The FDA has given another warm embrace to a biosimilar application – this time for Novartis AG unit Sandoz Inc.'s version of Amgen Inc.'s Enbrel (etanercept), a tumor necrosis factor blocker that first entered the US market in 1998.
In briefing documents released ahead of a July 13 meeting of the FDA's Arthritis Advisory Committee, regulators declared that Sandoz's data demonstrated its biosimilar, which currently goes under the moniker GP2015 while it's awaiting a trade name, was "highly similar" to
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Scrip for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?