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FDA Approves New COVID Vaccine

U.S. News & World Report · 56m

FDA Gives Full OK to Novavax COVID Shot for High-Risk Groups

Novavax had expected full approval for broader use by April 1, after the FDA reviewed data from a 30,000-person clinical trial showing the vaccine was safe and effective. But instead of a broad approval, the FDA asked the company to conduct more research.

Bloomberg on MSN · 36m

Novavax Soars After Covid Vaccine Secures Full FDA Approval

Novavax Inc. jumped after US regulators fully approved its Covid vaccine, easing investors’ concerns after the clearance was delayed and US Health and Human Services Secretary Robert F. Kennedy Jr. raised doubts about its efficacy.

Reuters on MSN · 4h

Novavax shares jump after long-awaited FDA approval of its COVID-19 vaccine

Novavax shares surged more than 17% before the bell on Monday, following the long-delayed approval of its COVID-19 vaccine from the U.S. health regulator, albeit with new conditions.

Alzheimer's, FDA and blood test

CNN on MSN · 2d

FDA greenlights first blood test to help diagnose Alzheimer’s disease in the US

The US Food and Drug Administration has given marketing clearance to a blood test to help diagnose Alzheimer’s disease, making the test the first to get signoff to aid in the early detection of the disease in the United States.

The American Journal of Mana… · 51m

FDA Clears First Blood Test for Early Detection of Alzheimer-Linked Amyloid Plaques

The FDA cleared marketing for the first in vitro diagnostic device that tests blood to aid in diagnosing Alzheimer disease.

Newsweek on MSN · 1d

New Alzheimer's Test Approved by FDA—What to Know

The new test, known as the Lumipulse G pTau217/ß-Amyloid 1-42 Plasma Ratio, detects amyloid plaques through blood testing, a type of protein indicative of Alzheimer's, the Alzheimer's Association explained in a Friday press release. These plaques can be seen in patients through a PET scan, according to the FDA.

2hon MSN

Baked Bean Recall Update as FDA Sets Highest Risk Level

Nearly 4,500 cases were pulled from shelves in 23 states after it was found that the affected cans had been mislabeled.

FDA, NIH Accelerate Shift Away From Animal Research as Experts Warn of Limitations

The FDA and NIH recently announced plans to phase out animal testing requirements for some therapies. While organoid and AI ...

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