Private company

Chimerix (United States)

Chimerix (United States) is a summary of material factors.1 It was founded in 2000.1 It is headquartered in Durham.1

Last updated Oct 20, 2026.

Overview

2000Founded1
  • IndustryPharmaceutical Preparations1
  • HeadquartersDurham1
  • Websitewww.chimerix.com
  • Incorporated inDE3
  • Business address2505 Meridian Parkway, Suite 100, Durham, Nc 277133
  • Filer categoryNon-accelerated filer, Smaller reporting company3

Below is a summary of material factors that make an investment in our common stock speculative or risky. Importantly, this summary does not address all of the risks and uncertainties that we face. Additional discussion of the risks and uncertainties summarized in this risk factor summary, as well as other risks and uncertainties that we face, can be found under “Risk Factors” in Part I, Item 1A of this Annual Report. The below summary is qualified in its entirety by that more complete discussion of such risks and uncertainties. You should consider carefully the risks and uncertainties described under “Risk Factors” in Part I, Item 1A of this Annual Report as part of your evaluation of an investment in our common stock.4 From its latest annual report

Financials

From the company’s reports to the SEC. Every number links to the filing it came from.

Key numbers, fiscal 2024

100.0%Gross margin5
-45550.5%Operating margin5
-41692.0%Net margin5
-34.6%Revenue growth, 20245
-72.6%Return on equity5
-$75.3MFree cash flow5

Where the money goes

Where each dollar of revenue went, fiscal 2024

  • Other costs100¢$212.0K

Out of $212.0K in revenue.5 The company lost money this year.

Financial statements

Revenue67895$212.0K in 2024−97% since 2018
0$10.0M$20.0M$30.0M$40.0M2018: $7.2M$7.2M20182019: $12.5M$12.5M2019+73%2020: $5.4M$5.4M2020−57%2021: $2.0M$2.0M2021−63%2022: $33.8M$33.8M2022+1609%2023: $324.0K$324.0K2023−99%2024: $212.0K$212.0K2024−35%
Gross profit895$212.0K in 2024−96% since 2020
0$10.0M$20.0M$30.0M$40.0M2020: $5.4M$5.4M20202021: $2.0M$2.0M2021−63%2022: $33.4M$33.4M2022+1587%2023: $324.0K$324.0K2023−99%2024: $212.0K$212.0K2024−35%
Operating income67895-$96.6M in 2024+35% since 2018
-$200.0M-$150.0M-$100.0M-$50.0M02018: -$71.6M-$71.6M20182019: -$116.0M-$116.0M2019+62%2020: -$44.5M-$44.5M2020−62%2021: -$173.4M-$173.4M2021+290%2022: -$60.4M-$60.4M2022−65%2023: -$93.1M-$93.1M2023+54%2024: -$96.6M-$96.6M2024+4%
Net income67895-$88.4M in 2024+27% since 2018
-$200.0M-$100.0M0$100.0M$200.0M2018: -$69.5M-$69.5M20182019: -$112.6M-$112.6M2019+62%2020: -$43.5M-$43.5M2020−61%2021: -$173.2M-$173.2M2021+298%2022: $172.2M$172.2M20222023: -$82.1M-$82.1M20232024: -$88.4M-$88.4M2024+8%
Fiscal year2018201920202021202220232024
Revenue$7.2M6$12.5M7$5.4M8$2.0M9$33.8M5$324.0K5$212.0K5
Cost of revenue$08$09$447.0K5$05$05
Gross profit$5.4M8$2.0M9$33.4M5$324.0K5$212.0K5
Research and development$55.2M12
Selling, general and admin
Operating expenses$175.4M9$93.8M5$93.4M5$96.8M5
Operating income-$71.6M6-$116.0M7-$44.5M8-$173.4M9-$60.4M5-$93.1M5-$96.6M5
Income before tax-$173.2M9$172.2M5-$82.1M5-$88.4M5
Income tax$06$07$08$09$36.0K5$05$05
Net income-$69.5M6-$112.6M7-$43.5M8-$173.2M9$172.2M5-$82.1M5-$88.4M5
Earnings per share-$2.037-$0.708-$2.049$1.975-$0.935-$0.995
Earnings per share (diluted)-$2.037-$0.708-$2.049$1.945-$0.935-$0.995
Shares (weighted, basic)84.9M shares987.6M shares588.6M shares589.7M shares5
Shares (weighted, diluted)84.9M shares988.8M shares588.6M shares589.7M shares5

Compare Chimerix (United States) with another company

Corporate structure

Chimerix (United States) sits at the top of its group. 1 entity, 1 country on record. Switch between the flow chart and the network, and select any entity to see its details.

