Creative Medical Technology Holdings (CELZ) risk factors, FY2024 10-K

Creative Medical Technology Holdings's FY2024 10-K, filed Mar 14, 2025, lists 30 risk factors in 5 groups. There is no earlier 10-K to compare against, so the most company-specific risks are listed below.

Risk factors listed
305 groups
Section length
6k wordsItem 1A

Creative Medical Technology Holdings's biggest risks in the FY2024 10-K

  • Creative Medical Technology Holdings faces ongoing financial losses and needs additional capital to fund its clinical trials.
  • The company depends heavily on clinical execution for cell platforms like CELZ-201 and ImmCelz, along with third-party manufacturers and key executives.

The risks most specific to Creative Medical Technology Holdings

  • Risks Related to our Financial Position and Capital Needs

    We have incurred recent losses and our future profitability is uncertain

    We incurred an operating loss of approximately $5.7 million for 2024 and $5.6 million for 2023, and expect losses to continue.

  • Risks Related to our Financial Position and Capital Needs

    Even with the proceeds from our recent securities offerings, we will need additional capital to fund our operations as planned

    Our operations used approximately $5.3 million in cash for 2024, leaving a combined cash and short-term U.S. treasuries balance of $5.9 million.

  • Risks Related to our Financial Position and Capital Needs

    We expect to continue to incur significant financial losses in the future as we seek to proceed with our Type I Diabetes (CELZ-201 CREATE-1) clinical trial, our AlloStemSpine® Chronic Lower Back Pain (CELZ-201 ADAPT) clinical trial, and our other planned clinical trials

    We expect significant financial losses as we advance our Type I Diabetes CELZ-201 CREATE-1 and AlloStemSpine Chronic Lower Back Pain CELZ-201 ADAPT clinical trials.

  • Risks Related to Product Development, Regulatory Approval and Commercialization

    We have limited experience in conducting and managing the clinical trials necessary to obtain regulatory approvals

    We have limited clinical trial experience, though our CaverStem and FemCelz products are exempt from FDA premarket review as autologous therapies.

  • Risks Related to Product Development, Regulatory Approval and Commercialization

    Our autologous products are currently not eligible for reimbursement from public or private insurers

    Our CaverStem and FemCelz products and procedures are paid for by patients and are not eligible for reimbursement from public or private insurers.

  • Risks Related to Product Development, Regulatory Approval and Commercialization

    We rely upon third parties for the manufacture of our CaverStem® and FemCelz® disposable kits and are dependent on their quality and effectiveness

    We rely on third parties to manufacture our CaverStem and FemCelz disposable kits and depend on their quality and error-free production.

  • Risks Related to Employee Matters

    We are dependent on our executive officers, and we may not be able to pursue our current business strategy effectively if we lose them

    Our success depends heavily on CEO Timothy Warbington and CFO Don Dickerson.

  • Risks Related To Our Common Stock

    Our failure to meet the continued listing requirements of The Nasdaq Capital Market could result in a delisting of our securities

    We effected a 1-for-10 reverse stock split in 2023 to meet Nasdaq's minimum bid price requirement and risk delisting if we fail continued listing rules.

All 30 risk factors

Headings as the filing states them, in filing order.

Risks Related to our Financial Position and Capital Needs

  1. 01We have incurred recent losses and our future profitability is uncertain
  2. 02Even with the proceeds from our recent securities offerings, we will need additional capital to fund our operations as planned
  3. 03We expect to continue to incur significant financial losses in the future as we seek to proceed with our Type I Diabetes (CELZ-201 CREATE-1) clinical trial, our AlloStemSpine® Chronic Lower Back Pain (CELZ-201 ADAPT) clinical trial, and our other planned clinical trials

Risks Related to Product Development, Regulatory Approval and Commercialization

  1. 04We may not be successful in our commercialization efforts for our proposed products and therapies, which may fail to achieve the degree of market acceptance by physicians, patients, healthcare payors and others in the medical community necessary for commercial success
  2. 05The results of our clinical trials may not support our product claims or may result in the discovery of adverse side effects
  3. 06We have limited experience in conducting and managing the clinical trials necessary to obtain regulatory approvals
  4. 07Clinical trials involve a lengthy and expensive process with an uncertain outcome, and results of earlier studies and trials may not be predictive of future trial results
  5. 08problems with investigator or patient compliance with the trial protocols
  6. 09Our autologous products are currently not eligible for reimbursement from public or private insurers
  7. 10The pharmaceutical business is subject to increasing government regulation and reform, including with respect to price controls, reimbursement, and access to therapies, which could adversely affect our future revenues and profitability
  8. 11United States federal and state privacy laws, and equivalent laws of other nations, may increase our costs of operation and expose us to civil and criminal sanctions
  9. 12Later discovery of previously unknown problems could limit our ability to market or sell our products or therapies and can expose us to product liability claims
  10. 13If we do not obtain required approvals in other countries in which we aim to market our products, we will be limited in our ability to export or sell the products in those markets
  11. 14We rely in part on third parties for research and clinical trials for our products and therapies
  12. 15We rely upon third parties for the manufacture of our CaverStem® and FemCelz® disposable kits and are dependent on their quality and effectiveness
  13. 16We may be unable to compete effectively with marketed therapies or drugs targeting similar indications to our products and therapies
  14. 17Our business and operations would suffer in the event of computer system failures or security breaches
  15. 18We are subject to risks arising from the global outbreak of the COVID-19 coronavirus
  16. 19We are subject to risks arising from the wars in Ukraine and the Gaza Strip

Risks Related to Our Intellectual Property

  1. 20We may not be able to protect our proprietary rights
  2. 21We are susceptible to intellectual property suits that could cause us to incur substantial costs or pay substantial damages or prohibit us from selling our product candidates
  3. 22We may need to initiate lawsuits to protect or enforce our intellectual property rights, which could be expensive and, if we lose, could cause us to lose some of our intellectual property rights, which would harm our ability to compete in the market

Risks Related to Employee Matters

  1. 23We are dependent on our executive officers, and we may not be able to pursue our current business strategy effectively if we lose them
  2. 24Our employees, clinical trial investigators, CROs, consultants, vendors and any potential commercial partners may engage in misconduct or other improper activities, including non-compliance with regulatory standards

Risks Related To Our Common Stock

  1. 25The market price of our common stock is highly volatile, and you could lose all or part of your investment
  2. 26general economic or political conditions in the United States or elsewhere
  3. 27If our shares of common stock are delisted from The Nasdaq Capital Market and become subject to the penny stock rules, it will be more difficult to trade our shares
  4. 28Our failure to meet the continued listing requirements of The Nasdaq Capital Market could result in a delisting of our securities
  5. 29We will indemnify and hold harmless our officers and directors to the maximum extent permitted by Nevada law
  6. 30Because we do not expect to pay dividends for the foreseeable future, investors seeking cash dividends should not purchase shares of common stock

Other Creative Medical Technology Holdings 10-Ks

  • FY2025 10-K risk factors
    30 risks2 reworded

    Annual cash use increased from $5.3 million to $5.9 million, and operating loss grew from $5.7 million to $6.1 million. Cash and short-term treasuries increased to $7.2 million backed by over $40 million in cumulative offerings.

    Filed Mar 20, 2026

About this page

The headings are the filing's own. The one-line readings and the overview are automated and can be wrong: read Item 1A of the 10-K for the exact wording.