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
- Diseases
- Acute myeloid leukemia
- 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
Sites (7)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Gabrail Cancer Center Coordinator of this site? Confirm its status | Canton | United States | Recruiting |
| Oncology Hematology Care Coordinator of this site? Confirm its status | Cincinnati | United States | Recruiting |
| University of Texas Southwestern Medical Center Coordinator of this site? Confirm its status | Dallas | United States | Recruiting |
| Colorado Blood Cancer Institute Coordinator of this site? Confirm its status | Denver | United States | Recruiting |
| University of Kansas Coordinator of this site? Confirm its status | Fairway | United States | Recruiting |
| MD Anderson Cancer Center Coordinator of this site? Confirm its status | Houston | United States | Recruiting |
| University of Miami Coordinator of this site? Confirm its status | Miami | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.