Interpace Biosciences Announces Full Year and Fourth Quarter 2021 Financial and Business Results
Interpace Biosciences reported its 2021 financial results, revealing a 28% increase in net revenue to $41.3 million. The fourth quarter also showed 13% growth in net revenue at $10.9 million. The company improved its net loss to $(14.9 million), up from $(26.5 million) in 2020. Cash collections surged by 31% to $43.1 million, and gross profit margins improved significantly. Despite challenges with insurance reimbursements for their Thyroid tests, CMS has confirmed retroactive billing adjustments for 2022. Interpace aims for continued growth and efficiency in 2022.
- Full-year net revenue increased 28% to $41.3 million.
- Fourth quarter net revenue improved 13% to $10.9 million.
- Net loss reduced to $(14.9 million) from $(26.5 million) in the prior year.
- Cash collections up 31% to $43.1 million, outpacing revenue.
- Gross profit margin improved to 43% from 33% in the previous year.
- Concerns over the reimbursement of the flagship Thyroid test, ThyGENext®.
- Did not achieve cash flow breakeven by the end of 2021.
● | 2021 Full Year Net Revenue of | |
● | 2021 Full Year Net Loss Improved | |
● | Full year Cash Collections improved by |
PARSIPPANY, NJ, March 31, 2022 (GLOBE NEWSWIRE) -- Interpace Biosciences, Inc. (“Interpace” or the “Company”) (OTCQX: IDXG) today announced financial results for the fiscal year and fourth quarter ended December 31, 2021 and provided a business and financial update.
“2021 has been a transformative year for Interpace,” said Thomas Burnell, President and CEO. Burnell added, “The Company established a sense of urgency and focus, right-sized its infrastructure, forged significant lending and investor relationships, and markedly grew revenue and improved overall profitability despite many unanticipated challenges.”
Thomas Freeburg, the Company’s CFO added, “During 2021, Interpace achieved significant improvement in overall profitability compared to the prior two successive years, with improved financial results across the board. We achieved substantial revenue growth and gross margin expansion while significantly reducing operating expenses. We intend to continue our focus on expense control, revenue growth, commercial payer reimbursement and expansion to drive further improvement in our profitability in 2022.”
Burnell continued, “While we did not fully achieve our lofty expectations of being cash flow breakeven by the end of 2021, and we entered 2022 with concerns related to reimbursement of the Company’s flagship Thyroid test, ThyGENext®, we have been notified by Centers for Medicare & Medicaid Services (CMS) and National Correct Coding Initiative (NCCI) that processing of claims for dates of service after January 1, 2022 will be completed beginning July 1, 2022 and are prepared to move forward with our planned growth strategy – with emphasis on expansion of the Company’s clinical diagnostics testing platform and portfolio, and a streamlined, more efficient approach to meeting the needs of our pharma services clients.”
Full-Year 2021 Financial Performance as Compared to Full-Year 2020
● | Net Revenue was | |
● | Gross Profit percentage was | |
● | Loss from Continuing Operations was |
● | Adjusted EBITDA was | |
● | Full year Cash collections improved by | |
● | December 31, 2020 cash balance was |
Fourth Quarter 2021 Financial Performance as Compared to the Fourth Quarter of 2020
● | Net Revenue was | |
● | Gross Profit percentage was | |
● | Loss from Continuing Operations was | |
● | Adjusted EBITDA was |
Recent Highlights
● | In January 2022, we announced the appointment of Vijay Aggarwal, Ph.D. to the Board of Directors effective February 1, 2022, replacing Eric B. Lev. Dr. Aggarwal and Mr. Lev were each designees of Ampersand 2018 Limited Partnership, a Series B Preferred stockholder of the Company. | |
● | In January 2022, the Company announced that CMS issued a new billing policy whereby CMS will no longer reimburse for the use of the Company’s ThyGeNEXT® and ThyraMIR® tests when billed together by the same provider/supplier for the same beneficiary on the same date of service. On February 28, 2022, the Company announced that the National Correct Coding Initiative (NCCI) program issued a response on behalf of CMS stating that the January 2022 billing policy reimbursement change for ThyGeNEXT® (0245U) and ThyraMIR® (0018U) tests has been retroactively reversed to January 1, 2022. CMS is currently reimbursing the Company for one of its two thyroid tests, and has agreed to retroactively reimburse for the second test once they have completed their internal administrative adjustments, confirming their acknowledgment that all tests will be reimbursed retroactive to January 1, 2022. As of the date of this filing, the Company has not yet realized the full cash collection benefit of current and retroactive Thyroid testing and such cash collections may be temporarily reduced or delayed until we resolve the matter with CMS. | |
● | During the fourth quarter of Fiscal 2021, the Company expanded commercial payor coverage of its proprietary Thyroid tests adding one new in-network contract. With the contracts added earlier in the year, Interpace now has contracts with 55 commercial payors. |
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, provides clinically useful molecular diagnostic tests, 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 five commercialized molecular tests and one test in a clinical evaluation program (CEP): PancraGEN® for the diagnosis and prognosis of pancreatic cancer from pancreatic cysts; PanDNA, a “molecular only” version of PancraGEN® that provides physicians a snapshot of a limited number of factors; ThyGeNEXT® for the diagnosis of thyroid cancer from thyroid nodules utilizing a next generation sequencing assay; ThyraMIR® for the diagnosis of thyroid cancer from thyroid nodules utilizing a proprietary gene expression assay; and RespriDX® that differentiates lung cancer of primary versus metastatic origin and for which the Company only has nominal revenues. 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 clinical evaluation program (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.
