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OncoMatch/Clinical Trials/NCT05362773

A Study of MGD024 in Patients With Relapsed or Refractory Hematologic Malignancies

Is NCT05362773 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies MGD024 for leukemia, acute myeloid.

Phase 1RecruitingMacroGenicsNCT05362773Data as of May 2026

Treatment: MGD024CP-MGD024-01 is a Phase 1, open-label, multi-center study of MGD024 as a single agent in participants with select blood cancers that have not responded to treatment with standard therapies or who have relapsed after treatment. The study is designed to determine the safety, tolerability, pharmacokinetics (affect of the body on the drug), pharmacodynamic (affect of the drug on the body), immunogenicity (development of antibodies against the drug), and preliminary anti-cancer effect of MGD024. Participants will receive treatment with MGD024 in consecutive 28-day cycles for a study treatment period of up to 12 cycles (approximately 1 year) or until treatment or study discontinuation criteria are met. Response assessments will be performed after Cycle 1 and then after every even numbered cycle starting with Cycle 2 until progression or study treatment discontinuation. Participants will be checked for side effects throughout the study.

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Extracted eligibility criteria

Cancer type

Acute Myeloid Leukemia

Myelodysplastic Syndrome

Hodgkin Lymphoma

Acute Lymphoblastic Leukemia

Chronic Myeloid Leukemia

Biomarker criteria

Required: IL3RA overexpression (at least 20% of malignant cells with CD123 expression)

Evidence of at least 20% of malignant cells with CD123 expression

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Min 1 prior line

Must have received: any prior anti-cancer therapy — relapsed or refractory

Relapsed after or refractory to at least one prior line of therapy and with no available potentially curative treatment option

Cannot have received: anti-CD123-directed agent

Exception: patients with BPDCN, who are allowed to have received prior tagraxofusp

Prior treatment with an anti-CD123-directed agent (except patients with BPDCN, who are allowed to have received prior tagraxofusp)

Lab requirements

Blood counts

acceptable laboratory values

Kidney function

acceptable laboratory values

Liver function

acceptable laboratory values

Cardiac function

acceptable heart function

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

US trial sites

  • Colorado Blood Cancer Network · Denver, Colorado
  • University of Maryland, Greenbaum Comprehensive Cancer Center · Baltimore, Maryland
  • Dana Farber Cancer Institute · Boston, Massachusetts
  • START - Midwest · Grand Rapids, Michigan
  • Washington University School of Medicine · St Louis, Missouri

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

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