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2024-511651-17-00RecruitingPhase 2

NMDSG-14B2

A phase II multicenter single-armed study using subject-specific minimal residual minimal disease markers to adopt treatment after allogeneic stem cell transplantation for subjects with myleodysplastic syndrome - MDS

Source: EU CTIS (euclinicaltrials.eu) · Last updated 27 May 2026

Next steps

Brief summary (registry, in English)

To prevent clinical events (relapse or non-relapse death) in minimal residual disease (MRD) positive subjects

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
200 (estimated)
First submitted
13 Feb 2024
Start date
21 Sept 2021
Lead sponsor
Karolinska University Hospital
EU CT number
2024-511651-17-00
EudraCT number
2021-003809-22

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 200
  • 11 sites in 4 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Uncontrolled hypertension, heart, liver, kidney related or other uncontrolled medical or psychiatric disorders

Other

  • No traceable genetic aberration identified either in screening next generation sequencing panel or next generation sequencing panel performed at diagnosis
  • Mental inability, reluctance or language difficulties that results in difficulty understanding the meaning of study participation

Who the study is looking for

  • Signed informed consent
  • Age ≥ 18 years
  • Subjects eligible for stem cell transplantation
  • Subjects having the disease myelodysplastic syndrome (MDS), mixed myelodysplastic/myeloproliferative syndrome or acute myeloid leukemia (AML) with myelodysplasia related dysplasia and 20-29% marrow blasts
  • All female subjects of childbearing potential have to have negative pregnancy test within 2 weeks prior to inclusion to the study

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (11)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Aarhus University HospitalAarhus NDenmarkRecruiting
RigshospitaletCopenhagen OeDenmarkRecruiting
HUS-YhtymaeHelsinkiFinlandRecruiting
Helse Bergen HFBergenNorwayRecruiting
Oslo University Hospital HFOsloNorwayRecruiting
Sahlgrenska University Hospital-Vaestra GoetalandsregionenGoteborgSwedenRecruiting
Karolinska University HospitalHuddingeSwedenRecruiting
Linkoping University Hospital Region OstergotlandLinkopingSwedenRecruiting
Region Skane Skanes UniversitetssjukhusLundSwedenRecruiting
Norrlands University HospitalUmeåSwedenRecruiting
Uppsala University HospitalUppsalaSwedenRecruiting

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This page is information, not medical advice. Discuss any trial with your doctor.