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Revumenib + 7+3 Induction and Midostaurin

Revumenib in Combination With 7+3 + Midostaurin in AML

  • RegistryNCT06313437
  • PhasePhase 1
  • StatusRecruiting
  • ConditionNewly Diagnosed NPM1- and FLT3-Mutated AML
  • SponsorRichard Stone, MD
How Revumenib + 7+3 + Midostaurin works1 min

The drug

What is being tested.

Menin inhibitor, 25 and 113 mg capsules, taken orally per protocol.

Antineoplastic agent, via intravenous (into the vein) infusion per protocol.

This is a single arm open label phase I trial of the menin inhibitor, revumenib, in combination with cytarabine and daunorubicin (7+3) chemotherapy and the multikinase inhibitor midostaurin for the frontline treatment of Nucleophosmin (NPM1) and FMS-like tyrosine kinase 3 (FLT3) mutated Acute Myeloid Leukemia (AML). Investigators are trying to determine the highest dose of revumenib that can be given safely in combination with these chemotherapy drugs.

The study

How the trial runs.

This research is being conducted to determine a safe and effective dose of revumenib that can be given in combination with standard induction (initial therapy to induce a remission) + FLT3 targeted therapy (midostaurin) and a single cycle of post-remission therapy + FLT3 targeted therapy (midostaurin) to participants with newly diagnosed Nucleophosmin (NPM1) and FMS-like tyrosine kinase 3 (FLT3) mutated Acute Myeloid Leukemia (AML).

The names of the study drugs involved in this study are: * Revumenib (SNDX-5613) (a type of menin inhibitor) * Midostaurin (a type of multi-kinase including FLT3 inhibitor) * Cytarabine (a type of antineoplastic agent) * Daunorubicin (a type of antineoplastic agent)

Live record on ClinicalTrials.gov →

Eligibility

Who the study is looking for.

  • Patients with AML who are newly diagnosed according to the WHO 2022 Classification and previously untreated except for hydroxyurea. ATRA pretreatment for suspected APL for less than 5 days is allowed. Eligible patients with AML arising from an antecedent hematologic disease (AHD) including MDS, may have been treated for their prior hematologic disease (except for allogenic transplant).
  • Patients must be ≥ 18 and < 75 years old.
  • Eastern Cooperative Oncology Group (ECOG) Performance status of 0 to 2.
  • Presence of FLT3-ITD and/or TKD mutation(s) AND NPM1 mutation in bone marrow or peripheral blood

Inclusion criteria as written on the registry, trimmed. The full list, with exclusions, is on the live record.

For you, or someone you love

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