Single-Dose Nirsevimab for Prevention of RSV in Preterm Infants

M Pamela Griffin, Nirsevimab Study Group, Dina Apele-Freimane (Member of the Working Group)

Research output: Contribution to journalArticlepeer-review

437 Citations (Scopus)
5 Downloads (Pure)

Abstract

BACKGROUND: Respiratory syncytial virus (RSV) is the most common cause of lower respiratory tract infection in infants, and a need exists for prevention of RSV in healthy infants. Nirsevimab is a monoclonal antibody with an extended half-life that is being developed to protect infants for an entire RSV season with a single intramuscular dose.

METHODS: In this trial conducted in both northern and southern hemispheres, we evaluated nirsevimab for the prevention of RSV-associated lower respiratory tract infection in healthy infants who had been born preterm (29 weeks 0 days to 34 weeks 6 days of gestation). We randomly assigned the infants in a 2:1 ratio to receive nirsevimab, at a dose of 50 mg in a single intramuscular injection, or placebo at the start of an RSV season. The primary end point was medically attended RSV-associated lower respiratory tract infection through 150 days after administration of the dose. The secondary efficacy end point was hospitalization for RSV-associated lower respiratory tract infection through 150 days after administration of the dose.

RESULTS: From November 2016 through November 2017, a total of 1453 infants were randomly assigned to receive nirsevimab (969 infants) or placebo (484 infants) at the start of the RSV season. The incidence of medically attended RSV-associated lower respiratory tract infection was 70.1% lower (95% confidence interval [CI], 52.3 to 81.2) with nirsevimab prophylaxis than with placebo (2.6% [25 infants] vs. 9.5% [46 infants]; P<0.001) and the incidence of hospitalization for RSV-associated lower respiratory tract infection was 78.4% lower (95% CI, 51.9 to 90.3) with nirsevimab than with placebo (0.8% [8 infants] vs. 4.1% [20 infants]; P<0.001). These differences were consistent throughout the 150-day period after the dose was administered and across geographic locations and RSV subtypes. Adverse events were similar in the two trial groups, with no notable hypersensitivity reactions.

CONCLUSIONS: A single injection of nirsevimab resulted in fewer medically attended RSV-associated lower respiratory tract infections and hospitalizations than placebo throughout the RSV season in healthy preterm infants. (Funded by AstraZeneca and Sanofi Pasteur; ClinicalTrials.gov number, NCT02878330.).

Original languageEnglish
Pages (from-to)415-425
Number of pages11
JournalThe New England journal of medicine
Volume383
Issue number5
DOIs
Publication statusPublished - 30 Jul 2020
Externally publishedYes

Keywords*

  • Antibodies, Monoclonal/administration & dosage
  • Antibodies, Monoclonal, Humanized/administration & dosage
  • Antiviral Agents/administration & dosage
  • Female
  • Hospitalization/statistics & numerical data
  • Humans
  • Incidence
  • Infant
  • Infant, Newborn
  • Infant, Premature
  • Injections, Intramuscular
  • Kaplan-Meier Estimate
  • Male
  • Poisson Distribution
  • Respiratory Syncytial Virus Infections/epidemiology
  • Respiratory Syncytial Virus, Human
  • Respiratory Tract Infections/epidemiology
  • Viral Fusion Proteins/antagonists & inhibitors

Field of Science*

  • 3.2 Clinical medicine

Publication Type*

  • 1.1. Scientific article indexed in Web of Science and/or Scopus database

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