Tenax Therapeutics (TENX) risk factors, FY2025 10-K

Tenax Therapeutics's FY2025 10-K, filed Mar 10, 2026, lists 46 risk factors in 6 groups. Against the prior year's 46: 2 new, 2 dropped, 11 substantially reworded.

Risk factors listed
466 groups
New this year
2vs 46 last year
Dropped
2since the prior 10-K
Substantially reworded
11of those kept
Section length
14k wordsItem 1A

What the changes say

  • Net operating losses surged from $19.5 million to $56.4 million, driving increased reliance on equity financing and share dilution.

What changed since the prior 10-K

New

  • NewRisks Related to Our Business and Our Operations

    collecting, analyzing and reporting final data from the clinical trials

    Clinical trials for products like levosimendan may be terminated or suspended by regulatory authorities like the FDA due to safety issues or protocol failures.

  • NewRisks Related to Owning Our Common Stock

    liability created by the Securities and Exchange Act of 1934, as amended (the “Exchange Act”) or the Securities Act of 1933, as amended (the “Securities Act”), or any other claim for which federal courts have exclusive jurisdiction

    Exclusive forum provisions limit stockholders from bringing claims outside designated judicial forums, potentially increasing costs and discouraging lawsuits.

Dropped

  • DroppedRisks Related to Our Dependence on Third Parties

    in a timely manner, we would experience a significant interruption in supply of levosimendan, which could negatively affect our clinical trial conduct and other product development efforts and timelines, financial condition, results of operations and cash flows

  • DroppedRisks Related to Intellectual Property

    difficult since it requires a showing of clear and convincing evidence to overcome the presumption of validity enjoyed by issued patents

Reworded

  • 68% rewrittenRisks Related to Our Dependence on Third Parties

    We do not own or operate any manufacturing facilities for the clinical- or commercial-scale production of our products

    Updated the notice requirement for sole manufacturing source Orion from 24 months to explicitly require 24 months notice to identify an alternative manufacturer for TNX-103.

  • 58% rewrittenRisks Related to Our Business and Our Operations

    any restrictions on the use of our products together with other medications

  • 52% rewrittenRisks Related to Owning Our Common Stock

    Our Bylaws contain an exclusive forum provision, which could limit our stockholders’ ability to obtain a favorable judicial forum for disputes with us or our directors, officers, employees, or agents

  • 43% rewrittenRisks Related to Intellectual Property

    We may incur substantial costs as a result of litigation or other proceedings relating to patent and other intellectual property rights and we may be unable to protect our rights to, or use, our technology

  • 40% rewrittenRisks Related to Our Financial Position and Need for Additional Capital

    We expect a number of factors to cause our operating results to fluctuate on a quarterly and annual basis, which may make it difficult to predict our future performance

  • 36% rewrittenRisks Related to Owning Our Common Stock

    Investors may experience dilution of their ownership interests because of the future issuance of additional shares of our common stock or securities convertible into common stock

    Updated share counts and warrant figures as of December 31, 2025, showing common stock increased to 9,314,130 shares and options increased to 6,616,432 shares.

  • 30% rewrittenRisks Related to Our Business and Our Operations

    Delays in the enrollment and completion of clinical testing could result in increased costs to us and delay or limit our ability to obtain regulatory approval for our product candidates

  • 30% rewrittenRisks Related to Our Financial Position and Need for Additional Capital

    We have incurred losses since our inception, expect to continue to incur losses in the foreseeable future, and may never become profitable

    Updated net operating losses for the year ended December 31, 2025 to $56.4 million, compared to $19.5 million for 2024.

  • 22% rewrittenRisks Relating to Our Industry

    We may not receive all of the anticipated market exclusivity benefits of imatinib’s orphan drug designation, if we prioritize imatinib development in the future

  • 21% rewrittenRisks Relating to Our Industry

    Our activities are and will continue to be subject to extensive government regulation, which is difficult to predict, expensive and time-consuming, and we will not be able to sell our products without regulatory approval

    Was: Our activities are and will continue to be subject to extensive government regulation, which is expensive and time-consuming, and we will not be able to sell our products without regulatory approval

  • 21% rewrittenRisks Related to Our Business and Our Operations

    The market may not accept our products

All 46 risk factors

Headings as the filing states them, in filing order.

Risks Related to Our Business and Our Operations

  1. 01We are limited in the number of products we can simultaneously pursue and therefore our survival depends on our success with a small number of product opportunities
  2. 02We currently have no approved drug products for sale, and we cannot guarantee that we will ever have marketable drug products
  3. 03Delays in the enrollment and completion of clinical testing could result in increased costs to us and delay or limit our ability to obtain regulatory approval for our product candidates30% rewritten
  4. 04collecting, analyzing and reporting final data from the clinical trialsNew
  5. 05lack of adequate funding to continue the clinical trial, including unforeseen costs due to enrollment delays, requirements to conduct additional trials and studies, and increased expenses associated with the services of our CROs and other third parties
  6. 06We are conducting two Phase 3 clinical trials, LEVEL and LEVEL-2 for oral levosimendan, which are expensive and time consuming, and the outcome of the clinical trials is uncertain
  7. 07The market may not accept our products21% rewritten
  8. 08any restrictions on the use of our products together with other medications58% rewritten
  9. 09Any collaboration we enter with third parties to develop and commercialize any future product candidates may place the development of our product candidates outside our control, may require us to relinquish important rights or may otherwise be on terms unfavorable to us

