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OpenTrials
Completed

NCT Number: NCT04682548

Estimating Prevalence of COVID-19 Infection and SARS-CoV-2 Antibodies in MS Patients

This non-interventional, biospecimen collection study is designed to help us better understand whether MS patients have impaired immune defenses to COVID-19 infection. The potential influence of immune modulating medications for MS will be considered through these exploratory studies. This study is also designed to provide context for interpretation of anti-SARS CoV2 serologies in MS patients during convalescence from COVID-19 infection.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

(Part A and B):

● Patient is outside of infectious period of COVID-19 defined as follows:

  • Patient with mild to moderate illness who are not severely immunocompromised:
  • At least 10 days have passed since symptoms first appeared and
  • At least 24 hours have passed since last fever without the use of fever-reducing medications and
  • Symptoms (e.g. cough, shortness of breath) have improved
  • Patient with severe to critical illness or who are severely immunocompromised:
  • At least 10 days and up to 20 days have passed since symptoms first appeared
  • At least 24 hours have passed since last fever without the use of fever-reducing medications and
  • Symptoms (e.g. cough, shortness of breath) have improved
  • Clinician-diagnosed MS treated or untreated with an approved DMT,
  • Ages 18 to 60,
  • EDSS 0 - 7,
  • Able to give informed consent,
  • Able to complete, or have someone help complete the patient questionnaire,
  • No high dose steroids, or IVIG, or PLEX use within 3 months of blood sample,
  • No convalescent plasma and/or polyclonal antibody treatments for COVID-19 within 3 months of blood sample collection.

Inclusion criteria

(Part B only)

  • COVID-19 positive patients, who received OCR within 6 months of COVID 19 infection,
  • EDSS 0 - 6.

Inclusion Critera (Redraws Only)

  • Completed standard of care COVID-19 vaccination series
  • On Ocrevus, glatiramer, interferon b, or not on any treatment disease-modifying treatment at the time of vaccination.

Exclusion criteria

(Part A and B):

  • Concurrent immunosuppressive therapy, active systemic cancer, primary or acquired immunodeficiency (i.e., CVID, HIV infection),
  • Active drug or alcohol abuse,
  • Other anti-CD20 therapy apart from OCR,
  • Uncontrolled diabetes mellitus,
  • End-organ failure (cardiac, pulmonary, renal, hepatic),
  • Systemic lupus erythematosus (SLE).

Exclusion criteria

(Part B only):

  • EDSS >6,
  • Active infection (e.g., hepatitis).

Exclusion criteria

(Healthy Controls Sample)

  • Concurrent immunosuppressive therapy, active systemic cancer, primary or acquired immunodeficiency (e.g. CVID, HIV infection),
  • Active ongoing drug or alcohol abuse,
  • Age >60 or <18,
  • Uncontrolled diabetes mellitus,
  • End-organ failure (cardiac, pulmonary, renal, hepatic),
  • SLE
  • No high dose steroids, or intravenous immunoglobulin (IVIG) or plasma exchange (PLEX) use within 3 months of blood sample collection,
  • No convalescent plasma and/or polyclonal antibody treatments for COVID-19 within 3 months of blood sample collection.

Treatment and study plan

Primary outcomes

  1. Seropositivie Rate Against SARS-CoV-2

    Time frame: Baseline, Day 0

    Seropositivity rate against SARS-CoV-2 (nucleocapsid and/or spike proteins, as available) as measured by the Roche DIA antibody assay in MS patients.

Secondary outcomes

  1. T Cell Response

    Time frame: Baseline, Day 0

    SARS-CoV-2 specific T cells will be measured using a well-validated assay such as ELISpot (enzyme-linked immune absorbent spot) to measure T cell responses to stimulation.

Other outcomes

  1. T Cell response

    Time frame: Baseline, Day 0

    SARS-CoV-2 specific T cells will be measured using a well-validated assay such as ELISpot (enzyme-linked immune absorbent spot) to measure T cell responses to stimulation.

  2. T Cell response

    Time frame: up to week 48 Post-Vaccination

    SARS-CoV-2 specific T cells will be measured using a well-validated assay such as ELISpot (enzyme-linked immune absorbent spot) to measure T cell responses to stimulation.

  3. SARS-CoV-2 Antibodies Level

    Time frame: Baseline, Day 0

    SARS-CoV-2 antibodies will be measured and assessed with Roche DIA Assay

  4. SARS-CoV-2 Antibodies Level

    Time frame: up to week 48 Post-Vaccination

    SARS-CoV-2 antibodies will be measured and assessed with Roche DIA Assay

Sponsors and collaborators

Lead sponsor

NYU Langone Health

Other

Registry information

Official study title

Estimating Prevalence of COVID-19 Infection and SARS-CoV-2 Antibodies in MS Patients With and Without Ocrelizumab Treatment, and Comparing Immune Responses to COVID-19 in MS Patients on Ocrelizumab and Healthy Controls

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Dec 23, 2020
Registry last updated
Nov 3, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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