๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-08-27

Dose Escalation Study of Teclistamab, a Humanized BCMA*CD3 Bispecific Antibody, in Participants With Relapsed or Refractory Multiple Myeloma (NCT03145181)

64007957MMY1001: A Phase 1/2, First-in-Human, Open-Label, Dose Escalation Study of Teclistamab, a Humanized BCMA x CD3 Bispecific Antibody, in Subjects With Relapsed or Refractory Multiple Myeloma

๐Ÿ”ต Active, Not Recruiting Phase1 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 dose(s) (RP2Ds) and schedule assessed to be safe for Teclistamab and to characterize the safety and tolerability of Teclistamab at the RP2Ds.

Who can join: Review the eligibility criteria below.

Location: City of Hope โ€” Duarte, 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 (13 Sites)

  • City of Hope โ€” Duarte, California
  • Colorado Blood Cancer Institute โ€” Denver, Colorado
  • Icahn School of Medicine at Mount Sinai Program for the Protection of Human Subjects โ€” New York, New York
  • Levine Cancer Institute โ€” Charlotte, North Carolina
  • University of Pennsylvania โ€” Philadelphia, Pennsylvania
  • Hospices Civils de Lyon HCL โ€” Lyon,
  • CHRU Tours Hopital Bretonneau โ€” Tours,
  • VU Medisch Centrum โ€” Amsterdam,
  • Hosp. Univ. Germans Trias I Pujol โ€” Badalona,
  • Hosp Clinic de Barcelona โ€” Barcelona,
  • Clinica Univ. de Navarra โ€” Pamplona,
  • Hosp Clinico Univ de Salamanca โ€” Salamanca,
  • Haematology Centre, R 51 โ€” Stockholm,

๐Ÿ“ž Contact the Study Coordinator

Phone: (800) 826-4673

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†—