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NCT06626893: AL-TOMICA

Integrative "Omics" Approaches for Leukemia Target Identification and Matched Therapeutic Intervention

Recruiting now NA Last updated 4 October 2024
What this trial tests

NA trial testing Functional tests in Myeloid Leukemia, Acute in 100 participants. Currently enrolling.

Timeline
1 March 2022
Primary endpoint
1 March 2025
1 March 2025

Quick facts

Lead sponsorAzienda Ospedaliero-Universitaria di Parma
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposebasic science
Enrollment100
Start date1 March 2022
Primary completion1 March 2025
Estimated completion1 March 2025
Sites8 locations across Italy

Drugs / interventions tested

Conditions studied

Sponsor

Azienda Ospedaliero-Universitaria di Parma — full company profile →

Who can join

18 and older, any sex, with Myeloid Leukemia, Acute or Leukemia, Acute Lymphoblastic. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this clinical trial is to use multiple "omics" sciences to more thoroughly investigate Acute Recurrent/Refractory Leukemias (LA R/R) after conventional therapy in order to identify new targets and/or therapeutic approaches, in patients with a diagnosis of Acute Myeloid Leukemia (AML), Acute Lymphoblastic Leukemia/ Lymphoblastic Lymphoma B(ALL-B), Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma T (ALL-T), Acute Biphenotypic Leukemia/II as defined by WHO( World Health Organization) 2016, relapsed or refractory after at least one line of therapy. The main question that the trial aims to answer is: "Can molecules with known biological activity be active and represent possible new therapeutic strategies in relapsed/refractory Acute Leukemias on the basis of response profiles identified through the integration of next-generation chemogenomic and functional analyses? " It is expected that a minimum of 100 patients, male and female, aged 18 years and older, will be included. To participate in the study, the patient must consent to the performance on biological specimen (peripheral blood and bone marrow) of genetic/molecular and/or "omics" investigations performed with modern sequencing techniques, such as Next Generation Sequencing, Single Cell RNA Seq (scRNAseq), RT-qPCR(Quantitative reverse transcription polymerase chain reaction). These investigations will aim to improve the understanding of the genetic and molecular alterations of her disease. In addition, your cells will be used in the laboratory to perform in vitro sensitivity studies (drug response profiling - DRP) that aim to simultaneously test a set of hundreds of drugs to assess sensitivity or resistance profiles of your disease cells with the aim of identifying specific new therapies that target specific cellular mechanisms. In addition, part of the biological sample will be used for investigations of the bone marrow microenvironment and the "secretome", i.e., cell signaling molecules and methods. In order to accomplish this study, samples from peripheral or bone marrow blood taken during routine investigations performed during follow-up and re-evaluation visits for the patient's disease as per normal clinical practice will be used. Among the investigations that will be performed on the blood sample will be the genetic/molecular and/or omics and preclinical investigations described above.

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Acute Myeloid Leukemia in Older Patients: From New Biological Insights to Targeted Therapies.
    Niscola P, Gianfelici V, Catalano G, Giovannini M, et al · · 2024 · cited 10× · PMID 39590121 · DOI 10.3390/curroncol31110490
  2. Single-cell RNA sequencing: enhancing the predictive accuracy of tumor immunotherapy efficacy.
    Zhou W, Huang Z, Wu Z, Tang M, et al · · 2025 · cited 3× · PMID 40857744 · DOI 10.1042/ebc20253017

Verify or expand the search:

Other trials of Functional tests

Trials testing the same drug.

Other recruiting trials for Myeloid Leukemia, Acute

Currently open trials in the same condition.

Other Azienda Ospedaliero-Universitaria di Parma trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06626893.

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