The National Medical Products Administration conditionally approves Sevatinib tablets for market launch

Recently, the National Medical Products Administration approved, through a priority review process and with conditional approval, the listing of Bayer HealthCare Pharmaceuticals Inc.'s new Class 1 innovative drug Sevatinib Tablets (brand name: Hexinno). This medication is indicated for the treatment of adult patients with unresectable locally advanced or metastatic non-small cell lung cancer (NSCLC) who have HER2 (ERBB2) activating mutations and have previously received at least one systemic therapy. The approval of this drug provides patients with a new treatment option. (National Medical Products Administration)

View Original
This page may contain third-party content, which is provided for information purposes only (not representations/warranties) and should not be considered as an endorsement of its views by Gate, nor as financial or professional advice. See Disclaimer for details.
  • Reward
  • Comment
  • Repost
  • Share
Comment
Add a comment
Add a comment
No comments
  • Pin