A Study to Assess the Potential Impact of Disease Modifying Therapies on COVID-19 Outcomes and the Antibody Response Following an Infection With SARS-CoV-2 in Patients With Multiple Sclerosis Within the Swiss Multiple Sclerosis Cohort.

Last updated: April 22, 2025
Sponsor: University Hospital, Basel, Switzerland
Overall Status: Completed

Phase

N/A

Condition

Memory Loss

Multiple Sclerosis

Scar Tissue

Treatment

data collection

analysis of blood samples

Clinical Study ID

NCT04760990
2020-02604; me20Mehling
  • Ages > 18
  • All Genders

Study Summary

This nested project of the Swiss Multiple Sclerosis Cohort (SMSC) is to assess the severity of COVID-19 and the magnitude of antibody response after infection with Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) in patients already treated or not with various immunotherapies for multiple sclerosis followed in the framework of the SMSC.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • all patients in the Swiss Multiple Sclerosis Cohort (SMSC)

Exclusion

Exclusion Criteria:

  • Patients with Neuromyelitis optica and Radiologically Isolated Syndrome will beexcluded

  • Existence of a documented refusal of further use of health-related personal dataand/or biological material

Study Design

Total Participants: 1181
Treatment Group(s): 2
Primary Treatment: data collection
Phase:
Study Start date:
February 01, 2021
Estimated Completion Date:
December 15, 2023

Study Description

This nested project of the Swiss Multiple Sclerosis Cohort (SMSC) is to assess the severity of COVID-19 and the magnitude of antibody response after infection with Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) in patients already treated or not with various immunotherapies for multiple sclerosis followed in the framework of the SMSC.

To assess the frequency and severity of SARS-CoV-2 infections and associated symptoms in the study population, data is collected from systematic questioning during the SMSC-visits and from serum samples collected every 6-12 months within the SMSC (for measurement of anti-SARS-CoV-2 antibodies in pre-pandemic reference samples and prospectively to determine the anti-SARS-CoV-2-serostatus during the study period).

Combining the information on anti-SARS- CoV-2 serostatus and infection history opens the opportunity to determine the number of patients without or with only mild vs. moderate to severe COVID-19 symptoms in large groups of patients with Multiple Sclerosis (MS) treated with immunotherapies targeting various components of the immune system.

Connect with a study center

  • Kantonsspital Aarau

    Aarau, 5001
    Switzerland

    Site Not Available

  • University Hospital Basel, Department of Neurology and Department of Biomedicine

    Basel, 4031
    Switzerland

    Site Not Available

  • Inselspital Bern

    Bern, 3010
    Switzerland

    Site Not Available

  • Hôpitaux Universitaires Genève

    Genève, 1205
    Switzerland

    Site Not Available

  • Lausanne University Hospital (CHUV)

    Lausanne, 1011
    Switzerland

    Site Not Available

  • Ospedale Regionale di Lugano

    Lugano, 6903
    Switzerland

    Site Not Available

  • Kantonsspital St. Gallen

    St. Gallen, 9007
    Switzerland

    Site Not Available

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