Calidi Biotherapeutics, Inc. (CLDI) Stock Price & How to Invest

Short answer

You can invest in Calidi Biotherapeutics (CLDI) by buying shares or fractional shares at any major broker, through an ETF that holds it, or as one holding in a thematic basket. Calidi is a clinical-stage immuno-oncology company developing virotherapies that use stem cells and engineered viruses to attack tumors, including CLD-101 (NeuroNova) for brain cancer, CLD-201 (SuperNova) for solid tumors, and a systemic, potentially redosable platform called RTNova (CLD-400). The thesis is that its stem-cell-shielded and systemically delivered oncolytic viruses could reach tumors that current virotherapies cannot. The biggest risk is that this is a highly speculative, pre-revenue micro-cap with very little cash, substantial doubt about its ability to continue as a going concern, a history of dilution and a reverse stock split, and value that hinges almost entirely on early-stage trial outcomes.

CLDI stock price

As of 2026-06-26, Calidi Biotherapeutics, Inc. (CLDI) last closed at $0.1630, down 93.9% over the past year. Over the past 52 weeks it has traded between $0.1500 and $11.98.

CLDI last close
$0.1630
1 day
+8.67%
1 month
-14.66%
1 year
-93.94%
52-week range
$0.1500 to $11.98
Last close
2026-06-26

Prices are daily closing prices from Yahoo Finance and may be delayed. For the live quote, check your broker or Calidi Biotherapeutics, Inc.'s investor relations page. Walnut is informational, not investment advice.

What does Calidi Biotherapeutics, Inc. (CLDI) do?

Calidi Biotherapeutics, Inc. is a clinical-stage immuno-oncology company based in San Diego, California, developing therapies that combine oncolytic viruses with cell-based delivery to target hard-to-treat cancers. Its approach is built on the idea of shielding therapeutic viruses inside stem cells so they can survive the immune system long enough to reach and destroy tumors. The pipeline includes CLD-101 (NeuroNova), studied in Phase 1 for high-grade glioma, an aggressive brain cancer; CLD-201 (SuperNova), an allogeneic stem-cell-loaded viral therapy for solid tumors such as soft tissue sarcoma, triple-negative breast cancer, and head and neck cancer; and RTNova (CLD-400), an earlier-stage systemic platform using an enveloped virotherapy designed for intravenous, potentially redosable delivery to metastatic and lung cancers. The company generates no product revenue and is years away from any potential approval.

Calidi became publicly traded in 2023 through a merger with a special purpose acquisition company (SPAC) and trades on NYSE American. Recent developments include FDA clearance of an investigational new drug application for CLD-201 in April 2025 and FDA Fast Track designation for CLD-201 in soft tissue sarcoma in July 2025, plus ongoing preclinical work on RTNova and a related lead candidate engineered to deliver an IL-15 immune-stimulating payload. The financial reality is stark: the company reported a net loss of about $25.6 million for 2025 and ended the year with roughly $5.6 million in cash, with about $6.9 million in cash and restricted cash reported as of March 31, 2026. It has flagged substantial doubt about its ability to continue as a going concern, carries a large overhang of warrants, and completed a 1-for-12 reverse stock split in August 2025 to maintain its share-price listing standard. Operations are funded through repeated, dilutive equity raises.

What's driving Calidi Biotherapeutics, Inc. (CLDI)?

1. Stem-Cell-Shielded Virotherapy Platform.

Calidi's core idea is to load oncolytic viruses inside stem cells so the viruses can evade the patient's immune defenses and reach tumors intact. This addresses a known limitation of conventional virotherapy, where the immune system can neutralize a virus before it acts. If validated in trials, the same delivery concept could in principle extend across multiple cancer types. Platform validation remains unproven in pivotal human studies, so this is a scientific thesis rather than an established result.

2. CLD-201 SuperNova and FDA Designations.

CLD-201 is an allogeneic, off-the-shelf stem-cell-loaded viral therapy aimed at solid tumors including soft tissue sarcoma, triple-negative breast cancer, and head and neck cancer. The FDA cleared its IND in April 2025 and granted Fast Track designation for the sarcoma indication in July 2025, which can mean more frequent FDA interaction and potential eligibility for expedited review. A first-in-human Phase 1 study is planned. These designations support development but do not guarantee that the therapy will prove safe or effective.

3. RTNova Systemic, Redosable Approach.

RTNova (CLD-400) is an earlier-stage platform using an enveloped virotherapy designed for intravenous delivery, which could allow systemic, potentially repeatable dosing to reach metastatic disease and lung cancer rather than only locally injected tumors. A related RedTail lead candidate is engineered to deliver an IL-15 immune-stimulating payload directly into the tumor microenvironment, with an IND targeted later. Because RTNova is preclinical, it carries the highest scientific uncertainty in the pipeline and is the furthest from any clinical readout.

