NCT06528301

A Phase 1, Multicenter, Open-label Study of UB-VV111 in Combination With Rapamycin in Relapsed/Refractory (R/R) CD19+ B-cell Malignancies

Study Summary

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).

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Interventions

UB-VV111GENETIC
UB-VV111 is a gene therapy that generates CD19 CAR T cells in the body.
rapamycinDRUG
Rapamycin is an FDA-approved drug.

Study Locations

FacilityCityStateCountry
City of HopeDuarteCaliforniaUnited States
The David and Etta Jonas Center for Cellular TherapyChicagoIllinoisUnited States
Washington University School of Medicine/Siteman Cancer CenterSt LouisMissouriUnited States
University of Nebraska Medical CenterOmahaNebraskaUnited States
University of Cincinnatti Medical CenterCincinnatiOhioUnited States
Fred Hutch Cancer CenterSeattleWashingtonUnited States
Royal North Shore HospitalSaint LeonardsNew South WalesAustralia
St. Vincent's Hospital MelbourneFitzroyVictoriaAustralia

Official Trial Information

View on ClinicalTrials.gov

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