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OncoMatch/Clinical Trials/NCT07011004

A Study of Natural Killer Cells in Combination With Atezolizumab in People With Acute Myelogenous Leukemia

Is NCT07011004 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies multiple treatments including Cytokine Induced Memory-Like Natural Killer Cells and Atezolizumb for acute myeloid leukemia refractory.

Phase 1RecruitingMemorial Sloan Kettering Cancer CenterNCT07011004Data as of May 2026

Treatment: Cytokine Induced Memory-Like Natural Killer Cells · Atezolizumb · CIML-NK cell therapyThe researchers are doing this study is to find the highest dose of cytokine-induced memory-like (CIML) natural killer (NK) cells in combination with the drug atezolizumab that causes few or mild side effects in people with relapsed/refractory acute myelogenous leukemia (AML). The researchers will also look at whether the treatment combination works against participants' cancer.

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Extracted eligibility criteria

Cancer type

Acute Myeloid Leukemia

Biomarker criteria

Allowed: FLT3 ITD mutation

Patients with FLT3-ITD or -TKD mutations must have received at least one commercially available inhibitor of FLT3.

Allowed: FLT3 TKD mutation

Patients with FLT3-ITD or -TKD mutations must have received at least one commercially available inhibitor of FLT3.

Allowed: NPM1 mutation

Patients with NPM1 mutation or rearrangements of MLL must be refractory to revumenib.

Allowed: KMT2A (MLL) rearrangement

Patients with NPM1 mutation or rearrangements of MLL must be refractory to revumenib.

Allowed: IDH1 mutation

Patients with mutations in IDH1 or IDH2 must be refractory to at least one commercially available inhibitor of IDH1 or IDH2, respectively.

Allowed: IDH2 mutation

Patients with mutations in IDH1 or IDH2 must be refractory to at least one commercially available inhibitor of IDH1 or IDH2, respectively.

Prior therapy

Min 2 prior lines

Must have received: combination chemotherapy (daunorubicin, anthracycline) — induction

Refractory to at least two attempts at prior induction therapy. An attempt is defined as either a single cycle of combination chemotherapy such as daunorubicin/anthracycline

Must have received: hypomethylating agent with venetoclax (hypomethylating agent, venetoclax) — induction

A single monthly cycle of a hypomethylating agent with venetoclax

Must have received: FLT3 inhibitor

Patients with FLT3-ITD or -TKD mutations must have received at least one commercially available inhibitor of FLT3.

Must have received: revumenib (revumenib)

Patients with NPM1 mutation or rearrangements of MLL must be refractory to revumenib.

Must have received: IDH1 inhibitor

Patients with mutations in IDH1 or IDH2 must be refractory to at least one commercially available inhibitor of IDH1 or IDH2, respectively.

Must have received: IDH2 inhibitor

Patients with mutations in IDH1 or IDH2 must be refractory to at least one commercially available inhibitor of IDH1 or IDH2, respectively.

Cannot have received: allogeneic hematopoietic cell transplantation

Prior allogeneic hematopoietic cell transplantation

Lab requirements

Kidney function

estimated or measured creatinine clearance > 50 ml/min

Liver function

serum bilirubin ≤ 5 mg/dl; ast and alt ≤ 2.5x uln unless thought to be disease related

Cardiac function

systolic lv ejection fraction ≥50% at rest and absence of new york heart association stage iii or iv congestive heart failure

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Memorial Sloan Kettering at Basking Ridge (Limited Protocol Activities) · Basking Ridge, New Jersey
  • Memorial Sloan Kettering Monmouth (Limited protocol activities) · Middletown, New Jersey
  • Memorial Sloan Kettering Bergen (Limited Protocol Activities) · Montvale, New Jersey
  • Memorial Sloan Kettering Suffolk - Commack (Limited protocol activities) · Commack, New York
  • Memorial Sloan Kettering West Harrison (Limited Protocol Activities) · Harrison, New York

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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