What the changes say
- No new risks were added, while the reverse-stock-split risk was removed after the July 7, 2025 split.
- Dilution disclosures now quantify 8,282,037 warrants, 2,785,363 options, and 300 restricted stock units.
- Common shares outstanding increased to 7,542,638, leaving 792,454,526 authorized shares available for issuance.
- Cash concentration risk now uses June 30, 2026 balances; management titles and program responsibilities were updated.
What changed since the prior 10-K
Dropped
- DroppedRisks Relating to Our Common Stock
We effected a reverse stock split on July 7, 2025, and such reverse stock split has caused and could further cause our stock price to decline relative to its value before the reverse stock split and decrease the liquidity of shares of our common stock
Reworded
- 49% rewrittenRisks Relating to Our Common Stock
You may experience future dilution as a result of future equity offerings or if we issue shares subject to options, warrants, stock awards or other arrangements
Adds specific outstanding warrant, option, and restricted-unit amounts and exercise-price ranges, replacing detailed Acuitas Warrant dilution language.
- 36% rewrittenRisks Relating to Our Business and Industry
The concentration of our assets within a certain financial institution could have a material adverse effect on its business, financial condition and results of operations
Updates the cash-balance date from July 31, 2025 to June 30, 2026; the substantive bank-failure risk is unchanged.
- 33% rewrittenRisks Relating to Our Common Stock
We may, in the future, issue additional shares of Common Stock, which would reduce investors’ percent of ownership and may dilute our share value
Updates issued shares from 1,917,061 to 7,545,474 and outstanding shares from 1,914,224 to 7,542,638, reducing remaining authorized shares.
- 27% rewrittenRisks Relating to Our Business and Industry
We depend upon our management and their loss or unavailability could put us at a competitive disadvantage which could have a material adverse effect on our business
Updates management roles, including Liver Disease and Long COVID Programs for Markham and Operations for Ahlem.
- 24% rewrittenRisks Relating to Our Business and Industry
We may expend our limited resources to pursue a particular drug candidate or indication and fail to capitalize on drug candidates or indications that may be more profitable or for which there is a greater likelihood of success
Changes only “research and development” to “R&D”; the resource-allocation risk is otherwise unchanged.
All 44 risk factors
Headings as the filing states them, in filing order.
Risks Relating to Our Business and Industry
- 01Successful development of biopharmaceuticals is highly uncertain and is dependent on numerous factors, many of which are beyond our control
- 02The concentration of our assets within a certain financial institution could have a material adverse effect on its business, financial condition and results of operations36% rewritten
- 03We have no products approved for commercial sale, have never generated any revenues and may never achieve revenues or profitability, which could cause us to cease operations
- 04We are a development stage company with a limited operating history, making it difficult for you to evaluate our business and your investment
- 05Since inception, we have not established any revenues or operations that would provide financial stability in the long term, and there can be no assurance that we will realize our plans on our projected timetable in order to reach sustainable or profitable operations
- 06Even if we successfully develop and market BIV201 and/or bezisterim (NE3107), we may not generate sufficient or sustainable revenue to achieve or sustain profitability, which could cause us to cease operations and cause you to lose all of your investment
- 07If we fail to obtain or maintain Orphan Drug exclusivity for BIV201, we will have to rely on other potential marketing exclusivity, and on our intellectual property rights, which may reduce the length of time that we can prevent competitors from selling generic versions of BIV201
- 08We will need to raise substantial additional capital in the future to fund our operations and we may be unable to raise such funds when needed and on acceptable terms, which could have a materially adverse effect on our business
- 09We have limited experience in drug development and may not be able to successfully develop any drugs, which would cause us to cease operations
- 10We may expend our limited resources to pursue a particular drug candidate or indication and fail to capitalize on drug candidates or indications that may be more profitable or for which there is a greater likelihood of success24% rewritten
- 11We have no manufacturing experience, and the failure to comply with all applicable manufacturing regulations and requirements could have a materially adverse effect on our business
- 12We do not currently have the sales and marketing personnel necessary to sell products, and the failure to hire and retain such staff could have a materially adverse effect on our business
- 13Even if we were to successfully develop approvable drugs, we will not be able to sell these drugs if we or our third-party manufacturers fail to comply with manufacturing regulations, which could have a materially adverse effect on our business
- 14We must comply with significant and complex government regulations, compliance with which may delay or prevent the commercialization of our product candidates, which could have a materially adverse effect on our business
- 15If we experience delays or discontinuations of our clinical trials by the FDA or comparable authorities in other countries, or if we fail to obtain registration or other approvals of our products or devices then we could be forced to cease our operations and you will lose all of your investment
