A Study of ASP2215 (Gilteritinib) by Itself, ASP2215 Combined With Azacitidine or Azacitidine by Itself to Treat Adult Patients Who Have Recently Been Diagnosed With Acute Myeloid Leukemia With a FLT3 Gene Mutation and Who Cannot Receive Standard Chemotherapy

Completed · Phase 3

Conditions studied: Acute Myeloid Leukemia (AML), Acute Myeloid Leukemia With FMS-like Tyrosine Kinase (FLT3) Mutation

In brief

This was a clinical study for adult participants who were recently diagnosed with acute myeloid leukemia or AML. AML is a type of cancer. It is when bone marrow makes white blood cells that are not normal. These are called leukemia cells. Some participants with AML have a mutation, or change, in the FLT3 gene. This gene helps leukemia cells make a protein called FLT3. This protein causes the leukemia cells to grow faster. For participants with AML who could not receive standard chemotherapy, azacitidine (also known as Vidaza®) was a current standard of care treatment option in the United States. This clinical study tested an experimental medicine called ASP2215, also known as gilteritinib. Gilteritinib worked by stopping the leukemia cells from making the FLT3 protein. This helped stop the leukemia cells from growing faster. This study compared two different treatments. Participants were assigned to one of these two groups by chance: a medicine called azacitidine, also known as Vidaza®, or an experimental medicine gilteritinib in combination with azacitidine. There was a twice as much chance to receive both medicines combined than azacitidine alone. The clinical study may help show which treatment helps patients live longer.

Key facts

Study ID

NCT02752035

Run by

Astellas Pharma Global Development, Inc.

People needed

183

Starts

2016-08-01

Expected to finish

2024-12-18

Last updated by the study team

2026-07-14

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subject is considered an adult according to local regulation at the time of obtaining informed consent.
• Subject has a diagnosis of previously-untreated AML according to World Health Organization (WHO) classification [Swerdlow et al, 2008] as determined by pathology review at the treating institution.
• Subject is positive for FLT3 mutation (internal tandem duplication [ITD] or tyrosine kinase domain [TKD] [D835/I836] mutation) (or for Korea only: ITD alone or ITD with concurrent TKD activating mutation) in bone marrow or whole blood as determined by central laboratory. Note: Only requirement of FLT3 mutation assessment by central laboratory is only applicable to the randomization portion of the study.
• Subject is ineligible for intensive induction chemotherapy by meeting at least 1 of the following criteria:
• Subject is ≥ 65 years of age and ineligible for intensive induction chemotherapy.
• Subject is ≥ 18 to 64 years of age and has any of the following comorbidities: [Ex-US Only]: Congestive heart failure (New York Heart Association {NYHA} class ≤ 3) or ejection fraction (Ef) ≤ 50%; [US Only]: Severe cardiac disorder e.g. congestive heart failure (New York Heart Association [NYHA] class ≤ 3) requiring treatment, ejection fraction ≤ 50%, or chronic stable angina; [Ex-US Only]: Creatinine > 2 mg/dL (177 µmol/L), dialysis or prior renal transplant; [US Only]: Creatinine clearance < 45 mL/min; ECOG performance status ≥ 2;
• [Ex-US Only]: Known pulmonary disease with decreased diffusion capacity of lung for carbon monoxide (DLCO) and/or requiring oxygen ≤ 2 liters per minute; [US Only] Severe pulmonary disorder (e.g., diffusion capacity of lung for carbon monoxide [DLCO] ≤ 65% or forced expiratory volume in the first second [FEV1] ≤ 65%); Prior or current malignancy that does not require concurrent treatment; Subject has received a cumulative anthracycline dose above 400 mg/m2 of doxorubicin (or cumulative maximum dose of another anthracycline). Any other comorbidity incompatible with intensive chemotherapy must be reviewed and approved by the Medical Monitor during screening and before randomization.
• Subject must meet the following criteria as indicated on the clinical laboratory tests:
• Serum AST and ALT ≤ 3.0 x Institutional upper limit of normal (ULN)
• Serum total bilirubin ≤ 1.5 x Institutional ULN
• Serum potassium ≥ Institutional lower limit of normal (LLN)
• Serum magnesium ≥ Institutional LLN Repletion of potassium and magnesium levels during the screening period is allowed.
• Subject is suitable for oral administration of study drug.
• Female subject is eligible to participate if female subject is not pregnant and at least one of the following conditions applies:
• Not a woman of childbearing potential (WOCBP); OR
• WOCBP agrees to follow the contraceptive guidance starting at screening and continue throughout the study period, and for at least 180 days after the final study drug administration.
• Female subject must agree not to breastfeed starting at screening and throughout the study period, and for 60 days after the final study drug administration.
• Female subject must not donate ova starting at screening and throughout the study period, and for 180 days after the final study drug administration.
• Male subject with female partners of childbearing potential must agree to use contraception as detailed in Contraception Requirements, starting at screening and continue throughout the study period, and for 120 days after the final study drug administration.
• Male subject must not donate sperm starting at screening and throughout the study period and for 120 days after the final study drug administration.
• Subject agrees not to participate in another interventional study while on treatment.

