Instant Report

Date: 04-Nov-2020

US FDA Approves TaiGens IND For TG-1000 To Treat Influenza A And B

TaiGen Biotechnology Company, Limited (TaiGen), a leading research-based and market-driven biotechnology company, announced that US Food and Drug Administration (FDA) has approved the Investigation New Drug (IND) application for TG-1000, a novel treatment for influenza A and B.

TG-1000 is a novel pan-influenza antiviral, which interrupts viral replication and transmission via a cap-snatching mechanism and is able to do this effectively against influenza-A, influenza-B, avian flu H7N9, and Tamiflu-resistant viruses. The first US patent for TG-1000 was successfully prosecuted and granted by the United States Patent and Trademark Office on Jan 14th, 2020.

Kuo-Lung Huang, the chairman and CEO of TaiGen notes, “Influenza is a life threatening disease with significant unmet medical needs and high medical burden. With the IND approval in place, we are ready and eager to extend the clinical study of TG-1000 to the US in the near future.”

According to Global Data, the global market for influenza antivirals reached US$ 2.34 billion in 2019 and is estimated to reach US$ 5.03 billion by 2026 at a CAGR of 11.5%. Currently the market is comprised primarily of the neuraminidase inhibitor oseltamivir and the newly developed endonuclease inhibitor baloxavir. With the recent introduction of baloxavir into the market, institutional investment analysts expect the market share of endonuclease inhibitors to increase at the expense of neuraminidase inhibitors. TaiGen’s TG-1000 is poised to take full advantage of this development.

TaiGen Biotechnology is a leading research-based and market-driven biotechnology company in Taiwan with a wholly-owned subsidiary in Beijing, China.