PHASE 1/2 STUDY OF LINVOSELTAMAB (ANTI-BCMA X ANTI-CD3BISPECIFIC ANTIBODY) IN PREVIOUSLY UNTREATED PATIENTSWITH SYMPTOMATIC MULTIPLE MYELOMA
Study of Linvoseltamab in Patients with Multiple Myeloma (NDMM)
Sponsor: Regeneron Pharmaceuticals, Inc.
Enrolling: Male and Female Patients
IRB Number: AAAU3354
U.S. Govt. ID: NCT05828511
Contact: Research Nurse Navigator: 212-342-5162 / cancerclinicaltrials@cumc.columbia.edu
Additional Study Information: This study is looking at people who have recently been newly diagnosed with a type of cancer called multiple myeloma (NDMM). The purpose of this study is to learn about the safety, tolerability (how your body reacts to the study drug), and effectiveness (tumor shrinkage) of linvoseltamab (called study drug) in participants with NDMM as a first step in determining if the study drug has a role to play in the treatment of NDMM. This study consists of 2 phases. Your study doctor will tell you which phase of the study you will be participating in. Linvoseltamab is not approved by the U.S. Food and Drug Administration (FDA) or any public health agency for any kind of treatment.
Investigator
Rajshekhar Chakraborty, MD
Do You Qualify?
Are you at least 18 years old? Yes No
Are you able to fill out surveys or questionnaires related to the study? Yes No
Are you able to attend appointments at the clinic and participate in study-related activities? Yes No
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For more information, please contact:
Research Nurse Navigator
cancerclinicaltrials@cumc.columbia.edu
212-342-5162