Interpace Biosciences Announces Second Quarter 2025 Financial and Business Results
Rhea-AI Summary
Interpace Biosciences (OTCQX:IDXG) reported mixed Q2 2025 financial results, with net revenue of $9.2 million, down 23% year-over-year. Despite overall revenue decline, the company achieved record thyroid testing performance, with volume up 16% and revenue up 25% year-over-year to $8.7 million.
The company reported a Q2 loss from continuing operations of $0.5 million, compared to income of $2.5 million in Q2 2024, primarily impacted by $1.2 million in one-time charges related to PancraGEN testing discontinuation. Cash collections remained strong at $10.8 million, and preliminary July 2025 revenue showed a 54% year-over-year increase to $3.3 million.
Interpace is transitioning to focus exclusively on thyroid testing, following the loss of PancraGEN reimbursement. The company maintains a positive outlook for Q3 2025 and beyond as a thyroid-only diagnostics business.
Positive
- Record thyroid test volume with 16% year-over-year growth
- Thyroid revenue increased 25% year-over-year to $8.7M
- Strong cash collections of $10.8M in Q2 2025
- Preliminary July 2025 revenue up 54% year-over-year to $3.3M
- Strategic investments in lab operational efficiency and AI automation
Negative
- Net revenue decreased 23% year-over-year to $9.2M
- Loss from continuing operations of $0.5M vs $2.5M income in prior year
- Gross profit margin declined to 57% from 65% year-over-year
- Loss of reimbursement for PancraGEN testing
- Cash and cash equivalents declined to $502K from $1.46M at year-end 2024
News Market Reaction 1 Alert
On the day this news was published, IDXG gained 0.53%, reflecting a mild positive market reaction.
Data tracked by StockTitan Argus on the day of publication.
| ● | Q2 Revenue of | |
| ● | Q2 Cash Collections of | |
| ● | Q2 Thyroid test volume up | |
| ● | Q2 Thyroid revenue of |
PARSIPPANY, NJ, Aug. 07, 2025 (GLOBE NEWSWIRE) -- Interpace Biosciences, Inc. (“Interpace” or the “Company”) (OTCQX: IDXG) today announced financial results for the second quarter ended June 30, 2025 and provided a business and financial update.
Second quarter Net Revenue was
“Despite the loss of reimbursement for the Company’s PancraGEN test, Q2 2025 represented another quarter of year-over- year double digit Thyroid volume and revenue growth,” stated Tom Burnell, President and CEO. “We are excited about the Company’s continued growth in revenue, profitability and cash flow as a thyroid only clinical diagnostics business, which will be more adequately reflected in Q3 and beyond”, added Burnell. Further, Burnell said, “the strength and resiliency of the Interpace team, coupled with their ability to anticipate and prepare for change, has made for a smooth transition away from the unwarranted challenges as a result of loss of PancraGEN reimbursement to a thriving thyroid testing business”.
Second Quarter 2025 Financial Performance
For the Second Quarter of 2025 as Compared to the Second Quarter of 2024
| ● | Net Revenue was | |
| ● | Gross Profit percentage was | |
| ● | Gross Profit percentage without one-time impact related to PancraGEN reimbursement loss was | |
| ● | Operating loss was | |
| ● | Loss from continuing operations was | |
| ● | Loss from continuing operations includes | |
| ● | Adjusted EBITDA was | |
| ● | Q2 2025 cash collections totaled |
About Interpace Biosciences
Interpace Biosciences is an emerging leader in enabling personalized medicine, offering specialized services along the therapeutic value chain from early diagnosis and prognostic planning to targeted therapeutic applications.
Clinical services, through Interpace Diagnostics, provide clinically useful molecular diagnostic tests and bioinformatics and pathology services for evaluating risk of cancer by leveraging the latest technology in personalized medicine for improved patient diagnosis and management. Interpace has three commercialized molecular tests and one test in a clinical evaluation program (CEP): ThyGeNEXT® for the diagnosis of thyroid cancer from thyroid nodules utilizing a next-generation sequencing assay; ThyraMIR®v2, used in combination with ThyGeNEXT®, for the diagnosis of thyroid cancer utilizing a proprietary microRNA pairwise expression profiler along with algorithmic classification; and RespriDX®, that differentiates lung cancer of primary versus metastatic origin. In addition, BarreGEN®, a molecular-based assay that helps resolve the risk of progression of Barrett’s Esophagus to esophageal cancer, is currently in a CEP, whereby we gather information from physicians using BarreGEN® to assist us in gathering clinical evidence relative to the safety and performance of the test and also providing data that will potentially support payer reimbursement.
