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FDA asks Sarepta to stop shipping gene therapy

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· 4h

Sarepta’s Risky Gamble: Gene Therapy Stays on Market Despite FDA Request

Facing mounting criticism, Sarepta recently announced plans to add a bold warning label to Elevidys.

· 20h · on MSN

Gene therapy maker Sarepta tells FDA it won’t halt shipments despite patient deaths

· 1d

Sarepta Says It Won't Comply With FDA Request to Stop Shipping Gene Therapy Elevidys

· 20h

Sarepta tells FDA it won’t halt shipments despite patient deaths

Drugmaker Sarepta Therapeutics said late Friday it won’t comply with a request from the Food and Drug Administration to halt all shipments of its gene therapy following the death of a third patient r...

· 1d

FDA to ask Sarepta to stop shipping Duchenne gene therapy

· 1d

Sarepta Therapeutics crisis is huge blow to Duchenne families, company

Juul's FDA approval doesn't clear fog of e-cigarette risks

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Las Vegas Sun · 58m

Juul’s FDA approval doesn’t clear fog of e-cigarette risks, especially for teens

The FDA has approved Juul’s continued sales of e-cigarettes, despite the health risks they present, especially with their popularity among teenagers.

· 2d · on MSN

FDA approves Juul e-cigarette and cartridge sales

· 2d · on MSN

Juul can continue selling its tobacco and menthol e-cigarettes, FDA says

1don MSN

Sarepta Shares Crash on Report That FDA Will Ask It to Stop Shipping Key Drug

The drop comes the day after the drugmaker said it would add a so-called black-box warning to its gene therapy Elevidys after two teenage boys receiving the treatment died earlier this year.

15h

FDA Announces Major Recall of Popular Deodorant

It's important to stay informed about recalls, because doing so truly impacts your life. Of course, the sooner you know about a recall, the better, because you can make sure to get rid of the suspecting item and keep everyone in your family safe.

Health and Me on MSN8h

"Obsolete And Unnecessary": FDA Set To Revoke 52 Nutrition And Labeling Rules

The FDA plans to revoke 52 outdated nutrition and labeling regulations to streamline food industry standards, citing them as obsolete and no longer necessary for modern practices.

GSK's Blood Cancer Drug Faces US Setback Due To FDA Panel's Eye Safety Warning

Oncologic Drugs Advisory Committee (ODAC) voted against the overall benefit/risk profile at the proposed dosage of GSK plc’s (NYSE:GSK) Blenrep (belantamab mafodotin-blmf) combinations. The belantamab mafodotin combinations were evaluated in adults with relapsed or refractory multiple myeloma who have received at least one prior line of therapy.

Food Business News1d

FDA targets 52 food standards of identity for termination

WASHINGTON — The US Food and Drug Administration aims to revoke 52 standards of identity (SOI) across a swath of food categories, claiming the regulations are “obsolete and unnecessary.”

FDA plans to revoke 52 food standards

The U.S. Food and Drug Administration has announced a plan to revoke 52 food standards after concluding they are "obsolete and unnecessary."