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Registry Study on Patient Characteristics, Biological Disease Profile and Clinical Outcome in Acute Myeloid Leukemia and Related Neoplasms - The Biology and Outcome (BiO)-Project

Launched by UNIVERSITY OF ULM · Dec 2, 2010

Trial Information

Current as of August 21, 2025

Recruiting

Keywords

Aml Registry Study Biology And Outcome Mds/Aml

ClinConnect Summary

The BiO-Project is a clinical trial that aims to understand more about acute myeloid leukemia (AML) and certain related blood disorders, including higher risk myelodysplastic syndromes (MDS). This study will involve adults who have recently been diagnosed with these conditions or have had them return after treatment. Researchers will collect information about the patients, including their medical history and genetic markers, and will track their health outcomes over a maximum of 10 years. They will also store biological samples, like blood and tissue, to help with future research.

To participate in this study, individuals must be at least 18 years old and have a suspected diagnosis of AML or related conditions. Participants will need to give their consent to share their information and samples. Throughout the study, participants can expect regular follow-ups and assessments to monitor their disease and quality of life. This research is being conducted at multiple sites in Germany and Austria and aims to improve understanding and treatment options for these serious blood disorders.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Patients with suspected diagnosis of acute myeloid leukemia and related neoplasms, newly diagnosed or relapsed/refractory, classified according to the International Consensus Classification
  • Age ≥ 18 years. There is no upper age limit.
  • Signed written informed consent
  • Exclusion Criteria:
  • Severe neurological or psychiatric disorder interfering with ability to give an informed consent
  • No consent for registration, storage and processing of the individual patient and disease characteristics and course as well as information of the family physician about study participation
  • No consent for biobanking of patient's biological specimens and performance of analyses on stored material.

About University Of Ulm

The University of Ulm is a leading academic institution located in Germany, renowned for its commitment to cutting-edge research and innovation in the fields of medicine and health sciences. As a clinical trial sponsor, the university leverages its robust network of researchers and clinical experts to advance medical knowledge and improve patient outcomes. With a focus on interdisciplinary collaboration, the University of Ulm conducts comprehensive clinical studies that adhere to the highest ethical standards and regulatory guidelines. Through its research initiatives, the university aims to contribute significantly to the development of new therapies and treatment modalities, fostering a deeper understanding of various health conditions.

Locations

Hamburg, , Germany

Augsburg, , Germany

Hannover, , Germany

Berlin, , Germany

Augsburg, , Germany

München, , Germany

Traunstein, , Germany

Düsseldorf, , Germany

Bad Saarow, , Germany

Minden, , Germany

Passau, , Germany

Landshut, , Germany

Karlsruhe, , Germany

Oldenburg, , Germany

Hamburg, , Germany

Bremen, , Germany

Stuttgart, , Germany

Bonn, , Germany

Graz, , Austria

Innsbruck, , Austria

Lebach, , Germany

Göttingen, , Germany

Ludwigshafen, , Germany

Darmstadt, , Germany

Braunschweig, , Germany

Ulm, , Germany

Oldenburg, , Germany

Wien, , Austria

Freiburg, , Germany

Hamm, , Germany

Hanau, , Germany

Hannover, , Germany

Heilbronn, , Germany

Lemgo, , Germany

Trier, , Germany

Wuppertal, , Germany

Homburg/Saar, , Germany

Magdeburg, , Germany

Esslingen, , Germany

Lüdenscheid, , Germany

Dortmund, , Germany

Aurich, , Germany

Flensburg, , Germany

München, , Germany

Karlsruhe, , Germany

Linz, , Austria

Linz, , Austria

Linz, , Austria

Rankweil, , Austria

Salzburg, , Austria

Aschaffenburg, , Germany

Berlin, , Germany

Berlin, , Germany

Berlin, , Germany

Bochum, , Germany

Düsseldorf, , Germany

Essen, , Germany

Frankfurt, , Germany

Fulda, , Germany

Gießen, , Germany

Goch, , Germany

Greifswald, , Germany

Göppingen, , Germany

Hamburg, , Germany

Herne, , Germany

Kaiserslautern, , Germany

Kiel, , Germany

Krefeld, , Germany

Lübeck, , Germany

Magdeburg, , Germany

Mainz, , Germany

Meschede, , Germany

Mutlangen, , Germany

Mühlheim, , Germany

Neuss, , Germany

Offenburg, , Germany

Recklinghausen, , Germany

Regensburg, , Germany

Saarbrücken, , Germany

Saarlouis, , Germany

Sande, , Germany

Stuttgart, , Germany

Stuttgart, , Germany

Trier, , Germany

Tübingen, , Germany

Ulm, , Germany

Villingen Schwenningen, , Germany

Offenbach, , Germany

Wernigerode, , Germany

Bochum, , Germany

Potsdam, , Germany

Salzburg, , Austria

Patients applied

JD

1 patients applied

Trial Officials

Hartmut Döhner, Prof. Dr.

Study Chair

University Hospital of Ulm

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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