- A company is conducting clinical trials and seeking drug approval for the U.S. market under the FDA.
The FDA approved the influenza vaccine for self-administration, while the CDC concurrently classified the previous influenza season as high-severity.
1 report, 1 independent
Updated Aug 15
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What happened
The FDA approved the influenza vaccine for self-administration, while the CDC concurrently classified the previous influenza season as high-severity.
Who's involved
What this event is mainly aboutKeep exploring
Part of
A company is conducting clinical trials and seeking drug approval for the U.S. market under the FDA.Also in this story
- A partnership with BARDA has accelerated the development of SCY-247 for the company.
- A company plans to submit regulatory applications to the FDA, EMA, and Australian TGA.
- Approval leads to procurement process initiation.
- UroGen Pharma Ltd., headquartered in Princeton, is seeking FDA approval for its products for the U.S. market.
The entities involved
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Centers for Disease Control and Prevention
government organization in Kampala, Uganda
- FDA
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AstraZeneca
British-Swedish pharmaceutical company
Related events
- Moderna and Merck are developing cancer vaccines in partnership, while Moderna is also seeking approval for its seasonal influenza vaccine.
- The FDA aligned vaccine formulas with global health recommendations provided by the World Health Organization.
- The American Academy of Pediatrics, American Medical Association, and CDC formed to provide clear vaccine guidance as government advice remains in flux.
Coverage
Newest first; wire copies grouped- Business WireFLUMIST (Influenza, Vaccine Live, Intranasal), the nation’s only nasal spray flu vaccine, now available for home delivery AstraZeneca launches the first FDA-approved influenza vaccine available for s