FDA Assigns Priority Review for Elacestrant in Metastatic Breast CancerAugust 11th 2022
If approved, elacestrant would be the first oral selective estrogen receptor degrader (SERD) as a second- or third-line treatment for patients with ER+/HER2- advanced or metastatic breast cancer. The PDUFA date is Feb. 17, 2023.
FDA Accepts BLA for Immunotherapy for Bladder CancerJuly 29th 2022
If approved, N-803 — with the brand name Anktiva — plus the Bacillus Calmette-Guérin vaccine would be the first immunotherapy combination for this indication in 23 years. The Prescription Drug User Fee Act target action date is May 23, 2023.