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Sarepta Therapeutics, FDA

Sarepta shares slide again as drugmaker bows to FDA pressure to pause gene therapy

Sarepta Therapeutics is pausing shipments of its gene therapy for muscular dystrophy following several patient deaths that have attracted attention from regulators.

MarketWatch · 3h

Sarepta Therapeutics’ stock slips further as company bows to FDA pressure to halt shipments

Sarepta Therapeutics shares traded lower in premarket trade on Tuesday, as the drugmaker relented to a Food and Drug Administration request to halt the shipments of a gene therapy.

Reuters · 13h

Sarepta to pause Elevidys gene therapy shipments in US

Sarepta Therapeutics said on Monday it will pause all shipments of Elevidys in the United States after two teenage boys with a rare condition called Duchenne muscular dystrophy, who had received the company's gene therapy,

FDA Appoints Biotech Exec

Associated Press News on MSN · 22h

FDA names former pharmaceutical company executive to oversee US drug program

The Food and Drug Administration named a longtime pharmaceutical executive to run the agency’s drug program. Dr.

UPI on MSN · 21h

Biotech exec George Tidmarsh picked as FDA's chief drug regulator

The U.S. Food and Drug Administration named ex-biotech exec George Tidmarsh as its chief drug regulator. FDA Commissioner Marty Makary called Tidmarsh an "accomplished physician-scientist and leader."

Reuters on MSN · 1d

FDA appoints George Tidmarsh as top drug regulator

By Sriparna Roy and Sneha S K (Reuters) -The U.S. Food and Drug Administration said on Monday it has appointed former biotech executive George Tidmarsh as the director of the Center for Drug Evaluation and Research.

FDA recalls Power Stick

TODAY on MSN · 19h

The FDA just recalled 67,000 cases of deodorant — here’s what you need to know

But one thing we’re confident about is that nobody wants to use a deodorant that has been recalled, which is why we are sharing this news: The Food and Drug Administration has issued a recall on 67,000 cases of Power Stick antiperspirant deodorant.

Austin American-Statesman on M… · 1d

FDA recalls over 67,000 cases of Power Stick deodorant due to manufacturing violations

What deodorant products are being recalled? Where were the recalled products sold? According to the recall notice, the Power Stick deodorants were sold nationwide. The deodorants

Yahoo · 1h

FDA recalls Power Stick; what to know about deodorant recall 2025

Pennsylvania-based A.P. Deauville, LLC is recalling several types of its Power Stick deodorant, due to a process issue.

CNET3h

What Is Pruritus? What the FDA Warning About Xyzal and Zyrtec Side Effects Means

Taking medication for an allergic reaction? You might face severely itchy skin as a side effect of Zyrtec or Xyzal, according ...

4hon MSN

FDA commissioner stirs debate over hormone therapy for menopause

A Food and Drug Administration expert panel has reignited a debate over whether hormone therapy should be used to treat ...

23hon MSN

FDA Issues Highest Risk Warning For Mushroom Recall

Mushrooms sold across two states have been recalled over fears they could be harboring listeria, a bug that "can cause ...

18h

FDA Approves Prefilled Syringe Presentation for Shingles Vaccine

Prefilled syringe eliminates the need to reconstitute separate vials prior to administration and simplifies the vaccine ...

Healio2h

FDA grants orphan drug designation to taladegib for IPF

The FDA granted an orphan drug designation to novel hedgehog pathway inhibitor taladegib, also known as ENV-101, for treating ...

1don MSN

FDA Suspends Muscular Dystrophy Drug After 3 Patient Deaths

The U.S. Food and Drug Administration ( FDA) has placed an immediate clinical hold on Sarepta Therapeutics' investigational ...

Medscape2h

FDA Panel Rejects Brexpiprazole-Sertraline Combo for PTSD

An FDA advisory panel concludes that the efficacy of brexpiprazole, when started concurrently with sertraline, has not been ...

15hon MSN

FDA Announces Massive Ice Cream Recall in 23 States

The Food and Drug Administration (FDA) makes sure to stay on top and notify people whenever a recall is put into place.

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Sarepta Therapeutics, FDA

FDA Appoints Biotech Exec

FDA recalls Power Stick

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