You may not qualify if…

• Subject was diagnosed as acute promyelocytic leukemia (APL).
• Subject has BCR-ABL-positive leukemia (chronic myelogenous leukemia in blast crisis).
• Subject has received previous therapy for AML, with the exception of the following:
• Emergency leukapheresis
• Hydroxyurea
• Preemptive treatment with retinoic acid prior to exclusion of APL ≤ 7 days
• Growth factor or cytokine support
• Steroids
• Subject has clinically active central nervous system leukemia.
• Subject has been diagnosed with another malignancy that requires concurrent treatment (with the exception of hormone therapy limited to those therapies that prevent recurrence and/or spread of cancer) or hepatic malignancy regardless of need for treatment.
• Subject requires treatment with concomitant drugs that are strong inducers of cytochrome P450 CYP3A/P-glycoprotein (P-gp).
• Subject requires treatment with concomitant drugs that are strong inhibitors or inducers of P-gp with the exception of drugs that are considered absolutely essential for the care of the subject.
• Subject requires treatment with concomitant drugs that target serotonin 5-hydroxytryptamine receptor 2B (5HT2BR) or sigma nonspecific receptor with the exception of drugs that are considered absolutely essential for the care of the subject.
• Subject has congestive heart failure classified as New York Heart Association Class IV.
• Subject with mean Fridericia-corrected QT interval (QTcF) > 480 ms at screening based on central reading.
• Subject with a history of Long QT Syndrome at screening.
• [Ex-US Only]: Subject has known pulmonary function tests with diffusion capacity of lung for carbon monoxide (DLCO) ≤ 50%, forced expiratory volume in the first second (FEV1) ≤ 60%, dyspnea at rest or requiring oxygen or any pleural neoplasm (Transient use of supplemental oxygen is allowed.)
• Subject has active hepatitis B or C or other active hepatic disorder.
• Subjects with positive hepatitis B surface antigen (HBsAg) or detectable hepatitis B DNA are not eligible.
• Subjects with negative HBsAg, positive hepatitis B core antibody and negative hepatitis B surface antibody will be eligible if hepatitis B DNA is undetectable.
• Subjects with antibodies to hepatitis C virus will be eligible if hepatitis C RNA is undetectable
• Subject has any condition which makes the subject unsuitable for study participation, including any contraindications of azacitidine.
• Subject has a known or suspected hypersensitivity to ASP2215, azacitidine or any components of the formulations used.
• [US Only]: Subject is ≥ 65 to 74 years of age, suitable for and willing to receive intensive induction chemotherapy.

Where it is running

• University of California, Irvine Medical Center — Orange, California, United States
• Robert H. Lurie Comprehensive Cancer Center — Chicago, Illinois, United States
• Rush University Medical Center — Chicago, Illinois, United States
• St. Louis University Cancer Center - Hematology/Oncology — St Louis, Missouri, United States
• Hackensack University Medical Center - John Theurer Cancer Center — Hackensack, New Jersey, United States
• Hematology-Oncology Associates of Northern NJ — Morristown, New Jersey, United States
• Roswell Park Cancer Institute — Buffalo, New York, United States
• Memorial Sloan-Kettering Cancer Center — New York, New York, United States
• Weill Cornell Medical College-New York Presbyterian Hospital — New York, New York, United States
• GHS Cancer Institute — Greenville, South Carolina, United States
• LDS Hospital — Salt Lake City, Utah, United States
• Site AU61004 — Liverpool, New South Wales, Australia
• Site AU61008 — Adelaide, South Australia, Australia
• Site AU61007 — Geelong, Victoria, Australia
• Site BE32007 — Brussels, Brussels Capital, Belgium
• Site BE32003 — Brussels, Bruxelles-Capitale, Region de, Belgium
• Site BE32006 — Ghent, Belgium
• Site CA15009 — Edmonton, Alberta, Canada
• Site CA15011 — Toronto, Ontario, Canada
• Site CA15002 — Toronto, Ontario, Canada
• Site CA15006 — Montreal, Quebec, Canada
• Site FR33003 — Nîmes, Gard, France
• Site FR33002 — Pessac, Gironde, France
• Site FR33015 — Rouen, Haute-Normandie, France
• UCLA David Geffen School of Medicine — Los Angeles, California, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.