The U.S. Food and Drug Administration (FDA) approved Journavx (suzetrigine) oral tablets on Thursday as a first-in-class ...
Vertex Pharmaceuticals Incorporated (Nasdaq: VRTX) today announced that the U.S. Food and Drug Administration (FDA) has approved JOURNAVXâ„¢ (suzetrigin ...
The Food and Drug Administration on Thursday approved a new type of nonopioid painkiller from Vertex Pharmaceuticals, NBC ...
The Vertex drug is a milestone after a long history of unsuccessful efforts to develop painkillers without the addictive ...
AstraZeneca’s Voydeya has become the first oral Factor D inhibitor to be approved by the FDA as a treatment for the rare disease paroxysmal nocturnal haemoglobinuria (PNH). Voydeya (danicopan ...
so there’s a clear need for new treatment options. The FDA approval is based on the APPLY-PNH and APPOINT-PNH trials, which showed that the drug was able to achieve “clinically meaningful ...
The Swiss drugmaker said the results add to the body of evidence showing the drug is safe and effective for adults with PNH. Fabhalta was approved by the FDA in 2023 for the treatment of adults ...