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Safety and Efficacy of Quizartinib in Children and Young Adults With Acute Myeloid Leukemia (AML), a Cancer of the Blood

Active, not recruiting · Phase 1, Phase 2 · NCT03793478

Conditions: Acute Myeloid Leukemia

At a glance

Research payments reported, 2025
$573,480
U.S. investigators named
19
Sites paid
20
Planned or actual enrollment
65

About the trial

Sponsor
Daiichi Sankyo (with Innovative Therapies For Children with Cancer Consortium, Children's Oncology Group)
Tested
Quizartinib (drug), Fludarabine (drug), Cytarabine (drug), Intrathecal (IT) triple chemotherapy prophylaxis (drug), Etoposide (drug)
Dates
Started 2018-08-15; completion 2027-05-01
Results posted
Not yet

Quizartinib is an experimental drug. It is not approved for regular use. It can only be used in medical research. Children or young adults with a certain kind of blood cancer (FLT3-ITD AML) might be able to join this study if it has come back after remission or is not responding to treatment.

From ClinicalTrials.gov, last updated 2026-04-01. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Daiichi Sankyo Inc. reported $573,480 in research payments for this study in 2025 (27 payments).

Products named: Vanflyta

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.