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FDA Approves Injection to Prevent HIV

FDA approves first twice-yearly injection that prevents HIV infection

The U.S. Food and Drug Administration (FDA) approved a new, twice-yearly shot — the first and only of its kind — to prevent HIV, the creator of the drug, Gilead Sciences, announced on Wednesday.Sold under the name Yeztugo,

CBS News on MSN · 16h

HIV prevention drug lenacapavir approved by FDA as twice-yearly injection

Clinical trials showed 99.9% of participants who received the drug, called Yeztugo from company Gilead Sciences, remained HIV negative.

Gizmodo · 15h

FDA Approves ‘Breakthough’ Drug to Prevent HIV

In clinical trials, researchers found Yeztugo to be highly effective as a twice-yearly form of pre-exposure prophylaxis.

FDA Announces New Vouchers to Cut Drug Reviews to 2 Months

The Baltimore Sun · 16h

FDA announces sweeping changes to speed up the drug review process

An FDA pilot program, known as the Commissioner’s Priority Voucher program, could drastically change the way pharmaceutical drugs reach the public and significantly cut down the time in

The Associated Press on MSN · 1d

FDA to offer faster drug reviews to companies promoting 'national priorities'

The Food and Drug Administration says it will begin offering faster reviews to new medicines that align with Trump administration priorities for Americans’ health

Bloomberg on MSN · 1d

FDA Announces New Vouchers to Cut Drug Reviews to Two Months

The US Food and Drug Administration announced a new national priority voucher plan that aims to cut drug review times to one to two months for companies it says are backing national interests.

STAT1d

FDA announces a new priority review program in bid to further administration goals

The FDA is launching a program to reward companies with accelerated drug review and speedy agency feedback, if their actions ...

MIT Technology Review6d

Here’s what food and drug regulation might look like under the Trump administration

Leaders of the FDA have published a list of new priorities for the agency. They want to deliver rapidly-approved cures and ...

17h

FDA’s removal of Ozempic, Wegovy from drug shortage list upheld

A federal judge on Wednesday ruled that the Food and Drug Administration’s (FDA) decision to remove popular GLP-1s from its drug shortage list, ending the sale of compounded versions of the ...

STAT23h

Vinay Prasad named chief medical and science officer at FDA

Vinay Prasad is taking on several big roles at the FDA, solidifying his position as a top adviser to Commissioner Marty ...

1don MSN

ProPublica Sued the FDA for Withholding Records About the Safety of Generic Drugs

The agency declined to quickly release documents that would identify drugs made at some of the most troubled foreign ...

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