Major holders of Chimerix (United States)

  • RA CAPITAL MANAGEMENT, L.P. Filed SCHEDULE 13G/A on Chimerix (United States), latest May 15, 2025 (3 filings since Sep 29, 2023)
  • GLAZER CAPITAL, LLC Filed SCHEDULE 13G on Chimerix (United States), latest Apr 17, 2025
  • Rubric Capital Management LP Filed SC 13G/A on Chimerix (United States), latest Feb 12, 2024 (4 filings since Feb 14, 2022)
  • Point72 Asset Management, L.P. Filed SC 13G/A on Chimerix (United States), latest Feb 14, 2023 (2 filings since Feb 14, 2022)
  • MONTANOVA CAPITAL, LLC Filed SC 13G/A on Chimerix (United States), latest Feb 13, 2023 (2 filings since May 2, 2022)
  • Opaleye Management Inc. Filed SC 13G/A on Chimerix (United States), latest Feb 13, 2023 (2 filings since Feb 1, 2022)
  • Peter Moll Filed SC 13G on Chimerix (United States), latest Jul 5, 2022
  • CANTEX PHARMACEUTICALS, INC. Filed SC 13G/A on Chimerix (United States), latest Feb 3, 2022
  • Chimerix (United States) Durham

Built from major holders from Schedules 13D and 13G. Each entity in the chart links to its source.

What it owns

What Chimerix (United States) reports owning in its annual reports to the SEC: buildings, land and equipment, real estate and locations, investments, intangible assets and inventory, at the end of its latest fiscal year and a year before.

Property and equipment

ItemLatestA year beforeChange
Property and equipment, before depreciation$5.4M5 Dec 31, 2024$5.4M5 Dec 31, 2023+0.1%
Accumulated depreciation$5.0M5 Dec 31, 2024$5.2M5 Dec 31, 2023−3.6%
Property and equipment, net$417.0K5 Dec 31, 2024$224.0K5 Dec 31, 2023+86.2%
Operating-lease assets (leased space)$951.0K5 Dec 31, 2024$1.5M5 Dec 31, 2023−35.8%

Properties, in its own words

Our corporate headquarters are located at 2505 Meridian Parkway, Suite 100, Durham, North Carolina 27713 in a facility we lease encompassing approximately 21,325 square feet of office space. The leases for this facility expire in July 2026. We separately lease laboratory space in Durham, North Carolina, encompassing a total of approximately 7,925 square feet. The lease for this laboratory space in Durham expires in July 2026.

We believe that our property and equipment are generally well maintained and in good operating condition.

Item 2 of the 10-K filed Mar 21, 2025.4

Leadership

Who has led Chimerix (United States), and when. Pick a name to see everywhere that person has worked.

Board members and other officers (31)

Timeline

  1. Apr 21, 20258-K Ended a material agreement; Completed an acquisition or sale; Listing notice or transfer51
  2. Mar 21, 20258-K Results of operations52
  3. Mar 5, 20258-K Entered a material agreement; Regulation FD disclosure53
  4. Mar 5, 20258-K Entered a material agreement54
  5. Mar 3, 20258-K Other events55
  6. Dec 30, 20248-K Entered a material agreement; New debt or obligation; Other events56
  7. Dec 10, 20248-K Regulation FD disclosure; Other events57
  8. Nov 14, 20248-K Executive or director change58
  9. Nov 7, 20248-K Results of operations; Regulation FD disclosure59
  10. Aug 13, 20248-K Results of operations; Regulation FD disclosure60
  11. Jul 3, 20248-K Listing notice or transfer61
  12. Jun 21, 20248-K Shareholder vote; Other events62
  13. Aug 1, 2023New chief executive Michael T. Andriole becomes CEO14
  14. Apr 9, 2019New chief executive Michael A. Sherman becomes CEO15
  15. Apr 11, 2014New chief executive M. Michelle Berrey becomes CEO16
  16. Apr 10, 2013New chief executive Kenneth I. Moch becomes CEO17
  17. 2000Founded Founded1

