Infection Surveillance of R/R Multiple Myeloma Patients Treated With Elranatamab as Clinical Practice in Italy
Starting soon
Conditions studied: Multiple Mieloma
In brief
The primary objective of this study is to measure the infection rate and presentation pattern in first 12 months of therapy with elranatamab as standard clinical practice in adult patients with Relapsed/Refractory Multiple Myeloma.
Key facts
- Study ID
- NCT07564128
- Run by
- Gruppo Italiano Malattie EMatologiche dell'Adulto
- People needed
- 50
- Starts
- 2026-08-01
- Expected to finish
- 2028-02-01
- Last updated by the study team
- 2026-05-04
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- adult patients (age >18 years) with no upper age limit
- confirmed Relapsed and Refractory Multiple Myeloma (RRMM) according to IMWG criteria (demonstrated disease progression on the last therapy (progressed on or within 60 days of last therapy).
- Patients must have received at least three (3) prior lines of therapy, including at least: one Immunomodulatory agent (e.g., Lenalidomide, Pomalidomide), one Proteasome Inhibitor (e.g., Bortezomib, Carfilzomib), one Anti-CD38 Monoclonal Antibody (e.g., Daratumumab, Isatuximab).
- Treatment with elranatamab within standard clinical practice
- Written informed consent signature
You may not qualify if…
- none
Full record on ClinicalTrials.gov
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