ClinicalTrials.gg
CompletedNCT03250338Updated Apr 9, 2026

Study Investigating the Efficacy of Crenolanib With Chemotherapy vs Chemotherapy Alone in R/R FLT3 Mutated AML

A Phase 3 interventional study of Crenolanib and Cytarabine in Relapsed/Refractory Acute Myeloid Leukemia With FLT3 Activating Mutations, sponsored by Arog Pharmaceuticals, Inc.. Completed at 62 sites in 6 countries. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-04-09.

Primary conditionnone(registry's first term: Recurrence)No conditionIs this wrong?Recurrence describes something many studies share rather than a condition a study is about. The study names no condition we can place it under, so it is not compared with other studies by condition.

Sponsored by Arog Pharmaceuticals, Inc. · Phase 3, Interventional, and Treatment

Phase
Phase 3
Study type
Interventional
Enrollment
106
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

This is a randomized, multi-center, double-blind, placebo-controlled study designed to evaluate the efficacy of crenolanib administered following salvage chemotherapy, consolidation chemotherapy, post bone marrow transplantation and as maintenance in relapsed/refractory AML subjects with FLT3 activating mutation.

02

Conditions studied

  • Relapsed/Refractory Acute Myeloid Leukemia With FLT3 Activating Mutations

Browse trials for

03

In context

Lead sponsor

Arog Pharmaceuticals, Inc. is the lead sponsor of 17 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Confirmed diagnosis of AML according to World Health Organization (WHO) 2016 classification
  2. Presence of FLT3-ITD and/or D835 mutation(s)
  3. Subjects must be primary or relapsed to intensive treatment for AML or refractory or relapsed after second line of treatment for AML
  4. Age ≥ 18 years and ≤ 75 years
  5. Adequate hepatic function
  6. Adequate renal functions
  7. performance status ≤ 3

Exclusion criteria

Exclusion Criteria:

  1. Known clinically active central nervous system(CNS) leukemia
  2. Severe liver disease
  3. Known, active infection with virus (HBV) or virus (HCV)
  4. Prior anti-leukemia therapy within the 14 days prior to randomization. Prior use of quizartinib or gilteritinib must be discontinued 21 days prior to randomization. Prior use of hydroxyurea or other palliative treatment for leukocytosis is allowed.
  5. Previous treatment with crenolanib or prior participation in clinical trial involving crenolanib.
Terms in these criteria, in plain language(5)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Relapsed and refractory

Relapsed: the illness came back after treatment had worked. Refractory: it did not respond to treatment, or stopped responding while still on it.

Line of therapy

A line of therapy is one course of treatment, which may combine several drugs. First-line is the first course given; second-line follows when that stops working or is not tolerated.

“Two prior lines” means two courses that count separately under the study’s rules — not simply two drugs. Ask the study team if you are unsure how yours are counted.

ECOG performance status

A scale of how much an illness limits everyday activity. For people being assessed to join a study, scores run from 0 (fully active) to 4; lower is more active.

0
Fully active, no restrictions.
1
Limited in strenuous activity, but walking and able to do light work, such as housework or office work.
2
Walking and able to look after yourself, but unable to work; up and about more than half of waking hours.
3
Able to look after yourself only in part; in bed or a chair more than half of waking hours.
4
Unable to look after yourself at all; in bed or a chair all day.

Studies most often ask for 0–1 or 0–2. Your doctor gives the score; the WHO scale uses the same steps. The full scale also has 5, which records death.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
106 participants (actual)

Study arms

  • Experimental
    Crenolanib

    Crenolanib following salvage chemotherapy

    Drug: Crenolanib · Drug: Cytarabine · Drug: Mitoxantrone · Drug: Fludarabine · Drug: Idarubicin · Drug: G-CSF

  • Placebo comparator
    Placebo

    Placebo following salvage chemotherapy

    Drug: Cytarabine · Drug: Mitoxantrone · Drug: Placebo Oral Tablet · Drug: Fludarabine · Drug: Idarubicin · Drug: G-CSF