Calendar

When it reported results

  1. Mar 21, 2025Reported quarterly or annual results52
  2. Nov 7, 2024Reported quarterly or annual results59
  3. Aug 13, 2024Reported quarterly or annual results60
  4. May 1, 2024Reported quarterly or annual results63
  5. Feb 29, 2024Reported quarterly or annual results64
  6. Nov 2, 2023Reported quarterly or annual results65
  7. Aug 3, 2023Reported quarterly or annual results66
  8. May 4, 2023Reported quarterly or annual results67

Upcoming dates from Nasdaq's calendar; past results from the company's 8-K filings (Item 2.02). The full markets calendar

Filings

235 filings to the SEC since October 2021: 5 annual reports, 10 quarterly reports, 45 major events, 101 insider forms, 19 large holders, 55 other. The latest 20:

  1. May 15, 2025SCHEDULE 13G/A EDGAR
  2. May 1, 202515-12G EDGAR
  3. Apr 22, 2025EFFECT EDGAR
  4. Apr 21, 20254 EDGAR
  5. Apr 21, 20254 EDGAR
  6. Apr 21, 20254 EDGAR
  7. Apr 21, 20254 EDGAR
  8. Apr 21, 20254 EDGAR
  9. Apr 21, 20254 EDGAR
  10. Apr 21, 20254 EDGAR
  11. Apr 21, 20254 EDGAR
  12. Apr 21, 20254 EDGAR
  13. Apr 21, 20254 EDGAR
  14. Apr 21, 20254 EDGAR
  15. Apr 21, 20254 EDGAR
  16. Apr 21, 20254 EDGAR
  17. Apr 21, 20254 EDGAR
  18. Apr 21, 202525-NSE EDGAR
  19. Apr 21, 2025S-8 POS EDGAR
  20. Apr 21, 2025S-8 POS EDGAR

The 235 filings since October 2021 can be filtered by form type and year here when JavaScript is on.

Every filing from the last five years, summarized. The full record is on SEC EDGAR.

Insider trades

29 open-market trades by officers, directors and large owners since October 2021: 13 buys and 16 sales. Grants, option exercises and gifts are left out.

DateWhoTradeSharesPriceValueFiling
Feb 13, 2025Melemed Allen S.CHIEF MEDICAL OFFICERSale3,065$4.50$13.8KForm 4
Feb 13, 2025Andriole Michael T.PRESIDENT AND CEOSale7,370$4.52$33.3KForm 4
Feb 13, 2025Alrutz Michael AlbertSVP AND GENERAL COUNSELSale1,600$4.52$7.2KForm 4
Feb 13, 2025Jakeman DavidVP OF FINANCE AND ACCOUNTINGSale300$4.53$1.4KForm 4
Feb 13, 2025LaSpaluto MichelleCHIEF FINANCIAL OFFICERSale2,260$4.51$10.2KForm 4
Jan 30, 2025Jakeman DavidVP OF FINANCE AND ACCOUNTINGSale2,800$4.10$11.5KForm 4
Jan 30, 2025LaSpaluto MichelleCHIEF FINANCIAL OFFICERSale1,015$4.11$4.2KForm 4
Jan 30, 2025Andriole Michael T.PRESIDENT AND CEOSale2,350$4.10$9.6KForm 4
Aug 8, 2024Andriole Michael T.PRESIDENT AND CEOSale1,285$0.83$1.1KForm 4
Feb 14, 2024Andriole Michael T.PRESIDENT AND CEOSale1,744$1.04$1.8KForm 4
Feb 14, 2024LaSpaluto MichelleCHIEF FINANCIAL OFFICERSale1,940$1.04$2.0KForm 4
Feb 14, 2024Jakeman DavidVP OF FINANCE AND ACCOUNTINGSale2,660$1.04$2.8KForm 4
Nov 17, 2023MIDDLETON FRED ADirectorBuy17,295$0.96$16.6KForm 4
Nov 10, 2023MIDDLETON FRED ADirectorBuy2,705$0.92$2.5KForm 4
Sep 28, 2023Jakeman DavidVP OF FINANCE AND ACCOUNTINGSale3,610$0.99$3.6KForm 4
Sep 25, 2023MIDDLETON FRED ADirectorBuy20,000$0.98$19.6KForm 4
May 18, 2023Andriole Michael T.PRESIDENT AND CEOBuy51,700$1.14$58.9KForm 4
May 12, 2023Sherman Michael A.Chief Executive OfficerBuy87,000$1.12$97.6KForm 4
May 10, 2023DEMSKI MARTHA JDirectorBuy18,000$1.11$20.0KForm 4
May 8, 2023Meyer Robert J.DirectorBuy8,750$1.14$10.0KForm 4

All 29 trades can be filtered by person here when JavaScript is on.