- 16We depend upon our management and their loss or unavailability could put us at a competitive disadvantage which could have a material adverse effect on our business27% rewritten
- 17We may not be able to attract and retain highly skilled personnel, which could have a materially adverse effect on our business
- 18The biotechnology and biopharmaceutical industries are characterized by rapid technological developments and a high degree of competition. We may be unable to compete with enterprises equipped with more substantial resources than us, which could cause us to curtail or cease operations
- 19There may be conflicts of interest among our officers, directors and stockholders
- 20We indemnify our officers and directors against liability to us and our security holders, and such indemnification could increase our operating costs
Risks Relating to Our Intellectual Property
- 21We may be unable to obtain or protect intellectual property rights relating to our product candidates, which could have a materially adverse effect on our business
- 22Patent terms may be inadequate to establish our competitive position on our drug candidates for an adequate amount of time
- 23We may not be able to protect our intellectual property rights throughout the world
- 24Changes in patent law could diminish the value of patents in general, thereby impairing our ability to protect our drug candidates
- 25We may become involved in lawsuits to protect or enforce our patents or other intellectual property, which could be expensive, time-consuming and unsuccessful, and issued patents directed towards our technology and drug candidates could be found invalid or unenforceable if challenged
- 26Furthermore, because of the substantial amount of discovery required in connection with intellectual property litigation, there is a risk that some of our confidential information could be compromised by disclosure during this type of litigation
- 27We may not identify relevant third-party patents or may incorrectly interpret the relevance, scope or expiration of a third-party patent, which might subject us to infringement claims or adversely affect our ability to develop and market our drug candidates
- 28Third parties may initiate legal proceedings alleging that we are infringing, misappropriating or otherwise violating their intellectual property rights, the outcome of which would be uncertain and could negatively impact the success of our business
- 29We may be subject to claims by third parties asserting that we or our employees have infringed, misappropriated or otherwise violated their intellectual property rights, or claiming ownership of what we regard as our own intellectual property
- 30We may be subject to claims challenging the inventorship of our patents and other intellectual property
- 31Intellectual property rights do not necessarily address all potential threats
- 32Intellectual property litigation may lead to unfavorable publicity that harms our reputation and causes the market price of shares of our Common Stock to decline
Risks Relating to Our Common Stock
- 33Our stock price is and may continue to be volatile and you may not be able to resell our Common Stock at or above the price you paid
- 34You may experience future dilution as a result of future equity offerings or if we issue shares subject to options, warrants, stock awards or other arrangements49% rewritten
- 35We may, in the future, issue additional shares of Common Stock, which would reduce investors’ percent of ownership and may dilute our share value33% rewritten
- 36The market price and trading volume of our Common Stock may be volatile
- 37Any failure to maintain effective internal control over financial reporting could harm us
- 38There is a limited trading market for our Common Stock, which could make it difficult to liquidate an investment in our Common Stock, in a timely manner
- 39The lack of public company experience of our management team could adversely impact our ability to comply with the reporting requirements of U.S. securities laws, which could have a materially adverse effect on our business
- 40We are considered a smaller reporting company that is exempt from certain disclosure requirements, which could make our stock less attractive to potential investors
- 41We are subject to the periodic reporting requirements of the Exchange Act, which require us to incur audit fees and legal fees in connection with the preparation of such reports. These additional costs will negatively affect our ability to earn a profit
- 42Because we do not intend to pay any cash dividends on our Common Stock, our stockholders will not be able to receive a return on their shares unless they sell them
- 43We are authorized to issue “blank check” preferred stock without stockholder approval, which could adversely impact the rights of holders of our securities
- 44Provisions in our Articles of Incorporation, our Bylaws, and Nevada law might discourage, delay or prevent a change in control of our company or changes in our management and, therefore, depress the trading price of our Common Stock
Other Biovie 10-Ks
- FY2025 10-K risk factors45 risks2 new2 dropped2 reworded
BioVie updated share figures following a 1-for-10 reverse stock split on July 7, 2025. Dilution disclosures now explicitly mention potential anti-dilution adjustments for Acuitas warrants. Cash concentration dates were updated to July 31, 2025.
Filed Aug 15, 2025 - FY2024 10-K risk factors45 risks
Biovie is a development-stage biopharmaceutical company with no approved products, commercial revenues, or manufacturing experience.
Filed Sep 30, 2024
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.