Actively Recruiting
Chemogenomic Profiling in Hematological Malignancies (HEM-Profiling 2021)
Led by Azienda Ospedaliero-Universitaria di Parma · Updated on 2026-03-03
250
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research focuses on various hematological malignancies as classified by the WHO 2016 guidelines, including acute and chronic leukemias, myeloproliferative and lymphoproliferative disorders, and myelodysplastic syndromes. It aims to study these blood cancers by analyzing bone marrow, peripheral blood, lymph node, or tissue samples collected both retrospectively and prospectively at the University Hospital of Parma. The study evaluates molecular and genetic characteristics to better understand these diseases and identify potential new treatments. Participants include patients with hematological malignancies who are either treatment-free or have relapsed or refractory conditions. Samples are collected from diagnostic procedures such as bone marrow aspirates, biopsies, and peripheral blood draws. Advanced genetic, molecular, and omics technologies like Nanostring, next-generation sequencing, and single-cell analysis are used to study these samples. This process includes examining molecular biomarkers and correlating anti-cancer responses with diagnostic and molecular features. Participants will undergo sample collection from existing or new diagnostic evaluations. Researchers will analyze these samples to assess the activity of bio-active compounds and investigational molecules at baseline. The study also monitors molecular biomarkers and diagnostic features to explore novel target therapies. Participation involves informed consent and may include follow-up visits. The goal is to improve understanding of hematological malignancies through comprehensive molecular profiling, with no intervention or treatment administered as part of the study.
CONDITIONS
Brief Title
Chemogenomic Profiling in Hematological Malignancies (HEM-Profiling 2021)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient aged over 1 year old, referred for evaluation to the University Hospital of Parma
- For retrospective study: patients previously diagnosed with hematological malignancies
- For prospective study: patients with suspected hematological malignancies requiring diagnostic assessment using blood, bone marrow, lymph node, or tissue biopsies
- Patients suspected of relapsed or refractory hematological disease needing diagnostic evaluation
- Patients progressing to blastic transformation from a chronic condition requiring diagnostic assessment
- Written informed consent obtained; for retrospective cases, consent signed during first follow-up visit
You will not qualify if you...
- Age less than 1 year old
- Patients unable to provide informed consent for any reason
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 2 weeks
Participants undergo diagnostic assessments including blood, bone marrow, lymph node, or tissue biopsies to evaluate hematological malignancies and molecular biomarkers.
1 to 2 visits depending on diagnostic procedures
Duration - Ongoing during the study period
Participants' samples are analyzed using genetic, molecular, and omics technologies to assess anti-cancer activity and identify novel target therapies.
Visits as needed for sample collection
Trial Site Locations
Total: 1 location
1
University of Parma
Parma, PR, Italy, 43126
Actively Recruiting
Research Team
G
Giovanni Roti, Associate Professor
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
BASIC_SCIENCE
Number of Arms
1
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