From Forms 4 filed with the SEC.

Major holders

Investors who own more than 5% of the shares must tell the SEC: a 13D if they may seek to influence the company, a 13G if they hold passively.

SEC filer profile

How Chimerix (United States) is registered with the Securities and Exchange Commission, from its EDGAR record and the cover page of its latest annual report.

  • Name on EDGARCHIMERIX INC2
  • CIK0001117480
  • Employer ID (EIN)33-09033954
  • Filer statusNon-accelerated filer not an emerging growth company; a smaller reporting company; not a shell company4
  • Incorporated inDelaware4
  • Fiscal year endsDecember 312
  • Industry code (SIC)2834 Pharmaceutical Preparations2
  • SEC reviewing officeOffice of Life Sciences, Division of Corporation Finance2
  • Business address2505 Meridian Parkway, Suite 100, Durham, NC 277132
  • Phone919.806.10742
  • Shares outstanding93,803,846 as of Apr 11, 202576
  • Public float$74.3M as of Jun 28, 20244
  • AuditorErnst & Young LLP, Raleigh, North Carolina PCAOB ID 42; no auditor attestation of internal control over financial reporting4
  • On EDGAR sinceAug 5, 20022
  • Filings916 in all: 4 (391), 8-K (156), SC 13G/A (43), 3 (42), 10-Q (36), CT ORDER (28), SC 13G (26), 144 (13)2
    All 52 form types

    S-8 (13), S-8 POS (13), 10-K (12), DEFA14A (12), DEF 14A (11), EFFECT (11), CORRESP (10), 424B5 (9), SC TO-T/A (9), 4/A (8), UPLOAD (7), POS AM (5), REGDEX (4), S-3 (4), S-3ASR (4), D (3), S-1/A (3), SC 14D9/A (3), SC14D9C (3), 10-K/A (2), 10-Q/A (2), 3/A (2), 424B3 (2), 424B4 (2), 8-K/A (2), S-1 (2), S-3/A (2), SC TO-C (2), SCHEDULE 13G (2), SCHEDULE 13G/A (2), SEC STAFF LETTER (2), 15-12G (1), 25-NSE (1), 5 (1), 8-A12B (1), CERTNAS (1), DRS (1), DRSLTR (1), FWP (1), POSASR (1), S-1MEF (1), SC 13D (1), SC 14D9 (1), SC TO-T (1)

  • Latest filingsAnnual report (10-K) Mar 21, 2025
    Quarterly report (10-Q) Nov 7, 2024
    Proxy statement (DEF 14A) Apr 26, 2024
    Latest 8-K (8-K) Apr 21, 2025

Securities registered for trading

ClassSymbolExchange
Common Stock, par value $0.001 per shareCMRXThe Nasdaq Global Market

From the cover page of the 10-K filed Mar 21, 2025 (Section 12(b) of the Exchange Act).4

Risk factors and legal proceedings

The risks Chimerix (United States) names in Item 1A of its 10-K filed Mar 21, 2025: 57 risks under these headings, as written.4

  • Risks Related to the Merger with Jazz Pharmaceuticals plc
  • The pending merger with Jazz Pharmaceuticals Public Limited Company (Jazz) is subject to a number of conditions beyond our control. We may not complete the pending merger with Jazz within the time frame we anticipate or at all, which could have an adverse effect on our business, financial results, and our stock price.
  • The pendency of the merger with Jazz could adversely affect our business, financial results and/or results of operations and may impair our ability to attract and retain qualified employees or retain or maintain relationships with our customers, suppliers, other business partners or governmental entities.
  • While the Merger Agreement is in effect, we are subject to restrictions on our business activities.
  • In certain instances, the Merger Agreement requires us to pay a termination fee to Jazz, which could require us to use available cash that would have otherwise been available for general corporate purposes.
  • We have incurred, and will continue to incur, direct and indirect costs as a result of the pending merger with Jazz.
  • Risks Related to Our Financial Condition and Need For Additional Capital
  • We have incurred significant losses in each year since our inception other than 2022. We anticipate that we will continue to incur significant losses for the foreseeable future.
  • Our ability to generate future revenues from product sales is uncertain and depends upon our ability to successfully develop, obtain regulatory approval for, and commercialize product candidates, and even if we generate future revenues, they may not be sufficient to lead to profitability.
  • If we fail to obtain additional financing, we could be forced to delay, reduce or eliminate our product development programs, seek corporate partners for the development of our product development programs or relinquish or license on unfavorable terms, our rights to technologies or product candidates.
  • If we draw down on our credit facility with Silicon Valley Bank, the terms of our loan and security agreement place restrictions on our operating and financial flexibility, and failure to comply with covenants or to satisfy certain conditions may result in acceleration of our repayment obligations and foreclosure on our pledged assets, which could significantly harm our liquidity, financial condition, operating results, business and prospects and cause the price of our securities to decline.
  • We routinely evaluate external assets to build our pipeline of product candidates and there can be no assurance that we will be successful in identifying or completing a transaction for a candidate, that any such transaction will result in additional value for our stockholders or that the process will not have an adverse impact on our business.
The other 47 risks
  • Risks Related to Clinical Development and Regulatory Approval
  • All of our product candidates are still under clinical development and may not obtain regulatory approval or be successfully commercialized.
  • We may be unable to obtain, or may be delayed in obtaining, regulatory approval for our most advanced clinical candidate: dordaviprone.
  • We depend on the successful completion of clinical trials for our product candidates, including dordaviprone. The positive clinical results obtained for our product candidates in prior clinical studies may not be repeated in future clinical studies.
  • Delays in clinical trials are common and have many causes, and any delay could result in increased costs to us and jeopardize or delay our ability to obtain regulatory approval and commence product sales.
  • Our product candidates may cause adverse effects or have other properties that could delay or prevent their regulatory approval or limit the scope of any approved label or market acceptance.
  • After the completion of our clinical trials, we cannot predict whether or when we will obtain regulatory approval to commercialize any of our product candidates and we cannot, therefore, predict the timing of any future revenue from any of our product candidates, including dordaviprone.
  • Failure by us or third-party collaborators to successfully develop, validate and obtain regulatory approval for companion diagnostics for use by oncologists could harm our ability to develop and commercialize dordaviprone.
  • The FDA may determine that dordaviprone or any of our other product candidates, even if approved for the designated rare pediatric disease prior to September 30, 2026, do not meet the eligibility criteria for a priority review voucher.
  • Following regulatory approval for any of our product candidates, including dordaviprone, we will still face extensive regulatory requirements and our products may face future development and regulatory difficulties.
  • We may never obtain approval for or commercialize any of our products outside of the United States, nor does approval of any of our products outside the United States mean we will ever obtain approval for or commercialize any of our products inside the United States, all of which could limit our ability to realize their full market potential.
  • Coverage and adequate reimbursement may not be available for dordaviprone, or any of our other current or future product candidates, which could make it difficult for us to sell profitably, if approved.
  • Our relationships with investigators, health care professionals, consultants, third-party payers, and customers may be subject to applicable anti-kickback, fraud and abuse and other healthcare laws and regulations, which could expose us to criminal sanctions, civil penalties, contractual damages, reputational harm and diminished profits and future earnings.
  • Recently enacted and future legislation may increase the difficulty and cost for us to obtain marketing approval of and commercialize our product candidates and affect the prices we may obtain.
  • Risks Related to Our Reliance on Third Parties
  • We rely on third-party manufacturers to produce our preclinical and clinical drug supplies, and we intend to rely on third parties to produce commercial supplies of any approved product candidates.
  • Manufacturing issues may arise that could increase product and regulatory approval costs or delay or impair commercialization of dordaviprone or our other product candidates.
  • The anticipated benefits of the sale of our TEMBEXA program and related assets may not be realized fully or at all or may take longer to realize than expected.
  • Emergent may not adequately perform according to the terms of the BARDA Agreement, and we might be required to guarantee performance of all obligations that Emergent assumed under novation.
