- Tonix reported that the first participant was dosed in a Phase 1 investigator-initiated pharmacodynamic study of TNX-1900, an intranasal potentiated oxytocin drug-device combination being evaluated for potential use in migraine and craniofacial pain.
- The study will assess trigeminal nerve-mediated forehead vasodilation by measuring skin blood flow responses to capsaicin and electrical stimulation using Laser Speckle Contrast Imaging.
- No clinical results were presented, and the company said results from the study will be used to guide future development of TNX-1900.
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. Tonix Pharmaceuticals Holding Corp. published the original content used to generate this news brief via EDGAR, the Electronic Data Gathering, Analysis, and Retrieval system operated by the U.S. Securities and Exchange Commission (Ref. ID: 0001999371-26-006915), on March 26, 2026, and is solely responsible for the information contained therein.
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