Actively Recruiting

Age: 18Years +
All Genders
ID07278921

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

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)

Follow-up

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

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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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