For more information, please visit Interpace Biosciences’ website at www.interpace.com.
Forward-looking Statements
This press release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, Section 21E of the Securities Exchange Act of 1934 and the Private Securities Litigation Reform Act of 1995, relating to the Company’s future financial and operating performance. The Company has attempted to identify forward-looking statements by terminology including “believes,” “estimates,” “anticipates,” “expects,” “plans,” “projects,” “intends,” “potential,” “may,” “could,” “might,” “will,” “should,” “approximately” or other words that convey uncertainty of future events or outcomes to identify these forward-looking statements. These statements are based on current expectations, assumptions and uncertainties involving judgments about, among other things, future economic, competitive and market conditions and future business decisions, all of which are difficult or impossible to predict accurately and many of which are beyond the Company’s control. These statements also involve known and unknown risks, uncertainties and other factors that may cause the Company’s actual results to be materially different from those expressed or implied by any forward-looking statements, including, but not limited to, the possibility that the Company’s estimates of future revenue, cash flows and adjusted EBITDA may prove to be materially inaccurate, the Company’s prior history of operating losses, the Company’s ability to adequately finance its business and seek alternative sources of financing, the Company’s ability to repay borrowings from BroadOak, the Company’s dependence on sales and reimbursements from its clinical services, the Company’s ability to retain or secure reimbursement including its reliance on third parties to process and transmit claims to payers and the adverse impact of any delay, data loss, or other disruption in processing or transmitting such claims, the Company’s revenue recognition being based in part on estimates for future collections which estimates may prove to be incorrect, and the Company’s ability to restructure itself in light of the loss of reimbursement for its PancraGEN product.
Additionally, all forward-looking statements are subject to the “Risk Factors” detailed from time to time in the Company’s Annual Report on Form 10-K for the fiscal year ended December 31, 2024, as amended, Current Reports on Form 8-K and Quarterly Reports on Form 10-Q filed with the Securities and Exchange Commission. Because of these and other risks, uncertainties and assumptions, undue reliance should not be placed on these forward-looking statements. In addition, these statements speak only as of the date of this press release and, except as may be required by law, the Company undertakes no obligation to revise or update publicly any forward-looking statements for any reason.
Contacts:
Investor Relations
Interpace Biosciences, Inc.
(855)-776-6419
Info@Interpace.com
INTERPACE BIOSCIENCES, INC.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(unaudited, in thousands, except per share data)
| Three Months Ended | Six Months Ended | |||||||||||||||
| June 30, | June 30, | |||||||||||||||
| 2025 | 2024 | 2025 | 2024 | |||||||||||||
| Revenue, net | $ | 9,232 | $ | 12,042 | $ | 20,747 | $ | 22,219 | ||||||||
| Cost of revenue | 3,956 | 4,236 | 8,101 | 8,102 | ||||||||||||
| Gross Profit | 5,276 | 7,806 | 12,646 | 14,117 | ||||||||||||
| Sales and marketing | 2,910 | 2,887 | 5,723 | 5,707 | ||||||||||||
| Research and development | 173 | 146 | 350 | 283 | ||||||||||||
| General and administrative | 2,661 | 2,141 | 5,211 | 4,381 | ||||||||||||
| Total operating expenses | 5,744 | 5,174 | 11,284 | 10,371 | ||||||||||||
| Operating (loss) income | (468 | ) | 2,632 | 1,362 | 3,746 | |||||||||||
| Interest accretion expense | - | (12 | ) | - | (30 | ) | ||||||||||
| Note payable interest | (49 | ) | (176 | ) | (127 | ) | (373 | ) | ||||||||
| Other (expense) income, net | (16 | ) | 71 | 4 | (12 | ) | ||||||||||
| (Loss) income from continuing operations before tax | (533 | ) | 2,515 | 1,239 | 3,331 | |||||||||||
| Provision for income taxes | - | 4 | 18 | 8 | ||||||||||||
| (Loss) income from continuing operations | (533 | ) | 2,511 | 1,221 | 3,323 | |||||||||||
