RecruitingPhase 2NCT06390956

Pirtobrutinib in Combination With Rituximab in Adults With Untreated Marginal Zone Lymphoma (PIONEER-MZL)

A Phase II Study of Pirtobrutinib in Combination With Rituximab in Adults With Untreated Marginal Zone Lymphoma


Sponsor

University of Utah

Enrollment

23 participants

Start Date

Feb 20, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this clinical trial is to learn if the drugs Pirtobrutinib and Rituximab are effective for the treatment of newly diagnosed marginal zone lymphoma.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a combination of two drugs — pirtobrutinib (a targeted cancer drug that blocks a protein called BTK) and rituximab (an antibody that targets cancer cells) — as a first treatment for a type of blood cancer called marginal zone lymphoma (MZL). **You may be eligible if...** - You are 18 or older - You have been diagnosed with marginal zone lymphoma (any subtype) confirmed by a biopsy - You have not had any systemic (whole-body) treatment for MZL before - Your blood counts, liver, and kidney function are within acceptable ranges **You may NOT be eligible if...** - You have had prior systemic drug treatment for MZL (prior antibiotics for certain infections or antiviral therapy is acceptable) - You have active cancer spreading to the brain or spinal fluid - You are pregnant or breastfeeding - You have a serious autoimmune condition requiring immune-suppressing medications 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

DRUGPirtobrutinib

Administered once daily as an oral medication.

DRUGRituximab

Rituximab is a sterile, clear, colorless, preservative-free liquid concentrate for intravenous (IV) administration. The product is formulated for intravenous administration in 9.0 mg/mL sodium chloride, 7.35 mg/mL sodium citrate dihydrate, 0.7 mg/mL polysorbate 80, and Sterile Water for Injection.


Locations(2)

Washington University

St Louis, Missouri, United States

Huntsman Cancer Institute at University of Utah

Salt Lake City, Utah, United States

View Full Details on ClinicalTrials.gov

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NCT06390956


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