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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
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

Full criteria on ClinicalTrials.gov

Sites (43)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Townsville University Hospital
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DouglasAustraliaUnknown status
Epworth Freemasons
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East MelbourneAustraliaUnknown status
Liverpool Hospital
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LiverpoolAustraliaUnknown status
Epworth Hospital
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RichmondAustraliaUnknown status
Slade Pharmacy
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RichmondAustraliaUnknown status
Calvary Mater Newcastle
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WaratahAustraliaUnknown status
Dr. Everett Chalmers Regional Hospital
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FrederictonCanadaUnknown status
CIUSSS de l'Est-de-l'Île-de-Montréal
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MontrealCanadaUnknown status
Centre intégré universitaire de santé et de services sociaux de l'Estrie - Centre Hospitalier Univer
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SherbrookeCanadaUnknown status
Winship Cancer Institute
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AtlantaUnited StatesUnknown status
Emory University Hospital Midtown
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AtlantaUnited StatesUnknown status
Emory University Hospital
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AtlantaUnited StatesUnknown status
University of Maryland
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BaltimoreUnited StatesUnknown status
MSK Basking Ridge.
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Basking RidgeUnited StatesUnknown status
Brigham and Women's Hospital
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BostonUnited StatesUnknown status
Dana-Farber Cancer Institute
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BostonUnited StatesUnknown status
MSK Commack.
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CommackUnited StatesUnknown status
Sylvester Comprehensive Cancer Center- The Lennar Foundation Medical Center
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Coral GablesUnited StatesUnknown status
University of Miami Hospital and Clinics Deerfield Beach
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Deerfield BeachUnited StatesUnknown status
Sylvester Comprehensive Cancer Center- Doral
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DoralUnited StatesUnknown status
MSK Westchester.
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HarrisonUnited StatesUnknown status
Indiana CTSI Clinical Research Center (ICRC)
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IndianapolisUnited StatesUnknown status
Indiana University Melvin and Bren Simon Comprehensive Cancer Center (IUSCCC)
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IndianapolisUnited StatesUnknown status
Indiana University Health University Hospital
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IndianapolisUnited StatesUnknown status
Dartmouth Hitchcock Medical Center
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LebanonUnited StatesUnknown status
Memorial Sloan Kettering Cancer Center - Investigational Drug Service Pharmacy
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Long Island CityUnited StatesUnknown status
University of Miami Hospital and Clinics
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MiamiUnited StatesUnknown status
Sylvester Comprehensive Cancer Center - Kendall
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MiamiUnited StatesUnknown status
Sylvester Comprehensive Cancer Center*
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MiamiUnited StatesUnknown status
MSK Monmouth.
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MiddletownUnited StatesUnknown status
Medical College of Wisconsin
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MilwaukeeUnited StatesUnknown status
MSK Bergen.
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MontvaleUnited StatesUnknown status
Dana-Farber Cancer Institute - Chestnut Hill
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NewtonUnited StatesUnknown status
Memorial Sloan Kettering Cancer Center - David H. Koch Center for Cancer Care (74th Street).
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New YorkUnited StatesUnknown status
Memorial Sloan Kettering Cancer Center - Main Campus
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New YorkUnited StatesUnknown status
Methodist Hospital
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OmahaUnited StatesUnknown status
Oncology Hematology West P.C. dba Nebraska Cancer Specialists
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OmahaUnited StatesUnknown status
Oncology Hematology West P.C. dba Nebraska Cancer - Methodist
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OmahaUnited StatesUnknown status
Sylvester Comprehensive Cancer Center Plantation
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PlantationUnited StatesUnknown status
University of Washington
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SeattleUnited StatesUnknown status
Fred Hutchinson Cancer Center
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SeattleUnited StatesUnknown status
MSK Nassau.
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UniondaleUnited StatesUnknown status
University of Massachusetts Chan Medical School
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WorcesterUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.