FTRE 10-K & 10-Q changes, risk factors and insider trading
Fortrea Holdings Inc. · Nasdaq · Services-Medical Laboratories · CIK 1965040 · All filings on SEC.gov
At a glance
What changed in the latest 10-K
Risk Factors
New heading “Changes in and uncertainty regarding U.S. regulations, government policies, government funding decisions, trade policies or tariffs could have a material adverse effect upon our business.”
New heading “Our revenues depend on the pharmaceutical, biotechnology and medical device industries and the expenditures they make in R&D; any reductions or delays in such expenditures could materially and adversely affect our business, financial condition, results of operations, and cash flows.”
New heading “Increasing attention to sustainability-related matters may impose additional costs on our business and expose us to new risks.”
New heading “Our stockholder rights agreement could discourage, delay, or prevent a change in control over us and may affect the trading price of our common stock.”
Removed heading “Risks Relating to General Matters”
Removed heading “We might not be able to engage in certain transactions and equity issuances until July 1, 2025.”
Removed heading “We are subject to a number of risks associated with the sale of certain assets relating to our Enabling Services segment, and these risks could adversely impact our operations, financial condition and business.”
Removed heading “Changes in our tax rates, the adoption of new U.S. or international tax legislation, or exposure to additional tax liabilities may adversely impact our financial results.”
Removed heading “Our revenues depend on the pharmaceutical, biotechnology and medical device industries.”
Removed heading “Our increasing focus on environmental, social, governance, and other sustainability matters could increase our costs, and inaction could harm our reputation and adversely impact our financial results.”
Largest changes
“Changes in and uncertainty regarding U.S. regulations, government policies, government funding decisions, trade policies or tariffs could have a material adverse effect upon our business.”see in full comparison
“Regulatory scrutiny of AI is increasing globally, and existing or future laws, regulations, standards or enforcement actions—many of which remain uncertain or may vary across jurisdictions—could restrict how we use AI, increase compliance costs, require changes to our operations, expose us to fines or litigation, or reduce the expected benefits of our investments in AI technologies. Any of the foregoing could adversely affect our business, financial condition or results of operations.”see in full comparison
“Significant political, trade, or regulatory developments in the jurisdictions in which we operate, such as those stemming from the U.S. administration, are difficult to predict and may have a material adverse effect on us. Similarly, changes in U.S. …”see in full comparison
“As described in the section entitled “Legal Proceedings” in this Annual Report on Form 10-K, a purported stockholder class action lawsuit has been filed against us and certain of our current and former directors and officers. We believe that the claims lack merit and intend to defend the lawsuits vigorously, but there can be no assurance that a favorable resolution will be obtained in any of these matters. …”see in full comparison
“We face increasing attention from investors, regulators, customers, and other stakeholders, who may have conflicting views on our positions, performance, and disclosures relating to environmental, social, governance, and other sustainability-related matters, and we are subject to legal and regulatory requirements relating to such positions, performance, and disclosures. In addition, sustainability-based customer standards, in particular in the EU, may impact our ability to compete successfully. …”see in full comparison
“As reported in our Form 10-Q for the quarter ended March 31, 2024, as filed with the SEC on May 24, 2024, management identified material weaknesses in our internal controls over financial reporting that existed because the company did not have sufficient resources which in turn led to an inability to effectively perform certain control activities and fulfill our internal control and accounting responsibilities. …”see in full comparison
Full comparison: every changed paragraph (113)
The following are certain risk factors that could affect our business, financial condition, results of operations, and cash flows. The risks that are highlighted below are not the only risks that we face. Investors should carefully consider each of the following risks and all of the other information contained in this Annual Report on Form 10-K. Some of theseThese risks relate principallyto, toamong ourother Spin from Labcorp, while others relate principally tothings, our business and the industry in which we operate or to the securities markets generally and ownership of our common stock. If any of the following risks actually occur, our business, financial condition, results of operations, or cash flows could be negatively affected.
•We operate in a highly competitive industry.
•We depend on third parties to provide services critical to our business.business and depend on them to comply with applicable laws and regulations.
•If we are unable to achieve and maintain effective internal controls, our business, financial condition, results of operations, and cash flows could be materially adversely affected.
•Changes in and uncertainty regarding U.S. regulations, government policies, government funding decisions, trade policies or tariffs could have a material adverse effect upon our business.
•A failure to identify and successfully close and integrate strategic acquisitions or close other strategic transactions could have a material adverse effect on our business objectives and our revenues and profitability.
•Failure to keep pace with rapid technological changes, including in the development or use of artificial intelligence,changes could adversely affect our business.
•Issues in the development, deployment and/or use of AI may result in reputational harm, liability, regulatory action or adversely affect our business, financial condition or results of operations.
•Changes in tax rates, laws or regulations or exposure to additional tax liabilities may adversely impact our financial results.
•Our revenues depend on the pharmaceutical, biotechnology, and medical device industries.industries and the expenditures they make in R&D; any reductions or delays could materially and adversely affect our business, financial condition, results of operations, and cash flows.
•Foreign currency fluctuations and our planned use of financial instruments to limit our exposure to currency fluctuations could expose us to risks and financial losses that may adversely affect our financial condition, liquidity and results of operations.
•Foreign currency fluctuations could have an adverse effect on our business.
•Costs associated with our debt and our debt covenants may limit cash flow available to invest in our business.
•We may not be able to access the capital and credit markets on terms that are favorable to us or at all.
Risks Relating to General Matters
•We are subject to a wide range of factors that impact global businesses like ours, including, among other things, macroeconomic trends, labor matters, adverse weather factors or other natural disasters, and damage or disruption to our facilities.
• Failure to establish and maintain effective internal control over financial reporting could materially and adversely affect us.
Risks Relating to Ownership of Our Common Stock
•Our stockholder rights agreement could discourage, delay, or prevent a change in control over us and may affect the trading price of our common stock.
•actions by governmental and/or regulatory authorities;
We experience termination, cancellation and non-renewal of contracts by our customers in the ordinary course of business, and the number and dollar value of cancellations can vary significantly from year to year. If any large customer materially decreases or terminates its relationship with us and we fail to add new customers or expand services to other existing customers to replace lost revenue, our business, financial condition, results of operations or cash flows could be materially adversely affected. For the year ended December 31, 2024,2025, our top ten customers based on revenue accounted for approximately 53%57% of our consolidated revenue and our top ten customers based on backlog accounted for approximately 51%54% of our total backlog. For the year ended December 31, 2024,2025, twoone customerscustomer accounted for approximately 14.3% and 10.5%18.1% of revenue. It is possible that an even greater portion of our revenues will be attributable to a smaller number of customers in the future, including as a result of our entering into strategic provider relationships with customers. Also, consolidation in our potential customer base results in increased competition for important market segments and fewer available customer accounts.
Access to data is foundational to any CRO,CRO. andIn throughaddition to leveraging our uniquein-house relationshipdata, Fortrea maintains relationships with Labcorp we have access to large datasets relevant to clinical trials under a patientbroad range of data providers that provide geographic, therapeutic and site data agreement (the “Patient and Site Data Agreement”). This Patient and Site Data Agreement is set to expire as of June 30, 2025, if not renewed. In addition, we source data from a number of third partiesdatasets, to support our services. With the continual evolution of data offerings and providers, we evaluate existing and new sources on an ongoing basis. An inability to purchase or access the necessary data (from Labcorp pursuant to the Patient and Site Data Agreement or from other third parties) now, or in the future, on commercially reasonable terms or at all, could have a material adverse effect on our business, financial condition and results of operations.
If we are unable to achieve and maintain effective internal controls, our business, financial condition, results of operations, and cash flows could be materially adversely affected.
As a public company, we are required to maintain internal controls over financial reporting and to report any material weaknesses in such internal controls. In addition, beginning with this Annual Report on Form 10-K, our independent registered public accounting firm is required to express an opinion as to the effectiveness of our internal controls over financial reporting. These reporting and other obligations place significant demands on our management and administrative and operational resources, including our accounting and IT resources. We were previously dependent on Labcorp’s systems to provide financial reporting and other financial and accounting information for periods prior to the Spin and through the period ending December 31, 2024. To fully separate ourselves from our Former Parent, we have (i) replaced / upgraded our systems, including our IT and enterprise resource planning systems, (ii) implemented additional financial, IT, and management controls, (iii) implemented new reporting systems and procedures, and (iv) hired additional management, IT, accounting, finance, legal, human resources, and other administrative staff and third-party service providers. If we are unable to achieve and maintain effective internal controls, our business, financial condition, results of operations, and cash flows could be materially adversely affected.
As reported in our Form 10-Q for the quarter ended March 31, 2024, as filed with the SEC on May 24, 2024, management identified material weaknesses in our internal controls over financial reporting that existed because the company did not have sufficient resources which in turn led to an inability to effectively perform certain control activities and fulfill our internal control and accounting responsibilities. Management has devoted substantial resources to the implementation of remediation efforts, as described most recently in the Company’s Quarterly Report on Form 10-Q for the quarter ended September 30, 2024. During the fourth quarter of 2024, the Company successfully completed the testing and evaluation necessary to conclude that, as of December 31, 2024, the previously identified material weaknesses have been remediated.
Building awareness of our brand is an ongoing initiative as we continue to conduct our business under the name Fortrea and certain associated brands, with the potential for new names and systems. Maintaining and continually enhancing the value of our brands is critical to the success of our business. Brand value is based in large part on customer perceptions. Success in promoting and enhancing brand value depends in large part on our ability to provide high-quality products. We may not improve upon the brand recognition associated with Labcorp and its historical or associated brands with customers, sites, suppliers, employees and candidates. If we fail to maintain and/or enhance brand recognition associated with the “Fortrea” name, it may affect our relationships with investigator sites or customers, which may adversely affect our ability to generate revenues and could impede our business in a highly competitive industry. Damage to our brand, reputation or loss of customer confidence in our brand or products could result in decreased demand for our products and have a negative impact on our business, results of operations or financial condition.
