RE: Short term SP not important9 Jan 2021 10:48
“ Investigational New Drug clearance and Expedited Regulatory Pathway granted from the FDA
Synairgen's Investigational New Drug (IND) application to the FDA to evaluate SNG001 as a treatment for patients with COVID-19, has been cleared, enabling Synairgen to initiate its SG018 trial in the US. Furthermore, the FDA has awarded SNG001 Fast Track status, enhancing the ability of Synairgen to interact with the FDA and shortening review timelines“