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NCT05100862 · ClinicalTrials.gov registry record · Phase 3

A Study of Zanubrutinib Plus Anti-CD20 Versus Lenalidomide Plus Rituximab in Participants With Relapsed/Refractory Follicular or Marginal Zone Lymphoma

A Phase 3 study of Marginal Zone Lymphoma and Relapsed/Refractory Follicular Lymphoma, sponsored by BeiGene.

Recruiting
Registry status
Phase 3
Development phase
780
Enrollment target
20
Study locations

NCT05100862 is a Phase 3 study of Marginal Zone Lymphoma and Relapsed/Refractory Follicular Lymphoma that is actively recruiting participants, run by BeiGene. The registered enrollment target is 780 participants, above the 87-participant average among 49 other Marginal Zone Lymphoma trials with a reported enrollment target (797% higher). The trial reports 20 study locations across 10 states.

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The verdict

NCT05100862, a Phase 3 study of Marginal Zone Lymphoma and Relapsed/Refractory Follicular Lymphoma, is actively recruiting participants, sponsored by BeiGene.

RECRUITING
Registry status
Phase 3
Development phase
780 participants
Enrollment target
20
Study locations

Study Summary

The purpose of the study is to compare the efficacy of zanubrutinib plus obinutuzumab versus lenalidomide plus rituximab (R\^2) in participants with relapsed/refractory (R/R) follicular lymphoma (FL), as measured by progression-free survival as determined by an independent review committee in accordance with the 2014 modification of the International Working Group on non-Hodgkin lymphoma (NHL) Criteria based on n positron emission tomography and computed tomography (PET/CT), and to compare the efficacy of zanubrutinib plus rituximab versus R\^2 in participants with R/R marginal zone lymphoma (MZL), as measured by progression free survival (PFS) assessed by IRC in accordance with CT-based Lugano 2014 Criteria.

Interventions

  • DRUG Zanubrutinib
  • DRUG Obinutuzumab
  • DRUG Rituximab
  • DRUG Lenalidomide

Study Locations (20)

California

  • Ucsf Fresno University of California San Francisco Fresno - Fresno
  • Kaiser Permanente Southern California - Irvine
  • Cancer and Blood Specialty Clinic - Los Alamitos
  • Los Angeles Cancer Network - Los Angeles
  • Valkyrie Clinical Trials - Los Angeles
  • UCLA Hematologyoncology - Los Angeles
  • Scripps Health - San Diego
  • Sharp Healthcare Sharp Memorial Hospital - San Diego

Florida

  • Baptist Md Anderson Cancer Center - Jacksonville
  • Ascension Sacred Heart - Pensacola

Kansas

  • Cotton Oneil Cancer Center - Topeka
  • Cancer Center of Kansas - Wichita

Maryland

  • Luminis Health Anne Arundel Medical Center - Annapolis
  • University of Maryland Greenebaum Comprehensive Cancer Center - Baltimore

Georgia

  • Northwest Georgia Oncology Centers Marietta - Marietta

Illinois

  • Cancer Care Specialists of Illinois - Decatur

Indiana

  • Fort Wayne Medical Oncology and Hematology - Fort Wayne

Iowa

  • Mission Cancer and Blood - Waukee

Trial Details

FieldValue
Enrollment Target 780 participants
Start Date 2022-03-10
Est. Completion 2030-06
Phase Phase 3

Sponsor

BeiGene

65 total trials

What the Registry Record Tells You About NCT05100862

The ClinicalTrials.gov registry entry for NCT05100862 describes a study currently listed as recruiting, categorized as Phase 3. The registered enrollment target is 780 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 87-participant average among 49 other Marginal Zone Lymphoma trials with a reported enrollment target (797% higher). The listed sponsor is BeiGene, which has 65 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Marginal Zone Lymphoma appearing as the primary indexed condition, and to 4 interventions - of which Zanubrutinib is the first listed.

NCT05100862 reports 20 study locations spanning 10 distinct geographic areas - top geographies include California, Florida, Kansas.

Frequently Asked Questions

What is clinical trial NCT05100862 about?

NCT05100862 is a clinical study titled "A Study of Zanubrutinib Plus Anti-CD20 Versus Lenalidomide Plus Rituximab in Participants With Relapsed/Refractory Follicular or Marginal Zone Lymphoma". The purpose of the study is to compare the efficacy of zanubrutinib plus obinutuzumab versus lenalidomide plus rituximab (R\^2) in participants with relapsed/refractory (R/R) follicular lymphoma (FL), as measured by progression-free survival as determined by an independent review committee in accord...

What is the current status of trial NCT05100862?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 780 participants. The study started on 2022-03-10. Estimated completion is 2030-06.

What conditions does trial NCT05100862 study?

This clinical trial studies the following conditions: Marginal Zone Lymphoma, Relapsed/Refractory Follicular Lymphoma.

What interventions are being tested in trial NCT05100862?

The interventions under investigation include: Zanubrutinib (DRUG), Obinutuzumab (DRUG), Rituximab (DRUG), Lenalidomide (DRUG).

Who is sponsoring clinical trial NCT05100862?

This trial is sponsored by BeiGene, which has 65 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05100862 being conducted?

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

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.