Actively Recruiting

Age: 18Years +
All Genders
ID07283224

Anonymization of Clinical Data From Pseudonymized Databases Collected as Part of Previous Clinical Trials on Multiple Myeloma

Led by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Updated on 2026-05-12

600

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research investigates multiple myeloma by analyzing previously collected genomic, clinical, and imaging data from past studies conducted at the Hematology Unit of IRCCS Azienda Ospedaliero-Universitaria di Bologna. The goal is to understand how these different types of information relate to disease outcomes and to create predictive models using artificial intelligence and machine learning that might forecast disease progression and treatment responses in the future. The study uses existing, pseudonymized data without requiring any new tests, procedures, or patient visits. The data includes genomic profiles from bone marrow and blood samples and imaging to describe disease distribution at baseline. Secondary measures will assess treatment response and early relapse within 18 months of therapy start. Participants are not actively involved since the study is retrospective and observational. Researchers will securely develop and store anonymized datasets for analysis. The main outcomes include detailed genomic descriptions and imaging data at baseline, with follow-up on therapy response and relapse rates. The study is planned to run until 2028.

CONDITIONS

Brief Title

Anonymization of Clinical Data From Pseudonymized Databases Collected as Part of Previus Clinical Trials on Multiple Myeloma

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Signed informed consent
  • Confirmed diagnosis of multiple myeloma
  • Previously enrolled in a spontaneous trial at the Hematology Unit of IRCCS AOU di Bologna since 2021 with pseudonymized datasets available
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Monitoring

Duration - Up to 6 years

Participants who underwent previous clinical trials are observed through analysis of anonymized clinical data collected from pseudonymized databases.

Trial Site Locations

Total: 1 location

1

IRCCS AOU Policlinico Sant'Orsola

Bologna, Bo, Italy, 40138

Actively Recruiting

Loading map...

Research Team

C

Carolina Terragna, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

Similar Trials

A Phase 1 Study of KTX-1001, an Oral, Selective MMSET Inhibi...

Multiple Myeloma

Actively Recruiting

22 locations

A Phase 1 Study to Evaluate the Safety of KLN-1010 Gene Ther...

Multiple Myeloma in Relapse

Actively Recruiting

7 locations

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here