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Calidi Biotherapeutics Provides Required NYSE American Disclosure

Key Takeaway: Calidi Biotherapeutics disclosed that its Financial Statements for 2025 included an audit report highlighting the assumption of continuing as a going concern. This disclosure is mandated by NYSE regulations and does not alter previous filings. The company is advancing its RedTail platform, targeting various cancers with its lead candidate, CLD-401.

Market Sentiment Analysis

POSITIVE FACTORS

  • Calidi Biotherapeutics is advancing its pipeline with innovative therapies.
  • The company is focused on addressing high unmet medical needs in cancer treatment.
  • The proprietary RedTail platform shows promise for targeted genetic medicine delivery.

CONCERNS & RISKS

  • The audit report emphasizes the company's need to continue as a going concern.
  • There are risks associated with raising sufficient capital for clinical trials.
  • Uncertainties exist regarding FDA approval for therapeutic candidates.

Full Press Release Details

SAN DIEGO, May 22, 2026 (GLOBE NEWSWIRE) -- Calidi Biotherapeutics, Inc. (NYSE American: CLDI) (“Calidi” or “the Company”), a biotechnology company pioneering the development of targeted genetic medicines, today advised that its Financial Statements included in its Annual Report on Form 10-K for the year ended December 31, 2025, contained an audit report from its Independent Registered Public Accounting Firm with an explanatory paragraph emphasizing that the Consolidated Financial Statements were prepared assuming that the Company will continue as a going concern. Release of this information is required by Section 610(b) of the NYSE American Company Guide and does not reflect any change or amendment to any of the Company’s filings for the fiscal year ended December 31, 2025.

About Calidi

Calidi Biotherapeutics (NYSE American: CLDI) is a biotechnology company pioneering the development of targeted therapies with the potential to deliver genetic medicines to distal sites of disease. The company’s proprietary RedTail platform features an engineered enveloped oncolytic virus designed for systemic delivery and targeting of metastatic sites. This advanced enveloped technology is intended to shield the virus from immune clearance, allowing virotherapy to effectively reach tumor sites, induce tumor lysis, and deliver potent genetic medicine(s) to metastatic locations.
CLD-401, the lead candidate from the RedTail platform, currently in IND-enabling studies, targets non-small cell lung cancer, head and neck cancer, and other tumor types with high unmet medical need. Calidi continues to advance its pipeline utilizing the RedTail platform including its novel approach to incorporate in situ T-cell engagers in solid tumors.
Calidi Biotherapeutics is headquartered in San Diego, California. For more information, please visit www.calidibio.com or view Calidi’s Corporate Presentationhere.

Forward-Looking Statements

This press release may contain forward-looking statements for purposes of the “safe harbor” provisions under the United States Private Securities Litigation Reform Act of 1995. Terms such as “anticipates,” “believe,” “continue,” “could,” “estimate,” “expect,” “intends,” “may,” “might,” “plan,” “possible,” “potential,” “predicts,” “project,” “should,” “towards,” “would” as well as similar terms, are forward-looking in nature, but the absence of these words does not mean that a statement is not forward-looking. These forward-looking statements include, but are not limited to, statements concerning key milestones, including certain pre-clinical data, planned clinical trials, and statements relating to the safety and efficacy of Calidi’s therapeutic candidates in development. Any forward-looking statements contained in this discussion are based on Calidi’s current expectations and beliefs concerning future developments and their potential effects and are subject to multiple risks and uncertainties that could cause actual results to differ materially and adversely from those set forth or implied in such forward-looking statements. These risks and uncertainties include, but are not limited to, the risk that Calidi is not able to raise sufficient capital to support its current and anticipated clinical trials, the risk that early results of clinical trials do not necessarily predict final results and that one or more of the clinical outcomes may materially change following more comprehensive review of the data, and as more patient data becomes available, the risk that Calidi may not receive FDA approval for some or all of its therapeutic candidates. Other risks and uncertainties are set forth in the section entitled “Risk Factors” and “Cautionary Note Regarding Forward-Looking Statements” in the Company’s annual report filed with the SEC on Form 10-K on March 27, 2026, as may be amended or supplemented by other reports we file with the SEC from time to time. We disclaim any obligation to update any forward-looking statement to reflect events or circumstances after the date of this press release or to reflect the occurrence of unanticipated events.

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Frequently Asked Questions

What does the audit report for Calidi Biotherapeutics indicate?

The audit report emphasizes that the financial statements assume the company will continue as a going concern.

What is the focus of Calidi's RedTail platform?

The RedTail platform aims to deliver genetic medicines to metastatic sites in various cancers.

What is CLD-401 targeting?

CLD-401 targets non-small cell lung cancer, head and neck cancer, and other high-need tumor types.

What are the risks mentioned in the press release?

Risks include potential difficulties in raising capital and uncertainties regarding FDA approval.

Last updated: May 22, 2026