RecruitingPhase 1NCT06824701

Tazemetostat in Combination With Zanubrutinib and Anti-CD20 Monoclonal Antibody in Relapsed or Refractory B-cell Non-Hodgkin Lymphoma

A Phase 1b Study of Tazemetostat in Combination With Zanubrutinib and Anti-CD20 Monoclonal Antibody in Relapsed or Refractory Indolent B-cell Non-Hodgkin Lymphomas (TARZAN Trial)


Sponsor

University of Utah

Enrollment

24 participants

Start Date

Sep 12, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this clinical trial is to learn if the study drug Tazemetostat combined with Zanubrutinib and anti-CD20 monoclonal antibody is safe and effective in treating patients with relapsed or refractory indolent B-cell non-Hodgkin lymphoma.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a combination of three drugs — tazemetostat (an epigenetic therapy), zanubrutinib (a targeted BTK inhibitor), and an anti-CD20 antibody (like rituximab or obinutuzumab) — for people with follicular lymphoma or other B-cell lymphomas that have relapsed or are difficult to treat. **You may be eligible if...** - You are 18 or older - You have follicular lymphoma or another B-cell lymphoma that has relapsed or not responded to prior treatment - You have received at least one prior therapy - You are in acceptable health (ECOG score 0–2) - Your organ function is within acceptable ranges **You may NOT be eligible if...** - You have active central nervous system lymphoma - You require anticoagulant therapy that may interact with study drugs - You have active autoimmune disease - You are pregnant or breastfeeding - You have a history of severe reactions to anti-CD20 therapy Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGTazemetostat

Tazemetostat will be self-administered BID as an oral treatment on a 28-day cycle.

DRUGZanubrutinib

Zanubrutinib will be self-administered BID as an oral treatment on a 28-day cycle.

DRUGRituximab

Rituximab or a biosimilar will be administered intravenously per standard of care.

DRUGObinutuzumab

Obinutuzumab will be administered intravenously on days 1, 8, 15 of cycle 1 and then day 1 of cycles 2 to 12.


Locations(1)

Huntsman Cancer Institute at University of Uta

Salt Lake City, Utah, United States

View Full Details on ClinicalTrials.gov

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NCT06824701


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