MAGNETISMM-2: Study of Elranatamab (PF-06863135) in Japanese Participants With Multiple Myeloma
- Sponsor
- Pfizer
- Study ID
- NCT04798586
- Phase
- PHASE1
- Status
- Completed
Conditions
- Relapsed or Refractory Multiple Myeloma
Eligibility Criteria
- Sex
- ALL
- Age
- 20 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Elranatamab (PF-06863135) — DRUGBCMA-CD3 bispecific antibody
Study Details
The purpose of this study is to confirm the safety and tolerability of elranatamab (PF-06863135) in Japanese participants with relapsed or refractory MM.
Key Dates
- Start date
- Mar 22, 2021
- Status verified
- May 2024
- Primary completion
- May 27, 2022
- Completion
- May 17, 2023
Study Design
- Enrollment
- 4 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Elranatamab (PF-06863135)BCMA-CD3 bispecific antibody
Primary Outcome Measure
Number of Participants With Dose Limiting Toxicities (DLTs) [ Time Frame: Up to 4 weeks ]
Related Studies
- A Study to Evaluate Mezigdomide, Bortezomib and Dexamethasone (MEZIVd) Versus Pomalidomide, Bortezomib and Dexamethasone (PVd) in Participants With Relapsed or Refractory Multiple Myeloma (RRMM)PHASE3 · Recruiting · Celgene · Los Alamitos, California
- A Study of JNJ-79635322 in Participants With Relapsed or Refractory Multiple Myeloma or Previously Treated Amyloid Light-chain (AL) AmyloidosisPHASE1 · Recruiting · Janssen Research & Development, LLC · Duarte, California
- Study of SIM0500 Alone in Participants With Relapsed or Refractory Multiple MyelomaPHASE1 · Recruiting · Jiangsu Simcere Pharmaceutical Co., Ltd. · Phoenix, Arizona
- A Study of mRNA-2808 in Participants With Relapsed or Refractory Multiple MyelomaPHASE1/PHASE2 · Recruiting · ModernaTX, Inc. · Birmingham, Alabama