FDA greenlights the unique combination of enfortumab vedotin (PADCEV®) and pembrolizumab (KEYTRUDA®), marking the first coalescence of an ADC and PD-1 inhibitor to combat progressive bladder carcinoma.
Federal regulations require that applicable clinical trials and NIH-funded clinical trials be registered no later than 21 days after enrollment of the first participant.
CSL, a major biotech player, announced that the FDA has accepted its application for the once-monthly hereditary angioedema preventative drug, garadacimab (CSL312).
Mucoadhesive drug delivery systems (MDDS) are designed to enhance the residence time of a drug at a specific site in the body, primarily on mucosal surfaces.
Suzhou Ribo Life Science recently inked a deal with Qilu Pharmaceutical, granting them rights to develop, produce, and market PCSK9 inhibitor drug RBD7022 (SR043) in Greater China.