Cytocom, Inc., a biopharmaceutical company creating next-gen immune therapies, received clearance from the U.S. FDA for its IND application for a Phase 2 trial to evaluate the safety and efficacy of CYTO-205 as a treatment to slow or halt the progression of SARS-CoV-2, the virus that causes COVID-19. CYTO-205 is designed to modulate immune system function, decrease elevated inflammatory responses associated with viral infection and inhibit viral replication in human lung cells.   The trial wil...