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Triple Combination of Pevonedistat and Venetoclax Plus Azacitidine in Adults With Acute Myeloid Leukemia Who Are Unfit for Intensive Chemotherapy

Trial Status: In Review

The purpose of this study is to determine whether the combination of pevonedistat + venetoclax + azacitidine improves event-free survival (EFS) compared with venetoclax + azacitidine in patients with newly diagnosed acute myeloid leukemia (AML) who are unfit for intensive chemotherapy.

Inclusion Criteria

  • Has morphologically confirmed diagnosis of AML (World Health Organization [WHO] criteria 2008). Participants may have newly diagnosed primary de novo AML or secondary AML (sAML), defined as AML after myelodysplastic syndromes (MDS) or myeloproliferative neoplasm (MPN), or therapy-related AML (t-AML) following cytotoxic therapy, and/or radiotherapy for a malignant or nonmalignant disease.
  • Has to be unfit for treatment with a standard Ara-C and anthracycline induction regimen due to age or co-morbidities defined by 1 of the following:
  • ≥75 years of age. OR
  • ≥18 to <75 years of age with at least one of the following:
  • Has Eastern Cooperative Oncology Group (ECOG) performance status of 2 or 3.
  • Has history of cardiac heart failure requiring treatment or ejection fraction ≤55% or chronic stable angina.
  • Has carbon monoxide lung diffusion capacity (DLCO) ≤65% or forced expiratory volume in 1 second (FEV1) ≤65% or significant history of chronic pulmonary obstructive disease.
  • Any other participant's comorbidity or disease condition that the physician judges to be incompatible with intensive chemotherapy must be reviewed and approved by the trial coordinator before study enrollment.
  • Has clinical laboratory values within the following parameters (repeat within 3 days before the first dose of study drug if laboratory values used for randomization were obtained more than 3 days before the first dose of study drug):
  • Total bilirubin ≤1.5 times the upper limit of the normal range (ULN) except in participants with Gilbert's syndrome. Participants with Gilbert's syndrome may enroll with direct bilirubin ≤3 times the ULN of the direct bilirubin. Elevated indirect bilirubin due to posttransfusion hemolysis is allowed.
  • Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤3.0 times the ULN.
  • Creatinine clearance (CrCl) ≥30 mL/min (calculated by the Cockcroft Gault formula).
  • Albumin >2.7 g/dL.
  • WBC count <25 × 10^9/L. Participants who are cytoreduced with leukapheresis or with hydroxyurea may be enrolled if they meet the eligibility criteria before starting therapy.

Exclusion Criteria

  • Has history of MPN with BCR-ABL1 translocation or AML with BCR-ABL1 translocation.
  • Has genetic diagnosis of acute promyelocytic leukemia.
  • Is eligible for intensive chemotherapy and/or allogeneic stem cell transplantation.
  • Has extramedullary AML without evidence of bone marrow involvement.
  • Had prior treatment with hypomethylating agents for AML (hypomethylating agent treatment for prior MDS is not exclusionary).
  • Has clinical evidence of or history of central nervous system involvement by AML.
  • Had diagnosed or treated for another malignancy (except for adequately treated carcinoma in situ of any organ or nonmelanoma skin cancer) within 1 year before randomization or previously diagnosed with another malignancy and have any evidence of residual disease that may compromise the administration of pevonedistat, venetoclax or azacitidine. Prior MDS is also allowed, but the participant cannot have received treatment for MDS within 14 days before first dose of any study drug.
  • Has a WBC count ≥25 × 10^9/L
  • Has uncontrolled human immunodeficiency virus (HIV) infection. Note: Known HIV positive participants who meet the following criteria will be considered eligible:
  • Cluster difference 4 (CD4) count >350 cells/mm^3.
  • Undetectable viral load.
  • Maintained on modern therapeutic regimens utilizing non-cytochrome P (CYP)-interactive agents.
  • No history of acquired immune deficiency syndrome (AIDS)-defining opportunistic infections.
  • Participant is known to be positive for hepatitis B or C infection, with the exception of those with an undetectable viral load within 3 months (hepatitis B or C testing is not required for eligibility assessment).
  • Has hepatic cirrhosis.
  • Has uncontrolled coagulopathy or bleeding disorder.
  • Has high blood pressure which cannot be controlled by standard treatments.
  • Has prolonged rate QTc interval ≥500 msec, calculated according to institutional guidelines.
  • Has left ventricular ejection fraction (LVEF) <40%.
  • As infection is a common feature of AML, participants with active infection are permitted to enroll provided that the infection is under control and no signs of systemic inflammatory response beyond low grade fever that makes participant clinically unstable in the opinion of the investigator. Participants with uncontrolled infection shall not be enrolled until infection is treated and brought under control.

North Carolina

Chapel Hill
UNC Lineberger Comprehensive Cancer Center
Status: IN_REVIEW

Ohio

Cleveland
Case Comprehensive Cancer Center
Status: IN_REVIEW

The drug being tested in this study is called Pevonedistat. Pevonedistat is being tested to treat people who have AML. This study will compare the improvement in EFS in pevonedistat + venetoclax + azacitidine combination arm group when compared with venetoclax + azacitidine. The study will enroll approximately 150 patients. Participants will be randomly assigned to one of the two treatment groups in 28-day treatment cycles and which will remain disclosed to the patient and study doctor during the study: - Pevonedistat 20 mg/m^2 + Venetoclax 400 mg + Azacitidine 75 mg/m^2 - Venetoclax 400 mg + Azacitidine 75 mg/m^2 This multi-center trial will be conducted worldwide. The overall time to participate in this study is approximately 4 years. Participants will attend the end-of-treatment visit 30 days after the last dose of study drug or before the start of subsequent anti-neoplastic therapy if that occurs sooner. Participants who discontinue study treatment without evidence of progressive disease (PD) will enter EFS follow-up or response follow-up (study visits every 3 months) or overall survival follow-up (contacted every 3 months to document subsequent therapies and survival status).

Trial Phase Phase II

Trial Type Treatment

Lead Organization
Takeda

  • Primary ID Pevonedistat-2002
  • Secondary IDs NCI-2020-02881, U1111-1239-7581, 2019-003117-33
  • Clinicaltrials.gov ID NCT04266795