Leukaemia Trial, Recruiting NCT06130787 Sponsor: University Hospital, Clermont-Ferrand Condition: Leukaemia
Back to Leukaemia

Leukaemia Trial, Recruiting

NCT06130787
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:

  • You are 18 years of age or older
  • You have been diagnosed with a specific type of blood cancer called CML (chronic myeloid leukemia) in its early stage, known as "chronic phase"
  • Your diagnosis was made no more than 3 months (90 days) before joining the trial
  • Your diagnosis has been confirmed by specific laboratory tests, including a test for the Philadelphia chromosome
  • A specific genetic marker in your blood (called BCR::ABL1) can be detected and measured by a lab test
  • You are starting your first-ever treatment for CML using a type of medication called a tyrosine kinase inhibitor (a targeted cancer drug)
  • You have not yet received any CML medications (including hydroxyurea) before your first blood sample is taken at diagnosis
  • You have signed consent forms for both parts of the study
  • You are able to read and understand French
  • You are covered by, or a dependent of someone covered by, French social security

Who may not be able to join:

  • Your CML is in a more advanced stage, called "accelerated phase" or "blast phase"
  • You do not wish to take part in the study
  • You have already started treatment before enrolling in the trial
  • You are under a legal protection order, guardianship, or have restricted personal freedoms (confirm with trial site)
  • You are currently pregnant or breastfeeding

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 5 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: Marc BERGER, University Hospital, Clermont-Ferrand

Phone: +33473754963

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
Registry
ClinicalTrials.gov
Start date
17 November 2023
Est. completion
17 November 2025

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Biological age determination; Individual fragility assessment; Individual fragility assessment; Tolerance of tyrosine kinase inhibitors; Tolerance of tyrosine kinase inhibitors; Tolerance of tyrosine kinase inhibitors; Tolerance of tyrosine kinase inhibitors; Tolerance of tyrosine kinase inhibitors

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: 5 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