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KO-Men-017: Ziftomenib in NPM1 Mutated or KMT2A Rearranged Acute Myeloid Leukemia - Clinical Trial

¿Cuál es el Propósito de este estudio?

We are doing this study to find the most effective, safe dose of an experimental drug called ziftomenib (the study drug). We want to know how well it works when it combined with either standard non-intensive (venetoclax + azacitidine) therapy or standard intensive (7+3) therapy for adults who have acute myeloid leukemia.

¿Cuál es la Condición que se está estudiando?

Untreated NPM1 Mutated or KMT2A Rearranged Acute Myeloid Leukemia (AML)

¿Quién puede participar en el Estudio?

Adults ages 18+ who:

  • Diagnosed with AML
  • Have a documented NPM1-m or KMT2A-r mutation
  • Have no history of BCR-ABL mutation

For more information, contact the study team at erin.murphy@duke.edu.

Grupo etario
Adultos

¿Qué Implica?

If you choose to join this study, you will participate in either the intensive or the non-intensive therapy groups. The study team will let you know which option is available to you when you are making your decision.

If you participate in the intensive therapy portion of the study, you will get a random assignment (fair, equal chance) to 1 of 3 groups:

  • Group 1: If you are in this group, your study regimen will be 7+3 in combination with the study drug during induction, ziftomenib+cytarabine consolidation, and then the study drug for maintenance
  • Group 2: If you are in this group, your study regimen will be 7+3 in combination with the study drug during induction, ziftomenib+cytarabine consolidation, and then a placebo (inactive substance with no drug in it) for maintenance
  • Group 3: If you are in this group, your study regimen will be 7+3 in combination with placebo during induction, placebo+cytarabine consolidation, and then placebo maintenance for maintenance

If you participate in the non-intensive therapy portion of the study, you will get a random assignment (fair, equal chance) to 1 of 2 groups:

  • Group 1: If you are in this group, your study regimen will be venetoclax + azacitidine in combination with the study drug
  • Group 2: If you are in this group, your study regimen will be venetoclax + azacitidine in combination with a placebo

During the study, your doctor may decide that a stem cell transplant is the best treatment option for you. If you do receive a stem cell transplant as part of your standard treatment, you may then go on to receive maintenance therapy after the stem cell transplant is complete.

Detalles del Estudio

Título Completo
Phase 3 Randomized, Double-blind, Placebo-controlled Studies Assessing Ziftomenib in Combination with Either Standard of Care Nonintensive (Venetoclax+Azacitidine) or Intensive (7+3) Therapy in Patients with Untreated NPM1 Mutated or KMT2A Rearranged Acute Myeloid Leukemia
Investigador Principal
Especialista en oncología hematológica
Número de Protocolo
IRB: PRO00118403
NCT: NCT07007312
Fase
Phase III
ClinicalTrials.gov
Estado de inscripción
Pronto disponible para inscripción