Clinical Trial 24124

• Overview

  Study Title:

  A Randomized Phase 2/3 Study Evaluating the Safety and Efficacy of Pivekimab Sunirine (PVEK) in Combination with Venetoclax and Azacitidine in Adult Subjects with Newly Diagnosed Acute Myeloid Leukemia (AML) Ineligible to Receive Intensive Chemotherapy

  Summary:

  Cancer is a condition where cells in a specific part of the body grow and reproduce uncontrollably. Acute myeloid leukemia (AML) is a cancer of the blood and bone marrow (the spongy tissue inside the bones) that affects white blood cells that helps to fight infections and also prevents normal blood cell production. This study will assess the adverse events and changes in the disease activity when Pivekimab Sunirine (PVEK) is given in combination with Venetoclax (VEN) and Azacitidene (AZA) in adult participants with AML ineligible to receive intensive chemotherapy. Pivekimab sunirine is a drug being evaluated in the treatment of AML.This is a Phase 2/Phase 3, study of PVEK. Phase 2 is open-label and randomized. Phase 3 is double-blind, randomized. Phase 2 and Phase 3 studies test potential new treatments in patients with a condition or disease. Open-label means that both patients and study doctors know which study treatment is given to patients in Phase 2 of the study. Double-blind means that neither the patients nor the study doctors know who is given which study treatment in Phase 3 of the study. Approximately 660 adult participants will be enrolled in 180 sites worldwide. In Phase 2 of the study, patients will be randomized to receive PVEK + VEN + AZA or standard of care treatment with VEN + AZA. In Phase 3, patients will be randomized to receive PVEK + VEN + AZA or a matching-placebo for PVEK plus VEN + AZA. PVEK is given as an infusion into the vein, AZA is given as an injection under your skin (subcutaneous) or as an infusion into the vein (intravenous) (depending on country where patient enrolls), and VEN is a tablet given by mouth. The total study duration is approximately 71 months. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic. The effect of the treatment will be checked by medical assessments, blood tests, and checking for side effects.

  Objective:

  Primary Objective: Phase 2: To evaluate if treatment with PVEK in combination with VEN + AZA improves complete remission (CR) rate as compared to standard of care with VEN + AZA in adult subjects with newly diagnosed AML ineligible to receive intensive chemotherapy. Phase 3: To assess the superiority of treatment with PVEK in combination with VEN + AZA in improving CR rate and prolonging overall survival (OS) compared to standard of care VEN + AZA in adult subjects with newly diagnosed AML ineligible to receive intensive chemotherapy. Secondary Objective: Phase 2: To assess if treatment with PVEK in combination with VEN + AZA, compared to VEN + AZA, improves composite CR + CRi and CR + CRh response rates. To assess if treatment with PVEK in combination with VEN + AZA, compared to VEN + AZA, improves the rate of CR, CR + CRi, and CR + CRh without measurable residual disease (CRMRD-, CR + CRiMRD-, CR + CRhMRD-). To assess if treatment with PVEK in combination with VEN + AZA, compared to VEN + AZA, improves duration of CR (DoCR). To assess if treatment with PVEK in combination with VEN + AZA, compared to VEN + AZA, improves overall survival (OS). To assess if treatment with PVEK in combination with VEN + AZA, compared to VEN + AZA, improves quality of life. Phase 3: To assess if treatment with PVEK in combination with VEN + AZA, compared to VEN + AZA, improves composite CR + CRi and CR + CRh response rates. To assess if treatment with PVEK in combination with VEN + AZA compared to VEN + AZA improves the rate of CR, CR + CRi, and CR + CRh without measurable residual disease (CRMRD-, CR + CRiMRD-, CR + CRhMRD-). To assess if treatment with PVEK in combination with VEN + AZA compared to VEN + AZA improves transfusion independence. To assess if treatment with PVEK in combination with VEN + AZA, compared to VEN + AZA, improves duration of CR (DoCR). To assess if treatment with PVEK in combination with VEN + AZA compared to VEN + AZA improves relapse-free survival (RFS). To assess if treatment with PVEK in combination with VEN + AZA compared to VEN + AZA improves quality of life.

• Treatments

  Therapies:

  Antibody-Drug Conjugate; BCL-2 inhibitor; Chemotherapy (NOS)

  Medications:

  Azacitidine (); Azacitidine (5-azacitidine); GDC-0199 (Venetoclax); Pivekimab Sunirine (); Pivekimab Sunirine/Placebo (); Venetoclax ()

• Inclusion Criteria

  Key Inclusion Criteria:
  • Participants must have newly diagnosed, untreated confirmed acute myeloid leukemia (AML) diagnosis as per the 5th edition of World Health Organization (WHO) criteria with a projected life expectancy of at least 12 weeks.
  • CD123-positive.
  • Ineligible for intensive induction therapy (chemotherapy).
  • ECOG performance status 0 to 2 for subjects ≥ 75 years of age or 0 to 3 for subjects ≥ 18 to 74 years of age.
  • White blood cell (WBC) count > Subjects must have adequate organ function.
  • Additional criteria may apply.

• Exclusion Criteria

  Key Exclusion Criteria:
  • Acute promyelocytic leukemia (APL), blast phase of CML or AML with t(9;22) or BCR:ABL1 fusion, transformation from myeloproliferative neoplasm (MPN), Chronic Myelomonocytic Leukemia (CMML), myelodysplastic/myeloproliferative neoplasm unspecified, or myeloid sarcoma.
  • Known active central nervous system (CNS) involvement with AML. Participants may have non-CNS extramedullary disease (excludes participants with myeloid sarcoma as the only disease manifestation at screening).
  • Participants with history of any malignancies within 2 years prior to screening with exception of: adequately treated in situ carcinoma of the cervix uteri or carcinoma in situ of the breast, in situ - carcinomas of bladder and esophagus; basal cell carcinoma of the skin or localized squamous cell carcinoma of the skin, and previous malignancy confined and surgically resected (or treated with other modalities) with curative intent and have no evidence of relapse within 2 years.
  • Participants must not have received a hypomethylating agent, any BCL-2 inhibitors including venetoclax, and/or chemotherapeutic agent for Myelodysplastic syndromes (MDS) or AML, CAR-T cell therapy, be currently participating in another clinical study, received any investigational treatment within 30 days prior to the first use of study combination product.
  • Female participant must not be pregnant or breastfeeding and is not considering becoming pregnant or donating eggs during the study and for approximately 7 months after the last dose of any study drug. Female participant of childbearing potential must agree to use at least 1 protocol specified method of birth control and male participant, if sexually active with female partner(s) of childbearing potential, must agree to practice the protocol-specified contraception.
  • Additional Criteria may apply.

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