• OraSure Technologies, Inc. Announces 2020 Full-Year and Fourth Quarter Financial Results and Provides COVID-19 Update

    المصدر: Nasdaq GlobeNewswire / 01 مارس 2021 16:15:00   America/New_York

    Full-Year 2020 Net Revenues of $172 Million Increased 11% Year-Over-Year, Driven by $50 Million in Sales of Oral Fluid Collection Devices for COVID-19 Molecular Testing

    COVID-19 Rapid Antigen Test clinical trials complete; OraSure plans to submit both a Prescription Self-Test and a Professional Test for EUA in Q1

    Management to Host Conference Call and Webcast Today at 5:00 p.m. ET

    BETHLEHEM, Pa., March 01, 2021 (GLOBE NEWSWIRE) -- OraSure Technologies, Inc. (NASDAQ: OSUR), a leader in point-of-care diagnostic tests, specimen collection devices, and microbiome laboratory and analytical services, today announced its financial results for the three months and year ended December 31, 2020.

    “OraSure continues to successfully navigate the pandemic, with a record-breaking fourth quarter and double-digit full-year revenue growth driven by a strong sequential quarterly increase in sales of our molecular sample collection kits for COVID-19 testing. We expect this strong sustained performance to persist as testing continues to be a key strategy to combat the ongoing pandemic. Our base business was resilient, with demonstrated strength in international HIV testing,” said Stephen S. Tang, Ph.D., President and Chief Executive Officer.

    Dr. Tang continued, “Importantly, we have made substantial progress on our COVID-19 Rapid Antigen Self-Test and oral fluid antibody test. We expect that OraSure’s COVID-19 activities will continue to accelerate the Company’s growth and significantly outweigh any negative impact of the pandemic on other parts of our business. We have locked the proprietary assay chemistry and completed development and clinical testing of our rapid antigen test for COVID-19. We accelerated the Prescription Self-Test trials and now plan to submit for both the Professional and Prescription Self-Test for Emergency Use Authorization (EUA) by the end of this month. We are also planning to resubmit two separate EUAs for our lab-based oral fluid antibody test, including additional analytical study data, as requested by the FDA, and look forward to bringing this important product to market as soon as possible.”

    Financial Highlights

    • Net revenues for the fourth quarter of 2020 were $62.9 million, a 27% increase from the fourth quarter of 2019. Net product and services revenues were $60.4 million, a 28% increase from the fourth quarter of 2019.
    • Net revenues for the full year 2020 were $171.7 million, an 11% increase over 2019.
    • Total product and service revenues for the Company’s molecular business unit were $40.3 million during the fourth quarter of 2020, an increase of 58% from the fourth quarter of 2019. This increase included $22.5 million in sales of sample collection devices for COVID-19 molecular testing.
    • Total product and service revenues for the Company’s molecular business unit were $102.8 million for the full year 2020, an increase of 45% from the full year 2019. The increase included $49.8 million in sales of sample collection devices for COVID-19 molecular testing.
    • Full year 2020 international sales of the Company’s HIV products grew 16% over the prior year driven by a 21% increase in HIV Self-Test sales in Africa. For the fourth quarter, HIV international revenue was $11.3 million, a 16% increase from the fourth quarter of 2019. This was a record quarter and year for sales of OraSure’s HIV self-tests internationally.
    • Net income for the fourth quarter of 2020 was $1.9 million, or $0.03 per share on a fully-diluted basis, compared to net income of $2.4 million, or $0.04 per share on a fully-diluted basis, for the fourth quarter of 2019.
    • Cash and investments totaled $257.1 million at December 31, 2020.

    COVID-19 Update

    Molecular/PCR:

    • Sales of sample collection devices for molecular/PCR COVID-19 testing in the fourth quarter showed sequential quarterly growth and persistence of commercial opportunity; the Company’s sample collection kits continued to be included in Emergency Use Authorizations (EUAs) granted to customers.
      • Use of DNA Genotek molecular sample collection kits continued to grow in back-to-work settings, back-to-school programs, laboratory testing and direct-to-consumer offerings. OraSure continues to build its customer base, with high-volume repeat orders from existing customers and demand from new customers.
        • The Company’s molecular collection kits are now included in eight EUAs granted by the U.S. Food and Drug Administration (FDA) to DNA Genotek customers for COVID-19 testing.
        • The Company’s ORAcollect® •RNA saliva collection device has been used in the more than one million COVID-19 tests administered by State University of New York campuses since the start of the 2020-2021 academic year. These tests were developed by DNA Genotek customer Quadrant Biosciences.
        • The Company’s OMNIgene·ORAL and ORAcollect® •RNA saliva collection devices have received interim authorization for use in COVID-19 testing from Health Canada.
        • Through OraSure’s customer Chronomics, the OMNIgene·ORAL is being utilized as a collection device for the UK Government’s “Test to Release for International Travel” COVID-19 testing program.

