Decoding the Inflammasome Influence on Treatment Response in Acute Myeloid Leukemia

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Other
Study Type: Observational
SUMMARY

The study is designed as a collection of biological samples of newly diagnosed acute myeloid leukemia (AML) patients treated in the clinical units involved. Samples of peripheral blood (PB) and bone marrow (BM) will be analyzed to determine the Inflammasome profile before and after a first-line chemotherapy treatment.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Any gender,

• Adults (\>18 years old),

• New suspect diagnosis of acute myeloid leukemia (ELN2022 Criteria)

• Capable of comprehend the study and the consent form,

• Willing to sign the informed consent for the study.

⁃ For the retrospective population we will select:

⁃ biological samples (BM Biopsies, BM Aspirates and PB) already banked upon research purpose informed consent and collected from the 01/06/2006 up to 01/06/2024 from adults patients with diagnosis of acute myeloid leukemia according to ELN2017 Criteria.

Locations
Other Locations
Italy
IRCCS Ospedale San Raffaele
RECRUITING
Milan
GOM Bianchi Melacrino Morelli
RECRUITING
Reggio Calabria
Contact Information
Primary
Sara Mastaglio, Haematologist MD
ciceri.clinicaltrials@hsr.it
+39 0226433917
Backup
Vincenzo Mercurio, Ph.D Trial Office Coordinator
regolatorio.scp@hsr.it
+390226439396
Time Frame
Start Date: 2025-02-22
Estimated Completion Date: 2026-08-31
Participants
Target number of participants: 80
Treatments
acute myeloid leukemia (AML) patients treated in the clinical units
acute myeloid leukemia (AML) patients treated in the clinical units
Related Therapeutic Areas
Sponsors
Leads: Ciceri Fabio
Collaborators: Azienda Ospedaliera Bianchi-Melacrino-Morelli

This content was sourced from clinicaltrials.gov