Veru Inc. reported its fiscal 2022 fourth quarter and full year financial results. The company is preparing for commercialization of sabizabulin, while also working to regenerate FC2 product sales.
U.S. FDA reviewing EUA application for sabizabulin to treat hospitalized COVID-19 patients at high risk for ARDS
European Medicines Agency’s (EMA) Emergency Task Force reviewing sabizabulin for emergency use in EU member states
Sabizabulin also under review for potential emergency authorization by MHRA (UK), TGA (Australia), and Health Canada
Veru preparing for U.S. and international commercialization and distribution of sabizabulin, and manufacturing capacity for drug supply in place
The statements in the release that are not historical facts are forward-looking statements which are based on the Company’s current expectations and subject to risks and uncertainties that may cause actual results to differ materially.