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Be Part of Research - Trial Details - A Study of ASP2215 Versus Salvage Chemotherapy in Patients With Relapsed or Refractory Acute Myeloid Leukemia (AML) With FMS-like Tyrosine Kinase (FLT3) Mutation

A Study of ASP2215 Versus Salvage Chemotherapy in Patients With Relapsed or Refractory Acute Myeloid Leukemia (AML) With FMS-like Tyrosine Kinase (FLT3) Mutation

Not Recruiting

Open to: ALL

Age: 18.0 - N/A

Medical Conditions

Leukemia
Leukemia, Myeloid
Leukemia, Myeloid, Acute


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


The purpose of this study is to determine the clinical benefit of ASP2215 therapy in participants with FMS-like tyrosine kinase (FLT3) mutated acute myeloid leukemia (AML) who are refractory to or have relapsed after first-line AML therapy as shown with overall survival (OS) compared to salvage chemotherapy, and to determine the efficacy of ASP2215 therapy as assessed by the rate of complete remission and complete remission with partial hematological recovery (CR/CRh) in these participants.

This study will also determine the overall efficacy in event-free survival (EFS) and complete remission (CR) rate of ASP2215 compared to salvage chemotherapy.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Oct 2015 Sep 2018

Publications

"Smith CC, Levis MJ, Perl AE, Hill JE, Rosales M, Bahceci E. Molecular profile of FLT3-mutated relapsed/refractory patients with AML in the phase 3 ADMIRAL study of gilteritinib. Blood Adv. 2022 Apr 12;6(7):2144-2155. doi: 10.1182/bloodadvances.2021006489."; "35130342"; "Perl AE, Larson RA, Podoltsev NA, Strickland S, Wang ES, Atallah E, Schiller GJ, Martinelli G, Neubauer A, Sierra J, Montesinos P, Recher C, Yoon SS, Hosono N, Onozawa M, Chiba S, Kim HJ, Hasabou N, Lu Q, Tiu R, Levis MJ. Follow-up of patients with R/R FLT3-mutation-positive AML treated with gilteritinib in the phase 3 ADMIRAL trial. Blood. 2022 Jun 9;139(23):3366-3375. doi: 10.1182/blood.2021011583."; "35081255"; "Perl AE, Martinelli G, Cortes JE, Neubauer A, Berman E, Paolini S, Montesinos P, Baer MR, Larson RA, Ustun C, Fabbiano F, Erba HP, Di Stasi A, Stuart R, Olin R, Kasner M, Ciceri F, Chou WC, Podoltsev N, Recher C, Yokoyama H, Hosono N, Yoon SS, Lee JH, Pardee T, Fathi AT, Liu C, Hasabou N, Liu X, Bahceci E, Levis MJ. Gilteritinib or Chemotherapy for Relapsed or Refractory FLT3-Mutated AML. N Engl J Med. 2019 Oct 31;381(18):1728-1740. doi: 10.1056/NEJMoa1902688. Erratum In: N Engl J Med. 2022 May 12;386(19):1868. doi: 10.1056/NEJMx220003."; "31665578"

INTERVENTIONAL

Intervention Type : DRUG
Intervention Description : tablet, oral

Intervention Arm Group : Gilteritinib;

Intervention Type : DRUG
Intervention Description : subcutaneous (SC) or intravenous (IV) injection

Intervention Arm Group : Salvage Chemotherapy;

Intervention Type : DRUG
Intervention Description : SC or IV injection

Intervention Arm Group : Salvage Chemotherapy;

Intervention Type : DRUG
Intervention Description : IV injection

Intervention Arm Group : Salvage Chemotherapy;

Intervention Type : DRUG
Intervention Description : SC (G-CSF) and IV (Fludarabine, Cytarabine, Idarubicin) injection

Intervention Arm Group : Salvage Chemotherapy;



You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Site GB44014
    Bournemouth
    BH7 7DW
  • Site GB44013
    Harrow
    HA1 3UJ
  • Site GB44003
    Manchester
    M13 9WL
  • Site GB44015
    Plymouth
    PL6 8DH


The study is sponsored by Astellas Pharma Global Development, Inc.




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Read full details for Trial ID: NCT02421939
Last updated 24 February 2025

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