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Signatures of Response and Resistance to Mosunetuzomab in Follicular Lymphomas (FL)

Signatures of Response and Resistance to Mosunetuzomab in Follicular Lymphomas (FL)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05529524
Enrollment
6
Registered
2022-09-07
Start date
2022-11-07
Completion date
2024-01-22
Last updated
2025-01-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Follicular Lymphoma

Keywords

Follicular Lymphoma, Mosunetuzomab, Resistance, CD20-CD3, Bispecific antibodies, Neoplasms, Lymphatic Diseases, Immunoproliferative Disorders

Brief summary

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.

Detailed description

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.

Interventions

None listed

Sponsors

Roche Pharma AG
CollaboratorINDUSTRY
The Lymphoma Academic Research Organisation
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

patients who participate to CELESTIMO study (NCT04712097)

Design outcomes

Primary

MeasureTime frameDescription
Capacity of sampling2 yearsnumber of samples collected

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026