Condition: Leukemia · Sponsor: Daiichi Sankyo
Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.
This study will compare the effects of Quizartinib versus placebo in combination with chemotherapy in participants with newly diagnosed FMS-like tyrosine kinase 3 (FLT3)-internal tandem duplication (ITD) negative acute myeloid leukemia (AML).
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
Key Inclusion Criteria: 1. Must be competent and able to comprehend, sign, and date an Ethics Committee (EC)- or Institutional Review Board (IRB)-approved ICF before performance of any trial-specific procedures or tests. 2. ≥18 years or the minimum legal adult age (whichever is greater) and ≤70 years (at Screening). 3. Newly diagnosed, morphologically documented primary AML based on the World Health Organization (WHO) 2016 classification (at Screening) 4. Eastern Cooperative Oncology Group (ECOG) performance status (at the time the participant signs their ICF) of 0-2. 5. Participant is a candidate for standard "7+3" induction chemotherapy regimen as specified in the protocol per investigator assessment Key Exclusion Criteria: 1. Diagnosis of acute promyelocytic leukemia (APL), French-American-British classification M3 or WHO classification of APL with translocation, t(15;17)(q22;q12), or BCR-ABL positive leukemia (ie, chronic myelogenous leukemia in blast crisis); participants who undergo diagnostic workup for APL and treatment with all-trans retinoic acid (ATRA), but who are found not to have APL, are eligible (treatment with ATRA must be discontinued before starting induction chemotherapy). 2. Diagnosis of AML secondary to prior chemotherapy or radiotherapy. 3. Diagnosis of AML with known antecedent myelodysplastic syndrome (MDS) or a myeloproliferative neoplasm (MPN) or MDS/MPNs including chronic myelomonocytic leukemia (CMML), atypical chronic myeloid leukemia (aCML), juvenile myelomonocytic leukemia (JMML) and others. 4. Participants with newly diagnosed AML with FLT3-ITD mutations (FLT3-ITD \[+\]) present at ≥5% VAF (or ≥0.05 SR) based on a validated FLT3 mutation assay. 5. Prior treatment for AML, except for the following allowances prior to Day 1 of chemotherapy: 1. Leukapheresis; 2. Treatment for hyperleukocytosis with hydroxyurea; 3. Cranial radiotherapy for central nervous system (CNS) leukostasis; 4. Prophylactic intrathecal chemotherapy
Reproduced word-for-word from the public registry record — the study team can answer questions about it.
| City of Hope Phoenix | Goodyear, Arizona, United States | — |
| Mayo Clinic - Phoenix | Phoenix, Arizona, United States | — |
| University of Arizona Cancer Center | Tucson, Arizona, United States | — |
| David Geffen School of Medicine | Los Angeles, California, United States | — |
| University of California Davis Health System | Sacramento, California, United States | — |
| Ucsf Helen Diller Family Comprehensive Cancer Center | San Francisco, California, United States | — |
| Stanford University School of Medicine- Parent | Stanford, California, United States | — |
| Colorado Blood Cancer Institute | Denver, Colorado, United States | — |
| Yale University | New Haven, Connecticut, United States | — |
| Sibley Memorial Hospital | Washington D.C., District of Columbia, United States | — |
| Mayo Clinic Hospital | Jacksonville, Florida, United States | — |
| Florida Hospital Cancer Institute - Kissimmee | Kissimmee, Florida, United States | — |
+ 272 more locations — full list on the registry record.
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