A PHASE II MULTICENTER OPEN -LABEL TRIAL OF TAGRAXOFUSP (TAG) IN COMBINATION WITH VENETOCLAX AND AZACITIDINE (VEN/AZA) IN ADULTS WITH PREVIOUSLY UNTREATED CD123+ ACUTE MYELOID LEUKEMIA (AML) WHO ARE INELIGIBLE FORINTENSIVE CHEMOTHERAPY

Contact:

NCT Number:

Protocol:

AAAV4214

Study Status:

Active/Enrolling

Population:

Adult

Phase:

II

The purpose of this study is to determine if tagraxofusp (Tag) in combination with venetoclax (Ven) and azacitidine (Aza) can safely treat cancer in patients who have not received study treatment for their acute myeloid leukemia (AML) before. The combination of Tag with Ven and Aza is experimental and this combination of all 3 drugs is not approved by the United States Food and Drug Administration (FDA) for the treatment for patients with AML.

Are you Eligible? (Inclusion Criteria)

  • Are you 18 years or older? -Are you able to give written informed consent and be able to comply with all study requirements which include taking the study drug and extra clinic visits and procedures? -Have you been diagnosed with acute myeloid leukemia (AML), a type of blood cancer, but have not started any treatment?

Specialty Area(s)

Leukemia, Acute Myeloid Leukemia, Immunotherapy

Principal Investigator

Trial Location(s)

CUIMC/Herbert Irving Pavilion
161 Fort Washington Avenue
New York, NY 10032