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FDA, gene and Skin Disorder

US FDA approves J&J's immune disorder drug

The U.S. Food and Drug Administration on Wednesday approved Johnson & Johnson's drug to treat a type of muscle-weakening disorder, which is expected to bring in blockbuster revenues and drive growth.

U.S. News & World Report · 22h

FDA Approves Zevaskyn for Rare, Genetic Skin Disorder

Zevaskyn is the first and only autologous cell-based gene therapy for recessive dystrophic epidermolysis bullosa

Becker's Hospital Review · 4h

FDA OKs gene therapy for skin condition

The FDA has approved Zevaskyn, the first gene-modified cellular therapy for treating wounds in patients with recessive dystrophic epidermolysis bullosis, a rare genetic skin disorder. Made by Abeona Therapeutics,

FDA, bread and recall

People on MSN · 2h

Bread Recalled Over 'Glass Fragments' as FDA Warns Consumption Could Cause 'Adverse Health Consequences'

Bread and rolls sold in six states have been recalled over 'glass fragments,' according to the U.S. Food and Drug Administration (FDA).

Fortune on MSN · 1d

FDA recalls bread that could contain ‘glass fragments’

The FDA is recalling bread that was found to have glass fragments on top of the rolls. Three kinds of bread from Upper Crust Bakery were impacted by the recall. The rolls were sold in Pennsylvania, California,

Fox Business on MSN · 1d

FDA issues urgent nationwide recall of bread sold in US found with 'glass fragments'

An urgent recall for hundreds of cases of frozen bread sold throughout the U.S. was issued after the FDA said "glass fragments" were found on top of the bread.

2hon MSN

Exclusive: Trump administration banned chosen names at FDA, CDC, NIH under new gender policy

Health and Human Services employees were told in March to remove 'nicknames' from email systems and signatures to comply with ...

1don MSN

FDA to undo some layoffs, after cuts to inspections and drug safety

Multiple current and laid-off FDA employees said the abrupt layoffs had resulted in delays and disruptions to the agency's ...

MedPage Today3h

FDA Approves Nipocalimab for Adult and Pediatric Myasthenia Gravis

The FDA approved nipocalimab (Imaavy) injection to treat adults and children ages 12 and older with generalized myasthenia ...

STAT11h

Will the FDA approve the first new drug to help people quit smoking in 20 years?

The drug cytisinicline could help expand options for quitting smoking, and if approved by the FDA, would be the first new ...

1don MSN

FDA scrutiny of Novavax COVID-19 vaccine sparks uncertainty about other shots

There’s new uncertainty about updated COVID-19 shots this fall after the Trump administration’s handling of a shot from ...

20hon MSN

FDA chief says they're looking at whether to approve COVID shots for next winter

The head of the Food and Drug Administration said Tuesday that the agency is now looking at whether it will still approve COVID-19 vaccines for next winter, citing a lack of data on booster shots.

Healio3h

FDA approves Imaavy for generalized myasthenia gravis in patients aged 12 years and older

The FDA has approved a monoclonal antibody to treat individuals aged 12 years and older with generalized myasthenia gravis ...

22h

FDA Chief Says He Won’t Reorganize Agency After Mass Layoffs (1)

The FDA doesn’t plan to execute a reorganization of the agency but will consolidate offices that handle travel, technology, ...

BioPharma Dive3h

J&J secures FDA OK for immune drug touted as future blockbuster

The company has predicted that Imaavy — now approved for generalized myasthenia gravis — could eventually earn more than $5 ...

6hon MSN

Trader Joe's, Gerber and Texas Pete among FDA recalls for April 2025. See full list

Many recalls are initiated due to the potential risk of contamination in the food product. Here's what was pulled from ...

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FDA, gene and Skin Disorder

FDA, bread and recall

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