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NeoGenomics provides cancer-focused genetic testing and information services to help diagnose and guide treatment for various cancers. Its tests include cytogenetics, FISH, flow cytometry, IHC, ISH, and molecular testing, run in CAP-accredited and CLIA-certified laboratories across multiple U.S. sites. Healthcare providers use the tests for diagnosis and treatment planning, while pharmaceutical companies use the Pharma Services division for clinical trials and drug development, with partnerships like QIAGEN for companion diagnostics. The company aims to advance oncology diagnostics and personalized medicine by delivering accurate, actionable results and supporting new cancer therapies.
Industries
Data & Analytics
Biotechnology
Healthcare
Company Size
1,001-5,000
Company Stage
IPO
Headquarters
Fort Myers, Florida
Founded
2002
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Total Funding
$1.2B
Above
Industry Average
Funded Over
8 Rounds
Health Insurance
401(k) Company Match
Employee Stock Purchase Plan
Tuition Reimbursement
Paid Vacation
Paid Holidays
Wellness Program
Hybrid Work Options
Why NeoGenomics (NEO) stock is up today. What Happened? Shares of oncology (cancer) diagnostics company NeoGenomics NEOjumped 15.8% in the afternoon session after the company reported second-quarter 2026 earnings that surpassed Wall Street expectations and raised its full-year financial guidance. The cancer-diagnostics company posted adjusted earnings of $0.05 per share on revenue of $201.7 million, beating analyst forecasts of $0.03 per share and $197.3 million in revenue. The top-line result represented an 11.2% increase compared to the same period in the previous year. Following the strong performance, NeoGenomics lifted its full-year outlook, now expecting revenue of around $804 million. Furthermore, its adjusted earnings per share guidance for the full year of $0.19 also came in ahead of analyst estimates. What Is The Market Telling Us NeoGenomics's shares are very volatile and have had 28 moves greater than 5% over the last year. But moves this big are rare even for NeoGenomics and indicate this news significantly impacted the market's perception of the business. The previous big move we wrote about was 20 days ago when the stock gained 3.4% on the news that the company announced the launch of the first FDA-approved immunohistochemistry (IHC) companion diagnostic test for patients with prostate cancer. The test, called PTEN IHC CDx, is designed to identify PTEN protein loss in patients with prostate adenocarcinoma. This detection is crucial as it helps determine which patients may be eligible for AstraZeneca's recently approved targeted therapy, TRUQAP. By providing a necessary diagnostic tool for a specific, modern treatment, NeoGenomics has established a clear commercial application for its product, linking it directly to patient care decisions and a major pharmaceutical therapy. NeoGenomics is up 32.9% since the beginning of the year, and at $15.63 per share, it has set a new 52-week high. Despite the year-to-date gain, investors who bought $1,000 worth of NeoGenomics's shares 5 years ago would now be looking at only $342.08. ONE MORE THING: 3 Hidden Platforms Growing 3X Faster than Amazon, Google, and PayPal. Amazon, Google, and Meta all followed the same playbook: Dominate an ignored market. Build an unbeatable moat. Scale until you're unstoppable. These three platforms are running that exact playbook right now. The early investors in Amazon made fortunes. The early investors in these could do the same.
