Oragenics (NYSE American: OGEN) provided a shareholder update outlining progress in its Phase IIa clinical trial of ONP-002 for concussion and mild traumatic brain injury in Australia, with active patient enrollment and dosing underway across multiple sites, while advancing U.S. regulatory preparations targeting a Type C FDA meeting request in the second quarter and IND submission by year-end 2026. The company also disclosed a letter of intent to pursue licensing of a complementary CNS-related medical device and reported a March 31, 2026, cash balance of $6.1 million.
To view the full press release, visit https://ibn.fm/tEk2C
About Oragenics, Inc.
Oragenics, Inc. is a clinical-stage biotechnology company developing brain-targeted therapeutics through proprietary intranasal delivery technology. The Company is working on advancing its lead candidate, ONP-002, as a potential first-in-class treatment for concussion and mild traumatic brain injury. Oragenics is working on commencing clinical trials in Australia for ONP-002 , with U.S. Phase 2b trials planned to follow. The Company’s intranasal delivery platform has potential applications across multiple neurological conditions, including Parkinson’s disease, Alzheimer’s disease, PTSD, and anxiety disorders. Oragenics is committed to developing innovative therapies that address significant unmet medical needs in neurological care. For more information, visit oragenics.com.
NOTE TO INVESTORS: The latest news and updates relating to OGEN are available in the company’s newsroom at https://ibn.fm/OGEN
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