We might not be able to engage in certain transactions and equity issuances until July 1, 2025.
Our ability to engage in certain transactions could be limited or restricted as a result of the Spin under the terms of the tax matters agreement entered into with Labcorp and in order to preserve, for U.S. federal income tax purposes, the qualification of the Spin and certain related transactions under Sections 355 and 368(a)(1)(D) of the Internal Revenue Code (the “Code”). Even if these transactions otherwise qualify for tax-free treatment to Labcorp’s stockholders under Section 355 of the Code, they may result in corporate-level taxable gain to Labcorp if there is a 50% or greater change in ownership, by vote or value, of shares of our stock, Labcorp’s stock or the stock of a successor of either occurring as part of a plan or series of related transactions that includes the Spin. Any acquisitions or issuances of our stock or Labcorp’s stock within two years of the Spin are generally presumed to be part of such a plan, although it may be possible to rebut that presumption.
Under the tax matters agreement that we entered into with Labcorp, we are required to comply with the representations and undertakings made in the Internal Revenue Service (“IRS”) ruling that Labcorp received in connection with the Spin and in materials submitted to the IRS in connection therewith and to the tax advisors in connection with the opinions Labcorp received regarding the intended tax treatment of the Spin and certain related transactions. The tax matters agreement also restricts our ability to take or fail to take any action if such action or failure to act could adversely affect the intended tax treatment. In particular, except in specific circumstances, until July 1, 2025, we are restricted from, among other things, (i) entering into any transaction pursuant to which all or a portion of our equity would be acquired, whether by merger or otherwise, and (ii) ceasing to actively conduct certain businesses or activities. These restrictions limit our ability to pursue certain transactions that we may believe to be in the best interests of our stockholders or that might increase the value of our businesses.
Epidemics, pandemics, or widespread public health crisis, such as COVID-19,crisis and associated economic repercussionsrepercussions, may have adverselyan impactedadverse impact on our business and results of operations, and may do so in the future.operations.
Epidemics, pandemics, or widespread public health crises, and associated economic repercussions, had a significant impact on our business and operations in the case of COVID-19 and may have an adverse impact our business and operations in the future. Such public health crises may have an adverse impact on our business and results of operations in a number of ways, including, but not limited to, the implementation of travel restrictions from U.S. and foreign governments; the shutdown of businesses in countries in which we operate; delays or challenges in patient enrollment and new clinical trial start-up; challenges in clinical site initiation due to difficulties in recruiting clinical site investigators and clinical site staff shortages; and the interruption of key clinical trial activities such as clinical trial site monitoring. These adverse effects could impact study participants and clinical sites and limit our ability to efficiently provide clinical trial services. In the past, we have been able to work with our customers to develop solutions to limit disruption to clinical trials while following required regulatory guidelines and maintaining quality to ensure the health and well-being of study participants, including alternative assessment methods such as virtual monitoring visits, but if we are unable to do so in the future, that could have an adverse impact on our business.
Pandemics, including the COVID-19 pandemic, and associated economic repercussions have significantly impacted our business and our operations. Other epidemics, pandemics, or widespread public health crises may impact our business and operations in the future. The possibility of epidemics or pandemics, including the spread of variants, could continue to adversely impact our business and results of operations in a number of ways, including, but not limited to:
•delays or difficulties in commencing new and operating ongoing clinical trials, including intermittent challenges accessing investigative sites, delays in enrolling patients, delays in obtaining approvals from regulatory authorities, and difficulty obtaining necessary pharmaceutical and other products and supplies;
•restrictions on the ability of our field teams to visit healthcare providers and difficulty securing appropriate personal protective equipment and testing and other tools required for client-facing engagements and visits to sites/healthcare providers;
•diversion of healthcare resources away from the conduct of clinical trials, including the diversion of hospitals serving as our clinical trial sites and hospital staff supporting the conduct of our clinical trials, as well as the reduction of our customers’ operating budgets;
•interruption of key clinical trial activities, such as clinical trial site data monitoring, due to social distancing requirements, quarantine and isolation protocols or interruption of clinical trial subject visits and study procedures, which may impact the collection and integrity of study data and ability to measure clinical trial endpoints;
•business disruptions at our customers;
•limitations on our employee resources, including because of quarantine and isolation protocols, sickness of employees or their families or the desire of employees to avoid contact with large groups of people;
•continued disruptions to our supply chain;
•diversion of management resources to focus on mitigating the impacts of pandemics;
•increased cybersecurity risks due to the number of employees that are working remotely in regions impacted by stay-at-home orders, increased levels of remote access creating additional opportunities for cybercriminals to exploit vulnerabilities and employees that may be more susceptible to phishing and social engineering attempts;
•increased cyber-attacks, such as phishing attacks by threat actors using the attention placed on a pandemic as a method for targeting our personnel; and
•strained technological resources due to the number of remote users.
These and other impacts of a pandemic could also have the effect of heightening many of the other factors described in these “Risk Factors” and other parts of this Annual Report on Form 10-K. TheDespite our efforts to manage the impacts of COVID-19 or other future outbreaks, including epidemics, pandemics or widespread public health crisis to the Company, the ultimate impactimpacts dependsdepend on the severity and duration of a pandemic, including the emergence and spread of variants, the continued availability and effectiveness of vaccines and treatments, and actions taken by governmental authorities and other third parties in response to the pandemic, each of which is uncertain, rapidly changing and difficult to predict. Any of these disruptions could adversely impact our business and results of operations.
We are subject to taxes in the U.S. and foreign jurisdictions. Our provision for income taxes is based on a jurisdictional mix of earnings, statutory tax rates and enacted tax rules, including transfer pricing. Enactment of, or changes in the interpretation of, tax legislation or income tax rates globally could materially impact our financial statements. Our effective tax rate and deferred income taxes could be impacted by changes in tax legislation globally.globally, and due to economic and political conditions, tax rates in various jurisdictions may be subject to significant change. The Inflation Reduction Act of 2022 (the “IRA”), enacted August 16, 2022, which, among other items, imposes a 15% alternative minimum tax on corporations with three-year average annual adjusted financial statement income exceeding $1 billion and introduces or extends a number of tax credits to promote clean energy development. We continue to monitor the effects of the IRA and other regulatory developments on our financial condition, operating results, and income tax rate.
Our future effective tax rates could be impacted by changes in the mix of earnings in countries with differing statutory tax rates, changes in the assessment regarding the realization of the valuation of deferred tax assets, or changes in tax laws and regulations or their interpretation.
In October 2021, the Organization for Economic Co-operation and Development (the "OECD") announced the OECD/G20 Inclusive Framework on Base Erosion and Profit Shifting (the "Framework"), which agreed to a two-pillar solution to address tax challenges arising from digitalization of the economy. In December 2021, the OECD released Pillar Two Model Rules defining the global minimum tax rules, which contemplate a minimum tax rate of 15%. An additional “top-up” tax would be incurred in instances where the 15% minimum tax rate is not achieved. To date, various jurisdictions have enacted, or are in the process of enacting, legislation on these rules, and the OECD continues to release additional guidance. While it is uncertain whether the U.S. will enact legislation to adopt the minimum tax directive, certainCertain countries in which we operate have adopted legislation, and other countries are in the process of introducing legislation to implement the minimum tax directive. Further, the OECD issued administrative guidance providing transition and safe harbor rules that could delay the impact of the minimum tax directive. We will continue to monitor the implementation of the Framework by the countries in which we operate. WeThere havewas calculated and accrued anno additional top-up tax due under the Pillar Two Framework in certain jurisdictions where the effective tax rate fell below the minimum threshold of 15%. This amount was not significant to the 2024 income tax provision for the Company.2025.
On July 4, 2025, new legislation commonly referred to as the One Big Beautiful Bill Act of 2025 (the “Tax Act”) was signed into law. The Tax Act includes substantial changes to the U.S. federal tax code and broader fiscal policy for tax year 2025 and forward. The Company has recorded any applicable impacts to its tax provision for the year ended December 31, 2025, which were not significant. There are several provisions of the Tax Act that do not go into effect until future tax years but are also not expected to have a significant impact on tax positions as currently recorded.
Failure to comply with national, state, local or international environmental, health and safety (“EH&S”) laws and regulations, could result in fines and penalties and loss of licensure, and have a material adverse effect upon our business.
We are subject to laws and regulations relating to the protection of the environment and human health and safety, including laws and regulations relating to the handling, transportation and disposal of medical specimens, infectious and hazardous waste and radioactive materials, as well as regulations relating to the safety and health of employees. Failure to comply with these laws and regulations could subject us to denial of the right to conduct business, fines, criminal penalties and/or other enforcement actions that could have a material adverse effect on our business. InThe addition,implementation of new or existing EH&S laws, regulations, and industry and customer standards, and any changes to them, which we cannot predict and which have historically become more stringent over time, could increase our costs and require us to reassess our business priorities. Administrative decisions, legal developments, or other governmental or judicial actions may influence the interpretation or enforcement of EH&S laws, regulations, and industry standards, and may thereby increase compliance or other costs, in the jurisdictions in which we operate. Any of these risks or costs, and our ability to assess, prepare for, and fully comply with future legislationEH&S laws or regulations, could imposehave additionala requirementsmaterial adverse effect on usour thatbusiness mayresults, becash costly.flows, financial condition, or prospects.