NeoGenomics lifts outlook as NGS Revenue jumps 26% and margins improve. 29 July 2026, 11:51 AM NGS growth and higher per-test revenue drive strong Q2 results. NeoGenomics (NASDAQ: NEO), a leader in oncology diagnostics, delivered a robust second quarter for 2026, with total revenue climbing 11% to $202 million. This performance was fueled by an impressive 26% year-over-year increase in next-generation sequencing (NGS) revenue, outpacing broader clinical services growth of 14%. The average revenue per clinical test rose sharply to $515 - up 12% over the prior year - despite only a modest 2% rise in clinical volume. | Key Metric | Q2 2026 | Q2 2025 | % Change | | Total Revenue | $202M | $181M | +11% | | NGS Revenue Growth | 26% | - | | Avg. Revenue per Test | $515 | $461 | +12% | | Clinical Test Volume | 363,498 | 356,630 | +2% | Operating leverage and margin expansion underpin profit reversal. Margin improvements were a standout, with gross profit up 19% to $92 million and adjusted EBITDA jumping 36% to $14 million. Key drivers were both the revenue mix shift to higher-margin NGS testing and disciplined expense controls: operating expenses fell 19% versus last year, largely on the back of avoiding prior-year impairment charges. Net income turned positive at $2 million, reversing a $45 million loss in the year ago quarter, though the quarter did include an $11 million gain from extinguishing debt. | Profitability Metric | Q2 2026 | Q2 2025 | % Change | | Gross Profit | $92M | $77M | +19% | | Gross Profit Margin (Adj.) | 48% | 45% | +2.6 pts | | Adjusted EBITDA | $14M | $11M | +36% | | Net Income | $2M | ($45M) | N/A | Guidance raised as NEO moves toward sustainable profitability. With business momentum accelerating, NeoGenomics raised its full-year 2026 outlook. The company now expects annual revenue of $802-$806 million - implying about 11% annual growth - and adjusted EBITDA of $56-$58 million, up more than 30% from last year. While a net GAAP loss is still forecasted for 2026 due to non-cash amortization and stock compensation, adjusted net income should be comfortably positive, as shown below: | 2026 Full-Year Outlook | Prior Guidance | Updated Guidance | Y/Y Change | | Revenue | $797-$803M | $802-$806M | +10-11% | | Adjusted EBITDA | $55-$57M | $56-$58M | +29-34% | | GAAP Net Loss | ($63M)-($50M) | ($42M)-($34M) | Improving | | Adjusted Net Income | Not previously disclosed | $22-$26M | - | Balance sheet fortified and commercial strategy refined. NeoGenomics ended the quarter with $146 million in cash and short-term investments after completing a $316 million offering of 0.75% convertible senior notes due 2032. A portion of the proceeds went toward retiring prior debt and mitigating dilution through capped call transactions, while $25 million was used for share repurchases. Operationally, the company launched a new dedicated commercial team for pathology and oncology, and advanced its RaDaR ST technology with additional Medicare reimbursement evidence submissions. Key takeaways: where does NEO go from here? The Q2 performance was underpinned by both top-line growth and expanding profit margins, thanks to mix shift toward higher-value genomic tests and cost efficiency. With revised guidance calling for double-digit revenue growth and a significant narrowing of losses, NeoGenomics appears to be executing on a strategy of sustainable, margin-driven expansion. While further profitability gains will depend on continued momentum in NGS and commercial execution, the company's reinforced balance sheet and raised outlook suggest that investors and analysts should monitor future volumes, per-test pricing, and reimbursement developments as key indicators of lasting value creation. For more details, readers can access the full results and financial filings on the NeoGenomics Investor Relations website. Contact Information: If you have feedback or concerns about the content, please feel free to reach out to Market Chameleon via email at [email protected]. About the Publisher - Marketchameleon.com: Marketchameleon is a comprehensive financial research and analysis website specializing in stock and options markets. Market Chameleon leverage extensive data, models, and analytics to provide valuable insights into these markets. Its primary goal is to assist traders in identifying potential market developments and assessing potential risks and rewards. NOTE: Stock and option trading involves risk that may not be suitable for all investors. Examples contained within this report are simulated and may have limitations. Average returns and occurrences are calculated from snapshots of market mid-point prices and were not actually executed, so they do not reflect actual trades, fees, or execution costs. This report is for informational purposes only, and is not intended to be a recommendation to buy or sell any security. Neither Market Chameleon nor any other