ELISA in Relapsed/Refractory MM

NCT ID: NCT06832865

Last Updated: 2025-02-18

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2026-08-01
• Study Completion Date: 2028-12-01

Brief Summary

This is an open-label phase 2 study of elranatamab in combination with isatuximab administered subcutaneously in patients with relapsed and refractory multiple myeloma (RRMM) who have received at least two prior lines of therapy and who have had previous treatment with both immunomodulatory drugs (IMiDs) and a proteasome inhibitor (PI). The subcutaneous injection method of isatuximab administration, including the device used to administer isatuximab, is investigational.

Detailed Description

This phase 2, single center, open-label study will enroll 30 patients with relapsed and refractory multiple myeloma (RRMM) who have received at least two prior lines of therapy and who have had previous treatment with both immunomodulatory drugs (IMiDs) and a proteasome inhibitor (PI). Participants with prior therapy with anti-CD38 and anti-B cell maturation antigen (BCMA) target except an anti-BCMA T cell engager (TCE) may be eligible.

This research is being done to see if the study drugs, elranatamab and isatuximab-irfc, reduce the risk of worsening disease and to evaluate the possible risks of the study drugs. Elranatamab is an FDA approved treatment for RRMM. Isatuximab is FDA approved as a treatment option for RRMM when administered intravenously (IV), however isatuximab will be administered as a subcutaneous (SC) infusion (injected under the skin) in this study which is not FDA approved and is investigational. Isatuximab will be administered subcutaneously using an investigational device called the on-body delivery system. The first six patients who complete Cycles 1 and 2 will be assessed for safety and adverse events prior to enrolling all other patients. The research involves screening for eligibility, study treatment and study visits, and follow-up visits. In the beginning (Day 1) of Cycle 1, there may be a 2-8 day inpatient visit so participants can be monitored during their first dose of isatuximab + elranatamab. Participants will receive study treatment until disease progression, unacceptable toxicity, or withdrawal, and will be followed every 3 months for 5 years after their final dose.

Conditions

Relapsed Refractory Multiple Myeloma (RRMM); Relapsed Refractory Multiple Myeloma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Elranatamab + Isatuximab-irfc

Elranatamab will be administered via subcutaneous (SC) injection usually into the abdomen or lower stomach at the following visits during each 28-day cycle:

• Cycle 1: Days 1, 4, 8, 15, 22
• Cycles 2-6: Days 1 and 15
• Cycles 7+: Day 1.

Isatuximab for SC administration will be administered via subcutaneous (SC) injection usually into the abdomen or lower stomach, using an investigational injector device called the on-body delivery system at the following visits during each 28-day cycle:

• Cycles 2-6: Days 1 and 15
• Cycles 7+: Day 1

This will continue as long as the participant is receiving treatment.

Group Type: EXPERIMENTAL

elranatamab

Intervention Type: DRUG

Subcutaneously injected study drug, usually into the abdomen or lower stomach. Each vial of elranatamab contains a sufficient amount of product to ensure an extractable volume of 1.9 mL at a concentration of 40 mg/mL. The dosing is as follows:

• Cycle 1 Day 1: 12 mg/0.3 mL
• Cycle 1 Day 4: 32 mg/0.8 mL
• Cycle 1 Day 8, 15, 22: 76 mg/1.9 mL
• Cycles 2-6, Day 1 and 15: 76 mg/1.9 mL
• Cycles 7+, Day 1: 76 mg/1.9 mL

Isatuximab SC

Intervention Type: DRUG

Isatuximab (SAR650984) is an IgG1 derived monoclonal antibody binding selectively the human CD38 membrane protein. Subcutaneously (SC) injected study drug with each vial containing 140 mg/mL (1400 mg/10mL) isatuximab. Isatuximab SC will be injected using the investigational OBDS and in the following doses:

• Cycles 2-6, Day 1 and 15: 1400 mg/10 mL
• Cycles 7+ Day 1: 1400 mg/10 mL

Isatuximab SC-OBDS

Intervention Type: DEVICE

The On Body Delivery System (OBDS) also called Isatuximab SC Wearable Injection System, is a sterile, single-use, disposable, elastomeric, user-filled investigational medical device. The OBDD has a reservoir for the drug product (isatuximab). A self-contained, integrated needle (with manual insertion and automatic retraction mechanism) is provided within the OBDS. The OBDS will be used to inject isatuximab each time the participant receives isatuximab in this study. Study drug administration will be done by trained medical professionals in the clinic. The OBDS device will be prepared by the medical professional, placed on the abdomen using the adhesive (sticky) pads that are on the device, the study drug (isatuximab) will be injected, and then the device will be removed.

