) or partial response (PR)
Time frame: Up to 2 years after UB-VV111 administration
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St Louis, Missouri, United States
University of Nebraska Medical Center
Omaha, Nebraska, United States
RECRUITINGUniversity of Cincinnatti Medical Center
Cincinnati, Ohio, United States
RECRUITINGFred Hutch Cancer Center
Seattle, Washington, United States
RECRUITINGRoyal North Shore Hospital
Saint Leonards, New South Wales, Australia
RECRUITINGSt. Vincent's Hospital Melbourne
Fitzroy, Victoria, Australia
RECRUITING