Actively Recruiting
Retrospective, Multicenter Observational Study to Evaluate the Response to Treatment With Mosunetuzumab in Relapsed/Refractory Follicular Lymphoma After at Least Two Lines of Therapy Within the Compassionate Use Program
Led by Andrés José Maria Ferreri · Updated on 2026-02-03
25
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate the response to treatment with Mosunetuzumab in adults with relapsed or refractory Follicular Lymphoma who have already received at least two lines of therapy. The study is retrospective and observational, collecting data from multiple centers to understand how Mosunetuzumab performs within a Compassionate Use Program. It focuses on patients with Follicular Non-Hodgkin Lymphoma treated under this program and overseen by lead sponsor Andrés José Maria Ferreri. Participants in this study have been treated with Mosunetuzumab, a drug administered as part of the Compassionate Use Program for those with relapsed or refractory Follicular Lymphoma after two or more prior therapies. The study collects information retrospectively and does not involve assigning treatments or interventions directly. The observation period includes up to one year from the start of treatment. During participation, researchers will evaluate treatment response using the Lugano criteria and measure disease-free survival over one year. They will also review overall survival and toxicity rates at 12 months. The study relies on patient records and treatment data without requiring additional procedures. Participants’ usual care continues as normal, and the total observation period lasts up to one year after treatment initiation.
CONDITIONS
Brief Title
Study to Evaluate the Response to Treatment With Mosunetuzumab in Relapsed/Refractory Follicular Lymphoma (FL) After at Least Two Lines of Therapy, Within the Compassionate Use Program (CUP).
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients (over 18 years) with follicular non-Hodgkin lymphoma
- Have undergone at least two lines of therapy
- Treated with Mosunetuzumab under a compassionate use program
- Signed informed consent for treatment
You will not qualify if you...
- Age under 18 years
- Patients with other types of cancer or lymphoma
- Patients not eligible for the Mosunetuzumab compassionate use program
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 1 year from treatment initiation
Participants receive Mosunetuzumab treatment under a compassionate use program.
Visit schedule according to compassionate use program (details not specified)
Duration - 12 months after starting treatment
Participants are monitored for disease-free survival, overall survival, and toxicity for up to 12 months after starting treatment.
Visit schedule for safety and response assessments (details not specified)
Trial Site Locations
Total: 1 location
1
IRCCS Ospedale San Raffaele
Milan, Italy, 20132
Actively Recruiting
Research Team
A
Andres JM Ferreri, Prof
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
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