NurExone to present at Moody Capital Solutions conference in New York
- NurExone Biologic Inc. to present at Moody Capital Solutions conference on September 9, 2026
- Yoram Drucker to lead investor presentation and one-on-one meetings in New York City
- Company focuses on exosome-based therapies for central nervous system injuries
- Lead product ExoPTEN has received Orphan Drug Designation for U.S. and Europe trials

*this image is generated using AI for illustrative purposes only.
NurExone Biologic Inc. (TSXV: NRX) will present at the Moody Capital Solutions 2026 Disruptive Growth & Life Sciences Conference on September 9, 2026.
The biotechnology company, which develops exosome-based regenerative therapies, announced its participation in the event taking place in New York City from September 9 to 10, 2026.
Presentation Details
Yoram Drucker, Co-Founder, Chairman and Vice President of Strategic Development, will deliver an investor presentation and participate in one-on-one meetings with investors.
| Detail | Information |
|---|---|
| Date | Wednesday, September 9, 2026 |
| Time | 9:10–9:30 a.m. EDT |
| Location | Room 1, The Westin New York Grand Central |
| Presenter | Yoram Drucker |
Drucker stated that NurExone is continuing preclinical development activities and preparing for potential clinical development. The company is also taking steps to support manufacturing and commercial capabilities for longer-term development.
Strategic Focus
The presentation will cover the company’s therapeutic-development activities, exosome platform, and U.S. manufacturing and commercial initiatives. NurExone aims to engage with the investment community regarding these areas.
About NurExone
NurExone is listed on the TSX Venture Exchange, OTCQB, and Frankfurt Stock Exchange. The company focuses on developing regenerative exosome-based therapies for central nervous system injuries.
Its lead product, ExoPTEN, has demonstrated preclinical data supporting clinical potential in treating acute spinal cord and optic nerve damage. The company has obtained Orphan Drug Designation to facilitate its roadmap towards clinical trials in the U.S. and Europe.
NurExone has established Exo-Top to anchor its North American activity and growth strategy. The company expects to offer solutions for quality exosomes and minimally invasive targeted delivery systems.
What specific preclinical milestones must NurExone achieve before initiating its first-in-human clinical trials for ExoPTEN?
How might the establishment of Exo-Top impact NurExone's cost structure and scalability for U.S. manufacturing compared to its current operations?
What are the key regulatory hurdles or timelines expected for advancing ExoPTEN from Orphan Drug Designation to IND approval in the U.S. and Europe?






