Pharma services, through Interpace Pharma Solutions, provides pharmacogenomics testing, genotyping, biorepository and other customized services to the pharmaceutical and biotech industries. Pharma services also advances personalized medicine by partnering with pharmaceutical, academic, and technology leaders to effectively integrate pharmacogenomics into their drug development and clinical trial programs with the goals of delivering safer, more effective drugs to market more quickly, while also improving patient care.
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 adverse impact of the COVID-19 pandemic on the Company’s operations and revenues, the substantial doubt about the Company’s ability to continue as a going concern, the possibility that the Company’s estimates of future revenue, cash flows and adjusted EBITDA may prove to be materially inaccurate, the Company’s history of operating losses, the Company’s ability to adequately finance its business, the Company’s ability to repay borrowings under its
Contacts:
Investor Relations
Interpace Biosciences, Inc.
(855)-776-6419
Info@Interpace.com
INTERPACE BIOSCIENCES, INC.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(in thousands, except per share data)
Three Months Ended | Years Ended | |||||||||||||||
December 31, | December 31, | |||||||||||||||
2021 | 2020 | 2021 | 2020 | |||||||||||||
(unaudited) | ||||||||||||||||
Revenue, net | $ | 10,853 | $ | 9,646 | $ | 41,314 | $ | 32,398 | ||||||||
Cost of revenue | 6,404 | 6,517 | 23,369 | 21,673 | ||||||||||||
Gross Profit | 4,449 | 3,129 | 17,945 | 10,725 | ||||||||||||
Sales and marketing | 2,482 | 2,478 | 10,067 | 9,254 | ||||||||||||
Research and development | 407 | 673 | 1,882 | 2,795 | ||||||||||||
General and administrative | 4,030 | 5,508 | 13,669 | 18,192 | ||||||||||||
Transition expenses | 111 | 1,780 | 2,585 | 2,578 | ||||||||||||
Loss on DiamiR transaction | 248 | - | 13 | - | ||||||||||||
Acquisition amortization expense | 728 | 1,115 | 4,064 | 4,461 | ||||||||||||
Change in fair value of contingent consideration | (281 | ) | (489 | ) | (338 | ) | (489 | ) | ||||||||
Total operating expenses | 7,725 | 11,065 | 31,942 | 36,791 | ||||||||||||
Operating loss | (3,276 | ) | (7,936 | ) | (13,997 | ) | (26,066 | ) | ||||||||
Interest accretion expense | (121 | ) | (135 | ) | (496 | ) | (549 | ) | ||||||||
Related party interest | (52 | ) | - | (424 | ) | - | ||||||||||
Other (expense) income, net | (241 | ) | (6 | ) | (496 | ) | 467 | |||||||||
Loss from continuing operations before tax | (3,690 | ) | (8,077 | ) | (15,413 | ) | (26,148 | ) | ||||||||
Provision (benefit) for income taxes | 17 | 10 | (667 | ) | 53 | |||||||||||
Loss from continuing operations | (3,707 | ) | (8,087 | ) | (14,746 | ) | (26,201 | ) | ||||||||
Loss from discontinued operations, net of tax | (22 | ) | (56 | ) | (197 | ) | (250 | ) | ||||||||
Net loss | (3,729 | ) | (8,143 | ) | (14,943 | ) | (26,451 | ) | ||||||||
Less adjustment for preferred stock deemed dividend | - | - | - | (3,033 | ) | |||||||||||
Net loss attributable to common stockholders | $ | (3,729 | ) | $ | (8,143 | ) | $ | (14,943 | ) | $ | (29,484 | ) | ||||
Basic and diluted loss per share of common stock: | ||||||||||||||||
From continuing operations | $ | (0.89 | ) | $ | (2.00 | ) | $ | (3.57 | ) | $ | (7.26 | ) | ||||
