Infectious Diseases
Are you sure you'd like to remove this alert? You will no longer receive email updates about this topic.
![](/-/media/editorial/stock-images/companies/sc2407_moderna_2193720145_1200.jpg?rev=c89b4bb6c799485a9b50c83d92d2d8ac&w=350&hash=ED8DAF507D3FD6D7DDCF2EF2E714D91A)
Amid Growing Pandemic Fears, Moderna Gets BARDA Funding For Flu Program
The biotech got a $176m award for its pandemic influenza vaccine program through BARDA’s Rapid Response Partnership Vehicle.
![](/-/media/editorial/buildings/corporate/v/valneva.jpg?rev=8d05e91d620f4de786861db25106fc52&w=350&hash=E7B818972F841084A98F438B06783229)
Valneva Cements Lead In Chikungunya Space With EU Nod
The green light from the European Commission for Ixchiq marks the third regulatory approval for the world’s first vaccine for chikungunya and extends the French biotech's lead over rival Bavarian Nordic.
![](/-/media/editorial/stock-images/miscellaneous/vaccine-injection-1200-shutterstock_1852449988.jpg?rev=6918e348f3274bb7bd3435cde85be1df&w=350&hash=B0730E3A6F1F8D8A1057A27F56AB4C50)
Moderna And GSK Hit By Declining RSV Vaccines Expectations
The efficacy of Moderna’s jab appears to fade faster than its rivals, while experts were surprised by an FDA panel’s recommendation to narrow the use of all three RSV vaccines.
![](/-/media/editorial/scrip/00_regular-column-images/sc2008_fivemustknowthings_1200_final.jpg?rev=e6ab2761c1e6477ebef4a5c11f824cfe&w=350&hash=85D113D905C9FDFC44BA47966C7DE910)
Quick Listen: Scrip's Five Must-Know Things
In this week's podcast edition of Five Must-Know Things: the outlook for 2025 launches; Merck confident in new pneumococcal vaccine; multiple US setbacks for Japanese firms; Stock Watch on Moderna missteps; and Sun’s North America head talks plans and strategy.
![](/-/media/editorial/scrip/2024/06/sc062024_hiv_prep_1200.jpg?rev=784a1e29091b4dcca1f845c4c569e295&w=350&hash=9FB44258BD43118F6BA6F55D29B0399C)
Gilead’s Twice-Annual Sunlenca Posts Zero Infection Rate In PrEP Trial
Lenacapavir is halfway to the pivotal data needed to file for twice-annual administration in PrEP, after demonstrating superiority against both background incidence of HIV infections and Truvada.
![](/-/media/editorial/hbw-insight/hbw-stock-images/money-sack-198026720_1200.jpg?rev=532f0504023c4d76a03e26e30401363d&w=350&hash=04627AEE0D632EE0E7FCD4521CAED84F)
Cagrisema Leads The Charge For 2025
2030 sales forecasts for Novo’s obesity hope are an order of magnitude larger than its closest rival among 2025’s expected debutantes.
![](/-/media/editorial/scrip/00_regular-column-images/sc2008_fivemustknowthings_1200_final.jpg?rev=e6ab2761c1e6477ebef4a5c11f824cfe&w=350&hash=85D113D905C9FDFC44BA47966C7DE910)
Quick Listen: Scrip's Five Must-Know Things
In this week's podcast edition of Five Must-Know Things: Boehringer best in MASH?; biopharma funding on an upswing?; Moderna’s combo jab; clinical trial recover from pandemic; and Astellas’s US commercial head speaks.
![](/-/media/editorial/stock-images/miscellaneous/vaccine-race-1830112673_1200.jpg?rev=ade2bff35f914b73a7c8a6c53a65837b&w=350&hash=64AB8E7A2278B9FE62EB24F0BA482F33)
Moderna Pips Pfizer/BioNTech In Combo Jab Race
The company reported a late-stage success with its COVID-19 and flu combo vaccine, and says it can hit the market next year.
![](/-/media/editorial/scrip/2024/06/sc2406_shionogi_rd_shutterstock_1924512509_1200.jpg?rev=7bb2eab95c854e2cb0cebd2ea718a660&w=350&hash=530748FD6AB0530ED1FD29EBEDBDF7E7)
Shionogi, Qpex Agree On Anti-Infective-Focused US R&D Site
Shionogi says first major US R&D site will enhance capabilities for both Shionogi and its 2023 acquisition Qpex, which prompted the Japanese firm to build on the San Diego company's close research collaborations with US government organizations.
![](/-/media/editorial/stock-images/diseases/sc2406_hepatitis_1994999621_1200.jpg?rev=668f0c0db08c425993c929b868a29e1d&w=350&hash=87A700E1D98F771CA3A6ADCE163EF8B2)
Vir Hopes To Take On Gilead’s Hepcludex After Positive Early Hepatitis D Results
The biotech presented preliminary data on chronic hepatitis D from the Phase II SOLSTICE study of tobevibart and elebsiran at the EASL meeting.
![](/-/media/editorial/buildings/corporate/s/sanofi-1200-shutterstock_2220893831.jpg?rev=0f2b4cba3740461f8c80892e5eda576d&w=350&hash=FE2DAEC462F216D487F0E4555BE7E5B6)
Sanofi’s $500m COVID-19 Deal Comes Four Years Too Late
But it rescues embattled Novavax.
![](/-/media/editorial/buildings/corporate/a/astrazenecaflags_rolandmagnusson_521453077_1200x675.jpg?rev=5b3b7036859f407d8abd36bc87d3c1b9&w=350&hash=C0906898D92BCD96C84E07167895BDDE)
A Job Well Done: AstraZeneca Bids Adieu To Vaxzevria As Demand Dries Up
The voluntary withdrawal of the license for the UK major's COVID-19 vaccine is due to a surplus of available updated jabs from other companies that target new variants and is not connected to the mis- and disinformation being peddled on the internet and elsewhere on very rare adverse events.
You must sign in to use this functionality
Authentication.SignIn.HeadSignInHeader
Email Article
All set! This article has been sent to my@email.address.
All fields are required. For multiple recipients, separate email addresses with a semicolon.
Please Note: Only individuals with an active subscription will be able to access the full article. All other readers will be directed to the abstract and would need to subscribe.