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Clinical Trials/NCT06764459
NCT06764459
Recruiting
Not Applicable

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

IRCCS Azienda Ospedaliero-Universitaria di Bologna1 site in 1 country20 target enrollmentMarch 15, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Myeloid Leukemia, Acute
Sponsor
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Enrollment
20
Locations
1
Primary Endpoint
Refractoriness to therapy
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

This study aims to analyze patients with mutated FLT3 AML treated with specific therapy by means of molecular characterization methods, to identify the presence of clones and subclones at onset and to be able to follow their evolution during therapeutic treatment.

Detailed Description

This study aims to analyze patients with mutated FLT3 AML treated with specific therapy by means of single-cell molecular characterization methods, to identify the presence of clones and subclones at onset and to be able to follow their evolution during therapeutic treatment. In this way, it is possible to study how the mutational profile varies under therapeutic pressure and identify any alterations responsible for resistance. It will thus be possible to define a panel of new molecular markers to be included in the diagnostic routine to identify early patients refractory/resistant to treatment with FLT3 inhibitors and thus improve the therapeutic approach of these patients.

Registry
clinicaltrials.gov
Start Date
March 15, 2023
End Date
December 31, 2026
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • FLT3 mutated

Exclusion Criteria

  • Respoder to therapy

Outcomes

Primary Outcomes

Refractoriness to therapy

Time Frame: At the end of the enrollment 3 years

Selected patients, as they are mutated in FLT3, following therapy with specific inhibitors must show refractoriness to treatment in order to continue the study and investigate in single cell the presence of clones or subclones responsible for any relapses.

Study Sites (1)

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