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CompletedNCT04682548Updated Nov 3, 2022

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

An observational study in Multiple Sclerosis and Covid19, sponsored by NYU Langone Health. Completed at 1 site in United States. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2022-11-03.

Sponsored by NYU Langone Health · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
920
Ages
18 Years to 60 Years
Sex
All
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Study summary

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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Conditions studied

  • Multiple Sclerosis
  • Covid19

Keywords

  • Disease-Modifying Therapy
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In context

COVID-19

7,640 studies on the registry are indexed under COVID-19; 488 are open to participants now.

This study's enrollment of 920 is above the median of 261 across 3,136 observational studies indexed under COVID-19.

Browse COVID-19 studies →

Lead sponsor

NYU Langone Health is the lead sponsor of 1,391 studies on the registry; 254 are open to participants now.

Of its 227 completed or terminated interventional studies of FDA-regulated products, 191 (84%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Projected study size is 1000 MS patients for primary objective and additional 40 non-autoimmune COVID-19 convalescent control and 20 COVID-19 negative healthy controls.

Eligibility criteria

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.
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
920 participants (actual)
Patient registry
No
Biospecimen retention
Samples with dna
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What researchers measure

Primary outcomes

  1. Seropositivie Rate Against SARS-CoV-2

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

    Time frame: Baseline, Day 0

Secondary outcomes

  1. T Cell Response

    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.

    Time frame: Baseline, Day 0

Other outcomes

  1. T Cell response

    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.

    Time frame: Baseline, Day 0

  2. T Cell response

    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.

    Time frame: up to week 48 Post-Vaccination

  3. SARS-CoV-2 Antibodies Level

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

    Time frame: Baseline, Day 0

  4. SARS-CoV-2 Antibodies Level

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

    Time frame: up to week 48 Post-Vaccination

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Study locations

1 site
  • NYU Langone Health
    New York, New York 10016, United States
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 3, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04682548
Lead sponsor
NYU Langone Health
Responsible party
Sponsor
First posted
Dec 23, 2020
Start date
Jan 5, 2021
Primary completion
Sep 15, 2022
Completion
Sep 15, 2022
Last update
Nov 3, 2022

Study contacts

Ilya Kister, MD
principal investigator · NYU Langone Health

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Nov 2022. You cannot join it, but the record below documents what was studied.

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