Sign in

NCT06528301RecruitingPhase 1

A Phase 1 Study of UB-VV111 With and Without Rapamycin in Relapsed/Refractory CD19+ B-cell Malignancies

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

Source: ClinicalTrials.gov · Last updated 15 Oct 2026

Brief summary (registry, in English)

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).

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
106 (estimated)
First submitted
25 Jul 2024
Start date
10 Mar 2025
Primary completion date
Mar 2029
Lead sponsor
Umoja Biopharma
NCT number
NCT06528301

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 106
  • From 10 Mar 2025 to the primary completion date, Mar 2029
  • 9 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Currently receiving treatment in another interventional clinical trial.

Other illness

  • History of or active human immunodeficiency virus (HIV)
  • Active hepatitis B or C
  • Systemic immunodeficiency diseases, except for well-controlled Type I diabetes or thyroid disease
  • Ongoing CNS disease that would preclude neurologic assessment
  • Uncontrolled angina or other acute heart disease

Lab values

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

Other

  • Women who are pregnant or breastfeeding
  • Current isolated central nervous system (CNS) involvement

Who the study is looking for

  • 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).
  • No serious concomitant diseases or active/uncontrolled infections
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • Adequate organ function
  • Patients who have previously received CD19-directed therapy must have biopsy confirming CD19 expression following completion of prior CD19-directed therapy.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (9)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
St Vincent's Hospital Melbourne
Coordinator of this site? Confirm its status
FitzroyAustraliaRecruiting
Royal North Shore Hospital
Coordinator of this site? Confirm its status
Saint LeonardsAustraliaRecruiting
The David and Etta Jonas Center for Cellular Therapy
Coordinator of this site? Confirm its status
ChicagoUnited StatesRecruiting
University of Cincinnatti Medical Center
Coordinator of this site? Confirm its status
CincinnatiUnited StatesRecruiting
City of Hope
Coordinator of this site? Confirm its status
DuarteUnited StatesRecruiting
START | Midwest
Coordinator of this site? Confirm its status
Grand RapidsUnited StatesRecruiting
University of Nebraska Medical Center
Coordinator of this site? Confirm its status
OmahaUnited StatesRecruiting
Fred Hutch Cancer Center
Coordinator of this site? Confirm its status
SeattleUnited StatesRecruiting
Washington University School of Medicine - Siteman Cancer Center
Coordinator of this site? Confirm its status
St LouisUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.