Interventions

elranatamab

Subcutaneously injected study drug, usually into the abdomen or lower stomach. Each vial of elranatamab contains a sufficient amount of product to ensure an extractable volume of 1.9 mL at a concentration of 40 mg/mL. The dosing is as follows:

• Cycle 1 Day 1: 12 mg/0.3 mL
• Cycle 1 Day 4: 32 mg/0.8 mL
• Cycle 1 Day 8, 15, 22: 76 mg/1.9 mL
• Cycles 2-6, Day 1 and 15: 76 mg/1.9 mL
• Cycles 7+, Day 1: 76 mg/1.9 mL

Intervention Type: DRUG

Isatuximab SC

Isatuximab (SAR650984) is an IgG1 derived monoclonal antibody binding selectively the human CD38 membrane protein. Subcutaneously (SC) injected study drug with each vial containing 140 mg/mL (1400 mg/10mL) isatuximab. Isatuximab SC will be injected using the investigational OBDS and in the following doses:

• Cycles 2-6, Day 1 and 15: 1400 mg/10 mL
• Cycles 7+ Day 1: 1400 mg/10 mL

Intervention Type: DRUG

Isatuximab SC-OBDS

The On Body Delivery System (OBDS) also called Isatuximab SC Wearable Injection System, is a sterile, single-use, disposable, elastomeric, user-filled investigational medical device. The OBDD has a reservoir for the drug product (isatuximab). A self-contained, integrated needle (with manual insertion and automatic retraction mechanism) is provided within the OBDS. The OBDS will be used to inject isatuximab each time the participant receives isatuximab in this study. Study drug administration will be done by trained medical professionals in the clinic. The OBDS device will be prepared by the medical professional, placed on the abdomen using the adhesive (sticky) pads that are on the device, the study drug (isatuximab) will be injected, and then the device will be removed.

Intervention Type: DEVICE

Other Intervention Names

PF-06863135; SAR650984; Isatuximab irfc; On Body Delivery System (Device); OBDS; Isatuximab Subcutaneous Injection Device (On Body Delivery System, OBDS); Isatuximab SC Wearable Injection System

Eligibility Criteria

Inclusion Criteria

• 1. This study will enroll patients with relapsed and refractory multiple myeloma who have had at least 2 prior lines of therapy including patients who have had previous treatment with both immunomodulatory drugs (IMiDs) and a proteasome inhibitor (PI). Prior therapy with anti-CD38 and anti-B cell maturation antigen (BCMA) target will be permitted except an anti-BCMA T cell engager. Patients cannot be refractory to an anti-CD38 antibody.
• 2. Measurable disease of multiple myeloma as defined by at least one of the following:

• a. Serum monoclonal protein ≥ 0.5 g/dL. Patients with IgD disease and lower amounts of monoclonal protein may be permitted to enroll with PI approval
• b. ≥ 200 mg of monoclonal protein in the urine on 24-hour electrophoresis
• c. Serum free light chain ≥ 100 mg/L (10 mg/dL) and abnormal serum free kappa to serum free lambda light chain (FLC) ratio (<0.26 or >1.65)
• 3. Age ≥18 years.

--a. The effects of elranatamab and isatuximab on the developing human fetus are unknown. For this reason and because anti-BCMA bispecific antibodies are known to be teratogenic, women of child-bearing potential must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation and 4 months after the last dose of elranatamab and 5 months after the last dose of isatuximab. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately.

