Respiratory syncytial virus

Calder Biosciences Inc. Publishes Next-Generation Vaccine Technology in Nature Communications

Retrieved on: 
Thursday, March 14, 2024

BROOKLYN, N.Y., March 14, 2024 /PRNewswire/ -- Calder Biosciences, Inc ., a next-generation vaccine company, has been published in a Nature Communications article ( https://www.nature.com/articles/s41467-024-46295-8 ) that debuts and validates the application of Calder's '3D Vaxlock' platform technology.

Key Points: 
  • BROOKLYN, N.Y., March 14, 2024 /PRNewswire/ -- Calder Biosciences, Inc ., a next-generation vaccine company, has been published in a Nature Communications article ( https://www.nature.com/articles/s41467-024-46295-8 ) that debuts and validates the application of Calder's '3D Vaxlock' platform technology.
  • Application of the technology not only dramatically improves potency, but also improves shelf-life of the vaccine at refrigerated temperatures that will facilitate distribution and delivery.
  • In the Nature Communications manuscript, Calder demonstrates that a high dose of their RSV vaccine achieves responses in aged, immunosenescent animals equivalent to responses in the young animal control group.
  • Calder also plans to apply its technology more generally in protein engineering, imparting thermostability as needed to additional subunit vaccines, biologics, or other targets.

The Access to Advanced Health Institute Receives up to $12.7 Million to Develop Novel NanoAlum Adjuvant Formulation for Better Protection Against Tuberculosis and Pandemic Influenza

Retrieved on: 
Thursday, March 7, 2024

Key Points: 
  • View the full release here: https://www.businesswire.com/news/home/20240307661956/en/
    This five-year prototype project will support AAHI’s development and optimization of “NanoAlum” – a novel nanoparticle adjuvant formulation, made from aluminum salts (“alum”).
  • Alum-adjuvanted vaccines have been less effective against diseases such as tuberculosis and influenza, which are more complex to target and can be challenging to manufacture because they require special sterilization methods.
  • AAHI’s NanoAlum formulation changes the size, shape, and charge of alum particles to enhance specific immune responses for better vaccine protection against complex diseases.
  • AAHI’s prototype project for MCDC will pair the combined 3M-052 and NanoAlum formulation with tuberculosis and pandemic influenza vaccine antigens.

Vir Biotechnology Provides Corporate Update and Reports Fourth Quarter and Full Year 2023 Financial Results

Retrieved on: 
Thursday, February 22, 2024

Vir Biotechnology, Inc. (Nasdaq: VIR) today provided a corporate update and reported financial results for the fourth quarter and full year ended December 31, 2023.

Key Points: 
  • Vir Biotechnology, Inc. (Nasdaq: VIR) today provided a corporate update and reported financial results for the fourth quarter and full year ended December 31, 2023.
  • Complete 24-week treatment data for 30 participants per regimen is expected in the fourth quarter of 2024.
  • The MARCH Part B trial is ongoing with 48-week end of treatment data expected in the fourth quarter of 2024.
  • Revenues: Total revenues for the quarter ended December 31, 2023 were $16.8 million compared to $49.4 million for the same period in 2022.

AMDI Receives a $5.3M NIH RADx® Tech Award to Finalize Development of Its 10 Minute RT-PCR Point-of-Care System and Respiratory Panel

Retrieved on: 
Wednesday, February 28, 2024

The funding will also be used to complete the first test panel for the Fast PCR system, targeting detection of multiple respiratory viruses: Influenza A and B, respiratory syncytial virus (RSV), and SARS-CoV-2.

Key Points: 
  • The funding will also be used to complete the first test panel for the Fast PCR system, targeting detection of multiple respiratory viruses: Influenza A and B, respiratory syncytial virus (RSV), and SARS-CoV-2.
  • The RADx Tech program was created to speed innovation and address critical public health challenges like the COVID-19 pandemic.
  • "AMDI is grateful for the recognition by the NIBIB for a second award that gives us the opportunity to complete the development of the Fast PCR System," said David Okrongly, CEO of AMDI.
  • The HBH technology removes the time constraints and costs associated with traditional sample prep", said Regis Peytavi, CTO of AMDI.

Steel Jupiter's Indoor Air Innovation Receives EPA Device Determination

Retrieved on: 
Tuesday, February 20, 2024

BETHLEHEM, Pa., Feb. 20, 2024 /PRNewswire/ -- Steel Jupiter has achieved a major development milestone with the recent issuance of a device determination from the U.S. Environmental Protection Agency (EPA) for the company's unique and innovative "Zinnia Technology-Coated MERV 8 Air Filter." The EPA's determination confirms that the Zinnia-coated filter operates through dual-action aerosol trapping mechanisms under the Federal Insecticide, Fungicide and Rodenticide Act (FIFRA).

