AZ And Merck Notch Another Win For Koselugo In Adults With NF1

The MEK inhibitor, already approved for pediatric patients with the rare condition neurofibromatosis type 1, showed benefits for adults in a Phase III trial.

(Shutterstock)
Key Takeaways
  • Koselugo showed a benefit in adult patients with the rare condition neurofibromatosis type 1 (NF1) in a Phase III trial.
  • The data position AstraZeneca and Merck to expand the MEK inhibitor into a larger patient population. The drug is approved for pediatric NF1 patients, but there are no treatments for adults. 
  • Koselugo generated $366m in sales during the first nine months of 2024, growing 49% from last year.

AstraZeneca and Merck & Co

Koselugo was approved by the US Food and Drug Administration in 2020 and

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 Clinical Trials

More from Rare Diseases