๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-08-25

Testing Teclistamab (TECVAYLI) in Combination With Iberdomide for Relapsed or Refractory Multiple Myeloma (NCT06465316)

A Phase 1b Trial of Teclistamab in Combination With Iberdomide for Relapsed/Refractory Multiple Myeloma

๐ŸŸข Recruiting Phase1 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: National Cancer Institute (NCI)

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

This phase Ib trial tests the safety, side effects, and best dose of iberdomide in combination with teclistamab in treating multiple myeloma that has come back after a period of improvement (relapsed) or that does not respond to treatment (refractory). Iberdomide is a medication that belongs to a group of drugs known as cereblon E3 ligase modulators. Iberdomide works by targeting and destroying proteins that help myeloma cancer cells to survive. A monoclonal antibody is a type of protein that can bind to certain targets in the body, such as molecules that cause the body to make an immune response (antigens). Immunotherapy with monoclonal antibodies, such as teclistamab, may help the body's immune system attack the cancer, and may interfere with the ability of cancer cells to grow and spread. Giving iberdomide in combination with teclistamab may be safe and tolerable in treating patients with relapsed or refractory multiple myeloma.

Who can join: Review the eligibility criteria below.

Location: Mayo Clinic Hospital in Arizona โ€” Phoenix, Arizona

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 (14 Sites)

  • Mayo Clinic Hospital in Arizona โ€” Phoenix, Arizona
  • Smilow Cancer Hospital-Derby Care Center โ€” Derby, Connecticut
  • Smilow Cancer Hospital Care Center - Guilford โ€” Guilford, Connecticut
  • Yale University โ€” New Haven, Connecticut
  • Yale-New Haven Hospital North Haven Medical Center โ€” North Haven, Connecticut
  • Mayo Clinic in Florida โ€” Jacksonville, Florida
  • Moffitt Cancer Center โ€” Tampa, Florida
  • University of Kansas Cancer Center โ€” Kansas City, Kansas
  • University of Kansas Cancer Center-Overland Park โ€” Overland Park, Kansas
  • University of Kansas Hospital-Westwood Cancer Center โ€” Westwood, Kansas
  • Mayo Clinic in Rochester โ€” Rochester, Minnesota
  • Ohio State University Comprehensive Cancer Center โ€” Columbus, Ohio
  • University of Oklahoma Health Sciences Center โ€” Oklahoma City, Oklahoma
  • VCU Massey Comprehensive Cancer Center โ€” Richmond, Virginia

๐Ÿ“ž Contact the Study Coordinator

Phone: (855) 776-0015

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

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. Contact the study coordinator using the phone/email above.
  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†—