Welcome to our dedicated page for Calidi Biotherapeutics SEC filings (Ticker: CLDI), a comprehensive resource for investors and traders seeking official regulatory documents including 10-K annual reports, 10-Q quarterly earnings, 8-K material events, and insider trading forms.
Clinical trial updates, cash-burn tables, and stem-cell delivery jargon make Calidi Biotherapeutics’ SEC disclosures tough to navigate. Missing a single 8-K data point on a Phase 1 read-out could mean mispricing the stock. Stock Titan’s AI-driven platform removes that risk by translating every Calidi Biotherapeutics SEC filing into clear, actionable language—while the document is still hitting EDGAR.
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Calidi Biotherapeutics, Inc. (NYSE American: CLDI) has filed a Form S-1 to register 6,355,650 shares of common stock for resale by existing holders. The bulk of the shares (6,053,000) are issuable upon exercise of Series G common warrants at an exercise price of $0.6954 per share (first exercisable 28 Sep 2025; expire 28 Mar 2033). A further 302,650 shares relate to warrants issued to placement agent Ladenburg Thalmann at $0.8125 per share (same first exercise date; expire 28 Sep 2030).
The company will not receive proceeds from the resale; cash would only be generated if warrant holders exercise for cash. At the last reported price of $0.2339 (2 Jul 2025) the warrants are out-of-the-money, but their future exercise could raise capital and dilute existing holders.
Calidi remains an emerging growth and smaller reporting company. It is also seeking shareholder approval to implement a reverse stock split between 1-for-2 and 1-for-19, after which historical share data will be adjusted.
Business profile. Calidi is a clinical-stage biotech developing three immuno-oncology platforms: RedTail (engineered vaccinia virus for systemic delivery of genetic medicines), SuperNova and NeuroNova (stem-cell-based oncolytic virus platforms). Lead candidate CLD-401 (IL-15 super-agonist payload) is targeted to enter Phase I by end-2026. The company currently has no approved products or revenue and highlights the need for substantial additional funding.
Governance changes. Former CEO & Chairman Allan Camaisa resigned effective 22 Apr 2025, becoming “CEO Emeritus” and remaining a Class III director. Eric Poma, Ph.D. was appointed CEO and Class I director, and James Schoeneck became Chairman. Camaisa receives a $500,000 12-month separation package plus consulting and COBRA payments.
The prospectus reiterates extensive risk factors typical of early-stage biotech firms, including capital needs, clinical uncertainty and potential NYSE American listing compliance.