HANSOH PHARMA's Aumseqa® Receives EU Marketing Authorization as Monotherapy

Stock News
Feb 20

HANSOH PHARMA (03692) announced that on February 12, 2026, the group's innovative drug Aumseqa® (Chinese brand name: Ameile®, overseas brand name: Aumseqa®) has been approved for marketing in the European Union as a monotherapy. The approval covers its use for: (i) the first-line treatment of adult patients with advanced non-small cell lung cancer (NSCLC) harboring epidermal growth factor receptor (EGFR) exon 19 deletions or exon 21 (L858R) substitution mutations, and (ii) the treatment of adult patients with advanced EGFR T790M mutation-positive NSCLC. This approval was granted by the European Commission (EC) based on a positive opinion from the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA).

Disclaimer: Investing carries risk. This is not financial advice. The above content should not be regarded as an offer, recommendation, or solicitation on acquiring or disposing of any financial products, any associated discussions, comments, or posts by author or other users should not be considered as such either. It is solely for general information purpose only, which does not consider your own investment objectives, financial situations or needs. TTM assumes no responsibility or warranty for the accuracy and completeness of the information, investors should do their own research and may seek professional advice before investing.

Most Discussed

  1. 1
     
     
     
     
  2. 2
     
     
     
     
  3. 3
     
     
     
     
  4. 4
     
     
     
     
  5. 5
     
     
     
     
  6. 6
     
     
     
     
  7. 7
     
     
     
     
  8. 8
     
     
     
     
  9. 9
     
     
     
     
  10. 10