TaiRx, Inc. (6580.TWO) develops and commercializes therapeutics primarily for cancer treatment and other diseases including inflammatory bowel conditions; core products and pipeline candidates include CVM-1118 (Foslinanib), an oral anti-cancer drug in Phase II clinical trials that received U.S. FDA Orphan Drug Designation for pancreatic neuroendocrine tumors (PNETs) in January 2025 granting seven years of market exclusivity upon approval; Zelnite, the only TFDA-approved selenium injection in Taiwan for treating selenium deficiency with high-dosage labeling updated and expanded in 2024; TRX-920, an oral delivery formulation of SN-38 for colon cancer; TRX-105, a preclinical molecule for colitis and inflammatory bowel disease symptoms; TRX-ADC, an antibody-drug conjugate with novel payload for cancer; TRX-NOC and TRX-711, additional investigational oncology assets; and nodal diagnostic devices plus antibody drugs. Founded in 2011 and headquartered at 6F-1, No. 66, San-Chung Road, Nankang District, Taipei City 115602, Taiwan, the company operates in the biotechnology sector targeting oncology and supportive care markets with products sold domestically through distributors and clinical programs advancing globally. Recent developments encompass CVM-1118's Orphan Drug Designation in 2025 and Zelnite label expansion in 2024; earlier efforts include a 2022 manufacturing partnership with Bora Pharmaceuticals for CVM-1118 Phase II trials and the 2018 formation of TaiRx US joint venture with BioHealth Innovation for nodal protein therapeutics and diagnostics.