  • We rely on third parties to conduct, supervise and monitor our clinical studies and related data, and if those third parties perform in an unsatisfactory manner, it may harm our business.
  • Risks Related to Commercialization of Our Product Candidates
  • The commercial success of dordaviprone, and any other product candidates, will depend upon the acceptance of these products by the medical community, including physicians, patients, pharmacists, health care payers or government agencies.
  • If we are unable to establish sales and marketing capabilities or enter into agreements with third parties to market and sell our product candidates, we may be unable to sustainably generate revenue.
  • If we obtain approval to commercialize any products outside of the United States, a variety of risks associated with international operations could materially adversely affect our business.
  • We face competition from other biotechnology and pharmaceutical companies and our operating results will suffer if we fail to compete effectively.
  • We may expend our limited resources to pursue a particular product candidate or indication and fail to capitalize on product candidates or indications that may be more profitable or for which there is a greater likelihood of success.
  • Risks Related to Our Intellectual Property
  • If we are unable to obtain or protect intellectual property rights related to our products and product candidates, we may not be able to compete effectively in our market.
  • Third-party claims of intellectual property infringement may prevent or delay our development and commercialization efforts or otherwise affect our business.
  • We may be involved in lawsuits to protect or enforce our patents, the patents of our licensors and licensees or our other intellectual property rights, which could be expensive, time consuming and unsuccessful.
  • Obtaining and maintaining our patent protection depends on compliance with various procedural, document submission, fee payment and other requirements imposed by governmental patent agencies, and our patent protection could be reduced or eliminated for non-compliance with these requirements.
  • Risks Related to Our Business Operations and Industry
  • Increasing demand for compassionate use or third-party supply of our unapproved therapies could impair or delay the completion of our controlled clinical trials or otherwise result in losses.
  • Competition for Phase 3 ACTION Study eligible patients from Investigator Initiated Clinical Trials (IITs) could result in losses.
  • If we fail to comply with the extensive legal and regulatory requirements affecting the health care industry, we could face increased costs, delays in the development of our product candidates, penalties and a loss of business.
  • Our future success depends on our ability to retain key executives and to attract, retain and motivate qualified personnel.
  • Potential product liability lawsuits against us could cause us to incur substantial liabilities and to limit commercialization of any products that we may develop.
  • Risks Related to Our Common Stock
  • The market price of our common stock is likely to be volatile, and you may not be able to resell your shares at or above your purchase price.
  • In the past we have not met, and may in the future not comply with all applicable requirements of Nasdaq, and if Nasdaq determines to delist our common stock, the delisting could adversely affect the market liquidity of our common stock and the market price of our common stock could decrease.
  • Our principal stockholders and management own a significant percentage of our stock and will be able to exert significant control over matters subject to stockholder approval.
  • Failure to establish and maintain adequate finance infrastructure and accounting systems and controls could impair our ability to comply with the financial reporting and internal controls requirements for publicly traded companies.
  • Future sales and issuances of our common stock or rights to purchase common stock, including pursuant to our equity incentive plans, could result in additional dilution of the percentage ownership of our stockholders and could cause our stock price to fall.
  • We have broad discretion in the use of the net proceeds from our financing transactions and may not use them effectively.
  • Volatility in our stock price could subject us to securities class action litigation.
  • Changes in tax laws or regulations that are applied adversely to us or our customers may have a material adverse effect on our business, cash flow, financial condition or results of operations.
  • Our effective tax rate may fluctuate, and we may incur obligations in tax jurisdictions in excess of accrued amounts.
  • Our ability to use our net operating loss carryforwards and certain other tax attributes may be limited.
  • Because we do not anticipate paying any cash dividends on our common stock in the foreseeable future, capital appreciation, if any, would be your sole source of gain.
  • Provisions in our corporate charter documents and under Delaware law could make it more difficult for a third-party to acquire us or increase the cost of acquiring us, even if doing so would benefit our stockholders and may prevent attempts by our stockholders to replace or remove our current management.
  • Risks Related to Data Privacy
  • We and the third parties with whom we work are subject to stringent and evolving U.S. and foreign laws, regulations, rules, contractual obligations, policies and other obligations related to data privacy and security. Our actual or perceived failure, or an actual or perceived failure by third parties with whom we work, to comply with such obligations could lead to regulatory investigations or actions; litigation; fines and penalties; disruptions of our business operations; reputational harm; loss of revenue or profits; and other adverse business consequences.
  • Risks Related to Information Technology
  • If our information technology systems or data, or those of third parties with whom we work, are or were compromised, we could experience adverse consequences resulting from such compromise, including but not limited to regulatory investigations or actions; litigation; fines and penalties; disruptions of our business operations; reputational harm; loss of revenue or profits; and other adverse consequences.
  • Increasing use of social media could give rise to liability, breaches of data security, or reputational damage.

Sources

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