First-ever rapid-acting insulin. This approval extends to a 3-milliliter single-patient-use prefilled pen and a 10-milliliter ...

Alvotech and Teva Pharmaceuticals announced the US Food and Drug Administration (FDA) has accepted for review a Biologics ...

The Trump administration is tearing down both regulations and the federal government that enforces them. The consequences will be enormous.

Gilead Sciences has won Food and Drug Administration priority review for its proposed lenacapavir twice-yearly shot to prevent HIV. Gilead on Tuesday said an FDA green light would make lenacapavir the ...

In addition to AVT06, which is a biosimilar candidate for Eylea ® (aflibercept) 2 mg, Alvotech is currently also developing AVT29, a biosimilar candidate for Eylea ® HD (aflibercept) 8 mg. Teva also ...

The discovery of this hormone paved the way for Ozempic, making the Gila monster an enormously profitable gift to modern ...

Samsung Bioepis Co., Ltd. today announced that the U.S. Food and Drug Administration (FDA) has approved the Biologics License Application (BLA) for OS ...

Outlook Therapeutics, Inc. (Nasdaq: OTLK), a biopharmaceutical company that achieved regulatory approval in the European Union (EU) and the United Kingdom (UK) for the first authorized use of an ...

Arizona’s Family Investigates found providers high on the job, two of them prescribing hundreds of opioids. Most of them are ...

These five tips from board-certified dermatologists tell you which type of sunscreen to use, how to apply it correctly, and when to reapply: Choose a sunscreen that has an SPF of 30 or higher, is ...

The study will enroll an initial cohort of six end-stage renal disease (ESRD) patients, expanding to up to 50 participants, and is intended to support a Biologics License Application (BLA) with the ...

The removal of the mandatory drug and neuropsychological testing applies exclusively in the application of the Philippine National Police (PNP) personnel of a new or renewal of license to own and ...