ICYMI: We recently announced results that expand our knowledge of NVX-CoV2373 and its ability to help protect from COVID19 over a longer period of time. Let's talk about what it means. Thread:
Our new data build on findings from our #UK Phase 3 #clinicaltrial (randomized, placebo-controlled, double-blind, with crossover), where we examined vaccine performance in 15K adults. Publication: nejm.org/doi/full/10.10…
There, we found an overall vaccine efficacy of 89.7%. A median of 55 days of surveillance was used for the final analysis. The Alpha (B.1.1.7) strain predominated during this time, with 86.3% efficacy vs Alpha.
Now, we're sharing data from an extended efficacy collection window from the UK Ph3 study: the 6-month period of 10 Nov 2020 - 10 May 2021, with a median of 101 days of surveillance. Alpha continued to dominate.
Our new analysis shows that the vaccine continues to demonstrate a reassuring top-line safety profile. Adverse events during this window were infrequent and balanced b/w vaccine & placebo groups.
In the primary efficacy analysis of this expanded timeframe, 158 cases were observed: 24 in the vaccine group, 134 in placebo group, for a vaccine efficacy of 82.7%.
A high level of vaccine efficacy was maintained over a 6-month period of surveillance, following the analysis used for EUA authorization (a median of 55 days of surveillance).
Further, in the expanded timeframe, all severe cases were in the placebo group, resulting in 100% efficacy against severe disease.
In examining protection against all COVID infection - symptomatic or asymptomatic (measured by PCR+ or anti-N seroconversion), we saw a vaccine efficacy of 82.5%.
Summary: Reassuring top-line safety profile. Clinical efficacy maintained over 6 months of surveillance. 100% efficacy against severe disease. 82.5% protection against all infection.
These encouraging findings suggest that NVX-CoV2373 may have a positive impact on disease transmission and protection over a longer period of time.
Thank you. Novavax is grateful to the thousands of people around the world who are volunteering for our vaccine studies. We thank the U.S. Government, @CEPIvaccines & other govts for their significant support of our work.
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Our new data build on findings from our #UK Phase 3 #clinicaltrial (randomized, placebo-controlled, double-blind, with crossover), where we examined vaccine performance in 15K adults. Publication: nejm.org/doi/full/10.10…
There, we found an overall vaccine efficacy of 89.7%. A median of 55 days of surveillance was used for the final analysis. The Alpha (B.1.1.7) strain predominated during this time, with 86.3% efficacy vs Alpha.
Now, we're sharing data from an extended efficacy collection window from the UK Ph3 study: the 6-month period of 10 Nov 2020 - 10 May 2021, with a median of 101 days of surveillance. Alpha continued to dominate.
Today we're thrilled to announce results of our PREVENT-19 Phase 3 pediatric expansion to adolescents (ages 12 through 17). Let's talk about the data and what they mean. Thread:
Today's results build on findings from the adult main study, investigating the safety & efficacy of NVX-CoV2373 in the United States and Mexico amidst an evolving #COVID19 pandemic: nejm.org/doi/full/10.10…#clinicaltrials
The pediatric expansion randomized adolescents age 12 through 17, in the U.S., in a 2:1 ratio to receive 2x 5μg doses of NVX-CoV2373, our investigational #vaccine candidate, or placebo, 21 days apart. Protocol: novavax.com/sites/default/…
We're thrilled to announce that PREVENT-19 (US/Mex Phase 3) results were submitted for publication. The manuscript is now available as a pre-print. Let's dive into what we found. Thread: medrxiv.org/content/10.110…
PREVENT-19 builds on observations from other/ongoing #clinicaltrials, investigating the safety & efficacy of NVX-CoV2373 in the United States and Mexico amidst an evolving #COVID19 pandemic. ir.novavax.com/2021-08-05-Nov…
The trial randomized adults age 18+ in a 2:1 ratio to receive 2x 5μg doses of NVX-CoV2373, our investigational #vaccine candidate, or placebo, 21 days apart. novavax.com/sites/default/…
According to @CDC, “on average, about 8% of the U.S. population gets sick from #flu each season.” There is an urgent need for improved flu #vaccines, particularly for older adults (>age 65), who bear higher disease burden. cdc.gov/flu/about/keyf…
Coverage of existing flu vaccines is >60% in the US, but recent flu seasons have shown vaccine effectiveness may be just 10-13% for one virus strain (A/H3N2) in older adults. ncbi.nlm.nih.gov/pmc/articles/P…
NEWS: Novavax Announces #COVID19 Vaccine Booster Data Demonstrating Four-Fold Increase in Neutralizing Antibody Levels Versus Peak Responses After Primary Vaccination ir.novavax.com/2021-08-05-Nov…
Following the primary vaccination series (21 days apart), a single booster dose at 6 months of NVX-CoV2373 induced a robust increase in anti-Spike antibody levels - up ~4.6-fold vs the response seen after the primary series.
The increased antibody response was consistent for both younger and older adults.
NEWS: Novavax and Serum Institute of India Announce Submission to Regulatory Agencies in India, Indonesia, Philippines for Emergency Use Authorization of Novavax’ Recombinant Nanoparticle #COVID19 Vaccine ir.novavax.com/2021-08-05-Nov…
The submissions were made to the Drugs Controller General of India (DCGI) and regulatory agencies in Indonesia and the Philippines.
“Today’s submission of our recombinant nanoparticle COVID-19 vaccine, the first protein-based option filed with any regulatory agency, represents a major milestone in Novavax’ transformation into a commercial global vaccine company,” said Stanley C. Erck, President and CEO