Smoldering Multiple Myeloma Clinical Trials

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Integrative Multi-omics Analysis to Predict Monoclonal Gammopathies Clinical Evolution

Status: Recruiting
Location: See all (4) locations...
Intervention Type: Other
Study Type: Observational
SUMMARY

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.

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

• Age \>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 (HV)

• Age \>60 years

• Diagnosis of osteoarthritis (OA)

• Scheduled for hospitalization for surgical treatment of OA (endoprosthesis or arthroplasty)

• Willing and able to provide written informed consent

Locations
Other Locations
Italy
Istituto Ortopedico Rizzoli IRCCS
ACTIVE_NOT_RECRUITING
Bologna
UO Ematologia Azienda Ospedaliero-Universitaria Policlinico Rodolico San Marco
ACTIVE_NOT_RECRUITING
Catania
UOC di Ematologia, Dipartimento di Oncologia, AOU Policlinico Paolo Giaccone
ACTIVE_NOT_RECRUITING
Palermo
S.C Ematologia - Azienda USL IRCCS di Reggio Emilia
RECRUITING
Reggio Emilia
Contact Information
Primary
Noemi Puccio
noemi.puccio@ausl.re.it
Time Frame
Start Date: 2025-03-17
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 60
Treatments
MGUS, SMM and MM patients
Patients with monoclonal gammopathy of undeterminated significance, smoldering multiple myeloma, or multiple myeloma
Healthy volunteers
Patients with a clinical and radiological diagnosis of osteoarthritis who undergo endo or arthro-prosthesis surgery
Sponsors
Collaborators: European Union, Ministero della Salute, Italy
Leads: Azienda USL Reggio Emilia - IRCCS

This content was sourced from clinicaltrials.gov