OPKO HEALTH, INC.
For the period ended Jun 30, 2025. Filed Jul 31, 2025.
View on SEC.govAbout this filing
A company's report for each of its first three quarters. The financial statements are not audited. It shows how the business has moved since the last annual report, and what management says changed.
Jun 30, 2025 · Filed Jul 31, 2025
What changed in Risk Factors?
Read the current filingPrevious report: 10-Q
Period ended 2025-03-31; filed 2025-05-01.
0001437749-25-014086
Item 1A. Risk FactorsCurrent report: 10-Q
Period ended 2025-06-30; filed 2025-07-31.
0000950170-25-100908
Item 1A. Risk FactorsThe baseline is this issuer’s latest earlier reporting period of the same form that was filed before the current report. A previous 10-Q is a different quarter, not a year-over-year comparison. Amendments are excluded.
Compared 7 previous paragraphs and 2 current paragraphs.
1 unchanged; 0 reworded; 1 added; 6 removed; 0 previous and 0 current paragraphs rearranged.
Tables are not compared: 0 previous and 0 current tables excluded. Dates, whitespace, punctuation and numbering changes are ignored; changes to financial figures remain significant.
A changed paragraph is not evidence that risk increased or decreased. An unchanged paragraph does not establish that risk stayed the same.
The current filing states there were no material changes to risk factors.
This is the filer’s own statement, not a conclusion from the comparison. Read its qualifications and the report it references.
Current filing’s statement
There have been no material changes to our risk factors as previously disclosed in our Form 10-K and our Quarterly Report on Form 10-Q for the quarter ended March 31, 2025.
Added paragraphs (1)
Current report
There have been no material changes to our risk factors as previously disclosed in our Form 10-K and our Quarterly Report on Form 10-Q for the quarter ended March 31, 2025.
Removed paragraphs (6)
Previous report
Unstable economic and market conditions may have adverse consequences on our business and financial condition.
Previous report
Our business performance may be impacted by a number of factors, including general economic conditions, the geopolitical environment, current or expected inflation, interest rate fluctuations, market volatility and the threat or imposition of broad-based tariffs. Significant developments or changes in national laws or policies to protect or promote domestic interests and/or address foreign competition, including laws and policies in areas such as trade, manufacturing, government purchasing, healthcare, intellectual property, regulatory enforcement and investment/development, can adversely affect our business and financial statements. The current U.S. administration has initiated or is considering imposing tariffs on certain goods. Consequently, certain foreign governments including China, have imposed or are considering imposing reciprocal tariffs on certain U.S. goods. While pharmaceutical products have largely been exempt from the most recent tariffs, such exemptions are likely to be terminated according to statements from the administration. We continue to evaluate the impacts of tariffs on our business and results of operations, but a trade war or other governmental action related to tariffs or international trade agreements or policies has the potential to disrupt our research activities, could raise our cost of goods, and could therefore adversely impact our business and financial condition.
Previous report
Changes in personnel and funding for government agencies, including the FDA, could negatively impact our business and financial condition.
Previous report
We rely on the FDA to provide feedback on clinical trials and development programs, review regulatory submissions and ultimately review and approve new products. Significant reductions to the FDA’s workforce and budget could constrain the FDA’s ability to timely and effectively provide feedback on our products. If disruptions at the FDA and other agencies delays the time necessary for our product candidates to be reviewed or approved, this delay could prevent our product candidates from being developed or commercialized in a timely manner or otherwise, if at all, which could adversely affect our business and financial condition.
Previous report
There is also substantial uncertainty as to whether or how the requirements and policies of government agencies including the FDA might be modified. Any significant changes to process or procedures of the FDA could present new challenges to the clinical development and approval process which can in turn affect our ability to timely bring products to market.
Previous report
Similarly, a portion of our business relies on funding from BARDA. There is significant uncertainty at this time as to whether such funding will remain available to us through clinical trials and for the development life of our product candidates. If the funding is reduced for studies related to the products or indications on which we are focused or on which researchers were or may have been considering applying for federal grants, our research and development initiatives could be delayed or otherwise affected.