Days ago Novartis posted a brief note on positive 16-week data about Cosentyx’s effects on non-radiographic axial spondyloarthritis, opening the door to an EMA submission in the indication. Now the pharma giant says it has the 52-week win needed to take to FDA regulators, too.
privacy policy | terms of use | contact us | advertise | pharma jobs | pharma blogs | facebook | twitter
Copyright © 2024,