(Reuters) -Rocket Pharmaceuticals said on Wednesday that the U.S. Food and Drug Administration has lifted the clinical hold on a mid-stage trial of its gene therapy, less than three months after it was halted due to a patient's death.

The Food and Drug Administration has authorized emergency use of animal drugs to treat and prevent infestations of the New World Screwworm, which poses an emerging threat to U.S. livestock and food security.

The FDA has approved Sisnos’s continuous glucose monitoring (CGM) system for consumer use beyond diabetes management, including weight management support.

But an FDA panel recently attacked SSRI’s – a class of antidepressant drugs – and their use during pregnancy. Some doctors say the panel is spreading misinformation about the drugs. L.A. Times science and medicine reporter Corinne Purtill joined Lisa McRee to explain.

NSCLC represents 80% of lung cancer cases and is the leading cause of cancer-related mortality globally. This designation is intended for patients with EGFR exon 19 deletions or e

The U.S. Food and Drug Administration has denied approval for PTC Therapeutics' oral medication for a rare genetic disorder with limited treatment options, the company said on Tuesday.

Sunscreen products marketed in mousse- or whipped cream-like formulations have not been tested to meet regulatory requirements.

A California company has created a first-of-its-kind eyedrop that corrects a certain type of vision impairment and could allow many Americans to ditch their corrective eyewear.