πŸ›οΈ Verified NIH Record β€’ Updated 2026-07-22

A Study of Ibrutinib With Rituximab in People With Untreated Marginal Zone Lymphoma (NCT04212013)

A Multicenter, Randomized, Double-blind, Placebo-controlled, Phase III Study of Ibrutinib in Combination With Rituximab in Subjects With Treatment NaΓ―ve Marginal Zone Lymphoma

πŸ”΅ Active, Not Recruiting Phase3 πŸ’Š Investigational Drug / Biologic Sponsor: Memorial Sloan Kettering Cancer Center

🩺 Plain-English Summary (8th-Grade Level)

The purpose of this study is to see if the combination of rituximab and ibrutinib can help people with marginal zone lymphoma who have not received treatment in the past. The study will also compare the combination of rituximab and ibrutinib with the combination of rituximab and placebo to see which combination works better.

Who can join: Review the eligibility criteria below.

Location: George Washington Cancer Center β€” Washington D.C., District of Columbia

Age range: 18 Years

πŸ§ͺ Interventions in This Study

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (10 Sites)

  • George Washington Cancer Center β€” Washington D.C., District of Columbia
  • Moffitt Cancer Center β€” Tampa, Florida
  • Mayo Clinic Cancer Center β€” Rochester, Minnesota
  • Memorial Sloan Kettering Basking Ridge β€” Basking Ridge, New Jersey
  • Memorial Sloan Kettering Monmouth β€” Middletown, New Jersey
  • Memorial Sloan Kettering Bergen β€” Montvale, New Jersey
  • Memorial Sloan Kettering Commack β€” Commack, New York
  • Memorial Sloan Kettering Westchester β€” Harrison, New York
  • Memorial Sloan Kettering Cancer Center β€” New York, New York
  • Memorial Sloan Kettering Nassau β€” Uniondale, New York

πŸ’° Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

πŸ’‘ How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Review the official NIH record below to find the coordinating site.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
πŸ›οΈ View Official NIH Record β†—