Loading...

Member Profile

Founded in 2001, TaiGen Biotechnology Co., Ltd. is a research-based and market-driven pharmaceutical company engaging in the development of novel therapeutics for infectious diseases. TaiGen has a wholly-owned Beijing subsidiary with proven capacities to conduct clinical trials and related registrations. TaiGen Biotechnology became a publicly listed company in Taipei Exchange (Ticker 4157.TWO) in January 2014.

TaiGen’s pipeline includes in-house discovered and developed new chemical entities: TG-1000, a novel antiviral for influenza, received China and US IND authorization in 2020. TaiGen successfully completed the unblinding of TG-1000 phase III clinical trial and filed New Drug Application (NDA) in mainland China in 2024. Taigexyn® capsule, a novel antibiotic, is the first NCEs developed by a Taiwanese company that received market approval and launched in mainland China and Taiwan. Taigexyn® intravenous formulation is also marketed in Taiwan and mainland China in 2020 & 2021 respectively, Taigexyn® IV becomes eligible for reimbursement in March as it passed the National Health Insurance Administration’s review and assessment on Feb 14 in Taiwan. Taigexyn is also granted three nationals prizes, SNQ, National Bio & Medicine Care Quality Award and National Innovation Award for Sustainability excellence. Taigexyn® is partnered in 35 countries worldwide. Licensed partners include GPCR for South Korea; R-Pharm for the Russian Federation and the Commonwealth of Independent States; Productos Científicos for Latin America; and Holding Distribution for distribution in Taiwan.


Product Pipelines

Please move your mouse cursor over abbreviations with periods to see their full names.

Company Milestones

   2014 TaiGen Biopharmaceuticals Holdings Ltd Publicly listed in Taipei Exchange (TPEx) since January 2014.
   2015 Received market approval of Nemonoxacin capsule from TFDA in January 2015.
   2016 Taigexyn® ( Nemonoxacin)capsule received CFDA market approval in June 2016 and launched in mainland China by Zhejiang Medicine Co. on October 23, 2016.
   2018 Taigexyn® intravenous and oral formulations successfully completed phase 3 clinical trial for community acquired pneumonia in Russia.
   2020 Received market approval of Nemonoxacin intravenous infusion from TFDA in October 2020.
   2021 Taigexyn® ( Nemonoxacin) intravenous infusion received NMPA market approval in June 2021
   2022 Taigexyn® ( Nemonoxacin) intravenous infusion became eligible for health insurance reimbursement price in March.
   2024 TaiGen successfully completed TG-1000 phase III trial and filed NDA in mainland China.