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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.

Phase 1/2RecruitingRegeneron PharmaceuticalsNCT06669247Data as of May 2026

Treatment: Linvoseltamab · REGN7945+LinvoseltamabThis 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)

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Extracted eligibility criteria

Cancer type

Multiple Myeloma

Performance status

ECOG 0–1(Restricted strenuous activity)

Eastern Cooperative Oncology Group (ECOG) performance status ≤1

Prior therapy

Min 3 prior lines

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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