๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-05-12

Testing the Safety of the Anti-cancer Drugs Tazemetostat and Belinostat in Patients With Lymphomas That Have Resisted Treatment (NCT05627245)

Phase 1/Expansion Study of Tazemetostat Plus Belinostat for the Treatment of Relapsed or Refractory Lymphoma

๐Ÿ”ต Active, Not Recruiting Phase1 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: National Cancer Institute (NCI)

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

This phase I trial tests the safety, side effects, and best dose of combination therapy with tazemetostat and belinostat in treating patients with lymphoma that has come back after a period of improvement (relapsed) or that does not respond to treatment (refractory). Tazemetostat is in a class of medications called EZH2 inhibitors. The EZH2 gene provides instructions for making a type of enzyme called histone methyltransferase which is involved in gene expression and cell division. Blocking EZH2 may help keep cancer cells from growing. Belinostat is in a class of medications called histone deacetylase inhibitors. Histone deacetylases are enzymes needed for cell division. Belinostat may kill cancer cells by blocking histone deacetylase. It may also prevent the growth of new blood vessels that tumors need to grow and may help make cancer cells easier to kill with other anticancer drugs. There is some evidence in animals and in living human cells that combination therapy with tazemetostat and belinostat can shrink or stabilize cancer, but it is not known whether this will happen in people. This trial may help doctors learn more about treatment of patients with relapsed or refractory lymphoma.

Who can join: Review the eligibility criteria below.

Location: University of California Davis Comprehensive Cancer Center โ€” Sacramento, California

Age range: 18 Years

๐Ÿงช Interventions in This Study

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

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

๐Ÿ“ All Participating Trial Locations (11 Sites)

  • University of California Davis Comprehensive Cancer Center โ€” Sacramento, California
  • Yale University โ€” New Haven, Connecticut
  • University of Kansas Clinical Research Center โ€” Fairway, Kansas
  • University of Kansas Cancer Center โ€” Kansas City, Kansas
  • University of Kansas Hospital-Westwood Cancer Center โ€” Westwood, Kansas
  • Rutgers Cancer Institute of New Jersey โ€” New Brunswick, New Jersey
  • NYP/Columbia University Medical Center/Herbert Irving Comprehensive Cancer Center โ€” New York, New York
  • Ohio State University Comprehensive Cancer Center โ€” Columbus, Ohio
  • University of Oklahoma Health Sciences Center โ€” Oklahoma City, Oklahoma
  • Huntsman Cancer Institute/University of Utah โ€” Salt Lake City, Utah
  • VCU Massey Comprehensive Cancer Center โ€” Richmond, Virginia

๐Ÿ’ฐ 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 ยง 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.

๐Ÿ’ก 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.
๐Ÿ›๏ธ View Official NIH Record โ†—