In addition, implementation of healthcare reform legislation that adds costs could limit the profits that can be made from the development of new drugs and medical products and devices. This could adversely affect R&D expenditures by such companies, which could in turn decrease the business opportunities available to us both in the U.S. and other countries. New laws or regulations may create a risk of liability, increase our costs or limit our service offerings. AtThe this time, it is unclear exactly how the newcurrent U.S. presidential administration willmay further impact the healthcare reform measures ofimplemented theunder previous Bidenadministrations Administration or whether the new Trump Administrationand could impose other reform efforts, including what, if any, impact such changeswhich could haveadversely onaffect our business. The Trump Administration has recently relied on executive orders in lieu of federal legislation to implement regulatory policy and objectives. We may be unable to anticipate changes in regulatory regimes of the U.S. federal government administration and, therefore, be unable to make timely operational or other changes, assuming we are in a position to effectively respond to any such change, which may not be the case, or to ensure compliance with federal regulations or orders. Executive orders or regulatory priorities issued or rescinded by the U.S. federal government administration may require additional capital expenditures or additional costs and may cause a delay or the abandonment of projects which could adversely affect our results of operations or financial condition.
We may also be required to comply with the data privacy and security laws of other countries in which we operate or with which we transfer and receive data. For example, in the European Economic Area, we are subject to the EU General Data Protection Regulation, and in the U.K., we are subject to the U.K. data protection regime consisting primarily of the GDPR and the U.K. Data Protection Act 2018, respectively, which include a range of compliance obligations for subject companies and imposes penalties for noncompliance of up to the greater of €20 million or 4% of worldwide revenue. The U.K. Data (Use and Access) Act 2025 (“DUA”) included further obligations for companies and imposes increased penalties for marketing and cookie non-compliance of up to £17.5 million or 4% of global annual turnover. We have established processes and frameworks to manage compliance with the GDPR.GDPR and DUA. Potential fines and penalties in the event of a violation of the GDPR and/or DUA could have a material adverse effect on our business and operations. In addition, similar data protection regulations addressing access, use, disclosure and transfer of personal data have been enacted or updated in regions where we do business, including in Asia, Latin America, and Europe. We expect to make changes to our business practices and to incur additional costs associated with compliance with these evolving and complex regulations.
In addition to data protection laws and regulations, government agencies have or are considering (or are adopting) other laws, regulations and guidelines that impact the processing of personal information. For example, the evolving landscape surrounding the use of AI and online advertising may lead to additional compliance costs and could increase our overall risk. Our employees and personnel may use generative AI technologies to perform their work, and the disclosure and use of personal data in generative AI technologies is subject to various privacy laws and other privacy obligations. Governments have passed and are likely to pass additional laws regulating generative AI.AI, such as the EU Artificial Intelligence Act 2024. Our use of this technology could result in additional compliance costs, regulatory investigations and actions, and lawsuits. If we are unable to use generative AI, it could make our business less efficient and result in competitive disadvantages.
Anti-corruption laws in the countries where we conduct business, including the U.S. Foreign Corrupt Practices Act (the “FCPA”), U.K. Bribery Act 2010 (the “Bribery Act”), and similar laws in other jurisdictions, prohibit companiescompanies, their employees, agents, representatives, business partners and theirthird-party intermediaries from engagingpromising, authorizing, making, offering or providing, directly or indirectly, improper payments or benefits to recipients in briberythe including improperly offering, promising, payingpublic or authorizingprivate thesector, giving ofincluding anything of value to individualsa or“foreign entitiesofficial” for the purposepurposes of corruptlyinfluencing official decisions or obtaining or retaining business.business, or otherwise obtaining favorable treatment. We operate in some parts of the world where corruption may be common and where anti-corruption laws may conflict to some degree with local customs and practices. We maintain an anti-corruption program including policies, procedures, training and safeguards in the engagement and management of third parties acting on our behalf. Moreover, we continue to evolve business processes, as regulations and business opportunities require, so that compliance risks are appropriately measured, mitigated, and effectively managed in alignment with appropriate risk tolerances. Despite these safeguards, we cannot guarantee protection from corrupt acts committed by employees or third parties associated with us. Violations or allegations of violations of anti-corruption laws could have a significant adverse effect on our business or results of operations.
Changes in and uncertainty regarding U.S. regulations, government policies, government funding decisions, trade policies or tariffs could have a material adverse effect upon our business.
Changes in regulations, government funding, government funding decisions, trade policies, pricing policies and tariffs imposed by the U.S. and other governments could have an impact on our business and our pharmaceutical, biotechnology and medical device customers.
Significant political, trade, or regulatory developments in the jurisdictions in which we operate, such as those stemming from the U.S. administration, are difficult to predict and may have a material adverse effect on us. Similarly, changes in U.S. administration policy or the policies of foreign countries that affect the geopolitical landscape could give rise to circumstances outside our control that could negatively impact our business operations, including movement of data, particularly given our international operations, or could subject us to additional risks and expenses including discriminatory or conflicting trade policies, sanctions or tariffs. The extent and duration of increased tariffs or sanctions and the resulting impact on general economic conditions and on our business are uncertain and depend on various factors, including but not limited to negotiations between the U.S. and affected countries, the responses of other countries or regions, and exemptions or exclusions that may be granted. The existing and any further trade restrictions, retaliatory trade measures, sanctions and additional tariffs could result in increased costs, disruptions in global shipping and supply chains, restrictions on access to markets and customers, inability to conduct clinical trials in other countries and impacts on our customers and their R&D budgets and priorities, all of which could adversely affect our results of operations or financial condition. In particular, the exposure among certain of our customers to tariffs, pricing mandates, and trade restrictions along with their limited ability to quickly relocate manufacturing may increase capital requirements and create additional pressure on such customers during what may be a period of reduced investment and could create a risk to growth, which could in turn impact our results of operations or financial condition. We and our customers may not be able to fully mitigate the impact of these operational issues, market forces and increased costs or pass price increases on to our customers. While tariffs, pricing, and other trade measures have not yet had a significant impact on our business or results of operations, we cannot predict further developments, and how they may adversely affect our results of operations or financial condition.
In addition, reductions in funding of government agencies and programs relevant to the pharmaceutical, biotechnology and medical device industries—such as the Food and Drug Administration, the National Institutes of Health, and Medicaid—or changes in funding priorities relevant to the pharmaceutical, biotechnology and medical device industries could adversely affect those industries, which could in turn have an effect on the demand for clinical trials and our business. At this time, it is unclear exactly how changes at the federal and state level, as well as any future changes that are made, will impact the industry, what changes will be made to the healthcare reform measures of prior administrations, or whether the government could impose other reform efforts, whether by statute, regulation or executive order, including what, if any, impact such changes could have on our business. We may be unable to anticipate changes in regulatory regimes of the governments where we operate and, therefore, be unable to make timely operational or other changes, assuming we are in a position to effectively respond to any such change, which may not be the case, or to ensure compliance with applicable regulations or orders, all of which could have a material adverse effect on our business. Further, the uncertainties described above may lead to slower decision making and/or could lead to fewer decisions to proceed with studies due to the increased risk profile.
Part of our strategy involves deploying capital to investments that enhance our business, which includes pursuing strategic acquisitions to strengthen our scientific capabilities and enhance therapeutic expertise, enhance global drug development capabilities, and increase presence in key geographic areas, or to enter into and consummate other strategic transactions, such as joint ventures, collaborations or divestitures. However, we may not be able to identify acquisition targets or other strategic arrangements that are attractive to us or that will have a meaningful impact on our operating results or to conduct other strategic transactions on terms that are acceptable to Fortrea, or at all.all, and we may not be able to realize the benefits of strategic transactions we have completed in the past or that we may complete in the future. Furthermore, the successful closing and integration of a strategic acquisitiontransactions entails numerous risks, including, among others:
Current or future acquisitions or other strategic transactions, if any, or any related integrationintegration, divestiture or transition efforts may not be successful, and we cannot provide assurance that our business will not be adversely affected by any future strategic transactions, including with respect to revenues and profitability. Similarly, any potential gains from strategic transactions, such as cost savings or other operational efficiencies may also not be realized.realized, or may be offset, partially or fully, by post-closing indemnification claims or other retained liabilities. Even if we are able to successfully integrate the operations of businesses that we may acquire in the future, we may not be able to realize the benefits that we expect from such acquisitions.
Management's Discussion & Analysis (MD&A)
Removed heading “Subsequent Event”
Removed heading “Credit Agreement Amendment”
Removed heading “Incremental Independent Public Company Expenses”
Largest changes
For the year ended December 31,see in full comparison2024,2025,the Company’sour effective tax rate was1.3%(0.3)% compared to(3.8)%1.3% for the year ended December 31,2023.2024. The effective tax rate for the year ended December 31,20242025 was lower thanthe Company’sour statutory tax rate primarily due to goodwill impairment with no tax benefit, an increase in the valuation allowance, non-deductible employee benefits,foreignwithholding taxes on 2025 non-U.S. earningstaxedthatatareratesnothigherpermanentlythan the U.S. statutory ratereinvested andU.S. tax on foreign income inclusions, partially offset by the U.S. R&D credit and certain state tax benefits. The effective tax rate for the year ended December 31, 2023 was lower than the Company’s statutory tax rate primarily due toforeign earnings taxed at rates higher than the U.S.statutoryrate,U.S. tax on foreign income inclusions, the base erosion and anti-abuse tax (“BEAT”) and non-deductible employee benefits,partially offset bythe U.S.R&Dcreditcredits and certain state tax benefits. The fluctuation in the effective tax rate for the year-to-date period was primarily due to goodwill impairment with no tax benefit, increased withholding taxes on 2025 non-U.S. earnings that are not permanently reinvested and increased non-deductible employee benefits offset by a reduction in the charge for valuation allowance.
