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Vermillion Reports Second Quarter 2016 Results Conference Call at 8:00 a.m. ET Today AUSTIN, Texas &#x2014

Key Takeaway: Vermillion Reports Second Quarter 2016 Results Conference Call at 8:00 a.m. ET Today AUSTIN, Texas August 10, 2016 Vermillion, Inc. (NASDAQ: VRML), a bio-analytical solutions company focused on gynecologic disease, reported its financial results for the second quarter ended Jun

Full Press Release Details

Vermillion Reports Second Quarter 2016 Results
Conference Call at 8:00 a.m. ET Today
AUSTIN, Texas August 10, 2016 Vermillion, Inc. (NASDAQ: VRML), a bio-analytical solutions company focused on gynecologic disease, reported its financial results for the second quarter ended June 30, 2016.
Valerie Palmieri, President and CEO of Vermillion, Inc., stated, We believe that our performance during the second quarter of 2016 has built a solid foundation for continued success throughout the remainder of the year, and that we are well positioned to enter the market expansion and growth' phase of our strategy this year, which will include the targeted launch of Overa.
Recent Corporate Developments:
Q2 2016 Financial Results
Total revenue in the second quarter of 2016 was $709,000 compared to $535,000 in the same year-ago quarter. The second quarter 2016 revenue included $554,000 from product sales of OVA1 by ASPiRA LABS and $155,000 of service revenue from ASPiRA IVD. Second quarter revenue in 2015 was comprised of $483,000 in OVA1 product revenue from Quest Diagnostics sales and $52,000 in OVA1 product revenue from ASPiRA LABS. ASPiRA IVD began operations in the second quarter of 2016, and thus there was no comparable service revenue in the prior year.
Product revenue in the second quarter of 2016 was derived from 2,345 OVA1 tests performed by ASPiRA LABS. ASPiRA LABS performed a total of 274 tests in the second quarter of the prior year in addition to the 3,829 OVA1 tests performed at Quest Diagnostics. Revenue on a per test performed basis increased to $236 in the second quarter of 2016 compared to $130 in the second quarter of 2015.
Cost of product revenue for the second quarter of 2016 totaled $527,000 and was consistent with the comparable prior year quarter. Cost of service revenue totaled $60,000 for ASPiRA IVD services.
Total operating expenses in the second quarter of 2016 decreased to $3.9 million compared to $4.8 million in the same year-ago quarter. The decrease was due primarily to lower sales personnel and personnel-related expenses following our February 2016 restructuring as well as lower research and development collaboration costs; partially offset by costs related to establishing the laboratory for ASPiRA IVD.
Net loss for the second quarter of 2016 was $3.7 million or $(0.07) per share, as compared to a net loss of $4.8 million or $(0.11) per share in the same year-ago quarter.
As of June 30, 2016, cash and equivalents totaled $11.1 million. We utilized a net $2.0 million in cash in the second quarter of 2016 after taking into account $2.0 million in disbursements received in April 2016 from a loan of up to $4.0 million from the State of Connecticut Department of Economic and Community Development. The Company is entitled to the remaining $2.0 million upon the achievement of certain future milestones. Net cash utilization of $3.2 - $3.7 million is expected in the third quarter of 2016.
Conference Call and Webcast
Vermillion's President and CEO Valerie Palmieri will host a call today to discuss results followed by a question and answer period.
Wednesday, August 10th @ 8:00am Eastern Time
Domestic:888-523-1228
International:719-457-2689
Replay, available through August 25th:
Domestic:877-870-5176
International:858-384-5517
Please call the conference telephone number five minutes prior to the start time. An operator will register your name and organization. If you have any difficulty connecting with the conference call, please contact Vermillion at (512) 519-0400.
Vermillion, Inc. is dedicated to the discovery, development and commercialization of novel high-value diagnostic and bio-analytical solutions that help physicians diagnose, treat and improve gynecologic health outcomes for women. Vermillion, along with its prestigious scientific collaborators, discovers, develops, and delivers innovative diagnostic and technology tools that help women with serious diseases. The company's initial in vitro diagnostic test, OVA1 , was the first FDA-cleared, protein-based In Vitro Diagnostic Multivariate Index Assay, and represented a new class of software-based liquid biopsy in vitro diagnostics. In March 2016, Vermillion received FDA clearance for Overa , a second generation OVA1 test with significantly improved specificity and ease of use. For additional information, including published clinical trials, visit www.vermillion.com.
Forward-Looking Statements
This press release contains forward-looking statements, as that term is defined in the Private Litigation Reform Act of 1995, that involve significant risks and uncertainties, including plans with respect to ASPiRA IVD, the targeted launch of Overa, and expected cash utilization in future periods. Words such as may, expects, intends, anticipates, believes, estimates, plans, seeks, could, should, continue, will, potential, projects and similar expressions are intended to identify forward-looking statements. The forward-looking statements contained in this press release are based on Vermillion's expectations as of the date of this press release. A variety of factors could cause actual
