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
๐ฉบ 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
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ 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,
๐ 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.
๐ฐ 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.
More studies in Hematological Malignancies
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- Feasibility of the Use of Weighted Blankets to Improve Sleep Among Patients With Hematological Malignancies โ Houston, Texas
- Phase II Study of CD5 CAR Engineered IL15-transduced Cord Blood-derived NK Cells in Conjunction With Lymphodepleting Chemotherapy for the Management of Aggressive T Cell Hematological Malignancies โ Houston, Texas
- A Study of Talquetamab in Participants With Relapsed or Refractory Multiple Myeloma โ Birmingham, Alabama
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๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.