CHMP backs Novartis's Zykadia for first-line use in lung cancer
Novartis's push to win approval for Zykadia as an initial treatment for a type of lung cancer got a lift on Friday with a positive recommendation from the European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP).
Zykadia is vying with Roche's Alecensa to become a first-line treatment for anaplastic lymphoma kinase (ALK)-positive lung cancer. Pfizer's Xalkori, with $561 million in 2016 sales, has approval in that setting.
In April, a Roche study showed Alecensa kept people alive longer without their disease progressing than Xalkori. Analysts have said that could give Roche an edge over Novartis, which has compared its drug to chemotherapy.
The CHMP nod for Zykadia will now be reviewed by the European Commission.
(Reporting by John Miller; Editing by Michael Shields)
Disclaimer: This site is primarily intended for healthcare professionals. Any content/information on this website does not replace the advice of medical and/or health professionals and should not be construed as medical/diagnostic advice/endorsement or prescription. Use of this site is subject to our terms of use, privacy policy, advertisement policy. © 2020 Minerva Medical Treatment Pvt Ltd