Oragenics Secures $16.5M in Funding, Plans Q3 2025 Trials for Concussion Treatment
PorAinvest
martes, 12 de agosto de 2025, 3:55 pm ET1 min de lectura
OGEN--
The funding will enable Oragenics to accelerate the clinical development of ONP-002, with the aim of becoming the first FDA-approved pharmacological treatment for concussion. The company has secured significant milestones in the second quarter of 2025, including Human Research Ethics Committee (HREC) approval in Australia, appointment of a Clinical Research Organization (CRO), and finalization of a cGMP manufacturing agreement with Sterling Pharma Solutions. These achievements position Oragenics to maintain a competitive edge in the rapidly growing intranasal neurotrauma space [1].
Oragenics aims to capitalize on the $8.9 billion global concussion market, which is projected to reach by 2027. The company's proprietary intranasal delivery system offers targeted, non-invasive drug administration directly to the brain, bypassing systemic circulation and reducing side effects. This technology has the potential to extend beyond concussion treatment to acute neurological emergencies and chronic neurodegenerative diseases [1].
The recent capital raise reflects growing investor confidence in Oragenics' transformational approach to neurotrauma treatment. The company plans to use the funds to accelerate clinical development, advance platform technology, strengthen manufacturing and regulatory capabilities, and support operational excellence and working capital needs [1].
References:
[1] https://www.quiverquant.com/news/Oragenics%2C+Inc.+Reports+Progress+on+Intranasal+Concussion+Treatment+ONP-002+and+Q2+2025+Milestones
STRL--
Oragenics raised $16.5 million in funding and plans to begin Phase IIa trials for its concussion treatment candidate, ONP-002, in Q3 2025. The company aims to enter the $8.9 billion global concussion market by 2027 and become the first FDA-approved pharmacological treatment for concussion. Oragenics has secured HREC approval in Australia, appointed a CRO, and finalized a cGMP manufacturing agreement to support clinical trials.
SARASOTA, Fla. - Oragenics, Inc. (NYSE American: OGEN) has raised $16.5 million in funding through a Series H Convertible Preferred Stock and Warrants offering. This capital infusion will support the company's lead candidate, ONP-002, a revolutionary intranasal treatment for concussion, as it prepares to enter Phase IIa trials in the third quarter of 2025 [1].The funding will enable Oragenics to accelerate the clinical development of ONP-002, with the aim of becoming the first FDA-approved pharmacological treatment for concussion. The company has secured significant milestones in the second quarter of 2025, including Human Research Ethics Committee (HREC) approval in Australia, appointment of a Clinical Research Organization (CRO), and finalization of a cGMP manufacturing agreement with Sterling Pharma Solutions. These achievements position Oragenics to maintain a competitive edge in the rapidly growing intranasal neurotrauma space [1].
Oragenics aims to capitalize on the $8.9 billion global concussion market, which is projected to reach by 2027. The company's proprietary intranasal delivery system offers targeted, non-invasive drug administration directly to the brain, bypassing systemic circulation and reducing side effects. This technology has the potential to extend beyond concussion treatment to acute neurological emergencies and chronic neurodegenerative diseases [1].
The recent capital raise reflects growing investor confidence in Oragenics' transformational approach to neurotrauma treatment. The company plans to use the funds to accelerate clinical development, advance platform technology, strengthen manufacturing and regulatory capabilities, and support operational excellence and working capital needs [1].
References:
[1] https://www.quiverquant.com/news/Oragenics%2C+Inc.+Reports+Progress+on+Intranasal+Concussion+Treatment+ONP-002+and+Q2+2025+Milestones

Divulgación editorial y transparencia de la IA: Ainvest News utiliza tecnología avanzada de Modelos de Lenguaje Largo (LLM) para sintetizar y analizar datos de mercado en tiempo real. Para garantizar los más altos estándares de integridad, cada artículo se somete a un riguroso proceso de verificación con participación humana.
Mientras la IA asiste en el procesamiento de datos y la redacción inicial, un miembro editorial profesional de Ainvest revisa, verifica y aprueba de forma independiente todo el contenido para garantizar su precisión y cumplimiento con los estándares editoriales de Ainvest Fintech Inc. Esta supervisión humana está diseñada para mitigar las alucinaciones de la IA y garantizar el contexto financiero.
Advertencia sobre inversiones: Este contenido se proporciona únicamente con fines informativos y no constituye asesoramiento profesional de inversión, legal o financiero. Los mercados conllevan riesgos inherentes. Se recomienda a los usuarios que realicen una investigación independiente o consulten a un asesor financiero certificado antes de tomar cualquier decisión. Ainvest Fintech Inc. se exime de toda responsabilidad por las acciones tomadas con base en esta información. ¿Encontró un error? Reportar un problema

Comentarios
Aún no hay comentarios