Salvage Treatment With Glofitamab in Patients Affected by Relapsed/Refractory Non-Hodgkin B-cell Lymphoma: a GIMEMA-FIL Study

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

The goal of this observational study is to evaluate the anti-lymphoma activity of glofitamab, administered according to the Compassionate Use Program, in relapsed/refractory B-NHL patients. The main question it aims to answer is the rate of patients in complete response.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
View:

• Patients who received glofitamab according to Compassionate Use Program AG42296

• Age \> 18 years

• Patients who received at least one dose of glofitamab between March 2022 and September 2023 in the context of the compassionate use program and who completed at least 1 year of observation after last glofitamab administration unless the patient died or was lost to follow up

• Patients who provided their consent according to local regulation to collect their data for study purposes, dead patients or patients lost to follow up for which any attempt has been made to collect their consent, according to local regulation on data privacy

Locations
Other Locations
Italy
Ematologia Istituto Nazionale Tumori
RECRUITING
Milan
Contact Information
Primary
Paola Fazi
p.fazi@gimema.it
0670390528
Backup
Enrico Crea
e.crea@gimema.it
0670390514
Time Frame
Start Date: 2023-12-22
Estimated Completion Date: 2025-12
Participants
Target number of participants: 96
Sponsors
Leads: Gruppo Italiano Malattie EMatologiche dell'Adulto

This content was sourced from clinicaltrials.gov

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