Karyopharm KPT-IST-391 (Relapsed/Refractory Multiple Myeloma) - Clinical Trial

¿Cuál es el Propósito de este estudio?

We are doing this study to find out if an experimental combination of drugs (selinexor, ruxolitinib, and methylprednisolone) is a safe and effective option for treating multiple myeloma that has come back after treatment or is not responding to treatment.

¿Cuál es la Condición que se está estudiando?

Relapsed/Refractory Multiple Myeloma

¿Quién puede participar en el Estudio?

Adults ages 18+ who:

  • Are diagnosed with multiple myeloma that has 1 of the following features: clonal bone marrow plasma cells >10% or biopsy-proven bony or extramedullary plasmacytoma
  • Did not have an adequate response to treatment that included the following drugs: anti-CD38 antibody, immunomodulatory agent, proteasome inhibitor

For more information, contact the study team at quinna.marshburn@duke.edu.

Grupo etario
Adultos

¿Qué Implica?

Everyone who takes part in this study will receive the study drug regimen. No placebo is used in this study.

If you choose to join, you will:

  • Take selinexor once per week
  • Take ruxolitinib twice per day
  • Take methylprednisolone every other day

Your progress will be assessed at the end of each 28-day period of taking the study regimen. These 28-day periods are called "cycles." The number of cycles you do in this study will depend on how you respond to the study drug regimen.

Detalles del Estudio

Título Completo
A phase I trial of selinexor, ruxolitinib and methylprednisolone for patients with relapsed/refractory multiple myeloma
Investigador Principal
Cristiana Costa Chase, DO
Especialista en oncología hematológica
Número de Protocolo
IRB: PRO00117038
NCT: NCT06225310
Fase
Fase I
ClinicalTrials.gov
Estado de inscripción
Abierto para inscripción
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