Athenex, Inc. today announced that it recently participated in a constructive meeting with the U.S. Food and Drug Administration (FDA) as scheduled, to discuss the clinical section of the New Drug Application (NDA) for oral paclitaxel and encequidar for the treatment of metastatic breast cancer. The Company is on track to submit the NDA in accordance with the FDA's guidance, and will provide a further update when the FDA’s official response to the filing becomes available.
View the full press release here: https://ir.athenex.com/news-releases/news-release-details/athenex-provides-update-oral-paclitaxel-fda-meeting