OncoMatch/Clinical Trials/NCT06669247
A Study to Assess the Safety and Anti-Tumor Activity of REGN7945 in Combination With Linvoseltamab in Adult Participants With Relapsed/Refractory Multiple Myeloma
Is NCT06669247 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies multiple treatments including Linvoseltamab and REGN7945+Linvoseltamab for relapsed/refractory multiple myeloma.
Treatment: Linvoseltamab · REGN7945+Linvoseltamab — This study is researching an experimental drug called REGN7945 in combination with another experimental drug called linvoseltamab, (also known as REGN5458) (each individually called a "study drug" or "study drugs" when combined). This study is the first time REGN7945 will be tested in humans. Linvoseltamab has previously been studied by itself (without other cancer drugs) in participants who had advanced multiple myeloma that returned and needed to be treated again after several other therapies had failed. The aim of the study is to see how safe, tolerable, and effective REGN7945 is when given in combination with linvoseltamab, compared with linvoseltamab alone. The study is looking at several other research questions, including: * What side effects may happen from taking the study drug(s) * How many people treated with REGN7945 and linvoseltamab compared to linvoseltamab alone have improvement of their multiple myeloma and by how much * How long people benefit from receiving REGN7945 in combination with linvoseltamab compared with linvoseltamab alone * How much study drug(s) is in the blood at different times * Whether the body makes antibodies against the study drugs(s) (which could make the study drug(s) less effective or could lead to side effects) * If there is any change in pain and cancer-related symptoms, how well people are able to function, and their quality of life when taking the study drug(s)
Check if I qualifyExtracted eligibility criteria
Cancer type
Multiple Myeloma
Performance status
ECOG 0–1(Restricted strenuous activity)
Eastern Cooperative Oncology Group (ECOG) performance status ≤1
Prior therapy
Must have received: anti-CD38 antibody
exposure to at least 1 anti-CD38 antibody
Must have received: immunomodulatory imide drug (IMiD)
exposure to at least 1...immunomodulatory imide drug (IMiD)
Must have received: proteasome inhibitor
exposure to at least 1...proteasome inhibitor (PI)
Lab requirements
Blood counts
adequate hematologic function
Kidney function
adequate renal function
Liver function
adequate hepatic function
Adequate hematologic, hepatic, and renal function
Structured fields extracted by AI. May contain errors — verify against the official protocol.
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