Acute Myeloid LeukemiaPhase 2NCT03836209
Gilteritinib vs Midostaurin in FLT3 Mutated Acute Myeloid Leukemia
A Phase 2 study testing Gilteritinib, Midostaurin and Daunorubicin in people with Acute Myeloid Leukemia, run by PrECOG, LLC. at 44 sites in United States.
Trial summary
Eligible untreated patients with FLT3 acute myeloid leukemia (AML) between the ages of 18 and 70 will be randomized to receive gilteritinib or midostaurin during induction and consolidation. Read more about this study
- Who is it for?
- Ages 18 to 70 years
- Conditions the study is for
- Acute Myeloid Leukemia
- What is being tested?
- Gilteritinib, Midostaurin and Daunorubicin
- Type of treatment
- Pill or oral medicine, Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 181 participants
- Where
- 44 sitesUnited States
- Study dates
- 6 Dec 2019to 30 Jun 2026
- Phase
- Phase 2
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 70 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Registration Criteria:
- Any patient undergoing bone marrow biopsy with suspicion of or known diagnosis of acute myeloid leukemia (AML) will be asked to sign a Prescreening Consent to allow for centralized testing of bone marrow/peripheral blood samples.
Randomization Eligibility Criteria:
- Patient must have previously untreated FLT3 mutated Non M3 AML (FLT3-TKD or FLT3-ITD allowed). ° Standard of care induction 7+3 chemotherapy may start prior to randomization using same regimen and doses as defined in the protocol while awaiting prescreening test results.
- Patient must have had no prior systemic therapy for AML, except as noted below:
- Hydroxyurea and emergent leukapheresis or preemptive treatment with retinoic acid prior to exclusion of Acute Promyelocytic Leukemia (APL) allowed.
- Prior therapy for myelodysplastic syndrome (MDS) or myeloproliferative neoplasms (MPN) (e.g., thalidomide or lenalidomide, interferon, jakafi, cytokines, 5-azacytidine or decitabine, histone deacetylase inhibitors).
- Initiation of standard of care 7+3 induction chemotherapy using same regimen and doses as defined in protocol while awaiting prescreening test results
- Patient may not have received hypomethylating agent within 21 days.
- Patient may not have M3 AML.
- Patient may not have AML with known Core Binding Factor -t(8;21), inv(16), t(16;16).
- Patient may not have known active Central Nervous System (CNS) leukemia. ° Prophylaxis with intrathecal chemotherapy is allowed prior to or during induction/consolidation.
- Patient must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0-3.
- Patient must be age ≥ 18 years to ≤ 70 years.
- Patient must be able to understand and willing to sign Institutional Review Board (IRB)-approved informed consent.
- Patient must be willing to provide mandatory bone marrow and blood samples for research.
- Patient must have adequate organ function as measured by the following criteria, obtained ≤ 48 hours prior to randomization except ECG and left ventricular ejection fraction (LVEF) which can be done ≤ 2 weeks prior to randomization:
- Serum creatinine ≤ 1.5x institutional upper limit of normal (ULN), or if serum creatinine outside normal range, then glomerular filtration rate (GFR) >40 mL/min as measured by Cockcroft-Gault formula.
- Alanine Aminotransferase (ALT) and Aspartate Aminotransferase (AST) ≤ 3x ULN, unless secondary to leukemia.
- Serum total or direct bilirubin <2 mg/dL, unless due to Gilbert's, hemolysis or leukemic infiltration.
- Fridericia-Corrected QT Interval (QTcF) interval ≤ 500 msec (using Friderica's correction).
- Left Ventricular Ejection Fraction >45%.
- The patient may not be known to have hypokalemia and/or hypomagnesemia that does not respond to supplementation.
- A female patient is eligible to participate if she is not pregnant and at least one of the following conditions apply:
- Not a woman of childbearing potential (WOCBP) OR
- WOCBP who agrees to follow the contraceptive guidance throughout the treatment period and for at least 180 days after the final study drug administration.
