Phase 2 Study for High-Risk Mantle Cell Lymphoma (MCL)

This study is investigating if adding glofitamab after initial treatment with acalabrutinib or zanubrutinib (BTKi drugs) and rituximab can help control high-risk mantle cell lymphoma (MCL). MCL is a type of cancer that affects white blood cells. You may be able to join if you have a confirmed diagnosis of MCL with specific genetic markers (CD20 positivity, t(11;14) translocation, and/or cyclin D1 overexpression). Researchers will be looking at how safe the treatment is and how well it clears the cancer, specifically checking for minimal residual disease (MRD) negativity. The study aims to enroll 30 participants, but its current recruitment status is unclear.

Study design
This is a Phase 2 interventional study, meaning it tests a new treatment approach in a small group of people. It plans to enroll 30 participants.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Safety and adverse events will be measured through study completion, which is an average of 1 year.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07257055

Phase 2 Study of BTKi-Rituximab Induction Followed by Glofitamab Consolidation in High Risk Untreated MCL Patients - WINDOW-4 Study

Recruiting
PHASE2Ages 18+InterventionalTreatment
M.D. Anderson Cancer Center
~30 participants
Updated 2026-05-20 on ClinicalTrials.gov
What's tested:AcalabrutinibRituximabGlofitamab

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Safety and adverse events (AEs)
Measured over Through study completion; an average of 1 year
Phase 2 Study
MCL
BTKi
Rituximab
Glofitamab
1 sites across 1 states
Texas1
  • Preetesh Jain, MD · PRINCIPAL_INVESTIGATOR · M.D. Anderson Cancer Center

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  • Safety and adverse events (AEs)Through study completion; an average of 1 year

    Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0