Via Nova Therapeutics Announces FDA clearance of Investigational New Drug (IND) application for VNT-101, a novel direct-acting antiviral against Influenza A virus
Excerpt from the Press Release:
OAKLAND, Calif., Sept. 21, 2023 /PRNewswire/ — Via Nova Therapeutics, Inc., a biotechnology company focused on discovering and developing therapeutics to treat viral infections with significant unmet medical need, today announced the clearance of its Investigational New Drug (IND) application from the U.S. Food and Drug Administration (FDA) for its Influenza A nucleoprotein inhibitor, VNT-101.
“We look forward to evaluating VNT-101 in the clinic,” said Don Ganem MD, Co-Founder and CEO of Via Nova Therapeutics. “This is an important step to developing a flu antiviral with a novel mechanism of action, and a milestone for Via Nova Therapeutics as we advance our first compound into the clinic.”
About the VNT-101 program
VNT-101 is a novel investigational small molecule being developed for treatment of seasonal influenza A infection. It is directed against a novel target, the influenza A nucleoprotein (NP).
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