NCT06215118Active, not recruitingPhase 1
A Study to Learn About the Effects of the Combination of Elranatamab (PF-06863135) and Iberdomide in Patients With Relapsed or Refractory Multiple Myeloma (MagnetisMM-30)
A PHASE 1B, OPEN-LABEL STUDY OF ELRANATAMAB IN COMBINATION WITH IBERDOMIDE IN PARTICIPANTS WITH RELAPSED REFRACTORY MULTIPLE MYELOMA
Source: ClinicalTrials.gov · Last updated 15 Sept 2026
Brief summary (registry, in English)
The main purpose of the study is to understand how safe and tolerable is elranatamab when given along with iberdomide. There are 2 parts to this study. Part 1 will look at how safe and tolerable is elranatamab when given with iberdomide. Part 2 will look at the correct amount of this combination that can be given to patients with relapsed or refractory multiple myeloma. Myeloma is a type of cancer that begins in plasma cells (white blood cells that produce antibodies). Refractory means a disease or condition that does not respond to treatment. Relapsed means the return of a disease after a period of improvement. All study medicines are given in cycles that last 28 days. Everyone taking part in this study will receive elranatamab as a shot under the skin. Iberdomide will be taken by mouth once a day for 21 days over a 28-day cycle. Participants will receive study medicine until: * their disease progresses or, * they experience unacceptable side effects or, * they choose to no longer take part in the study. The study will look at the experiences of people receiving the study medicines. This will help see if the study medicines are safe and can be used for multiple myeloma treatment.
- Status (registry)
- Active, not recruiting
- Phase (registry)
- Phase 1
- Study type
- Interventional
- Enrollment
- 100 (actual)
- First submitted
- 10 Jan 2024
- Start date
- 20 Feb 2024
- Primary completion date
- 16 Nov 2027
- Lead sponsor
- Pfizer
- Diseases
- Multiple myeloma
- NCT number
- NCT06215118
What you commit to
- Study type: Interventional · Phase 1
- Participants enrolled: 100
- From 20 Feb 2024 to the primary completion date, 16 Nov 2027
- 43 sites in 3 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Stem cell transplant within 12 weeks prior to enrollment or active graft vs host disease
- Any other active malignancy within 3 years prior to enrollment, except for adequately treated basal cell or squamous cell skin cancer, or carcinoma in situ
- Previous treatment with:
- BCMA-directed or CD3 redirecting therapy
- Administration of strong inhibitor or inducer of CYP3A4/5 within 2 weeks prior to dosing and during the study
- Administration with an investigational product within 30 days preceding the first dose of study intervention
Other illness
- Plasma cell leukemia, Smoldering multiple myeloma, Waldenström's macroglobulinemia, Amyloidosis, POEMS Syndrome
- Impaired cardiovascular function or clinically significant cardiovascular diseases
- Participants with any active, uncontrolled bacterial, fungal, or viral infection
- Participant is unable or unwilling to undergo protocol required thromboembolism prophylaxis
Other
- Iberdomide (CC-220) or Mezigdomide
Who the study is looking for
- Prior diagnosis of multiple myeloma as defined by IMWG criteria
- Measurable disease based on IMWG criteria as defined by at least 1 of the following:
- Serum M-protein ≥0.5 g/dL by SPEP
- Urinary M-protein excretion ≥200 mg/24 hour by UPEP
- Serum immunoglobulin FLC ≥10 mg/dL (≥100 mg/L) AND abnormal serum immunoglobulin kappa to lambda FL ratio (\<0.26 or \>1.65)
- Part 1: Received 2-4 prior lines of therapy for multiple myeloma, consisting of at least 1 immunomodulatory drug and 1 proteasome inhibitor.
- Part 2: Received 1-3 prior lines of therapy for multiple myeloma, consisting of at least 1 immunomodulatory drug and 1 proteasome inhibitor.