results and experience to differ materially from the anticipated results or other expectations expressed in such forward-looking statements. Factors that could cause actual results to materially differ from those projected in such forward-looking statements include but are not limited to: (1) Vermillion's ability to increase the volume of OVA1 sales; (2) Vermillion's ability to market its test through sales channels other than Quest Diagnostics, including ASPiRA LABS; (3) failures by third-party payers to reimburse OVA1 or changes or variances in reimbursement rates; (4) Vermillion's ability to secure additional capital on acceptable terms to execute its business plan; (5) Vermillion's ability to commercialize Overa both within and outside the United States; (6) in the event that Vermillion succeeds in commercializing Overa outside the United States, the political, economic and other conditions affecting other countries (including
foreign exchange rates); (7) Vermillion's ability to develop and commercialize additional diagnostic products and achieve market acceptance with respect to these products; (8) Vermillion's ability to compete successfully; (9) Vermillion's ability to obtain any regulatory approval for Vermillion's future diagnostic products; (10) Vermillion's or its suppliers' ability to comply with FDA requirements for production, marketing and post market monitoring of its products; (11) additional costs that may be required to make further improvements to Vermillion's manufacturing operations; (12) Vermillion's ability to maintain sufficient or acceptable supplies of immunoassay kits from its suppliers; (13) Vermillion's ability to continue to develop, protect and promote its proprietary technologies; (14) future litigation against Vermillion, including infringement of intellectual property and product liability exposure; (15) Vermillion's ability to retain key employees; (16) business interruptions; (17) legislative actions resulting in higher compliance costs; (18) changes in healthcare policy; (19) Vermillion's ability to comply with environmental laws; (20) Vermillion's ability to generate sufficient demand for ASPiRA LABS' services to cover its operating costs; (21) Vermillion's ability to comply with the additional laws and regulations that apply to it in connection with the operation of ASPiRA LABS; (22) Vermillion's ability to comply with FDA regulations that relate to its products and to obtain any FDA clearance or approval required to develop and perform laboratory developed tests; (23) ASPiRA IVD's lack of operating history; (24) ASPiRA IVD's ability to generate and maintain business; (25) fluctuations over time with respect to ASPiRA IVD's operating results; (26) ASPiRA IVD's ability to enter into profitable contracts; (27) ASPiRA IVD's ability to maintain effective information systems without significant interruption; ASPiRA IVD's ability to perform its services in compliance with contractual requirements, regulatory standards and ethical considerations; and (24) other factors that are described in Vermillion's Form 10-K for the year ended December 31, 2015 and Form 10-Q for the quarter ended March 31, 2016 as filed with the Securities and Exchange Commission (the SEC ). Vermillion expressly disclaims any obligation to update, amend or clarify any forward-looking statements to reflect events, new information or circumstances occurring after the date of this press release, except as required by law.
This release should be read in conjunction with the consolidated financial statements and notes thereto included in Vermillion's most recent reports on Form 10-K and Form 10-Q. Copies are available through the SEC's Electronic Data Gathering Analysis and Retrieval system (EDGAR) at www.sec.gov.
Investor Relations Contact:
LifeSci Advisors LLC
Consolidated Balance Sheets
(Amounts in Thousands, Except Share and Par Value Amounts)
June 30, December 31,
2016 2015
Assets
Current assets:
Cash and cash equivalents $ 11,062 $ 18,642
Accounts receivable 243 87
Prepaid expenses and other current assets 407 550
Inventories 80 87
Total current assets 11,792 19,366
Property and equipment, net 2,107 1,504
Other Assets - 90
Total assets $ 13,899 $ 20,960
Liabilities and Stockholders' Equity
Current liabilities:
Accounts payable $ 503 $ 988
Accrued liabilities 1,858 2,208
Deferred revenue 16 -
Short-term debt 180 -
Other current liabilities 32 155
Total current liabilities 2,589 3,351
Non-current liabilities:
Long-term debt 1,758 -
Other non-current liabilities 47 63
Total liabilities 4,394 3,414
Commitments and contingencies
Stockholders' equity:
Common stock, par value $0.001 per share, 150,000,000 shares authorized at
June 30, 2016 and December 31, 2015; 52,222,280 and 52,113,059 shares
issued and outstanding at June 30, 2016 and December 31, 2015, respectively 52 52
Additional paid-in capital 388,687 388,082
Accumulated deficit (379,234) (370,588)
Total stockholders' equity 9,505 17,546
Total liabilities and stockholders' equity $ 13,899 $ 20,960
Consolidated Statements of Operations
(Amounts in Thousands, Except Share and Per Share Amounts)
Three Months Ended June 30, Six Months Ended June 30,
2016 2015 2016 2015
Revenue:
Product $ 554 $ 535 $ 1,059 $ 1,170
Service 155 - 155 -
License - - - 316
Total revenue 709 535 1,214 1,486
Cost of revenue:
Product (1) 527 574 1,055 1,065
Service 60 - 60 -
Total cost of revenue 587 574 1,115 1,065
Gross profit 122 (39) 99 421
Operating expenses:
Research and development (2) 564 919 1,498 2,024
Sales and marketing (3) 1,628 2,559 3,908 4,776
General and administrative (4) 1,691 1,331 3,350 2,731
Total operating expenses 3,883 4,809 8,756 9,531
Loss from operations (3,761) (4,848) (8,657) (9,110)
Interest income (expense), net (8) 6 (5) 15
Other income (expense), net 20 (7) 16 109
Net loss $ (3,749) $ (4,849) $ (8,646) $ (8,986)
Net loss per share - basic and diluted $ (0.07) $ (0.11) $ (0.17) $ (0.21)
Weighted average common shares used to compute basic and diluted net loss per common share 52,151,440 42,985,954 52,132,288 43,050,872
Non-cash stock-based compensation expense included in cost of revenue and operating expenses:
(1) Cost of revenue $ 22 $ 10 $ 46 $ 19
(2) Research and development 22 32 53 63
(3) Sales and marketing 14 36 56 73
(4) General and administrative 319 121 445 209
Last updated: Aug 10, 2016