Leukaemia Trial, Recruiting NCT04869683 Sponsor: University Hospital, Brest Condition: Leukaemia
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Leukaemia Trial, Recruiting

NCT04869683
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Adults who have been diagnosed with, or are suspected of having, myelodysplastic syndrome (a type of blood/bone marrow disorder) at the time of diagnosis or during ongoing monitoring
  • People whose care is managed at the Cancer-Hematology Institute of Brest CHRU (a specific hospital centre in France)
  • People who have biological samples (such as blood or tissue) already stored in the hospital's biological resource centre (CRB)
  • People who have given their consent to participate in the trial

Who may not be able to join:

  • People who are under 18 years old, or who are pregnant
  • People who do not have biological samples stored in the hospital's biological resource centre (CRB)
  • People who have refused to participate, have not given consent, or are unable to give consent
  • People who are under a form of legal protection or guardianship (for example, under court-appointed guardianship or curatorship) (confirm with trial site)

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 26 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Nathalie Douet-Guilbert, MD,PhD, CHRU BREST

Phone: +33229020215

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
University Hospital, Brest
Registry
ClinicalTrials.gov
Start date
19 October 2022
Est. completion
19 October 2032

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Cohort MDS: epidemiologic MSD study

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov