Introgen Therapeutics Inc. has applied to the U.S. Food and Drug Administration (FDA) for priority review of Advexin p53 for the treatment of recurrent head and neck cancer.
Advexin combines the p53 tumor suppressor with a non-replicating, non-integrating adenoviral delivery system.
Application for priority review is based on results from Phase II and Phase III trials evaluating Advexin in the treatment of recurrent, end-stage, squamous-cell head and neck cancer.
Liquid Biopsies Replacing Tissue-based Tests and Improving Treatment
Liquid biopsies improve access to treatment options for many cancers and may replacing tissue tests & diagnostic imaging