Acute Myeloid Leukemia (AML) Clinical Trials

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Randomized Evaluation of Treosulfan Versus Melphalan Conditioning Followed by PTCy in Patients With AML and MDS Undergoing Allogeneic Transplantation

Status: Recruiting
Location: See all (17) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

The aim of this study is to compare the effectiveness and tolerability of two conditioning chemotherapies prior to allogeneic stem cell transplantation. The following will also be investigated: * Survival * Remission and Relapse rate * Engraftment or graft failure * Graft versus Host Disease (GvHD)

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Informed consent signed by the patient capable of giving

• Patient scheduled for allogeneic transplantation within the next 3 weeks

• Age ≥ 18 years

• AML or MDS according to WHO with indication for allogeneic HCT:

‣ AML in first or second complete remission (CR) or complete remission with incomplete hematologic recovery (CRi/CRh) or morphologic leukemia-free state (MLFS)

⁃ MDS according to WHO

• Increased risk for treatment-related toxicity by myeloablative conditioning according to at least one of the following criteria:

‣ Patients aged ≥ 50 years at transplant and/or

⁃ HCT-CI \> 2 and/or

⁃ AML or MDS scheduled for 2nd allogeneic HCT from different donor with minimum of 12 months after 1st allogeneic HCT

• Availability of a suitable donor:

‣ Matched sibling donor (MSD) or

⁃ matched unrelated donor (MUD, 10/10 HLA) or

⁃ mismatched unrelated donor (MMUD, single allele or antigen mismatch at HLA-A, -B, -C, or -DRB1 and no concurrent -DQB1 mismatch (9/10) shown by confirmatory typing) or

⁃ haploidentical family donor

• Planned GvHD prophylaxis with standard PTCy (with 50mg/kg body weight on days +3 and +4)

• No history of cardiac disease that preclude allogeneic HCT and absence of active symptoms, otherwise, documented left ventricular ejection fraction

⁃ 40 %.

• No need for supplementary oxygen on day of randomization

Locations
Other Locations
Germany
Universitätsklinikum Aachen, Medizinische Klinik IV
RECRUITING
Aachen
Klinikum Augsburg, Medizinische Klinik II
RECRUITING
Augsburg
Helios Klinikum Berlin Buch, Klinik für Onkologie und Palliativmedizin
RECRUITING
Berlin
Klinikum Chemnitz gGmbH; Klinik für Innere Medizin III
RECRUITING
Chemnitz
Universitätsklinikum Köln, Klinik I für Innere Medizin
RECRUITING
Cologne
Medizinische Fakultät der TU Dresden, Medizinische Klinik und Poliklinik I
RECRUITING
Dresden
Universitätsklinikum Frankfurt, Medizinische Klinik II
RECRUITING
Frankfurt Am Main
Universitätsklinikum Greifswald, Klinik und Poliklinik für Innere Medizin C
RECRUITING
Greifswald
Universitätsmedizin Halle (Saale), Klinik für Innere Medizin IV
RECRUITING
Halle
Universitätsklinikum Jena, Klinik für Innere Medizin II
RECRUITING
Jena
Universitätsklinikum Schleswig-Holstein, Campus Kiel, Klinik für Innere Medizin II
RECRUITING
Kiel
Universitätsklinikum Leipzig, Klinik und Poliklinik für Hämatologie, Zelltherapie, Hämostaseologie und Infektiologie
RECRUITING
Leipzig
Klinikum der Johannes Gutenberg Universität, III. Medizinische Klinik und Poliklinik
NOT_YET_RECRUITING
Mainz
Universitätsklinikum Münster, Medizinische Klinik A, KMT-Zentrum
RECRUITING
Münster
Klinikum Nürnberg, Campus Nord, Klinik für Innere Medizin 5
RECRUITING
Nuremberg
Universitätsklinik Rostock, Klinik und Poliklinik für Innere Medizin, Abt. für Hämatologie/Onkologie
RECRUITING
Rostock
Robert-Bosch-Krankenhaus, Hämatologie, Onkologie und Palliativmedizin
RECRUITING
Stuttgart
Contact Information
Primary
Prof. Friedrich Stölzel, MD
etal-5@ukdd.de
+49 431 500-22701
Backup
Desiree Kunadt, MD
etal-5@ukdd.de
+49 351 458 19523
Time Frame
Start Date: 2026-01-21
Estimated Completion Date: 2029-09
Participants
Target number of participants: 220
Treatments
Experimental: Treo - Arm
Treo d-4 - d-2 + Flud d-6 till d-2
Active_comparator: MEL - Arm
Mel d-2 + Flud d-6 till d-2
Sponsors
Leads: Technische Universität Dresden
Collaborators: medac GmbH

This content was sourced from clinicaltrials.gov