An Emergency Use Authorization (EUA) request has been submitted to the Food and Drug Administration (FDA) for the Novavax COVID-19 Vaccine, Adjuvanted as a homologous and heterologous booster to prevent COVID-19 caused by SARS-CoV-2 in adults 18 years of age and older.
The Novavax COVID-19 Vaccine is engineered from the genetic sequence of SARS-CoV-2 using the Company’s recombinant nanoparticle technology to generate antigen derived from the coronavirus spike (S) protein. The vaccine contains the Company’s saponin-based Matrix-M™ adjuvant technology to enhance and prolong immune responses.
The submission is supported by data from the randomized, placebo-controlled phase 3 PREVENT-19 trial (ClinicalTrials.gov Identifier: NCT04611802), which evaluated the efficacy, safety and immunogenicity of the Novavax COVID-19 Vaccine in participants 18 years of age and older in the US and Mexico. Participants received a booster dose of the Novavax COVID-19 Vaccine at least 6 months after the primary 2-dose series. Findings showed that the booster dose elicited robust antibody responses comparable to, or exceeding levels associated with the efficacy data in the primary series of the vaccine.
Additionally, the EUA submission included data from the multicenter, randomized, controlled phase 2 COV-BOOST trial, which showed that a heterologous booster dose of the Novavax COVID-19 Vaccine produced a significant antibody response.
As for safety, the Novavax COVID-19 Vaccine was associated with local and systemic reactions with a median duration of approximately 2 days. The incidence of medically attended adverse events, potentially immune-mediated medical conditions, and severe adverse events occurred infrequently following the booster dose.
“It’s important for people to have a choice as they evaluate how to stay protected against COVID-19, and boosters are an invaluable tool to build upon immunity obtained from previous vaccinations,” said Stanley C. Erck, President and CEO, Novavax. “Based on the data presented to the FDA’s VRBPAC and the CDC ACIP, we believe our vaccine offers a broad, long-lasting immune response against a range of variants.”
The FDA recently granted EUA to the Novavax COVID-19 Vaccine, Adjuvanted as a primary 2-dose series for the prevention of COVID-19 caused by SARS-CoV-2 in individuals 18 years of age and older. The vaccine is administered intramuscularly as a 2-dose primary series (0.5mL each), separated by 3 weeks.
The Novavax COVID-19 Vaccine is supplied as a suspension in a carton containing 10 multidose vials; each vial contains 10 doses of 0.5mL each.
Novavax submits application to the US FDA for Emergency Use Authorization for Novavax COVID-19 Vaccine, Adjuvanted as a booster in adults aged 18 and older. release. Novavax, Inc. Accessed August 15, 2022. https://www.prnewswire.com/news-releases/novavax-submits-application-to-the-us-fda-for-emergency-use-authorization-for-novavax- covid-19-vaccine-adjuvanted-as-a-booster-in-adults-aged-18-and-older-301605447.html
This article originally appeared on MPR