Coronavirus

Moderna Is Testing Its Covid-19 Vaccine on Young Children

Moderna Inc.

MRNA 4.87%

has begun studying its Covid-19 vaccine in children aged six months to 11 years in the U.S. and Canada, the latest effort to widen the mass-vaccination campaign beyond adults.

The Cambridge, Mass. company said Tuesday that the first children have received doses in the study, which Moderna is conducting in collaboration with the National Institute of Allergy and Infectious Diseases and a division of the Department of Health and Human Services.

“This pediatric study will help us assess the potential safety and immunogenicity of our COVID-19 vaccine candidate in this important younger age population,” Moderna Chief Executive

Stéphane Bancel

said.

The bulk of the U.S. Covid-19 vaccination campaign so far has focused on protecting adults, who are at higher risk of severe disease caused by the coronavirus than children. Moderna’s and

Johnson & Johnson’s

vaccines are authorized for use in adults 18 and older, while the vaccine from

Pfizer Inc.

and

BioNTech SE

is cleared for use in people 16 and older.

Efforts have begun to test the Covid-19 vaccines in children, who can still become infected, both to protect them from the virus and further build the population-level immunity to move past pandemic restrictions.

Federal health officials have suggested that if studies are positive, junior-high and senior-high students could get access to vaccines in the fall, followed by children of elementary-school age in early 2022.

Both Pfizer and Moderna last year started clinical trials testing their vaccines in adolescents aged 12 years and older. Both trials have fully enrolled subjects and the results are pending. J&J is planning to start pediatric testing of its vaccine.

The new Moderna study, which is a combined Phase 2 and 3 trial, will aim to enroll about 6,750 children and will be conducted in two parts, according to the company.

The first part of the trial will test different dose levels of the vaccine in children. Researchers will examine the safety and immune response to the various doses to determine which to carry into the second part of the study.

In the study’s second part, other study subjects will be randomly assigned to receive two doses of either Moderna’s vaccine or a placebo, 28 days apart. Researchers will track the safety, tolerability and effectiveness of the vaccine.

They will determine effectiveness of the vaccine in children either by using an immune-response marker known as a correlate of protection—if one is determined—or by comparing their immune responses to those seen in young adults, Moderna said.

Moderna didn’t give a timetable for completing the study.

Alerts and web-browser tools can help you book a Covid-19 vaccine appointment. WSJ’s Joanna Stern met up with Kris Slevens, an IT guy who has booked over 300 appointments for New Jersey seniors, to learn the best tricks to compete in the vaccine-booking Hunger Games. Photo illustration: Emil Lendof for The Wall Street Journal

Write to Peter Loftus at peter.loftus@wsj.com

Copyright ©2020 Dow Jones & Company, Inc. All Rights Reserved. 87990cbe856818d5eddac44c7b1cdeb8

Related posts

‘Time is of the essence’ on COVID-19 reduction: Transportation Secretary Pete Buttigieg

admin

8 Alaska youths experienced a rare and serious inflammatory syndrome after COVID-19 infections

admin

Vaccine efficacy – When covid-19 vaccines meet the brand new variants of the virus | Briefing

admin

Leave a Comment