Althoughsee in full comparisontheweCompany believesbelieve that the current assumptions and estimates used initsour goodwill impairment analysis are reasonable, supportable, and appropriate, continued efforts to maintain or improve the performance of these businesses could be impacted by unfavorable or unforeseen changes which could impact the existing assumptions used in the impairment analysis. Various factors could reasonably be expected to unfavorably impact existing assumptions: primarily delaysor lower demand resultinginlowernewcontractcustomer bookings and the related delayor reductioninrevenue,revenue from new customers, increases in customer termination activity or increases in operating costs. Accordingly, there can be no assurance that the estimates and assumptions made for the purposes of the goodwill impairmentand intangible assetanalysis will prove to be accurate predictions of future performance. It is possible that our conclusions regarding impairment or recoverability of goodwill in any reporting unit could change in future periods. There can be no assurance that the estimates and assumptions used in our goodwill impairment testing performed as of March 31, 2025 and June 30, 2025 will prove to be accurate predictions of the future, if, for example, (i) the businesses do not perform as projected, (ii) overall economic conditions in 2025 or future years vary from current assumptions (including changes in discount rates), (iii) business conditions or strategies for a specific reporting unit change from current assumptions, including loss of major customers, (iv) investors require higher rates of return on equity investments in the marketplace or (v) enterprise values of comparable publicly traded companies, or actual sales transactions of comparable companies, were to decline, resulting in lower multiples of revenues and EBITDA.
During the years ended December 31,see in full comparison2024, 20232025 and2022,2024, the Company recorded net restructuring charges of$50.1, $21.2,$44.1 and$25.9,$50.1, respectively, which are reflected within Restructuring and other charges in the consolidated and combined statements of operations. These charges are associated with Company actions toalign resources and restructure certain operations which includes eliminating redundant positions and aligning resources and facilities for cost improvements and to meet customer requirements. In addition, in the fourth quarter of 2024, the Company approved a restructuring plan tostreamline its operations and eliminate redundantpositions.positions,TheincludingCompany$3.2recordedanda restructuring charge$4.8 of$21.3impairment of facility relatedtoassetsthisduring2024 plan, which relate primarily to severance benefits2025 andare2024,accounted for under ASC 712, Compensation - Nonretirement Postemployment Benefits. Actions under these restructuring plans are expected to continue through 2025.respectively.
see in full comparisonManagementBased on the annual test performedits annual goodwill impairment testing as ofon October 1,2024.2024,TheitCompanywaselectedpreviouslyto perform a quantitative assessment on its two reporting units, Clinical Development and Clinical Pharmacology. Based upon the results of the quantitative assessment, the Company concludeddetermined that the fair values ofeachtheof itsCompany’s reporting units were greater than the carryingvalues.values, resulting in no impairment. For the Clinical Development reporting unit, the fair value of the business exceeded thebookcarrying value by approximately10%.10%For the Clinical Pharmacology reporting unit, the fair valueas oftheOctoberbusiness1,substantially exceeded the book value.2024.
During the year ended December 31,see in full comparison2024,2025, the Company's operations provided$262.8$113.5 of cash as compared to$168.4$262.8 in2023,2024,anaincreasedecrease of$94.4.$149.3. Thisincreasedecrease in cash flows from operating activities was primarily due to decreases in cash received from accounts receivable,includingdriven by the sale of receivables under the ReceivablesFacility,Facility during 2024, and an increase in cash used for accounts payable. These cash decreases were partially offset bythe decrease in net income and higherlower use of cash for prepaid expenses, taxes and interest, and an increase in net income exclusive of non-cash goodwill and other asset impairments, primarily driven by a decrease in selling, general and administrative expenses.
“In performing its annual goodwill impairment test as of October 1, 2025, the Company elected to perform the qualitative assessment on its two reporting units, Clinical Development and Clinical Pharmacology. Based on the results of the qualitative assessment, the Company concluded that the fair values of each of its reporting units were greater than the carrying values, resulting in no impairment.”see in full comparison
Full comparison: every changed paragraph (69)
The following discussion and analysis is intended to provide a summary of significant factors relevant to the financial performance and condition of Fortrea Holdings Inc., which we refer to in this discussion and analysis as “Fortrea,” the “Company,” “our” and “we”. Prior to the spin-off which was completed on June 30, 2023 (the “Spin” or “the Separation”), Fortrea existed and functioned as part of Labcorp Holdings Inc., which we refer to in this discussion and analysis as “Labcorp” or “Former Parent.” The following discussion and analysis of our financial condition and results of operations should be read in conjunction with our audited consolidated and combined financial statements and corresponding notes and other financial information included elsewhere in this Annual Report on Form 10-K. This discussion contains forward-looking statements that are based upon current expectations and are subject to uncertainty and changes in circumstances. Our actual results could differ materially from the results contemplated by these forward-looking statements due to a number of factors, including those discussed below and elsewhere in this Annual Report on Form 10-K, particularly in Part I, Item 1A. “Risk Factors.” Actual results may differ materially from these expectations. See “Cautionary Statement Concerning Forward-Looking Statements.”
Our team of approximately 15,50014,300 employees conductsis able to conduct operations in approximately 100 countries and delivers comprehensive phase I – IV clinical trial management, clinical pharmacology, and consulting services for our customers. Our offering is scaled to deliver focused and agile solutions to customers globally, streamlining the biopharmaceutical product, and medical device development process.
Subsequent Event
Credit Agreement Amendment
On February 28, 2025, the Company entered into an amendment (the “Second Credit Amendment”) to modify a financial covenant to provide the Company with additional flexibility under the Company’s credit agreement dated as of June 30, 2023 and as amended on May 3, 2024 (the “Existing Credit Agreement”), by and among the Company, certain subsidiaries of the Company and Goldman Sachs Bank USA (as administrative agent and collateral agent), governing the Company’s existing senior credit facility.
The Second Credit Amendment increased the Company’s maximum quarterly Total Leverage Ratio (as defined in the Existing Credit Agreement) from 5.30:1.00 to 6.00:1.00 for the fiscal quarters ending on September 30, 2025 through June 30, 2026, decreasing to 5.75:1.00 for the fiscal quarter ending on September 30, 2026, further decreasing to 5.50:1.00 for the fiscal quarter ending on December 31, 2026, and reverting to 5.30:1.00 thereafter.
In consideration of this adjustment, the Company paid a fee to consenting lenders and has agreed during the covenant adjustment period to certain additional limitations with respect to investments, restricted payments and liens.
Incremental Independent Public Company Expenses
These expenses were allocated to us based on direct usage when identifiable or, when not directly identifiable, on the basis of proportional net revenues or headcount or another reasonable driver, as applicable. We consider the basis on which the expenses have been allocated to reasonably reflect the utilization of services provided to, or the benefit received by, us during the periods presented. However, the allocations may not reflect the expenses we would have incurred as an independent company for the periods presented and may not be representative of future expenses that may be incurred. Actual costs that may have been incurred if we had been a standalone company would depend on a number of factors, including the organizational structure, whether functions were outsourced or performed by employees, and strategic decisions made in areas such as IT and infrastructure. For a period following the Separation, however, some of these functions have beenwere provided by Labcorp under the Transition Services Agreement. The actual costs of services represented by these allocations may vary significantly from the amounts allocated to us in the accompanying financial statements.
The actual costs of services represented by these allocations may vary significantly from the amounts allocated to us in the accompanying financial statements.
On March 9, 2024, the Company, together with its wholly-owned subsidiary, Fortrea Inc. (the “Seller”), entered into an Asset Purchase Agreement (the “Purchase Agreement”) with Endeavor Buyer LLC, an affiliate of Arsenal Capital Partners, pursuant to which the Seller agreed to sell, and to cause its affiliates to sell, certain assets relating to its Enabling Services Segment (the “Transaction”), including the sale of equity interests of Fortrea Patient Access Inc. and its subsidiaries and Endpoint Clinical, Inc. and its subsidiaries. The final adjusted purchase price for the Transaction was $340.0, subject to customary purchase price adjustments, with $295.0 paid at closing and $45.0 to be paid upon achievement of certain transition-related milestones, which includes certain services provided through a Transition Services Agreement. The Transaction closed during the second quarter of 2024. EstimatedThe proceedsfirst milestone payment in the amount of $285.2,$20.0 was received in the first quarter of 2025. The second and final milestone payment in the amount of $25.0 was received in the third quarter of 2025. The Transaction resulted in a loss on disposal of $19.6, subject to further adjustment based on customary purchase price adjustments.$19.6. The decision to sell such assets relating to the Enabling Services Segment represented a strategic shift that had a significant effect on the Company's results and operations and assets and liabilities for the periods presented. As a result, the Company has classified the assets related to the Enabling Services Segment as assets from discontinued operations and liabilities from discontinued operations on the consolidated balance sheet as of December 31, 2023. The operations of the Enabling Services Segment have been classified as income or loss from discontinued operations on the consolidated and combined statements of operations for all periods presented.operations.
The following Management’s Discussion and Analysis of Financial Condition and Results of Operations is intended to help you understand our results of operations for the years ended December 31, 2024, 20232025 and 2022.2024. For a comparison of our results of operations for the fiscal years ended December 31, 2024 and 2023, see “Part II, Item 7. Management’s Discussion and Analysis of Financial Condition and Results of Operations” of our Annual Report on Form 10-K for the fiscal year ended December 31, 2024, filed with the SEC on March 3, 2025.