4. Large Unmet Need in Hard-to-Treat Cancers.

Calidi targets cancers with poor prognoses and limited options, such as high-grade glioma and advanced solid tumors, where a differentiated mechanism could matter if it works. The addressable patient populations are meaningful, and immuno-oncology remains an active area of investment and partnership interest. However, addressing a large unmet need is only valuable if the therapy clears clinical trials and reaches the market, neither of which is assured for an early-stage company with limited resources.

What are the risks to Calidi Biotherapeutics, Inc. (CLDI)?

Calidi is a pre-revenue, clinical-stage micro-cap whose value depends almost entirely on early-stage trial outcomes, so a single clinical failure, safety signal, or program delay could sharply reduce the stock. The company has reported substantial doubt about its ability to continue as a going concern, ended 2025 with only about $5.6 million in cash against ongoing losses, and funds itself through repeated dilutive equity raises that erode existing shareholders; it also carries a large warrant overhang and completed a 1-for-12 reverse stock split in August 2025 to maintain its listing standard, with continued delisting risk if the share price falls again. There is no product revenue, no profit, and no certainty that any program will ever be approved or commercialized. This is among the most speculative categories of stock, and a total or near-total loss is a realistic outcome.

How is Calidi Biotherapeutics, Inc. (CLDI) valued? (approximate, Full-year 2025 results, with cash updated to March 31, 2026)

A simple financial snapshot. These are approximations and refresh quarterly; for current figures see Calidi Biotherapeutics, Inc.'s investor relations page or your broker.

  • Revenue: None (no approved products; pre-revenue clinical-stage)
  • Net loss (FY 2025): ~$25.6 million (vs. ~$23.8 million in 2024)
  • Cash & equivalents: ~$5.6 million at year-end 2025; ~$6.9 million cash and restricted cash at March 31, 2026
  • Cash runway: Very limited; company has flagged substantial doubt about going concern and relies on ongoing financings
  • Market cap: Micro-cap, roughly a few million dollars in early 2026; moves sharply on news and financings
  • Share structure: 1-for-12 reverse split effective August 2025; large warrant overhang (tens of millions of warrants outstanding)

A pre-revenue clinical biotech like Calidi cannot be valued on earnings, because there are none; metrics like P/E are not meaningful. Investors who study these companies typically weigh the cash runway against the quarterly burn rate, the timing and probability of upcoming clinical catalysts (such as trial starts, data readouts, and FDA designations), and the dilution required to fund the next stage of development. For Calidi specifically, the very low cash balance, going-concern doubt, reverse split, and heavy warrant overhang mean financing risk and dilution are central to any assessment, and the stock can swing dramatically on capital raises as much as on science.

Who competes with Calidi Biotherapeutics, Inc. (CLDI)?

Oncolytic-Virus and Virotherapy Companies

Calidi competes in the oncolytic-virus field with companies such as Replimune (REPL), which develops engineered herpes-based oncolytic immunotherapies, and CG Oncology (CGON), focused on a bladder-cancer oncolytic virus. The approved benchmark in the space is Amgen's Imlygic (talimogene laherparepvec). These peers are generally larger and better-capitalized than Calidi, and several have more advanced clinical programs.

Cell-Therapy and Immuno-Oncology Biotechs

Because Calidi uses stem cells to deliver its viruses, it also sits adjacent to the broader cell-therapy and immuno-oncology landscape, which includes a wide range of clinical-stage companies pursuing engineered cells and tumor-microenvironment approaches. Many of these are also pre-revenue and speculative, but the field as a whole competes for the same scientific talent, trial sites, partnership capital, and investor attention.

Biotech ETFs and Diversified Alternatives

Investors who want exposure to clinical-stage biotech without single-stock risk often use broad ETFs such as the SPDR S&P Biotech ETF (XBI) or the iShares Biotechnology ETF (IBB). Very small micro-caps like CLDI are rarely held in major ETFs, or appear only at tiny weights, so these funds provide diversified biotech exposure rather than direct Calidi exposure. A diversified fund spreads binary trial risk across many companies.

How to invest in Calidi Biotherapeutics, Inc. (CLDI)

There are three common ways to get CLDI exposure. Buy shares (or fractional shares) directly at any major broker. Hold an ETF that includes it, which spreads the position across many companies. Or build it into a focused thematic basket, so CLDI sits alongside other stocks that express the same thesis.

Walnut takes the basket route. Describe a thesis where CLDI fits (for example “AI infrastructure” or “dividend-growth large-caps”) and the AI proposes 5 to 6 constituents with target weights. You review the plan and fund it through your own broker when you're ready.

