For the first time, scientists say, they have evidence that using a biologic drug to remove sticky beta amyloid plaques from ...
FDA accepts Capricor's Biologics License Application for priority review, advancing deramiocel for DMD cardiomyopathy.
On March 19, the Food and Drug Administration granted traditional approval to pembrolizumab, or Keytruda, marketed by Merck (MRK), with ...
Rogaine was approved by the Food and Drug Administration in 1988, the first drug to win the agency’s endorsement for male ...
The company behind the drug, Sarepta Therapeutics, said that the patient suffered acute liver injury, a known side effect, The Associated Press reported. However, the "severity" of this case had not ...
The future of American drug innovation is threatened by US regulations that permit knockoff versions of new drugs to be sold to US consumers.
The exorbitant costs of drugs like Wegovy — especially compared to other countries — have prompted some insurers to tighten ...
ILUVIEN now approved for the treatment of chronic non-infectious uveitis affecting the posterior segment of the eye (NIU-PS) in addition to ...
I was not aware of it, and I should have been.”After a rise in complaints, in 2020 the FDA required drug manufacturers to add ...
The FDA approved a prefilled syringe format for Ani's purified Cortrophin Gel that should ease administration for MS patients ...
Treatments for dry eye disease, neuroendocrine tumors, chronic spontaneous urticaria, Barth syndrome, and migraine are under review.
Dima Hendricks has sickle cell disease, which is currently managed by an old medication, but she is hoping to take part in a ...
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