SARS-CoV-2

Vaxart Receives $9.27 Million BARDA Project NextGen Award to Prepare for Phase 2b Clinical Study Evaluating Its COVID-19 Oral Pill Vaccine Candidate

Retrieved on: 
Friday, January 19, 2024

SOUTH SAN FRANCISCO, Calif., Jan. 19, 2024 (GLOBE NEWSWIRE) -- Vaxart, Inc. (Nasdaq: VXRT) today announced that the United States Biomedical Advanced Research and Development Authority (BARDA) has awarded the Company $9.27 million to fund preparation for a 10,000 subject Phase 2b clinical study evaluating Vaxart’s oral pill XBB COVID-19 vaccine candidate against an approved mRNA vaccine comparator.

Key Points: 
  • “We are very honored to receive this BARDA award, which will support the innovative approach of our oral pill vaccine platform,” said Dr. Michael Finney, Vaxart’s Interim Chief Executive Officer.
  • “We believe our oral pill vaccine platform may ultimately hold the promise of revolutionizing how we fight pandemics and how we vaccinate against several infectious diseases.
  • Second, our previous research on other vaccine constructs found Vaxart’s oral pill vaccine to be cross-reactive against all tested SARS-CoV-2 variants and to trigger long-lasting immune responses, potentially offering broader, longer protection than the current first-generation vaccines.
  • Vaxart’s oral pill vaccine platform provides many of the features desired by BARDA, such as generating mucosal immunity and providing a cross-reactive response to many COVID variants.

Moleculin Announces 2023 Year-End Annamycin Clinical Trials Preliminary Data and 2024 Expectations for Multiple Data Readouts and Transition to Pivotal Phase 2B/3

Retrieved on: 
Wednesday, January 24, 2024

"Over the course of 2023, we delivered on our promise for a year of important data from our Annamycin clinical development programs.

Key Points: 
  • "Over the course of 2023, we delivered on our promise for a year of important data from our Annamycin clinical development programs.
  • We are well-positioned to continue building upon our encouraging growing body of preliminary clinical data and transition to pivotal Phase 2B/3 clinical trials by year-end 2024.
  • With our recent financing in December 2023, we have extended our runway into the fourth quarter of 2024, as well.
  • WP1122 successfully completed a Phase 1 clinical trial, which established a recommended safe dose for future potential Phase 1B or Phase 2 clinical trials.

CORBEVAX®, A COVID19 VACCINE DEVELOPED BY BIO E-INDIA BASED ON THE RBD PROTEIN ANTIGEN TECHNOLOGY FROM TEXAS CHILDREN'S HOSPITAL CENTER FOR VACCINE DEVELOPMENT, RECEIVES WORLD HEALTH ORGANIZATION EMERGENCY USE LISTING APPROVAL

Retrieved on: 
Monday, January 22, 2024

HOUSTON, Jan. 22, 2024 /PRNewswire/ -- Texas Children's Hospital announces today that Biological E's CORBEVAX®, a traditional, recombinant protein-based COVID-19 vaccine has received World Health Organization (WHO) approval under Emergency Use Listing (EUL). CORBEVAX® is developed and commercialized by Biological E Limited, an established global vaccine supplier based in Hyderabad, India, using Pichia pastoris yeast strain expressing Receptor Binding Domain (RBD) protein of SARS-CoV-2 engineered by Texas Children's Hospital Center for Vaccine Development (CVD) and Baylor College of Medicine (BCM),

Key Points: 
  • "The recombinant yeast strains enable production of the RBD protein which can be further utilized by vaccine researchers globally to develop & manufacture effective and low-cost vaccines.
  • By providing access to the yeast strains via non-exclusive licensing, we continue our mission to support global vaccine accessibility and availability."
  • Biological E subsequently developed large scale manufacturing technology for production of the RBD protein complying with Good Manufacturing Practices (GMP) as well as testing & characterization suitable for use as vaccine antigen.
  • The RBD protein was then used as an antigen and formulated with optimized adjuvants (Alum and CpG1018) to develop a COVID-19 candidate vaccine.

An RSV vaccine has been approved for people over 60. But what about young children?

Retrieved on: 
Wednesday, January 17, 2024

The Therapeutic Goods Administration (TGA) has approved a vaccine against respiratory syncytial virus (RSV) in Australia for the first time.

Key Points: 
  • The Therapeutic Goods Administration (TGA) has approved a vaccine against respiratory syncytial virus (RSV) in Australia for the first time.
  • RSV is a contagious respiratory virus which causes an illness similar to influenza, most notably in babies and older adults.

