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Moderna, Inc. (NASDAQ:MRNA) today announced that it has submitted an application to the U.S. Food and Drug Administration (FDA) for review of its Spikevax 2025-2026 formula, targeting the SARS-CoV-2 ...
The ultrasound catheter is being tested in the PreVail-PH2 study, an early feasibility trial enrolling PH patients with left ...
The FDA has approved Nucala (mepolizumab) as an add-on maintenance treatment for certain COPD patients whose disease isn't ...
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Medical Device Network on MSNQiagen and ID Solutions collaborate on dPCR assays for oncology researchID Solutions will produce and supply dPCR assays for use in non-clinical research on Qiagen's QIAcuity platforms.
The vaccine advisory committee for the Food and Drug Administration met Thursday to discuss potential changes to the formula for COVID-19 vaccines for 2025-2026.
A group of experts who advise the US Food and Drug Administration on its vaccine decisions voted unanimously Thursday to make a broad recommendation about which lineage of the coronavirus should be ...
Once upon a pandemic, Ivermectin was the controversial darling of DIY medicine — hailed as a miracle by some, horse-dewormer ...
By Jen Christensen, CNN The US Food and Drug Administration will now require Covid-19 vaccines from Pfizer/BioNTech and Moderna to use expanded warning labels with more information about the risk of a ...
Previously, updated COVID vaccines had been recommended annually by the CDC for everyone over the age of 6 months. The CDC ...
Healthy adults younger than 65 will no longer be eligible for COVID-19 shots starting in the fall, according to new federal ...
The U.S. Food and Drug Administration on Tuesday issued a recall alert concerning salmonella and cucumbers grown by a Palm Beach County grower. The same grower was linked to an outbreak in several ...
The US Food and Drug Administration is changing the way it approves Covid-19 vaccines for Americans — a move that will limit ...
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