- ECOG performance status 0-1
- Resolved acute effects of any prior therapy to baseline severity or CTCAE Grade ≤1
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (43)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Townsville University Hospital Coordinator of this site? Confirm its status | Douglas | Australia | Unknown status |
| Epworth Freemasons Coordinator of this site? Confirm its status | East Melbourne | Australia | Unknown status |
| Liverpool Hospital Coordinator of this site? Confirm its status | Liverpool | Australia | Unknown status |
| Epworth Hospital Coordinator of this site? Confirm its status | Richmond | Australia | Unknown status |
| Slade Pharmacy Coordinator of this site? Confirm its status | Richmond | Australia | Unknown status |
| Calvary Mater Newcastle Coordinator of this site? Confirm its status | Waratah | Australia | Unknown status |
| Dr. Everett Chalmers Regional Hospital Coordinator of this site? Confirm its status | Fredericton | Canada | Unknown status |
| CIUSSS de l'Est-de-l'Île-de-Montréal Coordinator of this site? Confirm its status | Montreal | Canada | Unknown status |
| Centre intégré universitaire de santé et de services sociaux de l'Estrie - Centre Hospitalier Univer Coordinator of this site? Confirm its status | Sherbrooke | Canada | Unknown status |
| Winship Cancer Institute Coordinator of this site? Confirm its status | Atlanta | United States | Unknown status |
| Emory University Hospital Midtown Coordinator of this site? Confirm its status | Atlanta | United States | Unknown status |
| Emory University Hospital Coordinator of this site? Confirm its status | Atlanta | United States | Unknown status |
| University of Maryland Coordinator of this site? Confirm its status | Baltimore | United States | Unknown status |
| MSK Basking Ridge. Coordinator of this site? Confirm its status | Basking Ridge | United States | Unknown status |
| Brigham and Women's Hospital Coordinator of this site? Confirm its status | Boston | United States | Unknown status |
| Dana-Farber Cancer Institute Coordinator of this site? Confirm its status | Boston | United States | Unknown status |
| MSK Commack. Coordinator of this site? Confirm its status | Commack | United States | Unknown status |
| Sylvester Comprehensive Cancer Center- The Lennar Foundation Medical Center Coordinator of this site? Confirm its status | Coral Gables | United States | Unknown status |
| University of Miami Hospital and Clinics Deerfield Beach Coordinator of this site? Confirm its status | Deerfield Beach | United States | Unknown status |
| Sylvester Comprehensive Cancer Center- Doral Coordinator of this site? Confirm its status | Doral | United States | Unknown status |
| MSK Westchester. Coordinator of this site? Confirm its status | Harrison | United States | Unknown status |
| Indiana CTSI Clinical Research Center (ICRC) Coordinator of this site? Confirm its status | Indianapolis | United States | Unknown status |
| Indiana University Melvin and Bren Simon Comprehensive Cancer Center (IUSCCC) Coordinator of this site? Confirm its status | Indianapolis | United States | Unknown status |
| Indiana University Health University Hospital Coordinator of this site? Confirm its status | Indianapolis | United States | Unknown status |
| Dartmouth Hitchcock Medical Center Coordinator of this site? Confirm its status | Lebanon | United States | Unknown status |
| Memorial Sloan Kettering Cancer Center - Investigational Drug Service Pharmacy Coordinator of this site? Confirm its status | Long Island City | United States | Unknown status |
| University of Miami Hospital and Clinics Coordinator of this site? Confirm its status | Miami | United States | Unknown status |
| Sylvester Comprehensive Cancer Center - Kendall Coordinator of this site? Confirm its status | Miami | United States | Unknown status |
| Sylvester Comprehensive Cancer Center* Coordinator of this site? Confirm its status | Miami | United States | Unknown status |
| MSK Monmouth. Coordinator of this site? Confirm its status | Middletown | United States | Unknown status |
| Medical College of Wisconsin Coordinator of this site? Confirm its status | Milwaukee | United States | Unknown status |
| MSK Bergen. Coordinator of this site? Confirm its status | Montvale | United States | Unknown status |
| Dana-Farber Cancer Institute - Chestnut Hill Coordinator of this site? Confirm its status | Newton | United States | Unknown status |
| Memorial Sloan Kettering Cancer Center - David H. Koch Center for Cancer Care (74th Street). Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| Memorial Sloan Kettering Cancer Center - Main Campus Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| Methodist Hospital Coordinator of this site? Confirm its status | Omaha | United States | Unknown status |
| Oncology Hematology West P.C. dba Nebraska Cancer Specialists Coordinator of this site? Confirm its status | Omaha | United States | Unknown status |
| Oncology Hematology West P.C. dba Nebraska Cancer - Methodist Coordinator of this site? Confirm its status | Omaha | United States | Unknown status |
| Sylvester Comprehensive Cancer Center Plantation Coordinator of this site? Confirm its status | Plantation | United States | Unknown status |
| University of Washington Coordinator of this site? Confirm its status | Seattle | United States | Unknown status |
| Fred Hutchinson Cancer Center Coordinator of this site? Confirm its status | Seattle | United States | Unknown status |
| MSK Nassau. Coordinator of this site? Confirm its status | Uniondale | United States | Unknown status |
| University of Massachusetts Chan Medical School Coordinator of this site? Confirm its status | Worcester | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.