Interventions

  • Crenolanib will be administered orally

    Also known as: Crenolanib besylate

  • HAM regimen FLAG-Ida

  • HAM regimen

  • DrugPlacebo Oral Tablet

    Placebo will be administered orally

  • FLAG-Ida regimen

  • FLAG-Ida regimen

  • DrugG-CSF

    FLAG-Ida regimen

06

What researchers measure

Primary outcomes

  1. Event-free survival (EFS)

    Time frame: 3 years

Secondary outcomes

  1. Overall Survival

    Time frame: 3 years

  2. Relapse-free Survival (RFS)

    Time frame: 3 years

  3. Complete remission rate (CR)

    Time frame: 3 years

  4. MRD negative complete remission rate

    Time frame: 3 years

07

Study locations

62 sites
  • City of Hope National Medical Center
    Sacramento, California 95817, United States
  • UC Davis Comprehensive Cancer Center
    Sacramento, California 95817, United States
  • University of Florida
    Gainesville, Florida 32610, United States
  • University of Chicago
    Chicago, Illinois 60637, United States
  • Kansas University
    Kansas City, Kansas 666160, United States
  • Karmanos Cancer Center
    Detroit, Michigan 48201, United States
  • Henry Ford Health System
    Detroit, Michigan 48202, United States
  • Roswell Park Cancer Institute
    Buffalo, New York 14263, United States
  • Wake Forest Baptist Medical Center
    Winston-Salem, North Carolina 27104, United States
  • University of Alberta
    Edmonton, Alberta T6G 2R3, Canada
  • Hospital Avicenne
    Bobigny, 93000, France
  • CHU Grenoble Alpes
    Grenoble, 38043, France
  • Hospital Center of Versailles (Le Chesnay)
    Le Chesnay, 78157, France
  • Hospital Claude Huriez - Chru Lille
    Lille, 59037, France
  • Institut Paoli-Calmettes
    Marseille, 13009, France
  • CHU de Nantes - Hôtel Dieu
    Nantes, 44093, France
  • University Hospital Nice L'Archet
    Nice, 06200, France
  • Hôpital St Louis
    Paris, 75010, France
  • CHU de Bordeaux
    Pessac, 33604, France
  • Centre Hospitalier Lyon Sud
    Pierre-Bénite, 69494, France
  • CHU de Poitiers
    Poitiers, 86021, France
  • Institut Universitaire du Cancer Toulouse
    Toulouse, 31059, France
  • Klinikum Chemnitz gGmbH
    Chemnitz, 09116, Germany
  • Technische Universität Dresden
    Dresden, Germany
  • Universitätsklinikum Essen (AöR)
    Essen, 45147, Germany
  • Universitätsklinikum Frankfurt
    Frankfurt, Germany
  • Universitätsklinikum Halle (Saale)
    Halle, Germany
  • Universitätsklinikum Münster
    Münster, 48149, Germany
  • Policlinico Tor Vergata
    Roma, RM 00133, Italy
  • AOU Policlinico Sant'Orsola-Malpighi
    Bologna, 40138, Italy
  • ASST Spedali Civili di Brescia
    Brescia, 25123, Italy
  • AOU Careggi
    Florence, 50134, Italy
  • IRST - Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori
    Meldola, 47014, Italy
  • IRCCS San Raffaele Hospital
    Milan, 20132, Italy
  • IRCCS Foundation Ca 'Granda Ospedale Maggiore Policlinico
    Milan, 20122, Italy
  • Istituto Europeo di Oncologia
    Milan, 20141, Italy
  • Aorn Antonio Cardarelli
    Naples, 80131, Italy
  • AOU Federico II
    Naples, 80131, Italy
  • AOU Maggiore della Carità
    Novara, 28100, Italy
  • AO Ospedali Riuniti Villa Sofia-Cervello
    Palermo, Italy
  • AO Ospedali Riuniti Marche Nord
    Pesaro, 61122, Italy
  • Ospedale Santa Maria delle Croci di Ravenna
    Ravenna, 48121, Italy
  • Fondazione Policlinico Universitario Agostino Gemelli
    Roma, 00168, Italy
  • A.O.U. Città della Salute e della Scienza di Torino
    Torino, 10126, Italy
  • AO Ordine Mauriziano di Torino
    Torino, 10128, Italy
  • Policlinico GB Rossi, University Hospital Verona
    Verona, 37134, Italy
  • AULSS n 8 Berica Ospedale San Bortolo
    Vicenza, 36100, Italy
  • Hospital U. Virgen del Rocio
    Seville, Andalusia 41013, Spain
  • Hospital U. Marques de Valdecilla
    Santander, Cantabria 39008, Spain
  • Hospital Universitario Central de Asturias (HUCA)
    Oviedo, Principality of Asturias 33011, Spain
  • Complejo Hospitalario Universitario A Coruna
    A Coruña, 15006, Spain
  • San Pedro de Alcantara Hospital
    Cáceres, 10003, Spain
  • Reina Sofia University Hospital
    Córdoba, 14004, Spain
  • Hospital Universitario de Donostia
    Donostia / San Sebastian, 20014, Spain
  • Hospital Ramon y Cajal
    Madrid, 28034, Spain
  • Fundacion Jimenez Diaz
    Madrid, 28040, Spain
  • Hospital 12 de Octubre
    Madrid, 28041, Spain
  • Hospital Universitario La Paz
    Madrid, 28046, Spain
  • Hospital Gregorio Maranon Servicio de Hematologia y Hemoterapia
    Madrid, Spain
  • Hospital Clinico Universitario de Salamanca
    Salamanca, 37007, Spain
  • Hospital Clinico Universitario de Santiago
    Santiago de Compostela, 15706, Spain
  • Hospital Universitario y Politecnico La Fe
    Valencia, 46026, Spain
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Aug 2018 to primary completion in Apr 2026, 91 months.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 11, 2017
First posted
Aug 15, 2017
StartActual
Aug 16, 2018
Primary completionActual
Apr 3, 2026
CompletionActual
Apr 3, 2026
Last update
Apr 9, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03250338
Lead sponsor
Arog Pharmaceuticals, Inc.
Responsible party
Sponsor
First posted
Aug 15, 2017
Start date
Aug 16, 2018
Primary completion
Apr 3, 2026
Completion
Apr 3, 2026
Last update
Apr 9, 2026

Study contacts

Eunice Wang, MD
principal investigator · Roswell Park Cancer Institute, Buffalo, New York, United States, 14263

Oversight

FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2026. You cannot join it, but the record below documents what was studied.

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Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

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Studies of the drug tested here: Crenolanib

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