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FDA, weight loss drugs

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 · 2h
FDA wants to limit compounded versions of weight loss drugs
The U.S. Food and Drug Administration on Thursday proposed excluding Novo Nordisk and Eli Lilly’s ‌weight-loss drugs from a key compounding list, potentially limiting large-scale production by outsour...

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 · 6h · on MSN
FDA moves to exclude weight loss drugs from compounding chemicals list
 · 13h · on MSN
US FDA proposes excluding weight-loss drugs from compounding list
 · 9h
US FDA proposes curbs on mass compounding of Novo, Lilly's weight-loss drugs
The U.S. Food and Drug Administration ​on Thursday proposed excluding Novo Nordisk (NOVOb.CO) and Eli Lilly's (LLY.N) weight-loss drugs from a key compounding list, potentially ‌limiting large-scale p...

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 · 10h
Eli Lilly Shares Jump 10% as Mounjaro, Zepbound Fuel Massive Growth
 · 10h
Lilly is selling $12.9 billion of GLP-1 drugs every three months — and expects to sell even more
 · 15h
Lilly rises after boosting 2026 outlook
CEO David Ricks touted the company’s oral weight loss therapy, Foundayo, launched earlier this month, which rivals Novo’s ( NVO) Wegovy pill.

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The Hour · 16h
Lilly: Q1 Earnings Snapshot
 · 1d
Eli Lilly Stock Could Rise Sharply After Earnings
12h

The FDA Just Approved a New Depression Treatment—and It Doesn’t Involve Medication

Known as transcranial direct-current stimulation, or tDCS, the technology is designed for at-home use, potentially offering a more accessible alternative to traditional therapies, according to The New York Times.
STAT
6h

Katherine Szarama named acting director of FDA’s vaccines and biologics center

Katherine Szarama, who joined the FDA last year to serve as Vinay Prasad’s deputy, will now fill his shoes at CBER.
8hon MSN

US FDA approves Axsome's drug for Alzheimer's-related agitation

By Kamal Choudhury and Mariam Sunny April 30 (Reuters) - The U.S. Food and Drug Administration has approved Axsome Therapeutics' drug to treat agitation in patients with Alzheimer's disease, the company said on Thursday,
2d

FDA set to pilot test real-time tracking of clinical trials

The Food and Drug Administration (FDA) is set to pilot test real-time clinical trials in the hopes of expediting results and feedback, federal health officials announced on Tuesday. At least two clinical trials by pharmaceutical companies AstraZeneca and Amgen will test the new system to alert FDA officials to study results in real time.
1d

America's infant formula supply is safe, FDA testing confirms

The FDA tested infant formula for contaminants, finding the U.S. supply is safe, but small exposures still matter for newborns.
1don MSN

FDA affirms safety of infant formula from heavy metals

The U.S. infant formula supply is largely safe from contaminants, according to new testing results announced Wednesday by the Food and Drug Administration (FDA). Between 2023 and 2025, FDA purchased and tested more than 300 infant formula samples at retail stores covering 16 brands.
1d

New Infant Formula Test Results Are Released by the FDA

The FDA has released the findings of a comprehensive test of infant formula in the U.S. CR's experts say some of the results raise questions.
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