Clinical trial Recruiting at 1 site Observational Ages 18 and up

Understanding the immune system and metabolism in patients with acute leukemia

Official title: Study of the Immunological Infiltrate and Immunometabolic Immunometabolic Profile of Patients with Acute Leukaemia

Run by IRCCS Azienda Ospedaliero-Universitaria di Bologna · NCT06814444 · Data updated 2026-11-12

This study looks at how the immune system and metabolism change in people with acute leukemia before and after treatment to see how these changes affect their response to therapy.

More Acute Leukemia trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment170 (estimated)
SponsorIRCCS Azienda Ospedaliero-Universitaria di Bologna
Academic / other
Drugs / interventionschemotherapy
Locations1 site (Bologna, Bologna)
StatusRecruiting
StartedNovember 11, 2023
Main results expectedDecember 11, 2029
Study endsDecember 11, 2030
Registry record updatedFebruary 7, 2025
Trial IDNCT06814444 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are adults aged 18 and older who have been diagnosed with acute leukemia and are eligible for treatment involving chemotherapy or innovative therapies.

Probably not a fit

Patients who do not have a diagnosis of acute leukemia or are not eligible for any treatment schemes will 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 observational study aims to characterize the immunophenotypic and immunometabolic profiles of patients diagnosed with acute leukemia, both before and after therapy. It will assess the relationship between the molecular and metabolic characteristics of leukemia cells and the surrounding immune system, identifying immune-modulatory mechanisms activated by malignant cells. Additionally, the study will explore how immunometabolic signatures correlate with therapy responses and investigate the role of extracellular vesicles in regulating immune cell metabolism. Samples will be collected from patients and healthy controls during routine care visits.

Why it matters

Potential benefit: If successful, this study could enhance the understanding of how the immune system interacts with leukemia, potentially leading to improved treatment strategies.

How similar studies have gone: While this approach is innovative, similar studies have shown promise in understanding the immune response in cancer, suggesting potential for success.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

PATIENT

* Diagnosis of Acute Leukaemia.
* Eligibility for a treatment scheme involving either conventional chemotherapy or innovative therapies, such as monoclonal antibodies, molecular therapies with specific targets, metabolic and immunological therapies.
* age ≥ 18 years.
* Signature of informed consent by patients at the time of diagnosis.

Healthy donors (AIL BOLOGNA ODV volunteers)

* age ≥ 18 years.
* Signature of informed consent.

Exclusion Criteria:

* no one

Where it's running

  • IRCCS Azienda Ospedaliero-Universitaria di Bologna
    Bologna, Bologna, Italy
    Recruiting

Study contacts

  • Principal investigator: Antonio Curti, MD — IRCCS Azienda Ospedaliero-Universitaria di Bologna
  • Study coordinator: Antonio Curti, MD
  • Email: antonio.curti2@unibo.it
  • Phone: +39 0512144074

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.