The United States reported the highest number of new cases of high- and low-grade serous ovarian cancer (HGSOC and LGSOC) in ...

Take advantage of TipRanks Premium at 50% off! Unlock powerful investing tools, advanced data, and expert analyst insights to help you invest with confidence. Verastem ( (VSTM)) has provided an update ...

Bildyos is supplied as a 60 mg/mL single-dose prefilled syringe and single-dose vial. Bilprevda is supplied as a 120 mg/1.7 mL single-dose vial. The US Food and Drug Administration (FDA) has approved ...

Bildyos is supplied as a 60mg/mL single-dose prefilled syringe and single-dose vial; Bilprevda is supplied as a 120mg/1.7mL single-dose vial. Bilprevda is indicated to prevent skeletal-related events ...

The US Food and Drug Administration has created a "green list" import alert to stop unapproved and unverified glucagon-like peptide 1 (GLP-1) drug ingredients from entering the United States.

On July 17, 2025, the FDA approved fluralaner oral solution (Exzolt; MSD Animal Health) for the treatment and control of Ornithonyssus sylviarum, also known as northern fowl mites, in laying hens and ...

Patients are advised to get a prescription from their doctor and to fill the prescription at a licensed pharmacy or use the FDA's BeSafeRx campaign to determine where to safely buy medications online.

(Reuters) - The U.S. Food and Drug Administration plans to fast-track reviews of four tobacco firms' nicotine pouches in a pilot program launching on Monday, amid pressure from the Trump ...

(This Sept. 8 story has been corrected to add the missing words 'from the risks' to the FDA statement, in paragraph 7) (Reuters) - The U.S. Food and Drug Administration plans to fast-track reviews of ...

Olomorasib combined with Keytruda targets KRAS G12C-mutant NSCLC, receiving FDA Breakthrough Therapy designation for its promising efficacy in early trials. The designation is based on LOXO-RAS-20001 ...