- Female patient must agree not to breastfeed or donate ova starting at treatment and throughout the study period, and for at least 180 days after the final study drug administration.
- A male patient must agree not to donate sperm starting at treatment and throughout the study period, and for at least 120 days after the final study drug administration.
- A male patient with female partner(s) of child-bearing potential must agree to use contraception during the treatment period, and for at least 120 days after the final study drug administration.
- Male patient with a pregnant or breastfeeding partner(s) must agree to remain abstinent or use a condom for the duration of the pregnancy or time partner is breastfeeding throughout the treatment period, and for at least 120 days after the final study drug administration.
- Patient may not have another malignancy that could interfere with the evaluation of safety or efficacy of this combination.
- Patient may not have a history of Long QT Syndrome.
- Patient may not have evidence of uncontrolled angina, severe uncontrolled ventricular arrhythmias, electrocardiographic evidence of acute ischemia, or congestive heart failure (CHF) New York Heart Association (NYHA) Class 3 or 4. Patient may also not have a history of CHF NYHA Class 3 or 4 in the past, unless a prescreening echocardiogram (ECHO) or multigated acquisition scan (MUGA) performed within 2 weeks prior to study entry with results of left ventricular ejection fraction >45%.
- Patient may not have had major surgery or radiation therapy within 4 weeks of registration.
- Patient may not require treatment with concomitant drugs that are strong inducers of CYP3A and P-gp.
- Patient with a known allergy to any of the study medications, their analogues, or excipients in the various formulations of any agent are not eligible.
- Patient with known gastrointestinal (GI) disease or prior GI procedure that could interfere with the oral absorption or tolerance of gilteritinib or midostaurin including difficulty swallowing are not eligible.
- Patient with any serious medical or psychiatric illness that could, in the investigator's opinion, potentially interfere with the completion of the treatment according to the protocol are not eligible.
- Patient may not participate in any other therapeutic clinical trials, including those with other investigational agents not included in this trial during treatment on this study without prior approval from PrECOG.
Trial locations and contacts
44 sites in 1 country.
44 sites in 1 country
United States44 sites
St. Joseph's Mercy Hospital
Ann Arbor, Michigan, 48106
Augusta University Medical Center
Augusta, Georgia, 30912
Johns Hopkins University
Baltimore, Maryland, 21287
Tufts Medical Center
Boston, Massachusetts, 02111
Massachusetts General Hospital
Boston, Massachusetts, 02114
University of Chicago Medical Center
Chicago, Illinois, 60451
Northwestern University Feinberg School of Medicine
Chicago, Illinois, 60611
University of Cincinnati Medical Center
Cincinnati, Ohio, 45267
University Hospitals Cleveland Medical Center
Cleveland, Ohio, 44106
University of California, San Francisco-Fresno (University Oncology Associates)
Clovis, California, 93611
Geisinger Medical Center
Danville, Pennsylvania, 17822
East Carolina University
Greenville, North Carolina, 27834
Penn State Milton S. Hershey Medical Center
Hershey, Pennsylvania, 17033
Franciscan Health Indianapolis
Indianapolis, Indiana, 46237
Mayo Clinic- Jacksonville, FL
Jacksonville, Florida, 32224
Northwell Health
Lake Success, New York, 11042
University of Kentucky Markey Cancer Center
Lexington, Kentucky, 40536
UCLA
Los Angeles, California, 90095
University of Wisconsin Clinical Science Center
Madison, Wisconsin, 53792
Marshfield Medical Center
Marshfield, Wisconsin, 54449
Medical College of Wisconsin
Milwaukee, Wisconsin, 53226
West Virginia University
Morgantown, West Virginia, 26506