Results of Continuing Operations for the years ended December 31, 2024, 20232025 and 20222024
The Company’s revenues for the year ended December 31, 2024,2025, were $2,696.4,$2,723.4, aan decreaseincrease of 5.1%1.0% over revenues of $2,842.5$2,696.4 in the corresponding period in 2023.2024. The change in revenues was due to aan decreaseincrease in organic revenues of 5.2%,0.8%, partially offset byand favorable foreign currency translation of 0.1%.0.2%. The Company defines organic growth as the change in revenues excluding the year over year impact of acquisitions, divestitures and currency. The 5.2%0.8% decreaseincrease in organic revenues was primarily driven by decreasedan increase in revenue in our clinical pharmacology business, including higher pass through costscosts. andThis increase was partially offset by lower serviceclinical development revenues resulting primarily from the lower quantity of new business wins prior to the Spin, along with the slower backlog burn rate and the mix of maturecomplex and longer duration studies in our portfolio.portfolio Theas decreasewell wasas partiallylower functional service provider revenue, which more than offset by an increase in revenue from clinicalnet pharmacologynew services.business, including higher pass through costs as projects progress through their lifecycle.
The Company’s revenues for the year ended December 31, 2023, were $2,842.5, an increase of 0.2% over revenues of $2,837.0 in the corresponding period in 2022. The increase in revenues was due to organic growth of 0.1% and favorable foreign currency translation of 0.1%. The increase in organic revenues was primarily driven by an increase in pass through costs offset by the mix and quantity of new business wins prior to the Spin and by the impact of a prior year FSP cancellation.
Direct costs decreased 4.0% in 2024 as compared with 2023 and increased as a percentage of revenues to 80.2% in 2024 as compared to 79.2% in 2023. The decrease in direct costs was primarily due to lower pass through costs as well as cost efficiencies gained from restructuring actions, which has better aligned our resource levels and geographic footprint with project requirements. These declines were partially offset by an increase in stock compensation and professional fees.
Direct costs increased 6.6%2.7% in 20232025, as compared with 20222024, and increased as a percentage of revenues to 79.2%81.5% in 20232025, as compared to 74.5%80.2% in 2022.2024. The increase in direct costs was primarily due to higheran increase in pass through costs, transitionstock services agreement costscompensation and personneldirect costsstudy related expenses, the reintroduction of variable compensation, and lower research and development tax credits. This increase was partially offset by lower headcount and personnel costs, including the removalbenefit of Formerrestructuring Parent corporate allocations and carve-out adjustments Fortrea received prior to the Spin.actions.
Selling, general and administrative expenses consist primarily of administrative payroll and related benefit charges, transition services agreement costs, information technology costs, other facility charges, advertising and promotional expenses, administrative travel and administrativecredit travel.loss provisions.
Selling, general and administrative expenses increaseddecreased 25.1%18.6% in 20242025, as compared to 2023.2024. The increasedecrease was primarily due to lower transition service agreement and information technology costs. This decrease was partially offset by an increase in professional fees and other costs to support the exitestablishment of theour Transitioncorporate Services Agreement with Labcorp and personnel and information technology costsfunctions as a stand-alone company.company as well as the reintroduction of variable compensation.
Selling, general and administrative expenses increased 7.7% in 2023 compared to 2022. The change in selling, general and administrative expenses was primarily due to an increase in personnel costs, credit loss provisions, transition service agreement costs and professional fees partially offset by elimination of prior year Former Parent corporate allocations and carve-out adjustments Fortrea received prior to the Spin.
Goodwill impairment for 2025 was $797.9. The impairment was specific to the Clinical Development reporting unit. There were no goodwill and other asset impairments for the year 2024.
During 2022, the Company recorded intangible asset impairment charges of $9.8. The Company concluded that the fair value was less than carrying value for one of its acquired technology related assets and recorded an asset impairment.
The decrease in depreciation expense for 2024,2025, as compared to 2023,2024, was due to a decrease in depreciable property, plant and equipment, primarily IT assets. The increase in depreciation expense for 2023, as compared to 2022, was primarily due to the increase in of property, plant and equipment, primarily IT assets, as part of the Spin.
The increase in amortization of intangibles and other assets in 2024, as compared to 2023, was not significant.
The decrease in amortization of intangibles and other assets in 2023,2025, as compared to 2022,2024, iswas primarilydue to certain intangible assets reaching the resultend of thetheir impairmentuseful oflives technology assets that occurred induring the fourthfirst quarter of 2022.2025.
During the years ended December 31, 2024, 20232025 and 2022,2024, the Company recorded net restructuring charges of $50.1, $21.2,$44.1 and $25.9,$50.1, respectively, which are reflected within Restructuring and other charges in the consolidated and combined statements of operations. These charges are associated with Company actions to align resources and restructure certain operations which includes eliminating redundant positions and aligning resources and facilities for cost improvements and to meet customer requirements. In addition, in the fourth quarter of 2024, the Company approved a restructuring plan to streamline its operations and eliminate redundant positions.positions, Theincluding Company$3.2 recordedand a restructuring charge$4.8 of $21.3impairment of facility related toassets thisduring 2024 plan, which relate primarily to severance benefits2025 and are2024, accounted for under ASC 712, Compensation - Nonretirement Postemployment Benefits. Actions under these restructuring plans are expected to continue through 2025.respectively.
The increasedecrease in interest expense for year ended December 31, 2024,2025, as compared with the corresponding period in 2023,2024, is primarily due to the higher overall debt balance, and the write-off of $12.2 of debt issuance costs associated with the pay down of debt in the quarter ended June 30, 2024, including the pay down of $70.2 on term loan A and $412.5 on term loan B.B, and the write-off of $12.2 of debt issuance costs associated with the pay down, which occurred during the six months ended June 30, 2024.
The increase in interest expense for year ended December 31, 2023, as compared with the corresponding period in 2022, is primarily due to the incurrence of indebtedness in June 2023, consisting of borrowings under the senior secured term loan facilities and the senior secured notes.
Foreign Exchange Gain (Loss) Gain
The change in foreign exchange gain (loss) gain for the year ended December 31, 2024,2025, as compared to the year ended December 31, 2023,2024, changedwas primarily due to the relativefluctuations weakening ofin the U.S. Dollar against the British Pound and the Euro.
The change in foreign exchange gain (loss) for the year ended December 31, 2023, as compared to the year ended December 31, 2022, was primarily due to the relative strengthening of the U.S. Dollar against the British Pound and the Euro, and the allocation of hedging losses from the Former Parent hedging program for 2023.
1 Not meaningful
The increasedecrease in other, net for the year ended December 31, 2024,2025, as compared to year ended December 31, 2023,2024, iswas primarily related to a change in the recognitionestimated amount of athe contingent consideration payment on a sale of a facility to a thirdthird-party. partyThis anddecrease was partially offset by income related to services provided under Transition Services Agreements.
The increase in other, net for the year ended December 31, 2023, as compared to year ended December 31, 2022, is primarily related to a gain on sale of assets sold in 2023.
Income Tax Expense (Benefit)
For the year ended December 31, 2024,2025, the Company’sour effective tax rate was 1.3%(0.3)% compared to (3.8)%1.3% for the year ended December 31, 2023.2024. The effective tax rate for the year ended December 31, 20242025 was lower than the Company’sour statutory tax rate primarily due to goodwill impairment with no tax benefit, an increase in the valuation allowance, non-deductible employee benefits, foreignwithholding taxes on 2025 non-U.S. earnings taxedthat atare ratesnot higherpermanently than the U.S. statutory ratereinvested and U.S. tax on foreign income inclusions, partially offset by the U.S. R&D credit and certain state tax benefits. The effective tax rate for the year ended December 31, 2023 was lower than the Company’s statutory tax rate primarily due to foreign earnings taxed at rates higher than the U.S. statutory rate, U.S. tax on foreign income inclusions, the base erosion and anti-abuse tax (“BEAT”) and non-deductible employee benefits, partially offset by the U.S. R&D creditcredits and certain state tax benefits. The fluctuation in the effective tax rate for the year-to-date period was primarily due to goodwill impairment with no tax benefit, increased withholding taxes on 2025 non-U.S. earnings that are not permanently reinvested and increased non-deductible employee benefits offset by a reduction in the charge for valuation allowance.
For the year ended December 31, 2023, the Company's effective tax rate was (3.8)% compared to 22.0% for the year ended December 31, 2022. The effective tax rate for the year ended December 31, 2022 was higher than the Company’s statutory tax rate primarily due to foreign earnings taxed at rates higher than the U.S. statutory rate, U.S. taxes on foreign income inclusions and state taxes, partially offset by benefits for permanently non-deductible items, employee benefits, the U.S. R&D credit and certain state benefits.
The Organization for Economic CooperationCo-operation and Development (the "OECD") has introduced new global minimum tax regulations, known as Pillar Two, that came into effect beginning on January 1, 2024. We will continue to monitor this development and its potential impact on our future tax rate. In 2024,2025, we havedid calculatednot andaccrue accrued an additionalany top-up tax under the Pillar Two Framework in certain jurisdictions whereas the effective tax rate fell below the minimum threshold of 15%. This amount was not significant to the total 2024 income tax provisionrates for theall Company.our non-US jurisdictions exceeded 16%.
On July 4, 2025, new legislation commonly referred to as the One Big Beautiful Bill Act of 2025 (the “Tax Act”) was signed into law. The Tax Act includes substantial changes to the U.S. federal tax code and broader fiscal policy for tax year 2025 and forward. We have recorded any applicable impacts to its tax provision for the year ended December 31, 2025, which were not significant. There are several provisions of the Tax Act that do not go into effect until future tax years but are also not expected to have a significant impact on tax positions as currently recorded.
