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Study identifier: NCT06681363 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Creation of a Biocollection of Patients With Acute Myeloid Leukemia (AML) or Lymphoid Leukemia (ALL) or High-risk Myelodysplastic Syndrome (MDS) Monitored at the Nantes University Hospital

Condition: Acute Myeloid Leucemia · High-risk Myelodysplastic Syndrome (MDS) · Acute Lymphoid Leukemia  ·  Sponsor: Nantes University Hospital

PhaseN/A
Planned participants1000
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The aim of the LANA bio-collection is to collect samples from patients with Acute Myeloid Leukemia (AML), Acute Lymphocytic Leukemia (ALL) or or high-risk myelodysplastic syndrome (MDS) to facilitate access to the leukemic or myelodysplastic cells for the research teams of the National Institute of Health and Medical Research (INSERM). To do this, an additional blood or bone marrow sample to those planned in the context of patient care will be collected after signing consent. These samples will then be sent directly to the INSERM teams for immediate analysis with the aim to conduct research aimed at a better understanding of AML, ALL or MDS and improving treatments

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

Talk to the study team

Pierre Perterlin  ·  +33 2 40 08 32 71  ·  Pierre.PETERLIN@chu-nantes.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Nantes University HospitalNantes, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT06681363