From discontinued operations | - | (0.01 | ) | (0.04 | ) | (0.06 | ) | |||||||||
Net loss per basic share of common stock | $ | (0.89 | ) | $ | (2.01 | ) | $ | (3.61 | ) | $ | (7.32 | ) | ||||
Weighted average number of common shares and | ||||||||||||||||
common share equivalents outstanding: | ||||||||||||||||
Basic | 4,181 | 4,043 | 4,135 | 4,029 | ||||||||||||
Diluted | 4,181 | 4,043 | 4,135 | 4,029 |
Selected Balance Sheet Data
($ in thousands)
December 31, | December 31, | |||||||
2021 | 2020 | |||||||
Cash, cash equivalents and restricted cash | $ | 3,314 | $ | 3,372 | ||||
Total current assets | 12,166 | 14,122 | ||||||
Total current liabilities | 15,682 | 18,233 | ||||||
Total assets | 38,427 | 45,681 | ||||||
Total liabilities | 34,309 | 28,228 | ||||||
Total stockholders’ deficit | (42,418 | ) | (29,083 | ) |
Selected Cash Flow Data
($ in thousands)
For the Years Ended | ||||||||
December 31, | ||||||||
2021 | 2020 | |||||||
Net loss | $ | (14,943 | ) | $ | (26,451 | ) | ||
Net cash used in operating activities | $ | (8,719 | ) | $ | (13,979 | ) | ||
Net cash used in investing activities | (315 | ) | (1,575 | ) | ||||
Net cash provided by financing activities | 8,976 | 16,605 | ||||||
Change in cash, cash equivalents and restricted cash | (58 | ) | 1,051 | |||||
Cash, cash equivalents and restricted cash – beginning | 3,372 | 2,321 | ||||||
Cash, cash equivalents and restricted cash – ending | $ | 3,314 | $ | 3,372 | ||||
Reconciliation of Adjusted EBITDA (Unaudited)
($ in thousands)
Three Months Ended | Years Ended | |||||||||||||||
December 31, | December 31, | |||||||||||||||
2021 | 2020 | 2021 | 2020 | |||||||||||||
Loss from continuing operations (GAAP Basis) | $ | (3,707 | ) | $ | (8,087 | ) | $ | (14,746 | ) | $ | (26,201 | ) | ||||
Bad debt (recovery) expense | - | 335 | (140 | ) | 585 | |||||||||||
Loss on DiamiR transaction | 248 | - | 13 | - | ||||||||||||
Receipt of HHS stimulus grant | - | - | - | (650 | ) | |||||||||||
Transition expenses | 111 | 1,780 | 2,585 | 2,578 | ||||||||||||
Legal and professional services | - | - | - | 495 | ||||||||||||
Depreciation and amortization | 1,024 | 1,399 | 5,374 | 5,501 | ||||||||||||
Stock-based compensation | 54 | 861 | 1,368 | 2,242 | ||||||||||||
Taxes expense(benefit) | 17 | 10 | (667 | ) | 53 | |||||||||||
Interest accretion expense | 121 | 135 | 496 | 549 | ||||||||||||
Financing interest and related costs | 468 | - | 950 | - | ||||||||||||
Mark to market on warrant liability | (87 | ) | 1 | 50 | (61 | ) | ||||||||||
Change in fair value of note payable | (58 | ) | - | (58 | ) | - | ||||||||||
Change in fair value of contingent consideration | (281 | ) | (489 | ) | (338 | ) | (489 | ) | ||||||||
Adjusted EBITDA | $ | (2,090 | ) | $ | (4,055 | ) | $ | (5,113 | ) | $ | (15,398 | ) |
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, acquisition related expenses, transition expenses, non-cash stock based compensation and ESPP plans, interest and taxes, and other non-cash expenses including asset impairment costs, bad debt expense, receipt of stimulus grants, loss on extinguishment of debt, goodwill impairment and change in fair value of contingent consideration, and warrant liability. The table above includes a reconciliation of this non-GAAP financial measure to the most directly comparable GAAP financial measure.
FAQ
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