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ONCOCYTE PROVIDES CORPORATE UPDATE AND REPORTS FOURTH QUARTER AND FULL YEAR 2018 FINANCIAL RESULTS
On track for commercial availability of DetermaVu™ in 2H 2019
Conference Call Today at 4:30 PM EDT
ALAMEDA, Calif., April 1, 2019 — OncoCyte Corporation (NYSE American: OCX), a developer of novel, non-invasive tests for the early detection of lung cancer, today reported financial and operating results for the fourth quarter and year ended December 31, 2018 and provided a corporate update.
“OncoCyte has made outstanding progress since our last quarterly update to investors, reporting positive results from our DetermaVu™ R&D Validation Study which demonstrated that DetermaVu™ is a commercially viable assay with the potential to change the treatment paradigm in lung cancer diagnostics,” said William Annett, President and Chief Executive Officer of OncoCyte. “Importantly, these results also confirmed the Company’s unique Immune System Interrogation approach provides an exquisitely sensitive and consistent signal for the diagnosis of early stage lung cancer. We are excited to investigate the broader application of this technology across multiple solid tumors moving forward and remain highly focused on executing the few remaining steps required for commercialization of DetermaVu™ later this year.”
|●||Successfully transitioned to the Ion Torrent next-generation sequencing platform for robust and reproducible results|
|●||Reported positive results from blinded, prospective R&D Validation Study demonstrating best-in-class performance with sensitivity of 90% and specificity of 75%|
|●||R&D Validation study served as proof of concept for unique Immune System Interrogation approach with potential applicability across many types of solid tumors|
|●||On-track to complete remaining validation studies by mid-year and make DetermaVu™ commercially available second half of 2019|
|●||Completed a successful equity raise for gross proceeds of $40.25 million which provides the resources to execute the development and commercialization of DetermaVu™|
Remaining Validation Pathway for DetermaVu™:
|●||1H 2019: Analytical Validation – with results expected shortly, this study will establish the performance characteristics of the system as established in the Clinical and Laboratory Standards Institute Guidelines that cover quantitation, precision, reproducibility and interfering substances|
|●||1H 2019: CLIA Laboratory Validation study – will rerun between 100 and 120 patient samples previously run in the R&D Validation study to confirm that the same positive results are obtained on the analytically validated systems|
|●||Mid-year 2019: Clinical Validation study – will run approximately 300 to 350 blinded, prospectively-collected blood samples to establish the DetermaVu™ performance in an independent, blinded data set as a final confirmation of test sensitivity and specificity in OncoCyte’s CLIA lab setting|
|●||2H 2019: Commercial availability of DetermaVu™|
|●||Post-launch (2020 initiation): Clinical Utility study – follow-on real world evidence study to demonstrate a net improvement in patient outcomes and cost savings for the healthcare system|
Fourth Quarter and Annual 2018 Financial Results
At December 31, 2018, OncoCyte had cash and cash equivalents of $8.0 million and marketable equity securities valued at $0.4 million, for a total of $8.4 million of liquid assets. The balance sheet was strengthened in February 2019 with the successful equity raise of $37.4 million in net proceeds from an underwritten public offering.
For the quarter ended December 31, 2018, OncoCyte reported a net loss of $4.5 million, or ($0.11) per share, compared to a net loss of $4.0 million, or ($0.13) per share, in the fourth quarter of 2017.
For 2018, OncoCyte reported a net loss of $15.8 million, or ($0.42) per share, compared to $19.4 million, or ($0.64) per share, in 2017.
Operating expenses for the three months ended December 31, 2018 were $4.0 million as reported, and were $3.5 million on an as adjusted basis. Operating expenses for 2018 were $15.2 million as reported and were $12.5 million on an as adjusted basis.
The reconciliation between GAAP and non-GAAP operating expenses is provided in the financial tables included with this earnings release.
Research and development expenses for the fourth quarter of 2018 were $1.2 million compared to $1.5 million for the same period in 2017, a decrease of $0.3 million. Research and development expenses for the year ended December 31, 2018 were $6.5 million, compared to $7.2 million during 2017, a decrease of $0.7 million. The decreases were primarily attributable to laboratory and other expenses related to diagnostic tests for diseases other than lung cancer as OncoCyte devoted substantially all of its research and development efforts to DetermaVu™ during 2018.
General and administrative expenses for the fourth quarter of 2018 were $2.6 million compared to $1.8 million for the same period in 2017. The $0.8 million increase was mainly attributable to personnel and related compensation, primarily related to the hiring of OncoCyte’s Chief Financial Officer and its Chief Operating Officer.
General and administrative expenses for the year ended December 31, 2018 decreased to $7.0 million from $9.2 million during 2017, a decrease of $2.2 million. During the year ended December 31, 2017, OncoCyte incurred a noncash expense of $4.1 million for the issuance of new warrants to certain investors who exercised outstanding warrants. OncoCyte did not incur a similar expense during 2018, Personnel and related compensation expenses increased by $1.1 million during 2018 primarily related to the hiring of the executives noted above, an increase of $0.5 million in legal, investor relations, financing and other related expenses, and an increase of $0.3 million in noncash stock-based compensation expense due to increased stock option grants.
