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RECRUITING Phase 1

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

NCT06528301 · View on ClinicalTrials.gov ↗

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).

Interventions

  • DRUG rapamycin
  • GENETIC UB-VV111

Study Locations (8)

California

  • City of Hope — Duarte

Illinois

  • The David and Etta Jonas Center for Cellular Therapy — Chicago

Missouri

  • Washington University School of Medicine/Siteman Cancer Center — St Louis

Nebraska

  • University of Nebraska Medical Center — Omaha

Ohio

  • University of Cincinnatti Medical Center — Cincinnati

Washington

  • Fred Hutch Cancer Center — Seattle

New South Wales

  • Royal North Shore Hospital — Saint Leonards

Victoria

  • St. Vincent's Hospital Melbourne — Fitzroy

Trial Details

FieldValue
Enrollment Target 106 participants
Start Date 2025-03-10
Est. Completion 2029-03
Phase Phase 1

Sponsor

Umoja Biopharma

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06528301

The ClinicalTrials.gov registry entry for NCT06528301 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 106 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Umoja Biopharma, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 4 conditions, with Lymphoma, B-Cell appearing as the primary indexed condition, and to 2 interventions — of which rapamycin is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06528301 reports 8 study locations spanning 8 distinct geographic areas — top geographies include California, Illinois, Missouri. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06528301 about?

NCT06528301 is a clinical study titled "A Phase 1 Study of UB-VV111 With and Without Rapamycin in Relapsed/Refractory CD19+ B-cell Malignancies". 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).

What is the current status of trial NCT06528301?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 106 participants. The study started on 2025-03-10. Estimated completion is 2029-03.

What conditions does trial NCT06528301 study?

This clinical trial studies the following conditions: Lymphoma, B-Cell, Chronic Lymphocytic Leukemia (CLL), Lymphoma, Non-Hodgkin (NHL), Lymphoma, Large B-Cell, Diffuse (DLBCL). These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06528301?

The interventions under investigation include: rapamycin (DRUG), UB-VV111 (GENETIC). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06528301?

This trial is sponsored by Umoja Biopharma, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06528301 being conducted?

This trial has 8 study locations across California, Illinois, Missouri, Nebraska, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial