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NCT05890352 · ClinicalTrials.gov registry record · Phase 2

Study Adding Drugs to Usual Treatment for Large B-Cell Lymphoma That Returned or Did Not Respond to Treatment

A Phase 2 study of Recurrent Diffuse Large B-Cell Lymphoma and Refractory Diffuse Large B-Cell Lymphoma, sponsored by SWOG Cancer Research Network.

Recruiting
Registry status
Phase 2
Development phase
227
Enrollment target
20
Study locations

NCT05890352: Recruiting Phase 2 study of Recurrent Diffuse Large B-Cell Lymphoma and Refractory Diffuse Large B-Cell Lymphoma, sponsored by SWOG Cancer Research Network.

NCT05890352 is a Phase 2 study of Recurrent Diffuse Large B-Cell Lymphoma and Refractory Diffuse Large B-Cell Lymphoma that is actively recruiting participants, run by SWOG Cancer Research Network. The registered enrollment target is 227 participants, above the 43-participant average among 43 other Recurrent Diffuse Large B-Cell Lymphoma trials with a reported enrollment target (428% higher). The trial reports 20 study locations across 4 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05890352, a Phase 2 study of Recurrent Diffuse Large B-Cell Lymphoma and Refractory Diffuse Large B-Cell Lymphoma, is actively recruiting participants, sponsored by SWOG Cancer Research Network.

RECRUITING
Registry status
Phase 2
Development phase
227 participants
Enrollment target
20
Study locations

Study Summary

This phase 2 trial studies the side effects and best dose of tazemetostat and zanubrutinib in combination with tafasitamab and lenalidomide, and to see how well these combinations work in treating patients with large B-cell lymphoma that returned or did not respond to earlier treatment. Tazemetostat is in a class of medications called EZH2 inhibitors. It helps to stop the spread of cancer cells. Zanubrutinib is in a class of medications called kinase inhibitors. It works by blocking the action of the abnormal protein that signals cancer cells to multiply. This helps stop the spread of cancer cells. tafasitamab is a monoclonal antibody that may interfere with the ability of cancer cells to grow and spread. Lenalidomide is in a class of medications called immunomodulatory agents. It works by helping the bone marrow to produce normal blood cells and by killing abnormal cells in the bone marrow. The addition of tazemetostat or zanubrutinib to tafasitamab and lenalidomide may be able to shrink the cancer or extend the time without cancer symptoms coming back.

Primary Outcome

Will be compared between participants randomized to control Arm 2 (tafasitamab + lenalidomide) versus (vs) experimental Arm 1 (tafasitamab + lenalidomide + tazemetostat), AND control Arm 2 vs experimental Arm 3 (tafasitamab + lenalidomide + zanubrutinib), respectively.

Interventions

  • PROCEDURE Biospecimen Collection
  • PROCEDURE Computed Tomography
  • PROCEDURE Magnetic Resonance Imaging
  • PROCEDURE Positron Emission Tomography
  • DRUG Lenalidomide

Study Locations (20)

California

  • Tower Cancer Research Foundation - Beverly Hills
  • City of Hope Comprehensive Cancer Center - Duarte
  • City of Hope Seacliff - Huntington Beach
  • City of Hope Antelope Valley - Lancaster
  • City of Hope at Long Beach Elm - Long Beach
  • Cedars Sinai Medical Center - Los Angeles
  • City of Hope Newport Beach - Newport Beach
  • City of Hope South Pasadena - South Pasadena
  • City of Hope South Bay - Torrance
  • City of Hope Upland - Upland

Illinois

  • University of Illinois - Chicago
  • University of Chicago Comprehensive Cancer Center - Chicago
  • Carle at The Riverfront - Danville
  • Carle Physician Group-Effingham - Effingham
  • Carle Physician Group-Mattoon/Charleston - Mattoon
  • UC Comprehensive Cancer Center at Silver Cross - New Lenox

Arizona

  • Banner University Medical Center - Tucson - Tucson
  • University of Arizona Cancer Center-North Campus - Tucson

Florida

  • Holy Cross Hospital - Fort Lauderdale
  • Mount Sinai Medical Center - Miami Beach

Trial Details

FieldValue
Enrollment Target 227 participants
Start Date 2023-09-26
Est. Completion 2029-01
Phase Phase 2
SWOG Cancer Research Network

270 total trials

What NCT05890352 shows while recruiting

NCT05890352 is an interventional study that assigns participants to a tested intervention. The registered 227 participants enrollment target is mid-sized for trials with a published cap, above the 43-participant average among 43 other Recurrent Diffuse Large B-Cell Lymphoma trials with a reported enrollment target (428% higher).

The record links to 6 conditions, with Recurrent Diffuse Large B-Cell Lymphoma appearing as the primary indexed condition, and to 5 interventions - of which Biospecimen Collection is the first listed.

NCT05890352 names 20 study sites across 4 states, led by California, Illinois, Arizona.

Frequently Asked Questions

What is clinical trial NCT05890352 about?

NCT05890352 is a clinical study titled "Study Adding Drugs to Usual Treatment for Large B-Cell Lymphoma That Returned or Did Not Respond to Treatment". This phase 2 trial studies the side effects and best dose of tazemetostat and zanubrutinib in combination with tafasitamab and lenalidomide, and to see how well these combinations work in treating patients with large B-cell lymphoma that returned or did not respond to earlier treatment. Tazemetostat...

What is the current status of trial NCT05890352?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 227 participants. The study started on 2023-09-26. Estimated completion is 2029-01.

What conditions does trial NCT05890352 study?

This clinical trial studies the following conditions: Recurrent Diffuse Large B-Cell Lymphoma, Refractory Diffuse Large B-Cell Lymphoma, High Grade B-Cell Lymphoma, High Grade B-Cell Lymphoma With MYC and BCL2 and/or BCL6 Rearrangements, Grade 3b Follicular Lymphoma.

What interventions are being tested in trial NCT05890352?

The interventions under investigation include: Biospecimen Collection (PROCEDURE), Computed Tomography (PROCEDURE), Magnetic Resonance Imaging (PROCEDURE), Positron Emission Tomography (PROCEDURE), Lenalidomide (DRUG).

Who is sponsoring clinical trial NCT05890352?

This trial is sponsored by SWOG Cancer Research Network, which has 270 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05890352 being conducted?

This trial has 20 study locations across Arizona, California, Florida, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Recurrent Diffuse Large B-Cell Lymphoma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05890352's enrollment target sits among peer trials

227 2nd of 43 the highest of 43 other Recurrent Diffuse Large B-Cell Lymphoma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Recurrent Diffuse Large B-Cell Lymphoma trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05890352, the US trial registry maintained by the National Library of Medicine. NCT05890352 (mid enrollment · wide site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.