HANSOH PHARMA (03692): Application for a market authorization of Dasatinib Mesylate Tablets accepted by the National Medical Products Administration.

date
20:27 27/02/2026
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GMT Eight
Hans Pharmaceuticals (03692) announced that on February 27, 2026, the group's new drug, sulfamethoxazole Damiertinib tablets in combination with sulfamethoxazole Amitenib tablets (Amelex), has been accepted for a new drug application (NDA) by the China National Medical Products Administration (NMPA). It is used to treat locally advanced or metastatic non-small cell lung cancer (NSCLC) patients with epidermal growth factor receptor (EGFR) gene mutation positive and EGFR tyrosine kinase inhibitor (TKI) therapy failure who also have mesenchymal-epithelial transition factor (MET) amplification. Sulfamethoxazole Damieratinib tablet (HS-10241) is an orally administered highly selective c-MET TKI independently developed by the group.
Hansoh Pharma (03692) announced that on February 27, 2026, the Group's new drug Methadimide Mesylate Tablets in combination with Amebimide Mesylate Tablets (Amelox) has received acceptance for the New Drug Application (NDA) from the National Medical Products Administration (NMPA) of China. This medication is intended for the treatment of locally advanced or metastatic non-small cell lung cancer (NSCLC) patients with positive epidermal growth factor receptor (EGFR) gene mutations who have failed treatment with EGFR tyrosine kinase inhibitors (TKIs) and have c-MET amplification. Methadimide Mesylate Tablets (HS-10241) is an orally administered, group-developed highly selective c-MET TKI.