TheWe Company managesmanage cash flow to fund and invest in operational growth, capital expenditures, and credit facility repayments. In connection with the Spin, we incurred indebtedness in an aggregate principal amount of $1,640.0, which consistsconsisted of borrowings under senior secured term loan facilities and senior secured notes. We have also entered into a senior secured revolving credit facility, which consists of a five-year facility in the principal amount of up to $450.0 as further discussed in Note 11, “Debt” to our consolidated and combined financial statements. During the year ended December 31, 2024, we paid down $70.2 on term loan A, and $412.5 on term loan B, respectively.
During the fourth quarter of 2025, we completed a tender offer to repurchase $75.7 of the Company’s outstanding 7.50% Senior secured notes due 2030. The tender offer complied with relevant provisions of the indenture governing the Notes relating to the Company’s requirement to repurchase a portion of the outstanding Notes following Fortrea’s sale of assets relating to its Enabling Services Segment.
During the year ended December 31, 2024, we paid down $70.2 on term loan A, and $412.5 on term loan B, respectively. We also have access to a senior secured revolving credit facility, which consists of a five-year facility in the principal amount of up to $450.0 as further discussed in Note 11, “Debt” to our consolidated and combined financial statements. As of December 31, 2025, there were no balances outstanding on the Company’s revolving credit facility and there were $2.3 in letters of credit issued under the letter of credit sublimit, resulting in $447.7 available for borrowing. The maximum revolver borrowing outstanding was $138.0 and $75.5 during the years ended December 31, 2025, and 2024, respectively.
On May 6, 2024, we entered into a three-year $300.0 accounts receivable securitization program (the “Receivables Facility”). Under this program, Fortrea Inc. conveys receivable balances to a wholly-owned, bankruptcy-remote special purpose entity, which in turn, may sell receivables to a third-party financial institution in exchange for cash. WeAs haveof December 31, 2025, the Company had sold $300.0 of receivablesreceivables, withwhich netwere proceedsderecognized of $297.9 underfrom the ReceivablesCompany’s Facility.consolidated balance sheet.
On February 24, 2026, the Company amended its Receivables Facility, which had been scheduled to terminate on May 6, 2027. The amended Receivables Facility is scheduled to terminate on February 23, 2029, unless terminated earlier pursuant to its terms.
We believe our existing cash and cash flows generated from operations, plus existing credit facilities, will be sufficient to cover the needs of our current and planned operations for at least the next 12 months. From time to time, we routinely evaluate strategic opportunities, including potential acquisitions, joint ventures or investments in complementary businesses. We may also access capital markets through the issuance of debt or equity, which we may use in connection with the acquisition of complementary businesses or other significant assets, or for other strategic opportunities, or general corporate purposes.
Cash Flows for the Year’s Ended December 31, 2024, 20232025 and 20222024
Cash and cash equivalents at December 31, 2024, 20232025 and 20222024 totaled $118.5, $108.6$174.6 and $110.4,$118.5, respectively. Cash and cash equivalents consist of highly liquid instruments, such as commercial paper, time deposits, and other money market instruments, which have maturities when purchased of three months or less.
During the year ended December 31, 2024,2025, the Company's operations provided $262.8$113.5 of cash as compared to $168.4$262.8 in 2023,2024, ana increasedecrease of $94.4.$149.3. This increasedecrease in cash flows from operating activities was primarily due to decreases in cash received from accounts receivable, includingdriven by the sale of receivables under the Receivables Facility,Facility during 2024, and an increase in cash used for accounts payable. These cash decreases were partially offset by the decrease in net income and higherlower use of cash for prepaid expenses, taxes and interest, and an increase in net income exclusive of non-cash goodwill and other asset impairments, primarily driven by a decrease in selling, general and administrative expenses.
During the year ended December 31, 2023, the Company's operations provided $168.4 of cash as compared to $82.7 in 2022, an increase of $85.7. Cash flows from operating activities benefited from moderation in growth of unbilled services and deferred revenue, along with lower cash used for accrued expenses, including lower incentive compensation payments, partially offset by a decrease in net income.
Net cash provided by investing activities for the year ended December 31, 20242025 was $251.6$14.4 as compared to net cash used for investing activities of $(31.8)$251.6 for the year ended December 31, 2023.2024. The $283.4$237.2 increasedecrease in net cash provided by (used for) investing activities for the year ended December 31, 2024,2025, was primarily due to $276.6 of net proceeds from the sale of the Enabling Services Segment andduring athe year overended December 31, 2024 offset by receipt of the first and second milestone payments related to the sale during the year decreaseended inDecember capital31, expenditures.2025. Capital expenditures were $25.5$25.2 and $40.3$25.5 for the years ended December 31, 20242025 and 2023,2024, respectively. Capital expenditures in 2025 and 2024 were 0.9% of revenues, primarily in connection with projects to support growth in the Company's core businesses. The Company intends to continue to pursue selective investments in key therapeutic areas, business areas and geographies to drive growth and to improve efficiency of the Company's operations. Such expenditures are expected to be funded by cash flow from operations.
Net cash used for investing activities for the year ended December 31, 2023 was $(31.8) as compared to net cash used for investing activities of $(54.0) for the year ended December 31, 2022. The $22.2 decrease in net cash used for investing activities was primarily due to a year over year decrease in capital expenditures. Capital expenditures were $40.3 and $54.4 for the years ended December 31, 2023 and 2022, respectively. Capital expenditures in 2023 were 1.4% of revenues, primarily in connection with projects to support growth in the Company's core businesses.
Net cash used for financing activities for the year ended December 31, 20242025 was $497.8$76.3 compared to cash used for financing activities of $140.8$497.8 for the year ended December 31, 2023.2024. Cash used for financing activities for the year ended December 31, 2025 was primarily related to the repurchase of a portion of the 7.50% Senior secured notes due 2030 as described above. Cash used for financing activities for the year ended December 31, 2024 was primarily related to principal payments on the term loan A and term loan B.
Net cash used for financing activities for the year ended December 31, 2023 was $140.8 compared to cash used for financing activities of $6.3 for the year ended December 31, 2022. Financing activities for year ended December 31, 2023 included proceeds from term loans and senior note offerings which were more than offset by the net transfers to Former Parent in connection with the Spin. Information regarding the net transfer is provided in Note 2, “Summary of Significant Accounting Policies” and Note 19, “Transactions with Former Parent” to the audited consolidated and combined financial statements.
We have chosen accounting policies that management believes are appropriate to accurately and fairly report our operating results and financial position in conformity with U.S. GAAP. We apply these accounting policies in a consistent manner. The Company’s critical accounting policies arise in conjunction with revenue recognition, business combinations, income taxes, and goodwillgoodwill, and indefinite-lived assets.
Fixed-price contracts are typically recognized as revenue over time based on a proportional-performance basis, using either input or output methods that are specific to the service provided. In an output method, revenue is determined by dividing the actual units of output achieved by the total units of output required under the contract and multiplying that percentage by the total contract value. When using an input method, revenue is recognized by dividing the actual costs incurred by the total estimated cost expected to complete the contract, and multiplying that percentage by the total contract value. Contract costs principally include direct labor and reimbursable out-of-pocket costs. The estimate of total costs expected to complete the contract requires significant judgment and estimates are based on various assumptions of events that often span several years. These estimates are reviewed periodically and any adjustments are recognized on a cumulative catch-up basis in the period they become known. During the years ended December 31, 20242025 and 2023,2024, reductions of approximately $61$16 and $60,$61, respectively, were recognized in revenue related to performance obligations partially satisfied in previous periods. DuringThe the2025 year ended December 31, 2022, revenue of approximately $72adjustment was recognizedprimarily fromdriven performanceby changes in estimated effort to complete customer contract obligations. The 2024 adjustment was driven by both changes in estimated effort to complete customer contract obligations that were partially satisfied in a previous period. Substantially all of these adjustments were associated withand changes in scope or price for full service clinical studies. The gross and net amounts of revenue recognized solely from changes in estimates were not material.price.
Fee-for-service contracts are typically priced based on transaction volume or time and materials. For volume based contracts the contract value is entirely variablevariable, and revenue is recognized as the specific product or service is completed. For services billed based on time and materials, revenue is recognized using the right to invoice practical expedient.
The Company maintains current receivable amounts with most of its customers. Fluctuations in accounts receivable, netnet, are attributable to a variety of factors including, but not limited to, the timing of cash receipts from customers, the Company’s assessment of collectability and corresponding provision for bad debt expenseexpense, and the inception, transition, modification or termination of customer relationships. The Company regularly monitors and assesses its risk of not collecting amounts owed by customers. This evaluation is based upon an analysis of current and past due amounts, along with relevant history and facts particular to the customer and the evaluation of the recoverability of amounts due. The Company records its allowance for credit losses based on the results of this analysis. The analysis requires the Company to make significant estimates and, as such, changes in facts and circumstances could result in material changes in the allowance for credit losses.
Prior to the Spin, the Company was included in the combined U.S. federal, state, and foreign income tax returns of Labcorp, where eligible. For the periods after Spin, the Company files income tax returns as a separate company. The income tax provisions,provisions and related deferred tax assets and liabilities reflected in our financial statements represent the Company as separate from Labcorp. The Company accounts for income taxes utilizing the asset and liability method. Under this method, deferred income taxes represent the expected future tax consequences of temporary differences between the financial statements carrying amount and the respective tax basis of assets and liabilities. Deferred tax assets and liabilities are measured using enacted tax rates expected to apply to taxable income in the years in which those temporary differences are expected to be recovered or settled. To the extent deferred taxes are recorded to accumulated other comprehensive income, we record the tax effect of any release of deferred taxes using either the specific identification approach or the portfolio approach based on the nature of the underlying item. We elected to not consider the estimated impact of potential future Corporate Alternative Minimum Tax liabilities for purposes of assessing valuation allowances on the Company’s deferred tax balances. The effect on deferred tax assets and liabilities of an enacted change in tax rates is recognized in income in the period that includes the enactment date.
