Actively Recruiting
Integrative Multi-omics Analysis to Predict Monoclonal Gammopathies Clinical Evolution
Led by Azienda USL Reggio Emilia - IRCCS · Updated on 2026-04-23
60
Participants Needed
4
Research Sites
93 weeks
Total Duration
On this page
Sponsors
A
Azienda USL Reggio Emilia - IRCCS
Lead Sponsor
E
European Union
Collaborating Sponsor
AI-Summary
What this Trial Is About
This prospective, multicenter, observational study aims to identify molecular and immunological markers associated with disease progression in patients with monoclonal gammopathy of undetermined significance (MGUS) and smoldering multiple myeloma (SMM). By integrating genomic, transcriptomic, immunophenotypic, and oral microbiome analyses, the study seeks to characterize the biological mechanisms underlying the transition to symptomatic multiple myeloma (MM). The study also includes in vitro modeling to investigate bone damage and immune dysfunction. Healthy volunteers (HV) undergoing joint replacement surgery for osteoarthritis will serve as controls. The ultimate goal is to improve early risk stratification and support future preventive strategies through a multi-omics approach. There is a pressing need for new strategies to identify high-risk individuals based on biological rather than purely clinical parameters. This study proposes an integrative, multi-omics approach to investigate the transition from MGUS/SMM to MM. By analyzing the immunome and oral microbiome alongside molecular profiling, the goal is to identify reliable biomarkers of progression. The resulting insights could be enable more accurate risk stratification and guide the design of future preventive clinical trials aimed at delaying or halting disease evolution.
CONDITIONS
Official Title
Integrative Multi-omics Analysis to Predict Monoclonal Gammopathies Clinical Evolution
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age over 18 years
- Male or female patients
- Histologically confirmed diagnosis of MGUS, SMM, or MM according to ESMO 2021 guidelines
- Willing and able to provide written informed consent
- Healthy volunteers over 60 years
- Diagnosis of osteoarthritis
- Scheduled for hospitalization for surgical treatment of osteoarthritis (endoprosthesis or arthroplasty)
- Willing and able to provide written informed consent
You will not qualify if you...
- Active current infection
- Autoimmune disease
- Women of childbearing potential unable to exclude pregnancy
- Use of high-dose corticosteroids within the past 7 days
- Prior joint surgery or severe joint deformity (healthy volunteers)
- Recent trauma, osteonecrosis, or osteoarthritis caused by prior or current joint infection (healthy volunteers)
- Metabolic disorders (healthy volunteers)
- Previous or current cancer diagnosis (healthy volunteers)
- Autoimmune diseases such as rheumatoid arthritis (healthy volunteers)
AI-Screening
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Trial Site Locations
Total: 4 locations
1
Istituto Ortopedico Rizzoli IRCCS
Bologna, Italy
Active, Not Recruiting
2
UO Ematologia Azienda Ospedaliero-Universitaria "Policlinico Rodolico San Marco"
Catania, Italy
Active, Not Recruiting
3
UOC di Ematologia, Dipartimento di Oncologia, AOU Policlinico "Paolo Giaccone"
Palermo, Italy
Active, Not Recruiting
4
S.C Ematologia - Azienda USL IRCCS di Reggio Emilia
Reggio Emilia, Italy
Actively Recruiting
Research Team
N
Noemi Puccio
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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