party makes warranties regarding results from its usage. Past performance does not guarantee future results. Please consult a financial advisor before executing any trades. You can read more about option risks and characteristics at theocc.com. The information is provided for informational purposes only and should not be construed as investment advice. All stock price information is provided and transmitted as received from independent third-party data sources. The Information should only be used as a starting point for doing additional independent research in order to allow you to form your own opinion regarding investments and trading strategies. The Company does not guarantee the accuracy, completeness or timeliness of the Information. Disclosure: This article was generated with the assistance of AI
NeoGenomics pays $9.8 million to settle kickback and Stark Law allegations. July 27, 2026 By: Allison Cook NeoGenomics Laboratories, a cancer-testing lab based in Fort Myers, Florida, has agreed to pay $9,813,260 to resolve False Claims Act allegations that it violated the Anti-Kickback Statute and the Stark Law, the Justice Department announced on July 20, 2026. The conduct ran from February 14, 2014, through December 31, 2022. Per the allegations, NeoGenomics gave 28 health care providers consulting help to build their own in-house testing labs and charged them less than that help was worth, allegedly to induce those providers to send lab work its way. It also paid outside consultants more when they steered more business to the lab, tying their compensation to the volume or value of referrals. Both arrangements funneled referrals that turned into Medicare and Medicaid claims, which the government treated as false. Of the $9.81 million, $6,542,173 is restitution. NeoGenomics self-reported the conduct through the HHS-OIG Provider Self-Disclosure Protocol on November 2, 2021, cooperated with the investigation, ended the arrangements, and received cooperation credit under the Justice Department's guidelines. The settlement is not an admission of liability. CONTACT US Please briefly describe the fraud you've observed, including who was involved, what happened, when it happened, where it happened, and how you know this information.
NeoGenomics Laboratories to pay $9.8 million to resolve FCA allegations relating to below-fair-market-value consulting services. July 27, 2026 Headlines that Matter for Companies and Executives in Regulated Industries Florida-based laboratory NeoGenomics Laboratories Inc. has agreed to pay $9,813,260 to resolve allegations that it violated the False Claims Act (FCA). The allegations centered on the company's provision of below-fair-market-value consulting services to health care providers that referred beneficiaries to NeoGenomics for laboratory testing. Additionally, the company was accused of paying variable referral-based compensation to independent consultants to secure new referring providers. According to the government, NeoGenomics operated a Laboratory Clinical Initiative program where it provided consulting services to 28 health care providers seeking to establish in-house flow cytometry and Fluorescence In-Situ Hybridization capabilities. The US Department of Justice (DOJ) maintained that NeoGenomics' program induced referrals for clinical laboratory tests in violation of the Anti-Kickback Statute (AKS) and that the financial arrangements created by these practices, along with the associated submission of claims, constituted violations of the Stark Law. NeoGenomics also allegedly contracted with independent consultants under terms that tied their compensation, at least in part, to the volume or value of referrals generated by the customers those consultants brought in. As part of the resolution, the DOJ recognized NeoGenomics' steps to cooperate during the investigation, along with its voluntary disclosures of its conduct to the DOJ. These efforts, along with remedial actions such as ending the consulting arrangements and terminating the employees involved, resulted in cooperation credit for NeoGenomics. The claims resolved by the settlement are allegations only and there has been no determination of liability. DEXYCU manufacturer to pay more than $4.7 million to resolve FCA allegations. On July 17, the DOJ announced that it reached a settlement with EyePoint, Inc. (formerly EyePoint Pharmaceuticals, Inc.), of Watertown, Massachusetts, to resolve AKS and FCA allegations tied to sales of its drug, DEXYCU. The DOJ alleges that EyePoint paid kickbacks to ambulatory surgery centers (ASCs) to induce the ASCs to purchase DEXYCU, which led to false claims for reimbursement from the federal government. The DOJ's allegations focused on two overarching schemes that took place between January 2019 and March 2023. First, in response to commercial insurance denying coverage of DEXYCU, EyePoint allegedly covered