Clinical Trials in Italy / NCT05839392
Recruiting
Not applicable
Novel Approaches to Target MECOM/EVI1 in AML
NCT05839392 · tracked via the Priya Life Science Italy tracker
Condition(s) studied
AML, Adult
Investigational drug(s) / intervention(s)
Biological characterization of AML with MECOM or atypical 3q26 rearrangements
Biological characterization of AML with MECOM or atypical 3q26 rearrangements: Peripheral blood and bone marrow withdrawal
Study summary
This is an academic, no-profit, multicenter, biological, non-pharmacologic study aimed at characterizing genome, transcriptome and proteome of patients affected by AML with MECOM or atypical 3q26 rearrangements.
Eligibility
Inclusion Criteria:
* AML with MECOM or atypical 3q26 rearrangements.
* Age ≥18.
* Signed written informed consent according to ICH/EU/GCP and national local laws.
Exclusion Criteria:
* None
Primary outcome measure(s)
- Identification of MECOM/EVI1 regulators or downstream effectors potentially druggable — At baseline
To assess the number of regulators or effectors of MECOM/EVI1
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Ematologia | Piacenza | Italy | Recruiting |
More Gruppo Italiano Malattie EMatologiche dell'Adulto trials in Italy
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Front-line VenObi Combination Followed by Ven or VenZan Combination in Patients With Residual Disease: a MRD Tailored Treatment for Young Patients With High-risk CLL
Active, not recruiting
Other trials for the same condition
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05839392 on ClinicalTrials.gov ↗ ← All trials in Italy