Oncolytics Biotech® Proposes Jurisdiction Change to Nevada
Oncolytics Biotech Inc. (Nasdaq: ONCY), a clinical-stage immunotherapy company focused on oncology, has announced its proposal to transition its jurisdiction of incorporation from Alberta, Canada, to the State of Nevada, U.S. This strategic decision aims to align with Oncolytics' growth goals in the U.S. market and enhance its operational efficiency.
Strategic Rationale Behind the Proposal
As Oncolytics evolves into a U.S.-focused clinical-stage oncology company, the shift to Nevada is intended to simplify its regulatory structure and improve access to U.S. capital markets. Jared Kelly, CEO of Oncolytics, commented, “We are a U.S.-focused oncology company with U.S.-based leadership, operations, and investors. This move simplifies our structure and enhances our capacity for future strategic opportunities, including partnerships and potential mergers and acquisitions.”
Background and Current Circumstances
Over recent years, Oncolytics has seen a significant shift in its operations, becoming predominantly U.S.-based. As of January 1, 2026, the Company is recognized as a domestic issuer under the U.S. Securities and Exchange Commission (SEC) regulations. This change led to increased regulatory complexities without added benefits, prompting management to reconsider its corporate domicile.
- Majority U.S.-based operations and management.
- Transition to domestic issuer status under SEC rules as of January 1, 2026.
- Objective: Enhance operational efficiency and access to capital markets.
Details of the Proposal and Shareholder Approval
The proposal to domesticate to Nevada is contingent upon shareholder approval. Shareholders of Oncolytics, as of December 9, 2025, will participate in a vote during a special meeting scheduled for January 15, 2026. This meeting will also address other transactions related to the jurisdiction change.
About Oncolytics Biotech Inc.
Oncolytics is currently developing pelareorep, an investigational RNA immunotherapeutic agent designed to induce anti-cancer immune responses. The agent has shown promising results in clinical studies targeting various types of cancer, including:
- First-line pancreatic cancer
- Metastatic breast cancer
- Anal and colorectal cancer
Pelareorep is under development in combination with chemotherapy and checkpoint inhibitors and has received Fast Track Designation from the FDA for metastatic pancreatic and breast cancers.
Investors and Additional Information
Oncolytics has filed a registration statement with the SEC regarding the proposed domestication. Shareholders are urged to review the definitive management circular/prospectus for critical information about the transaction. These documents can be accessed through the SEC website and Oncolytics' corporate site.
Forward-Looking Statements
This press release includes forward-looking statements related to Oncolytics’ future plans, including the proposed change of its jurisdiction. Investors should be aware of potential risks and uncertainties that may impact these forecasts.
For more information about Oncolytics and its proposed changes, visit www.oncolyticsbiotech.com or follow ONCY on social media.