When doctors began using the drug sotorasib in 2021 with high expectations for its innovative approach to attacking lung ...
Ahead of the FDA’s June target action date for Sarepta’s Duchenne muscular dystrophy gene therapy, ICER Chief Medical Officer David Rind blasted the regulator’s accelerated pathway in a JAMA viewpoint ...
Hundreds of dog and cat owners are complaining that their pet food is making their pets sick, some even dying.
There are four commercially available FDA-approved prescription antiviral treatment drugs recommended for influenza that are ...
In the first 2 years of the COVID-19 pandemic, shortages of 11% of generic active pharmaceutical ingredients (APIs) made by ...
On April 29, 2024, the US Food and Drug Administration (FDA ... review requirements for high-risk tests (i.e., tests subject to premarket approval requirements). FDA will continue to exercise ...
Federal regulators are challenging patents on 20 brand-name drugs, including the blockbuster weight-loss injection Ozempic, ...
Makers of medical tests that have long escaped government oversight will have about four years to show that their new ...
The US Food and Drug Administration has approved pivmecillinam (Pivya) tablets to treat uncomplicated urinary tract ...
(Reuters) -The U.S. health regulator approved on Monday ImmunityBio's combination ... Last year, the U.S. Food and Drug ...
A novel therapy for treating fear and anxiety in felines has been commercially launched. Pregabalin oral solution (Bonqat; Zoetis) is now available to veterinary clinics throughout the US and can be ...
The US FDA approval of Zeffdiffra and the global strategic partnerships between innovators are driving the development of drugs for MASH (1 Trusted Source MASH was earlier referred to as ...