A bit about RSV

  • There are two key groups of people we would like to protect from RSV: babies (up to about one year old) and people older than 60.
  • In babies and younger children, RSV generally causes a wheezing asthma-like illness (bronchiolitis), but can also cause pneumonia and croup.

RSV vaccines for older people

  • For older adults, there are actually several RSV vaccines in the pipeline.
  • The GSK and Pfizer RSV vaccines are similar.
  • Both vaccines have been shown to reduce illness from RSV by more than 80% in the first season after vaccination.

Protecting young children from RSV

  • To prevent other diseases, this can be overcome by giving multiple vaccine doses over time.
  • But the highest risk group for RSV are those in the first few months of life.
  • To protect this youngest age group from the virus, there are two potential strategies available instead of vaccinating the child directly.
  • Abrysvo, the Pfizer RSV vaccine, has been trialled in pregnant women.
  • In clinical trials, this vaccine has been shown to reduce illness in infants for up to six months.
  • It has been approved in pregnant women in the United States, but is not yet approved in Australia.

What now?

  • RSV, like influenza, is a major cause of respiratory illness, and the development of effective vaccines represents a major advance.
  • While the approval of the first vaccine for older people is an important step, many details are yet to be made available, including the cost and the timing of availability.


Allen Cheng receives funding from the National Health and Medical Research Council and the Australian Government. He is a member of the Australian Technical Advsory Group on Immunisation. The views expressed in this article may not reflect those of ATAGI.

ExeVir Bio Announces Positive Virus Neutralization Data for XVR012 Against Emerging COVID-19 Omicron Variants

Retrieved on: 
Monday, January 15, 2024

All authorized SARS-CoV-2 therapeutic antibodies that have been used in the clinic show severe to complete loss of virus neutralization potency against the currently circulating variants.

Key Points: 
  • All authorized SARS-CoV-2 therapeutic antibodies that have been used in the clinic show severe to complete loss of virus neutralization potency against the currently circulating variants.
  • ExeVir’s XVR012, a cocktail of XVR013m and XVR014, targets three distinct epitopes highly conserved across the broad sarbecovirus subgenus of Coronaviridae to minimize the risk for viral escape.
  • XVR013m is a heavy chain-only antibody targeting a unique membrane-proximal epitope in the S2 subunit of the spike protein.
  • ExeVir is currently gearing up to start the clinical development of both the combination XVR012, as well as its individual components XVR013m and XVR014.

RSV, flu and COVID: demystifying the triple epidemic of respiratory viruses

Retrieved on: 
Tuesday, January 16, 2024

Since 2022, a triple epidemic of respiratory viruses — RSV, influenza and SARS-CoV-2 — has been disrupting our daily lives. In addition, the media constantly reminds us of how this is straining emergency departments. How does the present respiratory virus season differ from seasons during the pre-COVID era? As a specialist in virus-host interaction, I would like to shed some light on the new dynamics of the respiratory virus season.The infamous SARS-CoV-2Despite limited access to screening tests, analysis of the number of hospital admissions shows that the virus is still going strong.

Key Points: 


Since 2022, a triple epidemic of respiratory viruses — RSV, influenza and SARS-CoV-2 — has been disrupting our daily lives. In addition, the media constantly reminds us of how this is straining emergency departments. How does the present respiratory virus season differ from seasons during the pre-COVID era? As a specialist in virus-host interaction, I would like to shed some light on the new dynamics of the respiratory virus season.

The infamous SARS-CoV-2

  • Despite limited access to screening tests, analysis of the number of hospital admissions shows that the virus is still going strong.
  • It has a strikingly efficient capacity to spread through aerosols, especially as we take refuge indoors to escape the cold.

Resurgence of seasonal flu

  • After a hiatus due to health measures, the influenza virus, which causes seasonal flu, has returned with the same force.
  • It is once again circulating in different variants belonging to Types (strains) A and B, although scientists believe that one Type B strain, the Yamagata lineage, has disappeared.

And what about RSV?

  • Bronchiolitis is characterized by the obstruction of the small airways, which can progress to wheezing or respiratory distress.
  • But RSV also severely affects the elderly and adults who are immunocompromised or have existing chronic conditions.
  • Admittedly, although these three viruses are attracting attention, other less publicized respiratory viruses are also circulating, demonstrating a diverse viral environment.

SARS-CoV-2 has turned everything upside down

  • The challenge is amplified by the extremely high transmission capacity of SARS-CoV-2 compared with influenza and RSV, which makes seasonal management much more complex.
  • But today, the picture has become even more complex with the continuing presence of SARS-CoV-2.

Beyond infection

  • In addition, it causes long-term consequences after infection, such as post-COVID syndrome (also known as long COVID), which affects millions of people.
  • The extent of the consequences of infection and reinfection on human health remains uncertain, as does the effectiveness of vaccines in limiting these effects.