• 4. ECOG performance status ≤2 (Karnofsky ≥60%, see Appendix A).
• 5. Participants must have adequate organ and marrow function as defined below:

• a. ANC ≥ 1000/μL. G-CSF is not permitted within 7 days of screening.
• b. Platelet count ≥ 50,000/µL. Platelet transfusion is not permitted within 7 days of screening.
• c. Hemoglobin ≥ 8 g/dL. Red blood cell transfusions are permitted to meet eligibility criteria.
• d. Calculated creatinine clearance of ≥ 30 mL/min by Cockcroft-Gault equation.
• e. Patient has adequate hepatic function, as evidenced by each of the following:

• Serum bilirubin values < 2 mg/dL; and
• Serum aspartate transaminase (ALT) and/or aspartate transaminase (AST) values< 2.5 × the upper limit of normal (ULN) of the institutional laboratory reference range. Patients with elevated bilirubin due to Gilbert's syndrome may be permitted with PI approval (i.e., total bilirubin <3 mg/dL and normal direct bilirubin).
• 6. Participants with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial.
• 7. Participants with known history or current symptoms of cardiac disease, or history of treatment with cardiotoxic agents, should have a clinical risk assessment of cardiac function using the New York Heart Association Functional Classification. To be eligible for this trial, participants should be class 2B or better.
• 8. Ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria

• 1. Patients with active plasma cell leukemia, POEMS syndrome, or amyloidosis are excluded from this trial.
• 2. Stem cell transplant within 12 weeks prior to enrollment, or active GVHD.
• 3. Ongoing Grade ≥2 peripheral sensory or motor neuropathy.
• 4. History of any grade peripheral sensory or motor neuropathy with prior BCMA directed therapy. History of GBS or GBS variants, or history of any Grade ≥3 peripheral motor polyneuropathy.
• 5. Previous treatment with an anti-BCMA bispecific T cell engager.

--a. Prior treatment with anti-BCMA CAR-T and/or ADC therapy is permitted; however, the participant cannot be refractory to this therapy if it was administered as the last line prior to study enrollment.

• 6. Participants who are receiving any investigational agents currently.
• 7. Participants who have had myeloma therapy or investigational drug within 2 weeks prior to start of treatment or those who have not recovered from adverse events due to agents administered more than 2 weeks earlier.
• 8. Known or suspected hypersensitivity to the study drug or any components of the device (e.g. adhesive which contains acrylic).
• 9. Impaired cardiovascular function or clinically significant cardiovascular diseases, defined as any of the following within 6 months prior to enrollment:

• a. Acute myocardial infarction, acute coronary syndromes (e.g., unstable angina, coronary artery bypass graft, coronary angioplasty or stenting, pericardial effusion);
• b. Clinically significant cardiac arrhythmias (e.g., uncontrolled atrial fibrillation or uncontrolled paroxysmal supraventricular tachycardia);
• c. Thromboembolic or cerebrovascular events (e.g., transient ischemic attack, cerebrovascular accident, deep vein thrombosis [unless associated with a central venous access complication] or pulmonary embolism);
• 10. Participants with known active HBV, HCV, HIV, or any active, uncontrolled bacterial, fungal, or viral infection. Active infections must be resolved at least 14 days prior to enrollment. Per institutional protocol, HBV DNA testing by PCR is mandatory for subjects at risk for HBV reactivation.
• 11. 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 and or other cancers treated with curative intent.
• 12. Other surgical (including major surgery within past 14 days prior to enrollment) medical or psychiatric condition including recent (within the past year) or active suicidal ideation/behavior or laboratory abnormality that may increase the risk of study participation or, in the investigator's judgment, make the participant inappropriate for the study.
• 13. Live attenuated vaccine within 30 days of the first dose of study intervention.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Pfizer

INDUSTRY

Sponsor Role: collaborator

Sanofi

INDUSTRY

Sponsor Role: collaborator

Massachusetts General Hospital

OTHER

Sponsor Role: lead

Responsible Party

Noopur Raje

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Noopur Raje, MD

Role: PRINCIPAL_INVESTIGATOR

Massachusetts General Hospital

Locations

Massachusetts General Hospital

Boston, Massachusetts, United States

Beth Israel Deaconess Medical Center

Boston, Massachusetts, United States

Countries

United States

Central Contacts

Noopur Raje, MD

Role: CONTACT

nraje@mgh.harvard.edu

617-724-1969

Facility Contacts

Noopur Raje, MD

Role: primary

nraje@mgh.harvard.edu

617-724-1969

David Avigan, MD

Role: primary

davigan@bidmc.harvard.edu

617-667-9920

Other Identifiers

24-727

Identifier Type: -

Identifier Source: org_study_id