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NCT06634394RecruitingPhase 1

APVO436 Phase 1b/2 Study in Patients With Newly Diagnosed AML

A Phase 1b/2 Open-Label Study of APVO436 in Combination With Venetoclax and Azacitidine in Patients With Newly Diagnosed Acute Myeloid Leukemia (AML)

Source: ClinicalTrials.gov · Last updated 11 May 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

A multi-center, open-label, dose-finding study of five dose levels of APVO436 in combination with venetoclax and azacitidine (ven/aza) in adult patients with newly diagnosed, CD123+ AML.

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
39 (estimated)
First submitted
4 Oct 2024
Start date
1 Oct 2024
Primary completion date
Oct 2027
Lead sponsor
Aptevo Therapeutics
NCT number
NCT06634394

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 39
  • From 1 Oct 2024 to the primary completion date, Oct 2027
  • 7 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patient has received treatment with the following:
    • A hypomethylating agent, venetoclax, and/or chemotherapeutic agent for AML, myelodysplastic syndrome (MDS), chronic myelomonocytic leukemia (CMML), or myelodysplastic/myeloproliferative neoplasms (MPS/MPN)
    • CAR-T cell therapy or history of allogeneic hematopoietic stem cell transplant (HSCT)
    • Experimental therapies for MDS or AML
  • Patient is receiving concurrent corticosteroid therapy as an anticancer drug (any dose).
  • Patient has known active CNS involvement with AML. Patients who received intrathecal chemotherapy for prophylaxis of AML in the CNS prior to enrollment may enroll in this study.

Other illness

  • Patient has history of MPN including myelofibrosis, essential thrombocythemia, polycythemia vera, chronic myeloid leukemia (CML) with or without BCR-ABL1 translocation, or AML with BCR-ABL1 translocation.
  • Patient has a current autoimmune disorder requiring immunosuppressive therapy such as systemic (oral or IV) steroid therapy \>10 mg methylprednisolone daily or its equivalent

Lab values

  • Creatinine clearance \<30ml/min based on Cockcroft-Gault or MDRD formular.
  • Bilirubin of \>3xULN in the absence of Gilbert's Syndrome.
  • AST and/or ALT \>3 times the ULN.

Other

  • Patient is currently participating in another interventional research study.
  • Patient has acute promyelocytic leukemia.

Who the study is looking for

  • 1\. Age ≥18 years. 2. Patient must have confirmation of AML based on 2016 World Health Organization (WHO) criteria and not been previously treated.
    • 3\. Patients must have CD123-positive AML as confirmed by local flow cytometry (or immunohistochemistry \[IHC\]). Confirmation at diagnosis is acceptable.
    • 4\. Patient must be considered ineligible for induction therapy defined by at least one of the following:
    • ≥75 years of age
    • Eastern Cooperative Oncology Group (ECOG) Performance Status of 2 or 3
    • Cardiac disorder (e.g., congestive heart failure requiring treatment, ejection fraction ≤ 50%, or chronic stable angina)
    • Pulmonary disorder (e.g., DLCO ≤65% or FEV1 ≤65%)
    • Creatinine clearance 30-45 mL/min based on Cockcroft-Gault or Modified of Diet in Renal Disease (MDRD) formular
    • Hepatic disorder with total bilirubin between 1.5 and 3 times the ULN 5. Patient must have a projected life expectancy of ≥12 weeks

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (7)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Gabrail Cancer Center
Coordinator of this site? Confirm its status
CantonUnited StatesRecruiting
Oncology Hematology Care
Coordinator of this site? Confirm its status
CincinnatiUnited StatesRecruiting
University of Texas Southwestern Medical Center
Coordinator of this site? Confirm its status
DallasUnited StatesRecruiting
Colorado Blood Cancer Institute
Coordinator of this site? Confirm its status
DenverUnited StatesRecruiting
University of Kansas
Coordinator of this site? Confirm its status
FairwayUnited StatesRecruiting
MD Anderson Cancer Center
Coordinator of this site? Confirm its status
HoustonUnited StatesRecruiting
University of Miami
Coordinator of this site? Confirm its status
MiamiUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.