๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-01-15

A Study of the Combination of Talquetamab and Teclistamab in Participants With Relapsed or Refractory Multiple Myeloma (NCT04586426)

A Phase 1b/2 Dose Escalation and Expansion Study of the Combination of the Bispecific T Cell Redirection Antibodies Talquetamab and Teclistamab in Participants With Relapsed or Refractory Multiple Myeloma

๐Ÿ”ต Active, Not Recruiting Phase1 / Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Janssen Research & Development, LLC

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

The purpose of this study is to identify the recommended Phase 2 regimen(s) (RP2R\[s\]) and schedule for the study treatment (Part 1), to characterize the safety of the RP2R(s) for the study treatment (Part 2) and to evaluate the anticancer activity of talquetamab + teclistamab in participants with relapsed or refractory multiple myeloma and extramedullary disease (EMD) (Part 3).

Who can join: Review the eligibility criteria below.

Location: University of Alabama at Birmingham, Comprehensive Cancer Center โ€” Birmingham, Alabama

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 (40 Sites)

Showing the first 25 of 40 sites.

  • University of Alabama at Birmingham, Comprehensive Cancer Center โ€” Birmingham, Alabama
  • University of Arkansas for Medical Sciences โ€” Little Rock, Arkansas
  • Colorado Blood Cancer Institute โ€” Denver, Colorado
  • Emory University โ€” Atlanta, Georgia
  • Mayo Clinic โ€” Rochester, Minnesota
  • Washington University St. Louis School Medicine Siteman Cancer Center โ€” St Louis, Missouri
  • Mount Sinai Medical Center โ€” New York, New York
  • Memorial Sloan Kettering Cancer Center โ€” New York, New York
  • Atrium Health โ€” Charlotte, North Carolina
  • Wake Forest University Baptist Medical Center (WFUBMC) - Comprehensive Cancer Center โ€” Winston-Salem, North Carolina
  • Cleveland Clinic โ€” Cleveland, Ohio
  • Oregon Health And Science University โ€” Portland, Oregon
  • The University of Texas MD Anderson Cancer Center โ€” Houston, Texas
  • St Vincents Hospital Melbourne โ€” Fitzroy,
  • Royal Perth Hospital โ€” Perth,
  • Arthur J E Child Comprehensive Cancer Centre โ€” Calgary, Alberta
  • Alberta Health Services โ€” Edmonton, Alberta
  • Princess Margaret Cancer Centre University Health Network โ€” Toronto, Ontario
  • McGill University Health Centre โ€” Montreal, Quebec
  • Hadassah Medical Center โ€” Jerusalem,
  • Sheba Medical Center โ€” Ramat Gan,
  • Tel Aviv Sourasky Medical Center โ€” Tel Aviv,
  • Kanazawa University Hospital โ€” Kanazawa,
  • Nagoya City University Hospital โ€” Nagoya,
  • Osaka University Hospital โ€” Osaka,

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.

Explore by condition: All Multiple Myeloma clinical trials

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†—