ASCs' costs through its "Assurance Program" by either offering to pay ASCs cash or by providing replacement product at no cost. Second, EyePoint effectively provided DEXYCU at no cost to patients whose commercial health insurance did not cover the drug by offering thousands of free samples to ASCs to use on patients who would otherwise pay out of pocket. As a result, the DOJ asserts that these free samples led ASCs to purchase more units of DEXYCU to be reimbursed by Medicare, Medicaid, and TRICARE and eliminate financial losses incurred by commercial insurers denying coverage. In connection with the settlement, EyePoint agreed to pay over $4.6 million and entered into a five-year Corporate Integrity Agreement with the US Department of Health and Human Services Office of Inspector General. EyePoint will pay an additional $25,478 to certain participating states. The case is captioned United States, et al. ex rel. AFCE, LLC v. EyePoint Pharmaceuticals, Inc., No. 21-cv-120171. The claims resolved by the settlement are allegations only and there has been no determination of liability. 30th Street Station contractor and owner agree to $7.2 million resolution arising from kickbacks paid to Amtrak official. Mark 1 Restoration Company and its owner Mark Snedden have agreed to pay $7,257,232.12 to resolve civil claims related to allegations that Mark 1 paid kickbacks to an Amtrak official in connection with a contract to renovate Philadelphia's 30th Street Station. The settlement requires Mark 1 and Snedden to pay $2,400,000 and to release Amtrak from any claim to $4,857,232.12 in additional funds that Amtrak retained or otherwise did not pay to Mark 1 after learning of the scheme. Pleadings from the related criminal proceedings provide detail about the alleged arrangement: Snedden and fellow Mark 1 executives conspired to furnish gifts and other items of value - including paid vacations, jewelry, cash, dinners, entertainment, a dog, and training for that dog - to the Amtrak employee responsible for overseeing the renovation project. The benefits conferred on the official totaled approximately $323,686. In return, the Amtrak employee allegedly leveraged his oversight role to secure contract modifications that artificially inflated project costs, ultimately resulting in more than $2 million in overbilling to Amtrak. Snedden has already pleaded guilty to criminal charges related to the kickback scheme, as have Mark 1 executives Donald Seefeldt, Lee Maniatis, and Khaled Dallo. The claims resolved by the settlement are allegations only and there has been no determination of liability. Louisiana company agrees to pay nearly $3 million to resolve allegations of PPP fraud. CAN USA, Inc., a Harvey, Louisiana-based inspection, repair, and maintenance services firm with offices in Hackensack, New Jersey, has agreed to pay $2,916,900 to resolve FCA allegations that it improperly obtained and received forgiveness of a Paycheck Protection Program (PPP) loan under the CARES Act. The DOJ contends that in January 2021, CAN USA applied for and received a $2 million Second Draw PPP loan despite exceeding the program's 300-employee eligibility threshold when its foreign affiliates' workforces were included, as the PPP rules required. In its loan application, CAN USA certified that it employed no more than 300 people; however, the United States alleges that CAN USA's combined domestic and international headcount surpassed that limit. After obtaining the loan, CAN USA sought and received full forgiveness of the $2 million principal plus accrued interest, effectively extinguishing its repayment obligation on funds to which it was not entitled. The case is captioned United States ex rel. Clearwater Metrics LLC v. CAN USA Inc., Civil Action No. 26-3469 (D.N.J.). The claims resolved by the settlement are allegations only and there has been no determination of liability.
NeoGenomics has launched PTEN IHC CDx, the first FDA-approved immunohistochemistry companion diagnostic test for patients with prostate adenocarcinoma. The test identifies PTEN protein loss in patients who may be eligible for AstraZeneca's recently approved targeted therapy TRUQAP. Prostate cancer is the most common cancer in men in the US, with more than 300,000 new cases and over 36,000 deaths annually. Of the approximately 35,000 patients diagnosed each year with mAPMN/S prostate cancer, about one in four have PTEN-deficient tumours. The test is available as a standalone order or as part of NEO PanTracer Pro for prostate cancer. It is performed by NeoGenomics pathologists across its national oncology laboratory network, delivering results in as few as one to two days.
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Industries
Data & Analytics
Biotechnology
Healthcare
Company Size
1,001-5,000
Company Stage
IPO
Headquarters
Fort Myers, Florida
Founded
2002
Find jobs on Simplify and start your career today