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Novavax to Participate in Fireside Chat at the SVB Securities Virtual Vaccine Forum

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Novavax, Inc. (Nasdaq: NVAX) will participate in a fireside chat during the SVB Securities Virtual Vaccine Forum on August 18, 2022, from 11:00 to 11:50 a.m. EDT. The discussion will focus on NVX-CoV2373, Novavax's recombinant nanoparticle protein-based COVID-19 vaccine candidate. Key participants include Filip Dubovsky, M.D., and John J. Trizzino. Novavax's COVID-19 vaccine has received multiple global authorizations and is under review for additional populations. The company is also evaluating a combination vaccine candidate and new Omicron strain-based vaccines.

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GAITHERSBURG, Md., Aug. 11, 2022 /PRNewswire/ -- Novavax, Inc. (Nasdaq: NVAX), a biotechnology company dedicated to developing and commercializing next-generation vaccines for serious infectious diseases, today announced that it will participate in a fireside chat during the SVB Securities Virtual Vaccine Forum. Novavax' recombinant nanoparticle protein-based COVID-19 vaccine candidate, NVX-CoV2373, will be a topic of discussion.

Fireside chat details:


Date:

Thursday, August 18, 2022


Time:

11:00 – 11:50 a.m. Eastern Daylight Time (EDT)


Moderator:

David Risinger, CFA


Novavax participants:

Filip Dubovsky, M.D., Executive Vice President, Chief Medical Officer and John J. Trizzino, Executive Vice President, Chief Commercial Officer and Chief Business Officer






Please contact your SVB Securities representative to view the session.

Novavax, Inc. (Nasdaq: NVAX) is a biotechnology company that promotes improved health globally through the discovery, development, and commercialization of innovative vaccines to prevent serious infectious diseases. The company's proprietary recombinant technology platform harnesses the power and speed of genetic engineering to efficiently produce highly immunogenic nanoparticles designed to address urgent global health needs. The Novavax COVID-19 vaccine, has received authorization from multiple regulatory authorities globally, including the U.S., European Commission and the WHO. The vaccine is currently under review by multiple regulatory agencies worldwide, including for additional indications and populations such as adolescents and as a booster. In addition to its COVID-19 vaccine, Novavax is also currently evaluating a COVID-seasonal influenza combination vaccine candidate in a Phase 1/2 clinical trial, which combines NVX-CoV2373 and NanoFlu*, its quadrivalent influenza investigational vaccine candidate, and is also evaluating an Omicron strain-based vaccine (NVX-CoV2515) as well as a bivalent format Omicron-based / original strain-based vaccine. These vaccine candidates incorporate Novavax' proprietary saponin-based Matrix-M adjuvant to enhance the immune response and stimulate high levels of neutralizing antibodies.

For more information, visit www.novavax.com and connect with us on LinkedIn.

*NanoFlu identifies a recombinant hemagglutinin (HA) protein nanoparticle influenza vaccine candidate produced by Novavax. This investigational candidate was evaluated during a controlled phase 3 trial conducted during the 2019-2020 influenza season. 

Contacts:
Investors
Novavax, Inc.
Erika Schultz | 240-268-2022
ir@novavax.com

Media
Ali Chartan | 240-720-7804
Laura Keenan Lindsey | 202-709-7521
media@novavax.com

Novavax Logo (PRNewsfoto/Novavax)

 

 

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SOURCE Novavax, Inc.

FAQ

What is Novavax's participation in the SVB Securities Virtual Vaccine Forum?

Novavax will participate in a fireside chat discussing its COVID-19 vaccine candidate NVX-CoV2373 on August 18, 2022.

Who are the key speakers from Novavax at the SVB Securities event?

Filip Dubovsky, M.D., and John J. Trizzino will represent Novavax during the chat.

What is NVX-CoV2373?

NVX-CoV2373 is Novavax's recombinant nanoparticle protein-based COVID-19 vaccine candidate.

When is the Novavax fireside chat scheduled?

The fireside chat is scheduled for August 18, 2022, from 11:00 to 11:50 a.m. EDT.

What progress has Novavax made with its COVID-19 vaccine?

Novavax's COVID-19 vaccine has been authorized by multiple regulatory bodies worldwide and is under review for various populations.

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Biotechnology
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