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Mosunetuzumab is a T-cell bispecific antibody targeting CD20 and CD3 aiming to redirect T cells to engage and eliminate malignant B cells. Bispecific antibodies (BsAb) are a promising treatment option which can induce long-term responses in refractory and relapsed B cell lymphoma patients. However, the factors determining the quality and duration of responses are poorly understood.
the objective is to produce a collection of great scientific interest for lymphoma research from CELESTIMO's clinical trial patients' samples to increase knowledge of treatment with mosunetuzumab's for patients with follicular lymphoma (FL). study population involves patients participating to CELESTIMO study in France. 10 sites are expected in this biobanking protocol study Biological samples will collected as part of routine care (tissue and blood already sampled in routine and/or CELESTIMO study) at screening, at C4, at C12 or at progressive disease/relapse.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Centre Hospitalier de La Cote Basque; Hematologie
Bayonne, France
Hopital Claude Huriez; Hematologie
Lille, France
Institut Paoli Calmettes
Marseille, France
CHU Saint Eloi; Service d'Hématologie Clinique
Montpellier, France
CHU NANTES - Hôtel Dieu; Service d'Hematologie Clinique
Nantes, France
CHU de Nîmes - Hôpital Carémeau
Nîmes, France
Hopital Saint Antoine; Hematologie Clinique
Paris, France
Hopital De La Miletrie; Hematologie Et Oncologie Medicale
Poitiers, France
CHU Pontchaillou
Rennes, France
Start Date
November 7, 2022
Primary Completion Date
January 22, 2024
Completion Date
January 22, 2024
Last Updated
January 24, 2025
6
ACTUAL participants
Lead Sponsor
The Lymphoma Academic Research Organisation
Collaborators
NCT06337318
NCT05006716
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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