Atlantic Health Systems/Morristown Medical Center
Morristown, New Jersey, 07962
Vanderbilt University
Nashville, Tennessee, 37232
Ochsner Clinic Foundation
New Orleans, Louisiana, 70121
Mount Sinai
New York, New York, 10029
Memorial Sloan Kettering Cancer Center
New York, New York, 10065
Weill Cornell Medicine New York Presbyterian Hospital
New York, New York, 10065
Kaiser Permanente Oakland
Oakland, California, 94611
University of Oklahoma Stephenson Cancer Center
Oklahoma City, Oklahoma, 73104
University of Nebraska Medical Center
Omaha, Nebraska, 68105
UC Irvine Health
Orange, California, 92868
University of Pennsylvania
Philadelphia, Pennsylvania, 19104
Thomas Jefferson University
Philadelphia, Pennsylvania, 19107
University of Pittsburgh Medical Center
Pittsburgh, Pennsylvania, 15232
Mayo Clinic- Rochester, MN
Rochester, Minnesota, 55905
University of Rochester Medical Center
Rochester, New York, 14642
Kaiser Permanente Roseville
Roseville, California, 95661
LDS Hospital
Salt Lake City, Utah, 84143
Kaiser Permanente Santa Clara
Santa Clara, California, 94115
HonorHealth Research Institute
Scottsdale, Arizona, 85258
MultiCare
Spokane, Washington, 99218
SUNY Upstate Medical University
Syracuse, New York, 13210
UW Cancer Center at ProHealth Care
Waukesha, Wisconsin, 53188
About this study
Official title: Randomized Trial of Gilteritinib vs Midostaurin in FLT3 Mutated Acute Myeloid Leukemia (AML)
Eligible untreated patients with FLT3 acute myeloid leukemia (AML) between the ages of 18 and 70 will be randomized to receive gilteritinib or midostaurin during induction and consolidation. Patients will also receive standard chemotherapy of daunorubicin and cytarabine during induction and high-dose cytarabine during consolidation.
Gilteritinib, is an oral drug that works by stopping the leukemia cells from making the FLT3 protein. This may help stop the leukemia cells from growing faster and thus may help make chemotherapy more effective. Gilteritinib has been approved by the Food and Drug Administration (FDA) for patients who have relapsed or refractory AML with a FLT3 mutation but is not approved by the FDA for newly diagnosed FLT3 AML, and its use in this setting is considered investigational.
Read more
Midostaurin is an oral drug that works by blocking several proteins on cancer cells, including FLT3 that can help leukemia cells grow. Blocking this pathway can cause death to the leukemic cells. Midostaurin is approved by the FDA for the treatment of FLT3 AML.
The purpose of this study is to compare the effectiveness of gilteritinib to midostaurin in patients receiving combination chemotherapy for FLT3 AML.
Read the detailed description
Approximately one third of patients with AML have a particular change in their leukemia cells (called a mutation) in a gene called FLT3. The presence of a FLT3 mutation can be used to direct treatment options.
This is an open-label phase II study. Patients will receive standard chemotherapy of daunorubicin and cytarabine during Induction and high-dose cytarabine during Consolidation. Patients will be randomized to gilteritinib or midostaurin. After approximately 90 patient's complete treatment, a review of the effectiveness of gliteritinib compared to midostaurin will be done. If gilteritinib is not as effective as midostaurin, the study may be stopped.
Bone marrow aspirate and biopsy will be done on Day 21 after start of Induction and after Induction to assess response. Patients with a complete response may proceed to consolidation chemotherapy. Another bone marrow aspirate and biopsy will be done after the first cycle of consolidation is complete.
Mandatory prescreening bone marrow and/or blood samples are required for FLT3 testing. Any left-over samples will be requested for future research (optional).
Mandatory bone marrow samples for research are required after Induction and if patient receives Consolidation, after the first cycle of Consolidation.
