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
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.
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 →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.
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.
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:
Patient with severe to critical illness or who are severely immunocompromised:
Symptoms (e.g. cough, shortness of breath) have improved
Inclusion Criteria (Part B only)
Inclusion Critera (Redraws Only)
Exclusion Criteria (Part A and B):
Exclusion Criteria (Part B only):
Exclusion Criteria (Healthy Controls Sample)
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
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
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
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
SARS-CoV-2 Antibodies Level
SARS-CoV-2 antibodies will be measured and assessed with Roche DIA Assay
Time frame: Baseline, Day 0
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
Plan to share: No
No publications or documents are linked to this record.
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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NYU Langone Health