Key Points: 
  • BETHLEHEM, Pa., Feb. 20, 2024 /PRNewswire/ -- Steel Jupiter has achieved a major development milestone with the recent issuance of a device determination from the U.S. Environmental Protection Agency (EPA) for the company's unique and innovative "Zinnia Technology-Coated MERV 8 Air Filter."
  • The EPA's determination confirms that the Zinnia-coated filter operates through dual-action aerosol trapping mechanisms under the Federal Insecticide, Fungicide and Rodenticide Act (FIFRA).
  • With the regulatory path now established, Steel Jupiter can proceed with its go-to-market plan, which includes performance testing multiple filter types across various real-world operational and environmental factors in simulated and actual settings, working with leading indoor air experts.
  • Steel Jupiter anticipates completing this final validation testing over the next several months.

Ginkgo Bioworks and SaponiQx Awarded MCDC Contract to Discover and Manufacture Next-Generation Vaccine Adjuvants Using Generative Molecular Design

Retrieved on: 
Thursday, February 15, 2024

Adjuvants are components of vaccines that help to enhance the magnitude, breadth, and duration of the immune response to vaccination.

Key Points: 
  • Adjuvants are components of vaccines that help to enhance the magnitude, breadth, and duration of the immune response to vaccination.
  • Currently, only a handful of adjuvants are available for human use in licensed vaccines.
  • Ginkgo will develop a first-generation Adjuvant Development Candidate (ADC) production method, using a heterologous production strain such as brewers' yeast, Saccharomyces cerevisiae.
  • Development of a first-generation ADC production method could facilitate further development of a sustainable mass-production manufacturing process for these complex adjuvants.

GSK’s RSV Vaccine, AREXVY, Accepted Under Priority Review in US for the Prevention of RSV Disease in Adults Aged 50-59 at Increased Risk

Retrieved on: 
Tuesday, February 6, 2024

GSK plc (LSE/NYSE: GSK) today announced that the US Food and Drug Administration (FDA) has accepted under Priority Review an application to extend the indication of GSK’s adjuvanted respiratory syncytial virus (RSV) vaccine to adults aged 50-59 who are at increased risk for RSV disease.

Key Points: 
  • GSK plc (LSE/NYSE: GSK) today announced that the US Food and Drug Administration (FDA) has accepted under Priority Review an application to extend the indication of GSK’s adjuvanted respiratory syncytial virus (RSV) vaccine to adults aged 50-59 who are at increased risk for RSV disease.
  • If approved, GSK’s RSV vaccine would be the first vaccine available to help protect this population.
  • AREXVY (Respiratory Syncytial Virus Vaccine, Adjuvanted) is currently approved in the US in adults aged 60 and over for the prevention of lower respiratory tract disease (LRTD) caused by RSV.
  • GSK used a Priority Review Voucher to reduce the US FDA review period of a supplemental Biologics License Application (sBLA) by four months.

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.

Clarivate Identifies Thirteen Potential Blockbuster Drugs and Gamechangers in Annual Drugs to Watch Report

Retrieved on: 
Monday, January 8, 2024

LONDON, Jan. 8, 2024 /PRNewswire/ -- Clarivate Plc (NYSE:CLVT), a global leader in connecting people and organizations to intelligence they can trust to transform their world, today announced the release of its annual Drugs to Watch™ report. The report provides in-depth predictive analysis of drugs with the potential for standout commercial and/or clinical success. The report, a key industry resource in the evolving healthcare landscape, has identified over 85 Drugs to Watch over the 11-year course of its publication.

Key Points: 
  • The report provides in-depth predictive analysis of drugs with the potential for standout commercial and/or clinical success.
  • The report, a key industry resource in the evolving healthcare landscape, has identified over 85 Drugs to Watch over the 11-year course of its publication.
  • Leveraging deep industry expertise and comprehensive therapeutic area differentiated data, this year's Drugs to Watch report identifies innovative medicines based on recent scientific breakthroughs poised to have extraordinary impacts on patient outcomes."
  • Included in Drugs to Watch 2023, a delayed U.S. launch meant that it remains a drug to watch for 2024.

Clarivate Identifies Thirteen Potential Blockbuster Drugs and Gamechangers in Annual Drugs to Watch Report

Retrieved on: 
Monday, January 8, 2024

LONDON, Jan. 8, 2024 /PRNewswire/ -- Clarivate Plc (NYSE:CLVT), a global leader in connecting people and organizations to intelligence they can trust to transform their world, today announced the release of its annual Drugs to Watch™ report. The report provides in-depth predictive analysis of drugs with the potential for standout commercial and/or clinical success. The report, a key industry resource in the evolving healthcare landscape, has identified over 85 Drugs to Watch over the 11-year course of its publication.

Key Points: 
  • The report provides in-depth predictive analysis of drugs with the potential for standout commercial and/or clinical success.
  • The report, a key industry resource in the evolving healthcare landscape, has identified over 85 Drugs to Watch over the 11-year course of its publication.
  • Leveraging deep industry expertise and comprehensive therapeutic area differentiated data, this year's Drugs to Watch report identifies innovative medicines based on recent scientific breakthroughs poised to have extraordinary impacts on patient outcomes."
  • Included in Drugs to Watch 2023, a delayed U.S. launch meant that it remains a drug to watch for 2024.