| Loss from discontinued operations, net of tax | (107 | ) | (74 | ) | (214 | ) | (178 | ) | ||||||||
| Net (loss) income | $ | (640 | ) | $ | 2,437 | $ | 1,007 | $ | 3,145 | |||||||
| Basic income (loss) per share of common stock: | ||||||||||||||||
| From continuing operations | $ | (0.12 | ) | $ | 0.57 | $ | 0.28 | $ | 0.76 | |||||||
| From discontinued operations | (0.02 | ) | (0.02 | ) | (0.05 | ) | (0.04 | ) | ||||||||
| Net income (loss) per basic share of common stock | $ | (0.14 | ) | $ | 0.56 | $ | 0.23 | $ | 0.72 | |||||||
| Diluted income (loss) per share of common stock: | ||||||||||||||||
| From continuing operations | $ | (0.12 | ) | $ | 0.57 | $ | 0.04 | $ | 0.76 | |||||||
| From discontinued operations | (0.02 | ) | (0.02 | ) | (0.01 | ) | (0.04 | ) | ||||||||
| Net income (loss) per diluted share of common stock | $ | (0.14 | ) | $ | 0.55 | $ | 0.04 | $ | 0.72 | |||||||
| Weighted average number of common shares and | ||||||||||||||||
| common share equivalents outstanding: | ||||||||||||||||
| Basic | 4,423 | 4,376 | 4,422 | 4,373 | ||||||||||||
| Diluted | 4,423 | 4,401 | 27,697 | 4,393 | ||||||||||||
Selected Balance Sheet Data (Unaudited)
($ in thousands)
| June 30, | December 31, | |||||||
| 2025 | 2024 | |||||||
| Cash and cash equivalents | $ | 502 | $ | 1,461 | ||||
| Total current assets | 9,504 | 11,773 | ||||||
| Total current liabilities | 7,149 | 10,615 | ||||||
| Total assets | 12,335 | 14,792 | ||||||
| Total liabilities | 13,548 | 17,009 | ||||||
| Total stockholders' deficit | (1,213 | ) | (2,217 | ) | ||||
Selected Cash Flow Data (Unaudited)
($ in thousands)
| For the Six Months Ended | ||||||||
| June 30, | ||||||||
| 2025 | 2024 | |||||||
| Net income | $ | 1,007 | $ | 3,145 | ||||
| Net cash provided by operating activities | $ | 1,755 | $ | 1,346 | ||||
| Net cash used in investing activities | (201 | ) | (225 | ) | ||||
| Net cash used in financing activities | (2,513 | ) | (2,600 | ) | ||||
| Change in cash and cash equivalents | (959 | ) | (1,479 | ) | ||||
| Cash and cash equivalents – beginning | 1,461 | 3,498 | ||||||
| Cash and cash equivalents – ending | $ | 502 | $ | 2,019 | ||||
Reconciliation of Adjusted EBITDA (Unaudited)
($ in thousands)
| Three Months Ended | Six Months Ended | |||||||||||||||
| June 30, | June 30, | |||||||||||||||
| 2025 | 2024 | 2025 | 2024 | |||||||||||||
| (Loss) income from continuing operations (GAAP Basis) | $ | (533 | ) | $ | 2,511 | $ | 1,221 | $ | 3,323 | |||||||
| Depreciation and amortization | 101 | 67 | 196 | 119 | ||||||||||||
| Stock-based compensation | 9 | 53 | 24 | 132 | ||||||||||||
| Severance & related expense | 524 | - | 692 | - | ||||||||||||
| Asset impairment - lab supplies | 198 | - | 198 | - | ||||||||||||
| Taxes expense | - | 4 | 18 | 8 | ||||||||||||
| Interest accretion expense | - | 12 | - | 30 | ||||||||||||
| Note payable interest | 49 | 176 | 127 | 373 | ||||||||||||
| Other expense/income, net | 10 | (14 | ) | 14 | (29 | ) | ||||||||||
| Change in fair value of note payable | 7 | (57 | ) | (18 | ) | 41 | ||||||||||
| Adjusted EBITDA | $ | 365 | $ | 2,752 | $ | 2,472 | $ | 3,997 | ||||||||
Non-GAAP Financial Measures
In addition to the United States generally accepted accounting principles, or GAAP, results provided throughout this document, we have provided certain non-GAAP financial measures to help evaluate the results of our performance. We believe that these non-GAAP financial measures, when presented in conjunction with comparable GAAP financial measures, are useful to both management and investors in analyzing our ongoing business and operating performance. We believe that providing the non-GAAP information to investors, in addition to the GAAP presentation, allows investors to view our financial results in the way that management views financial results.
In this document, we discuss Adjusted EBITDA, a non-GAAP financial measure. Adjusted EBITDA is a metric used by management to measure cash flow of the ongoing business. Adjusted EBITDA is defined as income or loss from continuing operations, plus depreciation and amortization, non-cash stock-based compensation, severance expense, interest and taxes, and other non-cash expenses including change in fair values of notes payable. The table above includes a reconciliation of this non-GAAP financial measure to the most directly comparable GAAP financial measure.