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
Recruiting
Observational Study
Acute Myeloid Leucemia
High-risk Myelodysplastic Syndrome (MDS)
Acute Lymphoid Leukemia
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 1,000 (estimated)
- Sponsor
- Nantes University Hospital · Other
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About This Trial
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…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patient of legal age affected by AML, ALL or MDS regardless of the time of treatment
* Patient who has signed the consent form.
* Patient affiliated with a social security system.
Exclusion Criteria:
* Minor patients.
* Adults under guardianship.
* Protected persons
Contacts