Clinical trial Recruiting at 1 site Observational Ages 18 and up

Analyzing genetic changes in patients with acute myeloid leukemia during treatment

Official title: Molecular Characterization of Patients With Acute Myeloid Leukemia and the Impact of Clonal Evolution in the Response to Therapeutic Treatments

Run by IRCCS Azienda Ospedaliero-Universitaria di Bologna · NCT06764459 · Data updated 2026-11-12

This study is trying to see how genetic changes in acute myeloid leukemia patients with FLT3 mutations affect their response to treatment, to help identify those who might not respond well.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment20 (estimated)
SponsorIRCCS Azienda Ospedaliero-Universitaria di Bologna
Academic / other
Locations1 site (Bologna)
StatusRecruiting
StartedMarch 15, 2023
Main results expectedDecember 31, 2025
Study endsDecember 31, 2026
Registry record updatedJanuary 30, 2025
Trial IDNCT06764459 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are patients diagnosed with FLT3 mutated acute myeloid leukemia.

Probably not a fit

Patients who respond well to therapy and do not have FLT3 mutations may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study focuses on patients with acute myeloid leukemia (AML) who have mutations in the FLT3 gene. It employs single-cell molecular characterization techniques to identify and track the evolution of cancer cell clones and subclones throughout treatment. By understanding how these genetic profiles change under therapeutic pressure, the study aims to uncover mechanisms of resistance to FLT3 inhibitors. Ultimately, the goal is to develop new molecular markers that can help identify patients who are likely to be resistant to treatment early on, thereby improving their therapeutic management.

Why it matters

Potential benefit: If successful, this study could lead to more personalized and effective treatment strategies for patients with FLT3 mutated AML.

How similar studies have gone: Other studies have shown promise in using molecular characterization to understand treatment resistance in leukemia, making this approach both relevant and potentially impactful.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* FLT3 mutated

Exclusion Criteria:

* Respoder to therapy

Where it's running

  • IRCCS Azienda Ospedaliero-Universitaria di Bologna Policlinico di Sant'Orsola
    Bologna, Italy
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.