Understanding the 'Durable Effect' Concept of B-cell Modulating Therapies

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-60
SponsorHeinrich-Heine University, Duesseldorf

About this trial

This prospective, observational clinical study aims to longitudinally assess peripheral immune cell profiles of patients with relapsing-remitting multiple sclerosis (RRMS) receiving anti-CD20 therapy with ofatumumab (OFA), ocrelizumab (OCR), ublituximab (UBX), and rituximab (RTX). Throughout the study, clinical data - including relapse events, patient scores, and neuropsychological parameters - will be collected, along with results from imaging techniques such as Optical Coherence Tomography (OCT) and Magnetic Resonance Imaging (MRI). This clinical data will be combined with immunological analyses, including multidimensional flow cytometry (mFC), bulk RNA sequencing (bulk-Seq), T and B cell receptor sequencing (TCR/BCR-Seq), proteomics, and immunoglobulin analysis. This approach aims to enable a detailed characterization of changes in the immune cell repertoire and their impact on the clinical disease course.

Eligibility criteria

Qualifiers

Diagnosed relapsing-remitting multiple sclerosis (RRMS) according to 2017 revised McDonald criteria

Current treatment with B cell modulating therapies or initiation/transition to B cell modulating therapies according to the "Summary of Product Characteristics (SmPC)"

EDSS score of 0.0 to 7.0

Disqualifiers

Previous treatment with alemtuzumab, cladribine, cyclophosphamide, mitoxantrone, azathioprine, mycophenolate mofetil, cyclosporine, methotrexate, total body irradiation or bone marrow transplantation

Medical, psychiatric, cognitive, or other conditions that, in the opinion of the investigator, impair the patient's ability to understand the patient information and give informed consent

Patients receiving immunosuppressive treatment for conditions other than MS or long-term corticosteroid treatment

Patients with confirmed infection by the Human Immunodeficiency Virus or Hepatitis C Virus

Trial design

Treatments tested in this trial

  • Anti-CD20 antibody

Treatment groups

100 Participants
are divided into 2 treatment groups

Sponsors and collaborators