NCT05675449Active, not recruitingPhase 1
A Clinical Trial of Four Medicines (Elranatamab Plus Carfilzomib and Dexamethasone or Maplirpacept) in People With Relapsed Refractory Multiple Myeloma
A PHASE 1B, OPEN-LABEL STUDY OF ELRANATAMAB IN COMBINATION WITH CARFILZOMIB PLUS DEXAMETHASONE AND ELRANATAMAB IN COMBINATION WITH PF-07901801 IN PARTICIPANTS WITH RELAPSED REFRACTORY MULTIPLE MYELOMA
Source: ClinicalTrials.gov · Last updated 13 Aug 2026
Brief summary (registry, in English)
The main purpose of the study is to evaluate the safety and tolerability of the combination of elranatamab and carfilzomib and dexamethasone or elranatamab and maplirpacept. There are 2 parts to this study. Part 1 will evaluate the safety and tolerability of elranatamab when given in combination with carfilzomib plus dexamethasone. Part 2 has 2 arms. The first will evaluate the safety and tolerability of elranatamab when given in combination with maplirpacept. The second will identify the optimal dose(s) of elranatamab plus maplirpacept. All study medicines are given over 4-week cycles. Everyone taking part in this study will receive elranatamab as a shot under the skin. Participants in Part 1 will also receive weekly carfilzomib as an IV infusion (given directly into a vein) and dexamethasone either by mouth (as a pill) or by IV infusion. Participants in Part 2 will receive elranatamab in combination with maplirpacept as an IV infusion (given directly into a vein) The investigators will examine the experiences of people receiving the study medicines. This will help determine if the study medicines are safe and can be used for multiple myeloma treatment. Participants will take part in this study for about 2 years after the first dose.
- Status (registry)
- Active, not recruiting
- Phase (registry)
- Phase 1
- Study type
- Interventional
- Enrollment
- 59 (actual)
- First submitted
- 7 Dec 2022
- Start date
- 14 Dec 2022
- Primary completion date
- 11 Mar 2026
- Lead sponsor
- Pfizer
- Diseases
- Multiple myeloma
- NCT number
- NCT05675449
What you commit to
- Study type: Interventional · Phase 1
- Participants enrolled: 59
- From 14 Dec 2022 to the primary completion date, 11 Mar 2026
- 36 sites in 2 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 versus 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.
- Part 1: Previous treatment with a BCMA-directed therapy.
- Part 2: Previous treatment with any anti-BCMA directed therapy, with the exception of CAR-T. Previous treatment with a CD47-SIRP alpha-directed therapy.
- Part 1: Prior treatment with carfilzomib
- Live attenuated vaccine within 4 weeks of the first dose of study intervention.
- Administration with an investigational product (e.g. drug or vaccine) concurrent with study intervention or within 30 days preceding the first dose of study intervention used in this study.
Other illness
- Plasma cell leukemia, Smouldering MM, Waldenströms macroglobulinemia, Amyloidosis, POEMS Syndrome, Primary refractory MM
- Impaired cardiovascular function or clinically significant cardiovascular diseases.
- Participants with any active, uncontrolled bacterial, fungal, or viral infection.
- Any of the following within 3 months of enrollment: erosive esophagitis, treatment resistant peptic ulcer, infectious or inflammatory bowel disease, pulmonary embolism or uncontrolled thromboembolic event.
- Intolerance to or participants who have had a severe (Grade ≥3) allergic or anaphylactic reaction to antibodies or therapeutic proteins
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.
- Urinary M-protein excretion ≥200 mg/24 hours.
- Serum immunoglobulin FLC ≥10 mg/dL (≥100 mg/L) AND abnormal serum immunoglobulin kappa to lambda FLC ratio (\<0.26 or \>1.65).
- Part 1: Received at least 1 but not more than 3 prior lines of therapy for multiple myeloma (induction therapy followed by stem cell transplant and consolidation/maintenance therapy will be considered as 1 line of therapy).
- Part 2: Received at least 3 prior lines of therapy for multiple myeloma who are refractory to at least one IMiD, one PI and one anti-CD38 antibody.
- ECOG performance status 0-1.
- Resolved acute effects of any prior therapy to baseline severity or CTCAE Grade ≤1.
- Not pregnant or breastfeeding and willing to use contraception.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (36)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Rambam Health Care Campus Coordinator of this site? Confirm its status | Haifa | Israel | Unknown status |
| Division of Hematology Hadassah Medical Center - Ein Kerem Coordinator of this site? Confirm its status | Jerusalem | Israel | Unknown status |
| The Research Fund of Hadassah Medical Organization (R.A.) Coordinator of this site? Confirm its status | Jerusalem | Israel | Unknown status |
| Rabin Medical Center Coordinator of this site? Confirm its status | Petah Tikva | Israel | Unknown status |
| Hematology Division Davidoff Center, Rabin Medical Center, Beilinson Hospital Coordinator of this site? Confirm its status | Petah Tikva | Israel | Unknown status |
| Emory University Administration Office 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 |
| 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 |
| Sylvester Comprehensive Cancer Center - Aventura Coordinator of this site? Confirm its status | Aventura | United States | Unknown status |
| The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Coordinator of this site? Confirm its status | Baltimore | United States | Unknown status |
| Johns Hopkins University Cancer Immunology/GI Oncology Coordinator of this site? Confirm its status | Baltimore | United States | Unknown status |
| Oncology Investigational Drug Service,Department of Pharmacy Services Coordinator of this site? Confirm its status | Baltimore | United States | Unknown status |
| Beverly Hills Cancer Center Coordinator of this site? Confirm its status | Beverly Hills | United States | Unknown status |
| Massachusetts General Hospital Coordinator of this site? Confirm its status | Boston | United States | Unknown status |
| Dana Farber/Mass General Brigham Cancer Care, Inc Coordinator of this site? Confirm its status | Boston | 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 |
| Sylvester Comprehensive Cancer Center - Coral Springs Coordinator of this site? Confirm its status | Coral Springs | 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 |
| Clinical Research Advisors (Encino Satellite Location) Coordinator of this site? Confirm its status | Encino | United States | Unknown status |
| Sylvester Comprehensive Cancer Center - Hollywood Coordinator of this site? Confirm its status | Hollywood | United States | Unknown status |
| University of Iowa Hospitals and Clinics Coordinator of this site? Confirm its status | Iowa City | United States | Unknown status |
| State University of Iowa, Division of Sponsored Programs Coordinator of this site? Confirm its status | Iowa City | United States | Unknown status |
| University of Arkansas for Medical Sciences Coordinator of this site? Confirm its status | Little Rock | United States | Unknown status |
| Clinical Research Advisors (West Hollywood Satellite Location) Coordinator of this site? Confirm its status | Los Angeles | United States | Unknown status |
| Clinical Research Advisors (Korea Town Satellite Location) Coordinator of this site? Confirm its status | Los Angeles | United States | Unknown status |
| Sylvester Comprehensive Cancer Center* Coordinator of this site? Confirm its status | Miami | United States | Unknown status |
| Griffin Cancer Research Building (GCRB) 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 |
| University of Miami Hospital and Clinics 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 |
| Vanderbilt University Medical Center Coordinator of this site? Confirm its status | Nashville | United States | Unknown status |
| Henry-Joyce Cancer Clinic Coordinator of this site? Confirm its status | Nashville | United States | Unknown status |
| Memorial Sloan Kettering Cancer Center - Main Campus Coordinator of this site? Confirm its status | New York | 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 |
| Sylvester Comprehensive Cancer Center Plantation Coordinator of this site? Confirm its status | Plantation | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.