Clear descriptions of potential risks and side effects will be required under rules that go into effect Nov. 20, even as the ...
The Mental Health Watchdog calls for reforms to protect public safety, citing decades of antidepressant, electroshock, and psychedelic drug risks.
The U.S. Food and Drug Administration (FDA) on Thursday approved the first new drug to treat people with ...
President-elect Donald Trump has named Robert F. Kennedy Jr. as his choice for the next secretary of the Department of Health ...
Executives and directors of Agenus Inc. misled the public about the results of clinical trials for the biotech’s cancer ...
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Oct 17 - The U.S. Food and Drug Administration has approved Avadel ... approved for the same condition as Lumryz, Xywav has the FDA's expanded nod to treat idiopathic hypersomnia, a rare ...
Research that was carried out by Baylor College of Medicine and Texas Children’s Hospital doctors have led to the U.S. Food ...
today announced that the U.S. Food and Drug Administration (FDA) has granted Rare Pediatric Disease designation to Papillon’s PPL-001, an experimental treatment for Friedreich's ataxia.
Set to become compulsory Nov. 20, the regulation isn't likely to make pharma ads easier for consumers to comprehend, but ...