About this trial

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).

Eligibility criteria

Qualifiers

18 years or older

Provides voluntary written informed consent

Relapsed or refractory large B-cell lymphoma (LBCL) or chronic lymphocytic leukemia (CLL)

Measurable disease according to Lugano 2014 criteria (LBCL) or iwCLL 2018 (CLL).

Disqualifiers

Women who are pregnant or breastfeeding

Current isolated central nervous system (CNS) involvement

Prior allogeneic bone marrow transplant, gene therapy, or adoptive cell transfer (exceptions include tumor-infiltrating lymphocytes and CAR T cells)

History of or active human immunodeficiency virus (HIV)

Trial design

Treatments tested in this trial

  • UB-VV111
  • rapamycin

Treatment groups

106 Participants
are divided into 2 treatment groups

Locations

8
Australia
Royal North Shore Hospital2065, Saint LeonardsNew South Wales, Australia
St. Vincent's Hospital Melbourne3065, FitzroyVictoria, Australia
United States
California
City of Hope91010, Duarte United States
Illinois
The David and Etta Jonas Center for Cellular Therapy60637, Chicago United States

Sponsors and collaborators

Umoja Biopharma

Lead sponsor