Polyrizon Submits FDA Pre-Request for Designation for PL-16 Nasal Spray

Reuters
Jan 02
Polyrizon Submits FDA Pre-Request for Designation for PL-16 Nasal Spray

Polyrizon Ltd. has announced the submission of a Pre-Request for Designation to the U.S. FDA for its PL-16 Viral Blocker, a hydrogel nasal spray designed to reduce exposure to respiratory viruses such as influenza and the common cold. This regulatory step could pave the way for PL-16 to achieve over-the-counter status, offering a non-pharmaceutical, physical barrier against viral infections. No grant or funding involving Polyrizon Ltd. or other beneficiary organizations is mentioned.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Polyrizon Ltd. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9618985-en) on January 02, 2026, and is solely responsible for the information contained therein.

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