Novel Approaches to Target MECOM/EVI1 in AML

ConditionAML, Adult
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorGruppo Italiano Malattie EMatologiche dell'Adulto

About this trial

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 criteria

This trial does not accept healthy volunteers

Qualifiers

AML with MECOM or atypical 3q26 rearrangements.

Age ≥18.

Signed written informed consent according to ICH/EU/GCP and national local laws.

Disqualifiers

None

Trial design

Design model

Single group

Treatments tested in this trial

  • Biological characterization of AML with MECOM or atypical 3q26 rearrangements

    Biological/Vaccine

    Peripheral blood and bone marrow withdrawal

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Identification of MECOM/EVI1 regulators or downstream effectors potentially druggable

To assess the number of regulators or effectors of MECOM/EVI1

Time frame
At baseline

Secondary outcomes

Other outcomes

Sponsors and contacts

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