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Study identifier: NCT05788679 Synced from ClinicalTrials.gov · July 29, 2026
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A Study Using Subject-specific MRD to Adopt Treatment After HSCT for Subjects With MDS

Condition: Myelodysplastic Syndromes · Acute Myeloid Leukemia With Myelodysplasia Related Disease and < 30% Blasts · Mixed Myelodysplastic/Myeloproliferative Disease  ·  Sponsor: Karolinska University Hospital

PhasePhase 2
Planned participants200
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this interventional study is to evaluate if pre-emptive intervention using Azacitidine and / or donor lymphocytes or tapering of immune suppression in measurable residual disease (MRD) positive subjects can prevent clinical relapse. Participants will undergo MRD surveillance and be subjected to intervention in case of MRD positivity. Results will be compared with NMDSG14B, part one, in which MRD was analyzed in included patients without recieving intervention.

This description comes directly from the study's public registry record.

Talk to the study team

Magnus Tobiasson, PhD  ·  0046858580000  ·  magnus.tobiasson@ki.se

Always discuss trial participation with your own doctor first.

Locations (1)

Department of Hematology, Karolinska University HospitalStockholm, SwedenRecruiting

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Source record: clinicaltrials.gov/study/NCT05788679