Leukaemia Trial, Recruiting NCT07061145 Sponsor: Azienda USL Reggio Emilia - IRCCS Condition: Leukaemia
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Leukaemia Trial, Recruiting

NCT07061145
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:

  • People who have been diagnosed with a specific type of blood cancer called chronic phase CML, where a particular genetic marker (called Philadelphia chromosome-positive and/or BCR-ABL-positive) is present
  • People who started their first-ever treatment for this condition using a type of medication called TKIs (targeted therapy drugs), between 1 January 2015 and 31 January 2022
  • People who were aged between 18 and 75 years old at the time they started that treatment
  • People who are male
  • People who had taken certain medications (Hydroxyurea or Anagrelide) before starting TKI therapy — this is permitted
  • People who are able to understand the study's goals and procedures and can make a free and voluntary choice about taking part
  • People who have signed a written consent form in line with required legal and ethical standards

Who may not be able to join:

  • People whose CML has progressed to a more advanced stage (known as accelerated phase or blast phase)
  • People who experienced a specific condition before starting TKI treatment (confirm with trial site for full details, as the condition is noted in the criteria but context is limited)

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 16 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: Isabella Capodanno, MD, Azienda USL - IRCCS di Reggio Emilia

Phone: 0522295511

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
Azienda USL Reggio Emilia - IRCCS
Registry
ClinicalTrials.gov
Start date
1 July 2025
Est. completion
1 July 2025

Where this trial is recruiting

🇮🇹 Italy

Primary endpoints

Cumulative incidence function (CIF) of ED

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: 16 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