Enbrel Biosimilar Market In Sandoz's Grasp; Will Cost, Litigation Derail It?

With the FDA giving an overwhelmingly positive review of Sandoz Inc.'s application for its biosimilar version of Enbrel (etanercept), which is sold in the US by Amgen Inc., the product appears to be headed to the US market – pending a likely blessing from the agency's advisory panel, which is meeting on July 13. But Sandoz must still get past litigation and convince prescribers and patients its etanercept biosimilar provides value over Enbrel.

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

More from Business

More from Scrip