Sales and marketing expenses for the fourth quarter of 2018 were $0.3 million compared to $0.6 million for the same period in 2017, a decrease of $0.3 million. Sales and marketing expenses for the full-year 2018 were $1.7 million compared to $2.4 million during 2017, a decrease of $0.7 million. These decreases were primarily due the decrease in consulting, marketing, and related expenses as OncoCyte concentrated its resources on the development of DetermaVu™ rather than on marketing related activities.
The Company will host a conference call today, April 1, 2019, at 4:30 pm EDT / 1:30 pm PDT to discuss the results along with recent corporate developments.
The dial-in number in the U.S./Canada is 877-407-9716; for international participants, the number is 201-493-6779. For all callers, please refer to Conference ID 13689139. To access the live webcast, go to the investor relations section on the Company’s website, http://investors.oncocyte.com/events-and-presentations.
DetermaVu™ is being developed as an intermediate step to confirm the absence of cancer after imaging modalities (LDCTs) that detect suspicious lung nodules and before downstream invasive procedures that determine if the nodules are malignant. OncoCyte estimates that a $4.7 billion annual market could develop in the U.S. for its confirmatory lung cancer liquid biopsy test, depending on market penetration and reimbursable pricing.
DetermaVu™ has the potential to dramatically reduce U.S. healthcare costs by billions of dollars each year by eliminating unnecessary biopsies, which, according to a recent Medicare study, cost on average $14,634 each. In addition, DetermaVu™ can provide great benefit to patients by avoiding invasive biopsies and the complications that arise in up to 24% of those procedures, and deaths that occur in up to 1% of cases.
DetermaVu™ is a trademark of OncoCyte Corporation.
About OncoCyte Corporation
OncoCyte is focused on the development and commercialization of novel, non-invasive blood (“liquid biopsy”) diagnostic tests for the early detection of lung cancer. Early detection of cancer can improve health outcomes, reduce the cost of care, and improve patients’ quality of life. Liquid biopsy diagnostic tests like those OncoCyte is developing may reduce the need for costlier and riskier diagnostic procedures such as invasive biopsy and cystoscopic procedures. OncoCyte is focusing its efforts on the development of DetermaVu™ as a non-invasive confirmatory diagnostic test for lung cancer. DetermaVu™ is being developed using proprietary sets of genetic molecular markers that differentially express in lung cancer. OncoCyte also plans to conduct research to identify additional molecular markers, acquire or license markers and related technology, and develop cancer tests based on those markers.
OncoCyte Forward Looking Statements
Any statements that are not historical fact (including, but not limited to statements that contain words such as “will,” “believes,” “plans,” “anticipates,” “expects,” “estimates” and similar expressions) are forward-looking statements. These statements include those pertaining to the implementation and results of research, development, clinical trials and studies, commercialization plans, future financial and/or operating results, and future opportunities for OncoCyte, along with other statements about the future expectations, beliefs, goals, plans, or prospects expressed by management. Forward-looking statements involve risks and uncertainties, including, without limitation, risks inherent in the development and/or commercialization of potential diagnostic tests or products, uncertainty in the results of clinical trials or regulatory approvals, the capacity of our third-party supplied blood sample analytic system to provide consistent and precise analytic results on a commercial scale, the need and ability to obtain future capital, and maintenance of intellectual property rights, and the need to obtain third party reimbursement for patients’ use of any diagnostic tests we commercialize. Actual results may differ materially from the results anticipated in these forward-looking statements and accordingly as such statements should be evaluated together with the many uncertainties that affect the business of OncoCyte, particularly those mentioned in the “Risk Factors” and other cautionary statements found in OncoCyte’s Securities and Exchange Commission filings. OncoCyte disclaims any intent or obligation to update these forward-looking statements, except as required by law.
