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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 · 21h

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 · 1d

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,

1st over counter combo COVID and flu test gets FDA approval

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.

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,

CNET on MSN · 1d

Is It COVID or Flu? FDA Gives 'Official' Authorization to Test That Will Tell You

FDA has upgraded its recall on eggs

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 ...

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.

YAHOO!News · 1d

FDA upgrades ongoing egg recall to Class 1 following multi-state Salmonella outbreak

A Class 1 recall is defined as a “situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death,” according to the FDA.

MedPage Today55m

Marstacimab Gets FDA Nod for Hemophilia A or B Without Inhibitors

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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 ...

8hon 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 ...

aha.org14m

FDA Issues Guidance for Compounding Certain Drug Products in Response to IV Solutions Supply Disruption

The Food and Drug Administration (FDA) today released guidance that is effective immediately for compounding certain parenteral drug products in response to the effects of recent hurricanes, including ...

Medscape1h

FDA Approves Pfizer's Hympavzi for Hemophilia A, B

The monoclonal antibody is the first non-factor, once-weekly treatment approved in the United States for hemophilia B.

23hon 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 ...

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 ...

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 ...

MedPage Today22h

Elamipretide for Barth Syndrome Survives FDA Advisory Vote

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