Mumbai: Unichem Labs has received five observations from the United States Food and Drug Administration (USFDA) at the ...
Health campaigners have written to U.S. regulators accusing Philip Morris International of misrepresenting past regulatory decisions, seeking to disrupt the launch of its flagship heated tobacco ...
Zai Lab Limited (ZLAB) and argenx (ARGX) announced that China's National Medical Products Administration or NMPA approved the Biologics License Application or BLA for efgartigimod alfa injection ...
VYVGART (efgartigimod alfa injection) is a human IgG1 antibody fragment that binds to the neonatal Fc reeptor (FcRn), resulting in the reduction of circulating IgG autoantibodies. It is the first ...
Researchers found that adherence and persistence in T2D patients using oral semaglutide is similar to DPP-4i, but semaglutide ...
Amsterdam, the Netherlands— argenx SE (Euronext & Nasdaq: ARGX) and Zai Lab Limited (Nasdaq: ZLAB; HKEX: 9688) today announced that China’s National Medical Products Administration (NMPA) approved the ...
That’s how experts describe the impact on health care of the U.S. Supreme Court’s recent decision in Loper Bright Enterprises v. Raimondo. That ruling overturned a decades-old ...
At least 58 people in at least 27 states have developed severe illness after consuming Diamond Shruumz products, including ...
VYVGART (efgartigimod alfa injection) (efgartigimod IV) is a human IgG1 antibody fragment that binds to the neonatal Fc receptor (FcRn), resulting in the reduction of circulating IgG autoantibodies.
(RTTNews) - Kyverna Therapeutics Inc. (KYTX) announced that its autologous, fully human CD19 chimeric antigen receptor or CAR T-cell product candidate, KYV-101, has been designated as a Regenerative ...
Stay informed to stay well when you get the FREE The Healthy by Reader's Digest daily email  What is a recall? A product ...
(RTTNews) - Eton Pharmaceuticals Inc's (ETON) New Drug Application or NDA for ET-400, a proprietary patented formulation of hydrocortisone oral solution, has been accepted by the U.S. Food and Drug ...