- Conditions
- Acute Myeloid Leukemia
- Being tested
- Gilteritinib, Midostaurin, Daunorubicin, Cytarabine
- Keywords
- Gilteritinib, Midostaurin, Daunorubicin, Cytarabine, FLT3, FLT3 Mutation, FLT3 Internal Tandem Duplication (ITD), FLT3 ITD, FLT3 Tyrosine Kinase Domain (TKD), FLT3 TKD
- Medical subject headings
- Leukemia, Myeloid, Acute
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
GilteritinibDrug
Also called ASP2215
Induction: 120 mg orally daily x 14 days starting on day 8
Consolidation: 120 mg orally daily x 14 days starting on day 8 of each cycle (up to 4 cycles)
MidostaurinDrug
Also called RYDAPT
Induction: 50 mg orally twice daily x 14 days beginning on day 8
Consolidation: 50 mg orally twice daily x 14 days beginning on day 8 of each cycle (up to 4 cycles)
DaunorubicinDrug
Also called Daunorubicin hydrochloride, Daunomycin, Rubidomycin, Cerubidine
First Induction: Daunorubicin 90 mg/m²/day IV Days 1,2,3
Second Induction, if needed: Daunorubicin 45 mg/m²/day IV Days 1,2,3
CytarabineDrug
Also called Cytosar-U, Ara-C, Arabinosyl, Cytosine Arabinoside
Induction: Cytarabine 100 mg/m²/day continuous infusion x 7 days starting Day 1
Second Induction, if needed: Cytarabine 100 mg/m²/day continuous infusion x 7 days starting Day 1
Consolidation: Cytarabine 3 g/m² (recommend 1.5 g/m² for age ≥ 55 or patients with decreased creatinine clearance) every 12 hours IV Days 1,3,5 or Days 1-3 for 6 doses for up to 4 cycles
| Study group | Role | What they receive |
|---|---|---|
| Arm A | Experimental | Induction: Daunorubicin, cytarabine and gilteritinib. Depending on response, second cycle of Induction may be given.
Consolidation: High-dose cytarabine and gilteritinib. Receives: Drug: Gilteritinib; Drug: Daunorubicin; Drug: Cytarabine |
| Arm B | Active comparator | Induction: Daunorubicin, cytarabine and midostaurin. Depending on response, second cycle of Induction may be given.
Consolidation: High-dose cytarabine and midostaurin. Receives: Drug: Midostaurin; Drug: Daunorubicin; Drug: Cytarabine |
What is being measured
The primary outcome is the main question the study is designed to answer.
FLT3 Mutation Negative Composite Complete Response (CRc) [Includes Complete Response (CR) or CR With Incomplete Hematologic Recovery (CRi)] at End of Induction
FLT3 mutation negative (evaluated by polymerase chain reaction [PCR]) Composite Complete Response (CRc) [includes CR and CRi] rate after induction treatment and complete MRD assessment. The cut points used for FLT3 mutation negative are 1% (equivalent to 10-2) for FLT3-TKD and 10-4 for FLT3-ITD.
Measured: 3 months
Secondary outcomes (6)
FLT3 Mutation Negative Complete Response (CR) Rate at End of Induction
CR evaluated by FLT3 testing after Induction
Measured: 3 months
Minimal Residual Disease (MRD)- CRc Rate at End of Induction
MRD- CRc evaluated by flow cytometry after Induction
Measured: 3 months
CRc (CR or CRi) Rate at End of Induction
CRc assessed in accordance with 2017 European LeukemiaNet (ELN)
Measured: 3 months
Event Free Survival (EFS)
EFS assessed in accordance with 2017 ELN
Measured: 68 months
Overall Survival (OS)
OS assessed in accordance with 2017 ELN
Measured: 68 months
Number of Participants Treatment-related Adverse Events as Assessed by CTCAE v5.0
Number of participants with abnormal laboratory values and/or adverse events
Measured: 10 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Feb 2019
- Study start6 Dec 2019
- Primary completion17 Oct 2023
- Study completion30 Jun 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Other trials for Acute Myeloid LeukemiaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Open-Label, Randomized trial of Daunorubicin/Cytarabine and High Dose Cytarabine + Gilteritinib vs Midostaurin for Induction and Consolidation. FLT3 mutated patients will be stratified based on TKD vs ITD. Patients who are FLT3 ITD will be further stratified by Signal Ratio (high vs. low of FLT3 Wild Type) and Nucleophosmin 1-Mutated (NPM1) \[positive vs negative\].
