The U.S. Food and Drug Administration (FDA) has approved Orgovyx (relugolix), an oral form of hormone therapy by Myovant Sciences, to treat adults with advanced prostate cancer. The approval, granted under priority review, was based on data from the HERO Phase 3 trial (NCT03085095), in which Orgovyx significantly increased the proportion of patients with sustained reductions in testosterone levels over nearly one year, compared with standard-of-care leuprolide acetate. Treatment also lowered the risk of major cardiovascular…
You must be logged in to read/download the full post.
The post FDA Approves Orgovyx, Oral ADT for Advanced Prostate Cancer appeared first on BioNewsFeeds.