The FDA’s approval of Arexvy for individuals aged 50-59 addresses a critical need in preventing severe respiratory ...
The Food and Drug Administration expanded the approval of GSK's respiratory syncytial virus vaccine to adults ages 50 to 59 ...
The FDA has approved GSK’s Arexvy shot for the prevention of lower respiratory tract disease caused by RSV in individuals 60 years of age and older, shortly after it was recommended for ...
If approved, the co-administration of Arexvy and Shingrix could provide a more convenient vaccination regimen for patients ...
The FDA's approval was based on three studies involving over 1,000 patients with moderate-to-severe eczema who were ...
Sanofi said the Food and Drug Administration has approved Sarclisa as a first line combined treatment option for adult patients with newly diagnosed multiple myeloma who aren't eligible for autologous ...
Zevra Therapeutics Inc. (ZVRA) made headlines yesterday with a landmark FDA approval for its innovative drug, MIPLYFFA, in the ...
The U.S. Food and Drug Administration has authorized the first-ever over-the-counter hearing aid software intended to be used ...