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).