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Viernes 2 oct 2026SEC · NASDAQ biomédico

Calendario›REGN›Linvoseltamab · LINKER-MM4

Linvoseltamab · LINKER-MM4

A Window of Opportunity Trial to Learn if Linvoseltamab is Safe and Well Tolerated, and How Well it Works in Adult Participants With Recently Diagnosed Multiple Myeloma Who Have Not Already Received Treatment

Ensayo de REGENERON PHARMACEUTICALS, INC. en Mieloma multiple.

Más ensayos de: Mieloma múltiple.

Fase
Fase 1/2
Estado
Reclutando pacientes
Participantes
149
previstos
Centros
32
Fin del objetivo primario
nov 2035
estimado por el promotor

Qué significa cada fase y cada estado.

Estudio de intervención, no aleatorizado, abierto. Comenzó en dic 2023.

Qué mide

Incidence of Dose-Limiting Toxicities (DLTs) (End of the Observation period; up to day 28) (del registro, en inglés)

Cómo lo describe el promotor

En el documentoEn inglés, del registroThis study is researching an experimental drug called linvoseltamab (called "study drug"). The study is focused on participants with newly diagnosed multiple myeloma (NDMM) who are eligible for high dose chemotherapy with autologous stem cell transplantation (transplant-eligible) or ineligible for autologous stem cell transplantation (transplant-ineligible). The aim of this clinical trial is to study the safety, tolerability (how the body reacts to the drug), and effectiveness (tumor shrinkage) of linvoseltamab in study participants with NDMM as a first step in determining if the study drug has a role in the treatment of NDMM. This study consists of 2 phases: * In Phase 1 Parts A and B, the study drug will be given to participants to study the side effects of the study drug and to establish the regimen (initial doses and full dose) of the study drug to be given to participants in Phase 2. * In Phase 1 Part C, the study drug will be given to participants to study the side effects when using different initial doses of the study drug. * In Phase 2, the study drug will be given to more participants to continue to assess the side effects of the study drug and to evaluate the activity of the study drug to shrink the tumor (multiple myeloma) in participants with NDMM. The study is looking at several research questions, including: * What side effects may happen from taking linvoseltamab? * What the right dosing regimen is for linvoseltamab? * How many participants treated with linvoseltamab have improvement of their disease and for how long? * The effects of linvoseltamab study treatment before and after transplant * 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).

Más ensayos de REGN

EnsayoFaseEstadoLectura de resultados
cemiplimabFase 2En marcha, sin reclutarmar 2025 (real)
Pozelimab + Cemdisiran · NIMBLEFase 3En marcha, sin reclutarjul 2025 (real)
Garetosmab · OPTIMAFase 3En marcha, sin reclutarjul 2025 (real)
Aflibercept 8 mg · ELARAFase 3En marcha, sin reclutarago 2025 (real)
Dupilumab · ENGAGEFase 2En marcha, sin reclutarfeb 2026 (real)
FianlimabFase 3En marcha, sin reclutarmar 2026 (real)

Todos los de REGN, en su ficha.

Ficha completa en ClinicalTrials.gov (NCT05828511), actualizada en may 2026.