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OncoMatch/Clinical Trials/NCT06292780

A Trial to Learn if Linvoseltamab is Safe and Works in Adults With Relapsed or Refractory Systemic Light Chain Amyloidosis (AL Amyloidosis)

Is NCT06292780 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies Linvoseltamab for relapsed/refractory systemic light chain amyloidosis.

Phase 1/2RecruitingRegeneron PharmaceuticalsNCT06292780Data as of May 2026

Treatment: LinvoseltamabThis study is researching an experimental drug called linvoseltamab ("study drug"). This study is focused on patients who have AL amyloidosis that has returned or have failed other therapies and need to be treated again. The study consists of 2 phases (Phase 1 and Phase 2): * In Phase 1, linvoseltamab will be given to a small number of participants to study the side effects of the study drug and to determine the recommended doses of the study drug to be given to participants in Phase 2. * In Phase 2, linvoseltamab will be given to more participants to continue to assess the side effects of the study drug and to evaluate the ability of linvoseltamab to treat AL amyloidosis. The study is looking at several other research questions, including: * How many participants treated with linvoseltamab have improvement in the abnormal proteins that cause organ problems and for how long * How many participants treated with linvoseltamab have improvement in the heart or kidney and for how long * What the right dosing regimen is for linvoseltamab * What side effects may happen from taking linvoseltamab * How much linvoseltamab is in the blood at different times * Whether the body makes antibodies against linvoseltamab (which could make the drug less effective or could lead to side effects)

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Extracted eligibility criteria

Cancer type

Multiple Myeloma

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Min 1 prior line

Lab requirements

Blood counts

adequate hematologic function, as described in the protocol

Kidney function

adequate renal function, as described in the protocol

Liver function

adequate hepatic function, as described in the protocol

Cardiac function

adequate cardiac function, as described in the protocol; NT-proBNP ≤8500 ng/L during screening

Adequate hepatic, hematologic, renal, and cardiac function, as described in the protocol; NT-proBNP ≤8500 ng/L during screening

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • City of Hope · Duarte, California
  • Colorado Blood Cancer Institute/SCRI · Denver, Colorado
  • Karmanos Cancer Institute · Detroit, Michigan
  • Roswell Park Comprehensive Cancer Center · Buffalo, New York
  • Ohio State University · Columbus, Ohio

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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