The importance of vaccines

  • The final distinction from the pre-pandemic period is the arrival of RSV vaccines.
  • However, these two vaccines have not yet been officially recommended.
  • The trio of vaccines against COVID-19, influenza and RSV will certainly help to reduce the severe symptoms associated with respiratory virus infections in the coming seasons.


Nathalie Grandvaux received research funding from the Canadian Institutes of Health Research (CIHR), the Natural Sciences and Engineering Research Council of Canada (NSERC), the Fonds de recherche du Québec - Santé (FRQS), the Canada Foundation for Innovation (CFI), the Fondation du centre hospitalier de l'Université de Montréal, and the Ministère de l'économie et de l'innovation du Québec.

Global qPCR Instruments Market Set to Reach $1.64 Billion by 2030, Driven by Advanced Diagnostics Demand and COVID-19 Screening Needs - ResearchAndMarkets.com

Retrieved on: 
Wednesday, January 10, 2024

The global qPCR instruments market size is expected to reach USD 1.64 billion by 2030.

Key Points: 
  • The global qPCR instruments market size is expected to reach USD 1.64 billion by 2030.
  • The market is driven by the introduction of novel advanced products and an increase in demand for highly efficient diagnostic equipment.
  • The demand for qPCR instruments and consumables is being driven by the spike in the incidence of SARS-CoV-2 infections globally.
  • North America dominated the global qPCR instruments market and accounted for the largest revenue share of 42.73% in 2022.

A UNIVERSAL CORONAVIRUS VACCINE COULD SAVE BILLIONS OF DOLLARS IF READY BEFORE NEXT PANDEMIC

Retrieved on: 
Thursday, January 11, 2024

NEW YORK, Jan. 11, 2024 /PRNewswire/ -- What if scientists had developed a universal coronavirus vaccine in the years prior to 2020 so that it was available at the start of the COVID-19 pandemic? A universal coronavirus vaccine targets parts of the virus that are common to either many or all coronaviruses, thereby offering some degree of protection against a range of strains. A new study suggests if such a vaccine were available at the start of the pandemic, it could have saved millions of lives, prevented suffering, and saved billions of dollars in direct medical and other costs until the strain-specific (i.e., SARS-CoV-2) vaccine went through the entire development, testing, and emergency use authorization process that lasted 10 months.

Key Points: 
  • NEW YORK, Jan. 11, 2024 /PRNewswire/ -- What if scientists had developed a universal coronavirus vaccine in the years prior to 2020 so that it was available at the start of the COVID-19 pandemic?
  • A universal coronavirus vaccine targets parts of the virus that are common to either many or all coronaviruses, thereby offering some degree of protection against a range of strains.
  • The experiments simulated what would happen if a universal coronavirus vaccine was available at the start of the COVID-19 pandemic.
  • A universal coronavirus vaccine was also shown to be highly cost-effective even if a more specific and more efficacious vaccine came to market.

Employee Locker Rooms Get Whole New Look, Feel, Functionality, and Level of Respect with Zippsafe Smart Storage

Retrieved on: 
Monday, January 8, 2024

Zippsafe replaces these bulky boxes with a series of soft textile bags that flex and expand to hold more and bulkier items.

Key Points: 
  • Zippsafe replaces these bulky boxes with a series of soft textile bags that flex and expand to hold more and bulkier items.
  • With its clean, modern aesthetic, Zippsafe also elevates the overall appeal of the locker room, making it a much more welcoming place for employees.
  • The Zippsafe smart locker system was launched in Europe in 2016 and is currently in use in a variety of healthcare settings, industrial facilities and office buildings.
  • For more information about how Zippsafe is reimagining the employee locker room experience, please visit www.zippsafe.com .

Cocrystal Pharma Provides an Update on the Clinical Development of its Novel, Broad-Spectrum Antiviral Investigational Candidates

Retrieved on: 
Thursday, January 4, 2024

CDI-988 is being evaluated for safety and pharmacokinetics in a randomized, double-blinded, placebo-controlled Phase 1 study in healthy subjects being conducted in Australia.

Key Points: 
  • CDI-988 is being evaluated for safety and pharmacokinetics in a randomized, double-blinded, placebo-controlled Phase 1 study in healthy subjects being conducted in Australia.
  • The Company reports favorable preliminary data from the single-ascending dose cohorts of the clinical study.
  • A randomized, double-blind, placebo-controlled Phase 2a clinical study with CC-42344 is underway in the United Kingdom.
  • In 2022 Cocrystal reported favorable safety and tolerability results in the healthy volunteer Phase 1 study with CC-42344 conducted in Australia .