NervGen Pharma Appoints Adam Rogers as CEO
NervGen Pharma announced its Board of Directors has unanimously appointed Adam Rogers, MD, as President and CEO, effective immediately. "Following a thorough evaluation during Adam's tenure as Interim CEO, the Board concluded that his leadership has been defined by results," said Craig Thompson, Independent Director and Member of the Nominating and Corporate Governance Committee. "Adam exemplifies the leadership qualities that NervGen requires, bringing the unique perspective of a practicing physician and seasoned biotech executive who understands the complexities and discipline inherent in advancing a novel therapy such as NVG-291. His leadership reflects a commitment to all stakeholders, from patients, families, and advocates, to shareholders and employees, aligned around the shared objective of bringing NVG-291 to market as the first approved pharmacologic treatment for spinal cord injury."
Trade with 70% Backtested Accuracy
Analyst Views on NGEN
About NGEN
About the author

- New CEO Appointment: NervGen Pharma has unanimously appointed Dr. Adam Rogers as the new president and CEO, effective immediately, following his successful tenure as interim CEO where he achieved key milestones.
- Successful Nasdaq Listing: Under Rogers' leadership, the company successfully listed on Nasdaq, marking a significant advancement in its capital market presence and laying the groundwork for future financing and business expansion.
- Product Development Progress: NervGen's lead candidate NVG-291 has advanced to late-stage development, potentially paving the way for commercialization and enhancing the company's competitive position in the market.
- Funding Initiative Launched: NervGen Pharma announced a $10 million non-brokered private placement aimed at providing funding for subsequent R&D and market promotion, reflecting the company's confidence in future growth.

- Nasdaq Listing: NervGen Pharma's common shares have been approved for listing on Nasdaq under the symbol "NGEN", marking a transition from the U.S. OTC market to a more liquid trading platform, which is expected to attract greater investor interest.
- Drug Development Progress: The company's lead drug, NVG-291, is in Phase 2 clinical trials, having received Fast Track designation from the FDA in October 2023, indicating its potential as the first pharmacologic therapy for spinal cord injury (SCI).
- Clinical Study Results: In the CONNECT SCI study announced on November 24, 2025, NVG-291 demonstrated significant improvements in function, independence, and quality of life for chronic SCI patients, further enhancing its market prospects.
- Future Plans: NervGen plans to hold an End-of-Phase 2 meeting with the FDA in early 2026 to align on the development and registration pathway for NVG-291, demonstrating the company's strong commitment to advancing SCI treatment.