The bottom line on Calidi Biotherapeutics, Inc. (CLDI)

Calidi Biotherapeutics is a pre-revenue, clinical-stage cancer-virotherapy company whose value depends on early trial data and its ability to keep funding operations. It behaves as a binary, highly speculative micro-cap: shares can move sharply on pipeline news or financing events, and the company has limited cash, ongoing dilution, and going-concern doubt that make outcomes extremely uncertain.

More on Calidi Biotherapeutics, Inc. (CLDI)

Whether CLDI is worth buying today depends more on your time horizon and what you already hold than on any single call. We walk through valuation, what would have to go right, and the risks in is CLDI a buy?, and where the stock could go from here in the CLDI stock forecast.

For income investors, whether CLDI pays a dividend and how the payout looks is covered in does CLDI pay a dividend?

Build a basket around CLDI with Walnut

Use Calidi Biotherapeutics, Inc. as one constituent in a thematic basket Walnut's AI helps you assemble. Describe a thesis you believe in, the AI proposes the holdings and weights, and you approve before any broker order.

FAQ

What does Calidi Biotherapeutics do?

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Calidi Biotherapeutics is a clinical-stage immuno-oncology company developing cancer therapies that combine oncolytic viruses with cell-based delivery. Its approach shields therapeutic viruses inside stem cells so they can evade the immune system and reach tumors. Its programs include CLD-101 (NeuroNova) for brain cancer, CLD-201 (SuperNova) for solid tumors, and an earlier-stage systemic platform called RTNova (CLD-400). The company is pre-revenue and has no approved products.

Does CLDI pay a dividend?

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No. Calidi Biotherapeutics does not pay a dividend. It is a pre-revenue, clinical-stage company that is unprofitable and burns cash, so it directs all available capital toward research and operations rather than returning money to shareholders. Any potential return from CLDI would have to come from share-price appreciation, not income, and the company's limited cash makes a dividend highly unlikely for the foreseeable future.

What are Calidi's main pipeline programs and catalysts?

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Calidi's lead programs are CLD-101 (NeuroNova) for high-grade glioma, studied in Phase 1, and CLD-201 (SuperNova), a stem-cell-loaded viral therapy for solid tumors that received an FDA IND clearance in April 2025 and Fast Track designation for soft tissue sarcoma in July 2025. RTNova (CLD-400) is a preclinical systemic platform. Potential catalysts include trial starts, early clinical data, FDA interactions, and financing announcements, all of which can move the stock sharply.

Why is CLDI stock so volatile?

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CLDI is a micro-cap clinical-stage biotech with no revenue, very little cash, and value tied to early trial outcomes, so its price reacts strongly to pipeline news, FDA decisions, and capital raises. Its small market value and low share price mean modest dollar flows can cause large percentage swings. The company has also done a reverse stock split and carries a large warrant overhang, both of which add to share-price instability.

Is Calidi at risk of running out of money or being delisted?

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Calidi has reported substantial doubt about its ability to continue as a going concern and ended 2025 with only about $5.6 million in cash against ongoing losses, so it depends on repeated, dilutive financings to keep operating. It completed a 1-for-12 reverse stock split in August 2025 to maintain its NYSE American share-price listing standard, and continued delisting risk exists if the share price falls again. These are real and serious risks for shareholders.

Which ETFs or baskets include CLDI?

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Very small micro-caps like Calidi are rarely included in major biotech ETFs, or appear only at tiny weights, so broad funds such as the SPDR S&P Biotech ETF (XBI) or iShares Biotechnology ETF (IBB) generally do not provide meaningful direct CLDI exposure. On Walnut, you could include CLDI as one holding in a thematic basket, for example alongside other oncolytic-virus or speculative biotech names, while keeping position sizing in mind given its risk.

Is CLDI a good stock?

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This is descriptive, not advice. The bull case is that Calidi's stem-cell-shielded and systemic virotherapy platforms could reach tumors current therapies cannot, supported by an FDA IND clearance and Fast Track designation for CLD-201. The bear case is that it is a highly speculative, pre-revenue micro-cap with going-concern doubt, very little cash, heavy dilution, a reverse split, and value that hinges on unproven early-stage trials, so a large or total loss is realistic. Whether it fits you depends on your own goals and risk tolerance.

Is CLDI a good stock to buy right now?

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This is informational, not a recommendation. Calidi is an extremely speculative clinical-stage biotech: it has no revenue, limited cash, substantial doubt about continuing as a going concern, and a history of dilution and a reverse stock split, while its potential rests on early-stage trial outcomes that may take years and could fail. Some investors treat such names as tiny, high-risk positions sized for a possible total loss, while others avoid them entirely. Walnut provides information, not investment advice.

Walnut is informational, not investment advice. Financial figures on this page are approximations; always verify current numbers with Calidi Biotherapeutics, Inc.'s investor relations page or your broker before making investment decisions.