Risks Related to Our Financial Position and Need for Additional Capital

  1. 10the costs of establishing sales, marketing and distribution capabilities for any product candidates for which we may receive regulatory approval
  2. 11We may be required to make milestone and royalty payments to the licensor of the levosimendan intellectual property in connection with the development and commercialization of levosimendan, which could adversely affect the profitability of levosimendan, if approved
  3. 12We expect a number of factors to cause our operating results to fluctuate on a quarterly and annual basis, which may make it difficult to predict our future performance40% rewritten
  4. 13our ability to attract and retain personnel, including our executive team, advisors and members of our Board of Directors; and
  5. 14We have incurred losses since our inception, expect to continue to incur losses in the foreseeable future, and may never become profitable30% rewritten

Risks Relating to Our Industry

  1. 15Intense competition might render our cardiovascular and pulmonary product candidates noncompetitive or obsolete
  2. 16Our activities are and will continue to be subject to extensive government regulation, which is difficult to predict, expensive and time-consuming, and we will not be able to sell our products without regulatory approval21% rewritten
  3. 17Discovery of previously unknown problems with our products, or unanticipated problems with our manufacturing arrangements, even after FDA and other regulatory approvals of our products for commercial sale, may result in the imposition of significant restrictions, including withdrawal of the product from the market
  4. 18We may not receive all of the anticipated market exclusivity benefits of imatinib’s orphan drug designation, if we prioritize imatinib development in the future22% rewritten
  5. 19Even after products are commercialized, we would expect to spend considerable time and money complying with federal, state, and foreign laws and regulations governing their sale, and, if we are unable to fully comply with such laws and regulations, we could face substantial penalties
  6. 20We are subject to uncertainty relating to healthcare reform measures and reimbursement policies that, if not favorable to our products, could hinder or prevent our products’ commercial success, if any of our product candidates are approved
  7. 21Governments outside the United States tend to impose strict price controls and reimbursement approval policies, which may adversely affect our prospects for generating revenue outside the United States
  8. 22Product liability lawsuits against us could cause us to incur substantial liabilities, limit sales of our existing products and limit commercialization of any products that we may develop
  9. 23the inability to commercialize any products that we may develop
  10. 24Our business and operations would suffer in the event of computer system failures, cyber-attacks or deficiencies in our cybersecurity

Risks Related to Our Dependence on Third Parties

  1. 25We do not own or operate any manufacturing facilities for the clinical- or commercial-scale production of our products68% rewritten
  2. 26If we fail to attract and retain senior management and key scientific personnel, we may be unable to successfully develop and commercialize our product candidates
  3. 27We expect to need to increase the size of our organization to further develop our product candidates, and we may experience difficulties in managing growth
  4. 28improve our operational, financial and management controls, reporting systems and procedures
  5. 29We currently have very limited marketing capabilities and no sales organization. If we are unable to establish sales and marketing capabilities on our own or through third parties, we will be unable to successfully commercialize our products, if approved, or generate product revenue
  6. 30unforeseen costs and expenses associated with creating and sustaining an independent sales and marketing organization
  7. 31business combinations or significant changes in a collaborator’s business strategy may adversely affect a collaborator’s willingness or ability to complete its obligations under any arrangement

Risks Related to Intellectual Property

  1. 32Our success will depend in part on obtaining and maintaining effective patent and other intellectual property protection for our product candidates and proprietary technology
  2. 33the patents of others may have an adverse effect on our business
  3. 34We rely on confidentiality agreements that, if breached, may be difficult to enforce and could have a material adverse effect on our business and competitive position
  4. 35We may incur substantial costs as a result of litigation or other proceedings relating to patent and other intellectual property rights and we may be unable to protect our rights to, or use, our technology43% rewritten
  5. 36Under current law, we may not be able to enforce all employees’ covenants not to compete and therefore may be unable to prevent our competitors from benefiting from the expertise of some of our former employees
  6. 37We may infringe or be alleged to infringe intellectual property rights of third parties

Risks Related to Owning Our Common Stock

  1. 38Our share price has been volatile, and may continue to be volatile, which may subject us to securities class action litigation in the future
  2. 39general economic and market conditions, including as a result of disruptive events broadly affecting society, and as a result of geopolitical uncertainties, including in the Middle East and the Russian invasion of and war against the country of Ukraine
  3. 40Investors may experience dilution of their ownership interests because of the future issuance of additional shares of our common stock or securities convertible into common stock36% rewritten
  4. 41Anti-takeover provisions in our corporate charter documents and under Delaware law could make an acquisition of us more difficult, which could discourage takeover attempts and lead to management entrenchment, and the market price of our common stock may be lower as a result
  5. 42authorize the Board, by a majority vote, to amend the Bylaws
  6. 43Our Bylaws contain an exclusive forum provision, which could limit our stockholders’ ability to obtain a favorable judicial forum for disputes with us or our directors, officers, employees, or agents52% rewritten
  7. 44liability created by the Securities and Exchange Act of 1934, as amended (the “Exchange Act”) or the Securities Act of 1933, as amended (the “Securities Act”), or any other claim for which federal courts have exclusive jurisdictionNew
  8. 45We have not paid cash dividends in the past and do not expect to pay dividends in the future. Any return on investment may be limited to the value of our common stock
  9. 46Our ability to use our net operating loss carryforwards and certain other tax attributes to offset future taxable income may be subject to certain limitations

Other Tenax Therapeutics 10-Ks

  • FY2024 10-K risk factors
    46 risks

    Tenax Therapeutics relies heavily on the clinical and commercial success of levosimendan for PH-HFpEF and imatinib for PAH. The company has a history of net operating losses, totaling $19.5 million in 2024, and operates with a very small team of just four full-time employees. Manufacturing is outsourced entirely to third parties, including Orion for levosimendan supply.

    Filed Mar 25, 2025

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.