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FDA, Genentech and metastatic breast cancer

FDA approves first once-weekly drug treatment regimen for hemophilia

Patients suffering from hemophilia received a "meaningful" advancement on Friday when federal regulators approved the first once-weekly treatment for the disease.

MarketWatch · 1d

Genentech Itovebi Gets FDA Approval for Treating Breast Cancer

Roche Group unit Genentech said that the Food and Drug Administration approved Itovebi for treating certain breast cancer. The approval is for Itovebi in combination with palbociclib and fulvestrant and for treating adults a certain locally advanced or metastatic breast cancer,

The Business Journals · 19h

FDA approves Genentech drug aimed at subset of breast cancer patients

A potential blockbuster cancer drug developed by Genentech Inc. and parent company Roche won regulatory approval Thursday to treat a subset of breast cancer patients, more than a month ahead of its scheduled decision date.

Joplin Globe · 23h

FDA Approves Genentech’s Itovebi, a Targeted Treatment for Advanced Hormone Receptor-Positive, HER2-Negative Breast Cancer With a PIK3CA Mutation

Genentech, a member of the Roche Group (SIX: RO, ROG; OTCQX: RHHBY), announced today that the U.S. Food and Drug Administration (FDA) approved Itovebi™ (inavolisib), in combination with palbociclib (Ibrance ® ) and fulvestrant,

FDA approves 1st combination COVID-flu test

CBS News on MSN · 1d

FDA authorizes over-the-counter combined COVID-19 and flu home test

Healgen Scientific's combined COVID-19 and flu test gives people a new way to check what's causing their symptoms, FDA says.

USA TODAY on MSN · 1d

FDA approves the first at-home test for COVID-19 and the flu, no prescription needed

The Food and Drug Administration has granted authorization of a COVID-19 and flu test that can be used without a prescription. The authorization, announced Monday, uses a nasal swab to detect the proteins from SARS-CoV-2 and Influenza A and B, or the viruses are found in COVID-19 and the flu.

Houston Chronicle on MSN · 1d

First over the counter combo COVID and flu test gets FDA approval

The public will no longer need a prescription or a visit to a health provider to take take a combined COVID and flu test at home. The U.S. Food and Drug Administration on Thursday announced it has authorized the use of the Healgen Rapid Check COVID-19/Flu A&B Antigen Test,

FDA has upgraded its recall on eggs

TODAY on MSN · 1d

FDA says egg recall over salmonella can have 'serious' health effects: Avoid these brands

Eggs sold in three states have been recalled due to possible salmonella contamination. Here's what consumers need to know about symptoms, brands and more.

al.com · 1d

Check your fridge for these brands: FDA has upgraded its recall on eggs

The Food and Drug Administration has escalated an ongoing egg recall to its most serious class. On Sept. 6, the Centers for Disease Control and Prevention sent out an initial recall for eggs produced by Wisconsin-based Milo’s Poultry Farms LLC because ...

SFGATE on MSN · 2d

Eggs sicken 2 in California as FDA bumps recall up to highest threat level

California has been linked to a Food and Drug Administration recall of 4 million eggs. On Sept. 6, the Center for Disease Control and Prevention first announced Milo’s Poultry Farms LLC, based in Wisconsin,

US FDA approves Pfizer's drug for rare bleeding disorder

The U.S. Food and Drug Administration approved Pfizer's once-a-week injection for the two main types of a rare bleeding ...

3hon MSN

Pfizer wins FDA approval for hemophilia B drug that will be first once-weekly treatment

The new drug would allow patients to produce the needed clotting protein for an extended period, reducing the need for ...

6hon MSN

Lemonade Recall Update As FDA Sets Risk Level

More than 13,000 cans of lemonade are being recalled due to a labeling mishap.Cans of Minute Maid Zero Sugar Lemonade are ...

21hon MSN

The FDA Just Recalled Nearly 10 Million Pounds of Ready-to-Eat Meat and Poultry Nationwide

According to the FDA announcement, the recall includes approximately 9,986,245 pounds of ready-to-eat meat and poultry ...

Ferguson urges decision on mifepristone lawsuit against FDA

Washington state Attorney General Bob Ferguson has filed a summary judgment motion in an ongoing lawsuit, involving ...

1don MSN

Cattle Feed Recall Update as FDA Sets Highest Risk Level

The U.S. Food and Drug Administration (FDA) has given the highest risk classification to several recalled animal feed ...

EatingWell on MSN3h

Here's What the FDA Wishes You Knew About Apple Cider

Related: Slow-Cooker Hot Cider with Brandy. But you may have heard that if apple cider isn’t properly processed, it can make ...

MedPage Today20h

Elamipretide for Barth Syndrome Survives FDA Advisory Vote

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