Alex Smith joins Oxeia investor webinar on concussion therapy

Oxeia Biopharmaceuticals will hold a June 18 investor webinar with former NFL quarterback Alex Smith as it promotes OXE103, an investigational treatment for persistent post-concussion symptoms. The event comes as the company says the therapy could become the first FDA-approved drug designed specifically for concussion recovery. Why it matters: - Oxeia Biopharmaceuticals is pitching OXE103 as a potential new treatment for persistent post-concussion symptoms, a condition with no FDA-approved drug therapy. - The company is trying to draw investors ahead of its next development phase and highlight a possible path to a first-in-class concussion recovery drug. What happened: - Oxeia will host a live investor webinar on June 18, 2026, from 2:00 p.m. to 2:45 p.m. EDT. - The event will feature CEO Dr. Michael Wyand, Board Member and former NFL quarterback Alex Smith, and Co-Founder and trauma surgeon Dr. Vishal Bansal. - The company says the webinar will focus on OXE103 and what it believes could become the first FDA-approved drug specifically developed for concussion recovery. - Registration is available through the webinar link . The details: - Oxeia describes OXE103 as an investigational therapy for persistent post-concussion symptoms. - The company says its development package includes a licensing agreement for Daiichi Sankyo clinical data, with nine completed studies across multiple indications and four Phase 1 safety trials. - Daiichi Sankyo’s prior ghrelin studies enrolled more than 300 patients and generated human safety and tolerability data for ghrelin, the hormone behind OXE103. - The FDA has confirmed that no additional preclinical or safety studies are required before OXE103 can advance to Phase 2b, according to the company. - Oxeia says a Phase 2a pilot study produced an 85% responder rate, compared with 33% for standard care alone. - The company says its leadership team has been part of biotechnology exits totaling about $9 billion. - Oxeia is a clinical-stage biotechnology company developing OXE103 for persistent post-concussion symptoms. - The company’s leadership has participated in exits including Arena Pharmaceuticals’ acquisition by Pfizer and Kythera Biopharmaceuticals’ acquisition by Allergan. Between the lines: - Alex Smith’s involvement gives Oxeia a prominent sports figure with personal relevance to concussion recovery, which can help the company reach both investors and a broader public audience. - The mix of prior clinical data, FDA feedback and an early responder signal suggests Oxeia is trying to position OXE103 as more de-risked than many early-stage biotech programs. - The Reg CF structure and explicit risk disclosure indicate the raise is speculative and aimed at retail investors willing to take on high uncertainty. What’s next: - Oxeia said company leadership will discuss the science behind OXE103, upcoming milestones and the regulatory path during the webinar. - The company is expected to keep advancing toward Phase 2b if development stays on track. - OXE103 remains investigational and has not been approved by the U.S. Food and Drug Administration. The bottom line: - Oxeia is using Alex Smith’s profile and a June 18 investor event to build interest in a concussion therapy program it says is closer to the FDA path than most early-stage biotech candidates.

Disclaimer: This article was produced by AGP Wire with the assistance of artificial intelligence based on original source content and has been refined to improve clarity, structure, and readability. This content is provided on an “as is” basis. While care has been taken in its preparation, it may contain inaccuracies or omissions, and readers should consult the original source and independently verify key information where appropriate. This content is for informational purposes only and does not constitute legal, financial, investment, or other professional advice.

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