What this study is
The novel coronavirus (SARS-CoV-2) infection (COVID-19) has caused a worldwide pandemic. There is still much that is unknown regarding the virus, especially its effects on pregnancy, the fetus, and the neonate. This study seeks to evaluate adverse pregnancy and neonatal outcomes related to COVID-19 infection.
The FDA has authorized emergency use authorization for the SARS-CoV-2 messenger ribonucleic acid (mRNA) vaccines from Pfizer and Moderna. Pregnant women were excluded from the Phase III clinical trials of the mRNA vaccines. There are no studies that have evaluated functional antibody responses, antibody reactivity to variant viruses, T cell frequencies or activity, or protection against infection or development of COVID-19. Having a more detailed understanding of how pregnancy and lactation alters the longevity, specificity, and activity of antiviral antibody and T cell-mediated immune responses to COVID-19 mRNA vaccines is essential for the FDA to inform future recommendations and regulation of these vaccines.
What's being tested
- mRNA COVID-19 vaccine (Pfizer or Moderna)
Intervention · BIOLOGICAL
mRNA vaccine received at any time during pregnancy course
Study details
- Sponsor
- Johns Hopkins University
- Conditions
- COVID-19 · Pregnancy; Infection
- Enrolling
- 300 people
- Starts
- 2020-04-13
- Est. completion
- 2028-05-05
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 14 Years – 55 YearsSex FEMALEHealthy volunteers AcceptedVaccine Arm
You may qualify if
- All pregnant women receiving their prenatal care from the Johns Hopkins Hospital or Johns Hopkins Bayview Medical Center, who are planning to receive an mRNA COVID vaccine and/or a third dose booster during their pregnancy.
You can't join if
- Prior COVID-19 infection.
Sample Collection Arm
You may qualify if
- All pregnant women admitted to the Johns Hopkins Hospital or Johns Hopkins Bayview Medical Center for delivery and their newborn (at birth), will be considered for enrollment.
- Pregnant patients with a positive COVID-19 test during their pregnancy or at the time of admission to Labor & Delivery.
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (1)
1 openJohns Hopkins Hospital
Baltimore, Maryland, United States
- William C Golden, M.D.. · Contact410-955-4588cgolden@jhmi.edu
- Kimberly Jones-Beatty, DNP, CNM · Contactkjone111@jhmi.edu
- Sabra Klein, PhD · Sub-investigator
- Andrew Pekosz, PhD · Sub-investigator
- Andrea Cox, MD, PhD · Sub-investigator
- Heba Mostafa, PhD · Sub-investigator
Recruiting
Study team
Sponsor
Johns Hopkins University
Study ID IRB00246472
Principal investigator
William C Golden, MD
Johns Hopkins University
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.