RecruitingPhase 3NCT04628026
Phase III Study of Induction and Consolidation Chemotherapy With Venetoclax in Patients With Newly Diagnosed AML or MDS-EB-2
Studying Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- University of Ulm
- Principal Investigator
- Hartmut Doehner, MDUniversity of Ulm
- Intervention
- Venetoclax(drug)
- Enrollment
- 650 target
- Eligibility
- 18-75 years · All sexes
- Timeline
- 2022 – 2032
Study locations (30)
- Tirol Kliniken GmbH, Innsbruck, Austria
- Kepler Universitaetsklinikum GmbH, Linz, Austria
- Ordensklinikum Linz GmbH, Linz, Austria
- Landeskrankenhaus (LKH) Rankweil, Interne E am Landeskrankenhaus Rankweil, Rankweil, Austria
- Gemeinnuetzige Salzburger Landeskliniken Betriebsgesellschaft mbH, Salzburg, Austria
- Hanusch Krankenhaus Der Wiener Gebietskrankenkasse, Vienna, Austria
- Ziekenhuis Aan De Stroom, Antwerp, Belgium
- Az St-Jan Brugge-Oostende A.V., Bruges, Belgium
- Universitair Ziekenhuis Brussel, Brussels, Belgium
- Katholieke Universiteit te Leuven, Leuven, Belgium
- Algemeen Ziekenhuis Delta, Roeselare, Belgium
- CHU UCL NAMUR - Mont Godinne, Yvoir, Belgium
- North Estonia Medical Centre Foundation, Tallinn, Estonia
- Tartu University Hospital, Tartu, Estonia
- Helsinki University Central Hospital Meilahden Kolmiosairaala, Helsinki, Finland
- +15 more locations on ClinicalTrials.gov
Collaborators
Stichting Hemato-Oncologie voor Volwassenen Nederland
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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