- Masking
- None (open label)
- Enrolment
- 181 participants (actual)
Sponsor and investigators
- Lead sponsor
- PrECOG, LLC.
- Sponsor type
- University, hospital or other
- Collaborators
- Astellas Pharma Inc
- Responsible party
- Sponsor
- Investigators
- Selena Luger, MD, Study chair, University of Pennsylvania
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03836209
- Sponsor's protocol ID
- PrE0905
- Status last verified
- Jul 2026
- First submitted
- 7 Feb 2019
- Last updated
- 23 Jul 2026
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- No: Data is proprietary.
Study at a glance
From the registry record, last updated by the sponsor on 23 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Randomized Trial of Gilteritinib vs Midostaurin in FLT3 Mutated Acute Myeloid Leukemia (AML)
- ClinicalTrials.gov ID
- NCT03836209
- Acronym / sponsor ID
- PrE0905
- Conditions
- Acute Myeloid Leukemia
- Keywords
- Gilteritinib, Midostaurin, Daunorubicin, Cytarabine, FLT3, FLT3 Mutation, FLT3 Internal Tandem Duplication (ITD), FLT3 ITD
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 181 participants (actual)
- Lead sponsor
- PrECOG, LLC.University, hospital or other
- Collaborators
- Astellas Pharma Inc
- Study start
- 6 Dec 2019 (actual)
- Primary completion
- 17 Oct 2023 (actual)
- Study completion
- 30 Jun 2026 (actual)
- First posted
- 11 Feb 2019 (actual)
- Results
- Posted 28 Feb 2025
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Eligible untreated patients with FLT3 acute myeloid leukemia (AML) between the ages of 18 and 70 will be randomized to receive gilteritinib or midostaurin during induction and consolidation. Patients will also receive standard chemotherapy of daunorubicin and cytarabine during induction and high-dose cytarabine during consolidation.
Gilteritinib, is an oral drug that works by stopping the leukemia cells from making the FLT3 protein. This may help stop the leukemia cells from growing faster and thus may help make chemotherapy more effective. Gilteritinib has been approved by the Food and Drug Administration (FDA) for patients who have relapsed or refractory AML with a FLT3 mutation but is not approved by the FDA for newly diagnosed FLT3 AML, and its use in this setting is considered investigational.
Midostaurin is an oral drug that works by blocking several proteins on cancer cells, including FLT3 that can help leukemia cells grow. Blocking this pathway can cause death to the leukemic cells. Midostaurin is approved by the FDA for the treatment of FLT3 AML.
The purpose of this study is to compare the effectiveness of gilteritinib to midostaurin in patients receiving combination chemotherapy for FLT3 AML.
Detailed description
Approximately one third of patients with AML have a particular change in their leukemia cells (called a mutation) in a gene called FLT3. The presence of a FLT3 mutation can be used to direct treatment options.
This is an open-label phase II study. Patients will receive standard chemotherapy of daunorubicin and cytarabine during Induction and high-dose cytarabine during Consolidation. Patients will be randomized to gilteritinib or midostaurin. After approximately 90 patient's complete treatment, a review of the effectiveness of gliteritinib compared to midostaurin will be done. If gilteritinib is not as effective as midostaurin, the study may be stopped.
Bone marrow aspirate and biopsy will be done on Day 21 after start of Induction and after Induction to assess response. Patients with a complete response may proceed to consolidation chemotherapy. Another bone marrow aspirate and biopsy will be done after the first cycle of consolidation is complete.
Mandatory prescreening bone marrow and/or blood samples are required for FLT3 testing. Any left-over samples will be requested for future research (optional).