We are subject to income taxes in the U.S. and various foreign jurisdictions. The Company is not currently under tax examination by the Internal Revenue Service (“IRS”) as a separate taxpayer. We are no longer subject to U.S. state income tax audits prior to 2018.2017. ThereWe are subject to ongoing foreign income tax audits as a separate taxpayer in various jurisdictions ranging from 2018 - 2022. While we believe we have adequately accrued for all tax positions, amounts assessed by taxing authorities could be greater than what we have recorded in our financial statements. Accordingly, additional income tax provisions on federal, state and foreign income tax-related matters could be recorded in the future as revised estimates are made or the underlying matters are settled or otherwise resolved. Since the timing of resolution of income tax audits are uncertain, it is difficult to predict with certainty the range of reasonably possible significant increases or decreases in the liability related to uncertain tax positions that may occur within the next twelve months.
With limited exception, the Company has considered the earnings of its foreign subsidiaries prior to 2024 to be indefinitely invested outside the United States on the basis of limited foreign cash reserves and plans for the reinvestment of those subsidiary earnings. Our foreign undistributed earnings are computed under the U.S. federal tax earning and profits (“E&P”) principles. The determination of the amount of deferred tax liability that would be recorded for these earnings if they were not indefinitely reinvested is not practicable at this time. In 2024,2025, management has recorded a deferred tax liability related to applicable foreign withholding taxes on approximately $95.3$133.5 of undistributed 2024 U.S. GAAP earnings and profits of its foreign subsidiaries as the Company does not intend to reinvest these earnings will not be indefinitely reinvested outside the United States.
What changed in the latest 10-Q
Risk Factors
There have been no material changes to the risk factors described in our Annual Report on Form 10-K for the year ended December 31, 2025, as filed with the SEC on February 26, 2026 (our “Annual Report”). For a discussion of the risks relating to our business, see the Part I, Item 1A “Risk Factors” section of our Annual Report and the “Cautionary Statement Concerning Forward-Looking Statements” set forth in Part I, Item 2 of this Form 10-Q.
No wording changes found in this section.
Full comparison: every changed paragraph (0)
Management's Discussion & Analysis (MD&A)
Largest changes
During thesee in full comparisonthreesix months endedMarchJune31,30, 2026, the Company’s operationsusedprovided$17.0$11.9 of cash as compared to$124.2$102.4 of cash used by operations during thethreesix months endedMarchJune31,30, 2025. Thedecreaseincrease in cashusedprovided of$107.2$114.3 for thethreesix months endedMarchJune31,30, 2026 was primarily due toan increase in cash received from accounts receivable,a decrease in cash used for accountspayable,payable and interest, as well as anincreaseimprovement in netincomelossexclusive ofexcluding non-cashgoodwillincome andotherexpenseasset impairments.items. These cash increases were partially offset by higher use of cash for accruedexpenses, including variable compensation.expenses.
“Direct costs decreased 5.4% during the six months ended June 30, 2026 as compared with the corresponding period in 2025. The change in direct costs was due to a decrease in organic direct costs of 6.9%, partially offset by unfavorable foreign currency translation of 1.5%. Direct costs decreased as a percentage of revenues to 80.0% during the six months ended June 30, 2026 as compared to 81.6% in the corresponding period in 2025. …”see in full comparison
“Selling, general and administrative expenses decreased by 17.8% during the six months ended June 30, 2026 as compared with the corresponding period in 2025. The decrease was primarily due to lower information technology and personnel costs, including the benefit of restructuring actions, as well as lower credit loss provisions. These decreases were partially offset by a year over year increase in variable compensation expense.”see in full comparison
Thesee in full comparisonchangedecline in restructuringand other chargesexpense for the three and six months endedMarchJune31,30, 2026, as compared to the correspondingperiodperiods in 2025, wasnotprimarilysignificant.due to the planned progression of the Company’s restructuring programs, which resulted in lower restructuring charges.
There were no goodwill and other asset impairments for the three and six months endedsee in full comparisonMarchJune31,30, 2026. Goodwill impairment for the three and six months endedMarchJune31,30, 2025 was$488.8$309.1 and $797.9, respectively. This impairment was specific to the Clinical Development reporting unit.
Three and Six Months Endedsee in full comparisonMarchJune31,30, 2026 compared with Three and Six Months EndedMarchJune31,30, 2025
Full comparison: every changed paragraph (25)
Fortrea, a Delaware corporation incorporated on January 31, 2023, is a leading global contract research organization (“CRO”) providing biopharmaceutical product and medical device development solutions to pharmaceutical, biotechnology and medical device customers. We offer customers highly flexible delivery models that include Full Service, Functional Service Provider (“FSP”), and Hybrid Service structures. We have a rich history of providing clinical development services for over 30 years across more than 20 therapeutic areas, first as Covance and later as Labcorp Drug Development. On June 30, 2023, we completed the Spin from Labcorp. We leverage our global scale, scientific and therapeutic expertise, clinical data insights, technology innovation,innovation (including Fortrea Intelligent TechnologyTM), industry network and decades of experience as a standalone company and as a business unit prior to the Spin to deliver tailored solutions to our customers. With what we believe is a distinctive market offering, Fortrea meets growing global demand for clinical development services.
Our backlog consists of anticipated future revenue from business awards that either have not started, or that are in process and have not been completed. Our backlog also reflects any cancellation or adjustment activity related to these awards. The average duration of our contracts will fluctuate from period to period based on the contracts comprising our backlog at any given time. The majority of our contracts contain early termination provisions that typically require notice periods ranging from 30 to 90 days. We adjust backlog for foreign currency fluctuations and exclude from backlog amounts that have been recognized as revenue in our statements of operations. Our backlog was $7.8 billion as of MarchJune 31,30, 2026.
Three and Six Months Ended MarchJune 31,30, 2026 compared with Three and Six Months Ended MarchJune 31,30, 2025
Revenues
The Company’s revenues for the three months ended MarchJune 31,30, 2026 were $636.5,$678.2, a decrease of 2.3%4.5% from revenues of $651.3$710.3 in the corresponding period in 2025. The change in revenues was due to a decrease in organic revenues of 3.2%4.9%, andpartially offset by favorable foreign currency translation of 0.9%.0.4%. The 3.2%4.9% decrease in organic revenues was due to lower pass through costs as well as lower demand for our functional service provider business. These decreases were partially offset by an increase in fullour serviceclinical revenue,pharmacology business, driven by an increase in net new business.business and study mix.
The Company’s revenues for the six months ended June 30, 2026 were $1,314.7, a decrease of 3.4% from revenues of $1,361.6 in the corresponding period in 2025. The change in revenues was due to a decrease in organic revenues of 4.0%, partially offset by favorable foreign currency translation of 0.6%. The 4.0% decrease in organic revenues was due to lower pass through costs as well as lower demand for our functional service provider business. These decreases were partially offset by an increase in our clinical pharmacology business, driven by an increase in net new business and study mix.
Direct costs decreased 4.1%6.6% during the three months ended MarchJune 31,30, 2026 as compared with the corresponding period in 2025. The change in direct costs was due to a decrease in organic direct costs of 6.3%7.4%, andpartially offset by unfavorable foreign currency translation of 2.2%.0.8%. Direct costs decreased as a percentage of revenues to 80.6%79.5% during the three months ended MarchJune 31,30, 2026 as compared to 82.1%81.2% in the corresponding period in 2025. The 6.3%7.4% decrease in organic direct costs was primarily due to lower pass through and stock-based compensation costs, as well as lower personnel costs, including the benefit of restructuring actions. These decreases were partially offset by a year over year increase in variable compensation expense.expense and clinical pharmacology study related costs.
Direct costs decreased 5.4% during the six months ended June 30, 2026 as compared with the corresponding period in 2025. The change in direct costs was due to a decrease in organic direct costs of 6.9%, partially offset by unfavorable foreign currency translation of 1.5%. Direct costs decreased as a percentage of revenues to 80.0% during the six months ended June 30, 2026 as compared to 81.6% in the corresponding period in 2025. The 6.9% decrease in organic direct costs was primarily due to lower pass through and stock-based compensation costs, as well as lower personnel costs, including the benefit of restructuring actions. These decreases were partially offset by a year over year increase in variable compensation expense and clinical pharmacology study related costs.
Selling, general and administrative expenses decreased by 17.5%18.2% during the three months ended MarchJune 31,30, 2026 as compared with the corresponding period in 2025. The decrease was primarily due to lower information technology and personnel costs, including the benefit of restructuring actions.actions, as well as lower credit loss provisions. These decreases were partially offset by a year over year increase in variable compensation expense.
Selling, general and administrative expenses decreased by 17.8% during the six months ended June 30, 2026 as compared with the corresponding period in 2025. The decrease was primarily due to lower information technology and personnel costs, including the benefit of restructuring actions, as well as lower credit loss provisions. These decreases were partially offset by a year over year increase in variable compensation expense.
The change in depreciation expense for the three and six months ended MarchJune 31,30, 2026, as compared to the corresponding periodperiods in 2025, was not significant.
The change in amortization of intangibles and other assets duringfor the three and six months ended MarchJune 31,30, 2026, as compared to the corresponding periodperiods in 2025, was not significant.
There were no goodwill and other asset impairments for the three and six months ended MarchJune 31,30, 2026. Goodwill impairment for the three and six months ended MarchJune 31,30, 2025 was $488.8$309.1 and $797.9, respectively. This impairment was specific to the Clinical Development reporting unit.
The changedecline in restructuring and other chargesexpense for the three and six months ended MarchJune 31,30, 2026, as compared to the corresponding periodperiods in 2025, was notprimarily significant.due to the planned progression of the Company’s restructuring programs, which resulted in lower restructuring charges.