LifeSci Advisors, LLC
|December 31, 2018||December 31, 2017|
|Cash and cash equivalents||$||8,034||$||7,600|
|Marketable equity securities||428||760|
|Prepaid expenses and other current assets||180||168|
|Total current assets||8,642||8,528|
|Intangible assets, net||-||746|
|Machinery and equipment, net||614||822|
|Deposits and other noncurrent assets||262||120|
|LIABILITIES AND STOCKHOLDERS’ EQUITY|
|Amount due to BioTime and affiliates||$||2,101||$||2,099|
|Accrued expenses and other current liabilities||2,109||1,042|
|Loan payable, current||800||800|
|Capital lease liability, current||385||338|
|Total current liabilities||5,561||4,454|
|Loan payable, net of deferred financing costs, noncurrent||347||1,070|
|Capital lease liability, noncurrent||187||289|
|Preferred stock, no par value, 5,000 shares authorized; none issued and outstanding||-||-|
|Common stock, no par value, 85,000 shares authorized; 40,664 and 31,452 shares issued and outstanding at December 31, 2018 and December 31, 2017, respectively||74,742||59,968|
|Accumulated other comprehensive loss||-||(888||)|
|Total stockholders’ equity||3,423||4,403|
|TOTAL LIABILITIES AND STOCKHOLDERS’ EQUITY||$||9,518||$||10,216|
STATEMENTS OF OPERATIONS
(IN THOUSANDS, EXCEPT PER SHARE DATA)
|Three Months Ended December 31,||Year Ended December 31,|
|Research and development||$||1,204||$||1,507||$||6,514||$||7,174|
|General and administrative||2,573||1,785||7,007||9,232|
|Sales and marketing||270||600||1,681||2,443|
|Total operating expenses||4,047||3,892||15,202||18,849|
|Loss from operations||(4,047||)||(3,892||)||(15,202||)||(18,849||)|
|OTHER EXPENSES, NET|
|Interest expense, net||(50||)||(68||)||(216||)||(217||)|
|Unrealized loss on marketable equity securities||(498||)||-||(427||)||-|
|Other income (expense), net||96||-||91||(309||)|
|Total other expenses, net||(452||)||(68||)||(552||)||(526||)|
|Basic and diluted net loss per share||$||(0.11||)||$||(0.13||)||$||(0.42||)||$||(0.64||)|
|Weighted average shares outstanding: basic and diluted||40,664||31,440||37,850||30,195|
STATEMENTS OF CASH FLOWS
|Year Ended December 31,|
|CASH FLOWS FROM OPERATING ACTIVITIES:|
|Adjustments to reconcile net loss to net cash used in operating activities:|
|Amortization of intangible assets||121||242|
|Amortization of prepaid maintenance||18||-|
|Impairment charge for intangible assets||625||-|
|Loss on sale of BioTime shares||-||309|
|Dividend income from AgeX Therapeutics common stock received as dividend-in-kind||(96||)||-|
|Unrealized loss on marketable equity securities||427||-|
|Warrants issued to certain shareholders as inducement to exercise of warrants||-||4,074|
|Amortization of debt issuance costs||77||83|
|Changes in operating assets and liabilities:|
|Amount due to BioTime and affiliates||2||(753||)|
|Prepaid expenses and other current assets||(11||)||115|
|Accounts payable and accrued liabilities||1,002||(48||)|
|Net cash used in operating activities||(11,649||)||(13,385||)|
|CASH FLOWS FROM INVESTING ACTIVITIES:|
|Net proceeds from sale of BioTime shares||-||934|
|Purchase of equipment||(31||)||(91||)|
|Net cash provided by (used in) investing activities||(31||)||843|
|CASH FLOWS FROM FINANCING ACTIVITIES:|
|Proceeds from exercise of stock options||58||610|
|Proceeds from exercise of warrants||-||7,774|
|Proceeds from sale of common shares||10,000||-|
|Financing costs to issue common shares||(65||)||-|
|Proceeds from sale of common shares and warrants||3,592||-|
|Financing costs to issue common shares and warrants||(290||)||-|
|Proceeds from issuance of loan payable, net of financing costs||-||1,982|
|Repayment of loan payable||(800||)||(133||)|
|Repayment of capital lease obligation||(381||)||(265||)|
|Net cash provided by financing activities||12,114||9,968|
|NET INCREASE (DECREASE) IN CASH AND CASH EQUIVALENTS||434||(2,574||)|
|CASH AND CASH EQUIVALENTS:|
|At beginning of the year||7,600||10,174|
|At end of the year||$||8,034||$||7,600|
Non-GAAP Financial Measures
This earnings release includes operating expenses prepared in accordance with accounting principles generally accepted in the United States (GAAP), and includes certain historical non-GAAP operating expenses. In particular, OncoCyte has provided non-GAAP total operating expenses, adjusted to exclude noncash stock-based compensation, depreciation and amortization, and an impairment charge for intangible assets. Non-GAAP financial measures are not meant to be considered in isolation or as a substitute for comparable financial measures prepared in accordance with GAAP. However, OncoCyte believes the presentation of non-GAAP total operating expenses, when viewed in conjunction with our GAAP total operating expenses, is helpful in understanding OncoCyte’s ongoing operating expenses and its programs.
Furthermore, management uses these non-GAAP financial measures in the aggregate to establish budgets and operational goals, to manage OncoCyte’s business and to evaluate its performance and its programs.
Reconciliation of Non-GAAP Financial Measure
Adjusted Operating Expenses
|Amounts In Thousands||Amounts In Thousands|
For the Three
December 31, 2018 (unaudited)
December 31, 2018 (unaudited)
|GAAP Operating Expenses - as reported||$||4,047||$||15,202|
|Stock-based compensation expense||(400||)||(1,479||)|
|Impairment charge for intangible assets||-||(625||)|
|Depreciation and amortization expense||(130||)||(577||)|
|Non-GAAP Operating Expenses, as adjusted||$||3,517||$||12,521|
The following information was filed by Oncocyte Corp (OCX) on Monday, April 1, 2019 as an 8K 2.02 statement, which is an earnings press release pertaining to results of operations and financial condition. It may be helpful to assess the quality of management by comparing the information in the press release to the information in the accompanying 10-Q Quarterly Report statement of earnings and operation as management may choose to highlight particular information in the press release.
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