Vasomune Therapeutics Receives U.S. FDA Fast Track Designation for AV-001

Vasomune Therapeutics, Inc., recently announced that the U.S. Food and Drug Administration (FDA) granted Fast Track designation for AV-001 for the prevention or treatment of moderate-to-severe ARDS in patients hospitalized with viral and/or bacterial respiratory infections. AV-001 is a first-in-class fully synthetic PEGylated peptide targeting the Tie2 receptor which plays a critical role in vascular stability, barrier integrity and endothelial quiescence, particularly within the pulmonary space.

Vasomune Therapeutics is an OBIO® member, an alumnus of our CAAP® program, and presented at the OBIO® Investment Summit.

Previous
Previous

Esprit-ai, Perley Health and OBIO® partner on a ground-breaking project to Support High Quality Dementia Care in long-term care homes

Next
Next

Oncoustics Awarded INOVAIT Focus Fund to Accelerate AI-Driven Liver Diagnostics at Point of Care