The decrease in interest expense for the three and six months ended MarchJune 31,30, 2026, as compared with the corresponding periodperiods in 2025, was due to lower average debt outstanding during the first quarterand second quarters of 2026, driven by the repurchase of $75.7 of senior secured notes in 2025 and zerono borrowingborrowings on the revolverrevolving incredit facility during the quarter,first half of 2026, as well as lower effective interest rates on term loan A and term loan B.
The change in foreign exchange gain (loss) for the three and six months ended MarchJune 31,30, 2026 compared to the foreign exchange gain (loss) for three and six months ended MarchJune 31,30, 2025, was primarily due to the fluctuations in the U.S. Dollar against the British Pound and the Euro.
The changedecline in other, net for the three and six months ended MarchJune 31,30, 2026, as compared with the corresponding periodperiods in 2025, was notprimarily significant.due to income recognized in the prior-year periods related to services provided under transition services agreements that terminated in 2025.
For the three months ended MarchJune 31,30, 2026, the Company's effective tax rate was (91.91000.0)% compared to (2.71.1)% for the corresponding period in 2025. For the six months ended June 30, 2026, the Company's effective tax rate was (172.6)% compared to (2.1)% for the corresponding period in 2025. The fluctuationfluctuations wasin the quarter-to-date and year-to-date periods were primarily due to goodwill impairment with no associated tax benefit and BEAT for the three and six months ended MarchJune 31,30, 2025 and the impact of valuation allowance primarily related to expected interest deductibility limitations for the three and six months ended MarchJune 31,30, 2026.
The Company manages cash flow to fund and invest in operational growth, capital expenditures, and credit facility repayments. In connection with the Spin, we incurred indebtedness in an aggregate principal amount of $1,640.0, which consists of borrowings under senior secured term loan facilities and senior secured notes. We have also entered into a senior secured revolving credit facility, which consists of a five-year facility in the principal amount of up to $450.0 as further discussed in Note 6, “Debt” to our condensed consolidated financial statements. As of MarchJune 31,30, 2026, there was no balance outstanding on the Company’s revolving credit facility and there were $2.3 in letters of credit issued under the letter of credit sublimit, resulting in $447.7 available for borrowing. The maximum revolver borrowing outstanding was $— and $98.5$135.5 during the threesix months ended MarchJune 31,30, 2026 and 2025, respectively.
On May 6, 2024, we entered into a three-year $300.0 accounts receivable securitization program (the “Receivables Facility”). Under this program, Fortrea Inc. conveys receivable balances to a wholly-owned, bankruptcy-remote special purpose entity, which in turn, may sell receivables to a third-party financial institution in exchange for cash. As of MarchJune 31,30, 2026, the Company had sold $300.0 of receivables, which were derecognized from the Company’s consolidated balance sheet.
Cash Flows for the threeSix months ended MarchJune 31,30, 2026 and 2025
Cash and cash equivalents at MarchJune 31,30, 2026 and 2025 totaled $147.5$168.6 and $101.6,$81.2, respectively. Cash and cash equivalents consist of highly liquid instruments, such as commercial paper, time deposits and other money market instruments, which have maturities when purchased of three months or less.
During the threesix months ended MarchJune 31,30, 2026, the Company’s operations usedprovided $17.0$11.9 of cash as compared to $124.2$102.4 of cash used by operations during the threesix months ended MarchJune 31,30, 2025. The decreaseincrease in cash usedprovided of $107.2$114.3 for the threesix months ended MarchJune 31,30, 2026 was primarily due to an increase in cash received from accounts receivable, a decrease in cash used for accounts payable,payable and interest, as well as an increaseimprovement in net incomeloss exclusive ofexcluding non-cash goodwillincome and otherexpense asset impairments.items. These cash increases were partially offset by higher use of cash for accrued expenses, including variable compensation.expenses.
Net cash used for investing activities for the threesix months ended MarchJune 31,30, 2026 was $8.0$15.0 as compared to net cash provided by investing activities of $16.1$8.6 for the threesix months ended MarchJune 31,30, 2025. The $24.1$23.6 decreaseincrease in net cash (used for) provided by investing activities for the threesix months ended MarchJune 31,30, 2026 was primarily due to receipt of the first milestone payment related to the sale of the Enabling Services Segmentsegment during the threesix months ended MarchJune 31,30, 2025 and a period over period increase in capital expenditures. Capital expenditures were $8.0$17.0 and $2.9$10.4 for the threesix months ended MarchJune 31,30, 2026 and 2025, respectively. Capital expenditures for the threesix months ended MarchJune 31,30, 2026 were 1.3% of revenues, primarily in connection with projects to support growth in the Company's core businesses. The Company also intends to continue to pursue selective investments in key therapeutic areas, business areas and geographies to drive growth and to improve efficiency of the Company's operations. Such expenditures are expected to be funded by cash flow from operations.
Net cash provided by financing activities for the threesix months ended MarchJune 31,30, 2026 was $— compared to cash provided by financing activities of $88.4$49.4 for the threesix months ended MarchJune 31,30, 2025. Cash provided by financing activities for the threesix months ended MarchJune 31,30, 2025 was primarily related to net proceeds from the revolving credit facility. The Company did not draw on the revolving credit facility during the threesix months ended MarchJune 31,30, 2026.
FTRE insider buying and selling (Form 4)
Since 2026-04-11, insiders reported open-market purchases in 0 Form 4 filings and open-market sales in 10 filings (6 insiders, 8 trade dates, 246,119 shares, about $4.5M). Net open-market shares: -246,119 (purchases minus sales); net value about -$4.5M.Totals add up every open-market (code P and S) line in those filings, using the prices reported in the filings. Awards, option exercises, tax withholding and gifts are listed below but not counted.
| Trade date | Insider | Transaction | Shares | Price | Value |
|---|---|---|---|---|---|
| 2026-09-09 | Russell Carrie Elizabeth |
Open-market sale | 246 | $16.85 | $4.1K |
| 2026-09-09 | Morais Mark A. |
Open-market sale | 3,149 | $16.85 | $53.1K |
| 2026-09-08 | Russell Carrie Elizabeth |
Option exercise | 850 | — | — |
| 2026-09-08 | Morais Mark A. |
Option exercise | 7,157 | — | — |
| 2026-08-19 | Morais Mark A. |
Open-market sale | 4,892 | $18.19 | $89.0K |
| 2026-08-18 | Morais Mark A. |
Option exercise | 11,313 | — | — |
| 2026-08-06 | Thakral Anshul |
Open-market sale | 55,882 | $18.17 | $1.0M |
| 2026-08-06 | Thakral Anshul |
Open-market sale | 55,975 | $18.06 | $1.0M |
| 2026-08-05 | Thakral Anshul |
Open-market sale | 49,452 | $19.03 | $941.1K |
| 2026-08-05 | Thakral Anshul |
Open-market sale | 50,417 | $19.28 | $972.0K |
| 2026-08-04 | Thakral Anshul |
Option exercise | 416,666 | — | — |
| 2026-08-03 | Sanders Machelle |
Open-market sale | 9,700 | $18.01 | $174.7K |
| 2026-07-20 | Smith David Ross |
Option exercise | 6,598 | — | — |
| 2026-06-10 | Sanders Machelle |
Option exercise | 38,817 | — | — |
| 2026-06-10 | Smith David Ross |
Shares withheld for tax | 18,244 | $16.34 | $298.1K |
| 2026-06-10 | Smith David Ross |
Option exercise | 38,817 | — | — |
| 2026-06-10 | Pesicka Edward A |
Option exercise | 38,817 | — | — |
| 2026-06-10 | Morais Mark A. |
Open-market sale | 4,674 | $16.82 | $78.6K |
| 2026-06-10 | Ray Amrit |
Option exercise | 38,817 | — | — |
| 2026-06-10 | Russell Erin L |
Option exercise | 38,817 | — | — |
| 2026-06-02 | Morais Mark A. |
Open-market sale | 4,866 | $15.49 | $75.4K |
| 2026-06-02 | Mcconnell Jill G. |
Open-market sale | 4,866 | $15.49 | $75.4K |
| 2026-06-01 | Morais Mark A. |
Option exercise | 11,006 | — | — |
| 2026-06-01 | Mcconnell Jill G. |
Option exercise | 11,006 | — | — |
| 2026-05-18 | Parks Robert |
Open-market sale | 2,000 | $13.44 | $26.9K |
| 2026-05-14 | Neupert Peter M |
Option exercise | 148,536 | — | — |
Well-known investors holding FTRE (13F)
| Investor | Quarter | Shares | Reported value | % of their 13F | Change vs prior quarter |
|---|---|---|---|---|---|
| AQR Capital Management (Cliff Asness) | 2026-06-30 | 2,980,474 | $51.9M | 0.02% | Reduced 10% |
| Renaissance Technologies | 2026-06-30 | 1,289,609 | $22.4M | 0.03% | Reduced 10% |
| Citadel Advisors (Ken Griffin) | 2026-06-30 | 1,023,010 | $17.8M | 0.01% | Added 101% |
| Millennium Management (Israel Englander) | 2026-06-30 | 626,489 | $10.9M | 0.01% | Added 148% |
| Two Sigma Investments | 2026-06-30 | 215,937 | $3.8M | 0.0% | Reduced 52% |
| Point72 Asset Management (Steve Cohen) | 2026-06-30 | 352,372 | $3.3M | — | Sold out |
| D. E. Shaw & Co. | 2026-06-30 | 127,123 | $2.2M | 0.0% | Added 140% |
| Gotham Asset Management (Joel Greenblatt) | 2026-06-30 | 101,013 | $1.8M | 0.0% | New position |