Mandatory bone marrow samples for research are required after Induction and if patient receives Consolidation, after the first cycle of Consolidation.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- Open-Label, Randomized trial of Daunorubicin/Cytarabine and High Dose Cytarabine + Gilteritinib vs Midostaurin for Induction and Consolidation. FLT3 mutated patients will be stratified based on TKD vs ITD. Patients who are FLT3 ITD will be further stratified by Signal Ratio (high vs. low of FLT3 Wild Type) and Nucleophosmin 1-Mutated (NPM1) [positive vs negative].
| Arm | Type | Receives |
|---|---|---|
| Arm A | Experimental | Drug: Gilteritinib, Drug: Daunorubicin, Drug: CytarabineInduction: Daunorubicin, cytarabine and gilteritinib. Depending on response, second cycle of Induction may be given. Consolidation: High-dose cytarabine and gilteritinib. |
| Arm B | Active comparator | Drug: Midostaurin, Drug: Daunorubicin, Drug: CytarabineInduction: Daunorubicin, cytarabine and midostaurin. Depending on response, second cycle of Induction may be given. Consolidation: High-dose cytarabine and midostaurin. |
Who may qualify
- Ages
- 18 to 70 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| GilteritinibAlso: ASP2215Induction: 120 mg orally daily x 14 days starting on day 8 Consolidation: 120 mg orally daily x 14 days starting on day 8 of each cycle (up to 4 cycles) | Drug | Arm A |
| MidostaurinAlso: RYDAPTInduction: 50 mg orally twice daily x 14 days beginning on day 8 Consolidation: 50 mg orally twice daily x 14 days beginning on day 8 of each cycle (up to 4 cycles) | Drug | Arm B |
| DaunorubicinAlso: Daunorubicin hydrochloride, Daunomycin, Rubidomycin, CerubidineFirst Induction: Daunorubicin 90 mg/m²/day IV Days 1,2,3 Second Induction, if needed: Daunorubicin 45 mg/m²/day IV Days 1,2,3 | Drug | Arm A, Arm B |
| CytarabineAlso: Cytosar-U, Ara-C, Arabinosyl, Cytosine ArabinosideInduction: Cytarabine 100 mg/m²/day continuous infusion x 7 days starting Day 1 Second Induction, if needed: Cytarabine 100 mg/m²/day continuous infusion x 7 days starting Day 1 Consolidation: Cytarabine 3 g/m² (recommend 1.5 g/m² for age ≥ 55 or patients with decreased creatinine clearance) every 12 hours IV Days 1,3,5 or Days 1-3 for 6 doses for up to 4 cycles | Drug | Arm A, Arm B |
Primary outcome
FLT3 Mutation Negative Composite Complete Response (CRc) [Includes Complete Response (CR) or CR With Incomplete Hematologic Recovery (CRi)] at End of Induction
Time frame: 3 months
FLT3 mutation negative (evaluated by polymerase chain reaction [PCR]) Composite Complete Response (CRc) [includes CR and CRi] rate after induction treatment and complete MRD assessment. The cut points used for FLT3 mutation negative are 1% (equivalent to 10-2) for FLT3-TKD and 10-4 for FLT3-ITD.
6 secondary outcomes
FLT3 Mutation Negative Complete Response (CR) Rate at End of Induction
Time frame: 3 months
Minimal Residual Disease (MRD)- CRc Rate at End of Induction
Time frame: 3 months
CRc (CR or CRi) Rate at End of Induction
Time frame: 3 months
Event Free Survival (EFS)
Time frame: 68 months
Overall Survival (OS)
Time frame: 68 months
Number of Participants Treatment-related Adverse Events as Assessed by CTCAE v5.0
Time frame: 10 months
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 23 Jul 2026.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Individual participant dataSharing planned: No. Data is proprietary.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Selena Luger, MD study chair
University of Pennsylvania
44 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Gilteritinib, Midostaurin and Daunorubicin in people with Acute Myeloid Leukemia, run by PrECOG, LLC. at 44 sites in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 23 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 44 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 28 Feb 2025). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
FLT3 Mutation Negative Composite Complete Response (CRc) [Includes Complete Response (CR) or CR With Incomplete Hematologic Recovery (CRi)] at End of Induction (time frame: 3 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Jul 2026.