    Antigen:

    • OraSure has finalized all product development and completed clinical studies for its COVID-19 Rapid Antigen Self-Test and now plans FDA EUA submission for both Professional and Prescription Self-Test in the first quarter.
      • OraSure has locked the proprietary assay chemistry and completed development of its COVID-19 Rapid Antigen Self-Test and has collected all clinical study data to now submit both the Professional version and Prescription Self-Test version for EUA in the first quarter of 2021.
      • Subject to receipt of EUA, this product would test for active COVID-19 infection using nasal samples self-collected from the lower nostrils. The COVID-19 Rapid Antigen Self-Test is designed to be performed anytime, anywhere, with no instrumentation, batteries or laboratory analysis needed to interpret results. 
      • Subject to regulatory approvals, the Company intends to market its Prescription Self-Test for use by individual consumers (with prescription) at home, or in any location by employers/universities on- or off-site, or by physicians, or public health via remote testing, and its Professional Test for use at drive-through sites, physician offices, public health testing sites, and employer/university health centers.
      • After the Company submits the Professional Test and Prescription Self-Test for EUA, it intends to continue plans to pursue an OTC claim.
      • The Company will be manufacturing at risk and intends to launch the tests without delay, subject to authorization.

    Antibody:

    • OraSure is working with the FDA to secure Emergency Use Authorization for its lab-based OraSure SARS-CoV-2 Antibody ELISA. Currently no COVID-19 antibody tests that use oral fluid samples have received Emergency Use Authorization. OraSure’s test could be the first. Oral fluid samples minimize healthcare professionals’ need for personal protective equipment and reduces their exposure to potentially infected patients as compared to blood draws; the test could aid health officials in community surveillance efforts and seroprevalence studies.
      • With this test, individuals would use the OraSure Oral Antibody Collection Device to self-collect an oral fluid sample under the observation of a healthcare professional. The sample would then be placed into the buffer vial for storage and transport, and then later dispensed onto the OraSure SARS-CoV-2 ELISA microplate for testing in a laboratory. This lab-based antibody test can aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating prior infection.
      • At the request of the FDA, the Company plans to resubmit two separate EUAs for the test, one covering the oral fluid specimen collector and one for the microplate assay. In addition, the FDA has requested that additional analytical studies be conducted on sample collection and stability.
      • OraSure continues to sell its antibody test for research use only, which has led to interest from several companies and labs regarding seroprevalence studies in cities or university populations.

    Manufacturing:

    • OraSure’s initiative to increase manufacturing capacity to meet demand for COVID-19 sample collection kits and tests continues on schedule. Additional expansion planned to support Rapid Antigen Self-Test.
      • Previously the Company had disclosed that it was expanding manufacturing capacity for the Rapid Antigen Self-Test to 70 million tests per year in the third quarter of 2021 (including tests for HIV, HCV and Ebola).
      • OraSure now plans additional expansion of 50 million Rapid Antigen Self-Tests, bringing capacity to 120 million tests per year (including tests for HIV, HCV and Ebola) by the second quarter of 2022. The Company expects this additional capacity to support sales outside of the U.S.
      • As previously disclosed, the Company is expanding capacity of its molecular sample collection devices to a rate of approximately 75 million units annually in the second quarter of 2021 and further to 80 million units in the third quarter, including non-COVID kits.
      • Also as previously disclosed, installation of new lines for the oral-fluid antibody test will bring total capacity to 20 million units per year by the fourth quarter, including existing products.

    Financial Results for the Three Months Ended December 31, 2020

    Net revenues for the fourth quarter of 2020 of $62.9 million increased 27% from the comparable period of 2019, primarily as a result of strong sales of molecular sample collection kits for COVID-19 testing and increased international sales of the Company’s HIV Self-Test partially offset by declines in revenues of our other product lines largely due to the impact of COVID-19.

    Gross profit percentage was 61% for the three months ended December 31, 2020 compared to 60% for the three months ended December 31, 2019. Gross profit in the current quarter benefited from an improved product mix associated with higher gross profit percentage product sales.

    For the three months ended December 31, 2020, operating expenses were $30.3 million, an increase of $4.1 million from the $25.8 million reported for the three months ended December 31, 2019, largely due to increased investment in the development of the Company’s COVID products.

    The Company generated operating income of $7.9 million in the fourth quarter of 2020 compared to operating income of $4.1 million in the fourth quarter of 2019.

    During the fourth quarters of 2020 and 2019, the Company recorded income tax expense of $5.7 million and $2.1 million, respectively. Income tax expense in both periods largely consisted of foreign taxes due related to our Canadian subsidiary.

    First Quarter 2021 Guidance

    The Company expects first quarter 2021 net revenues to range from $55.0 million to $60.0 million.

    Financial Data (Unaudited)

      Three Months Ended  Year Ended 
      December 31,  December 31, 
      2020  2019  2020  2019 
    Results of Operations                
    Net revenues $62,855  $49,668  $171,721  $154,605 
    Cost of products and services sold  24,671   19,829   69,853   60,022 
    Gross profit  38,184   29,839   101,868   94,583 
    Operating expenses:                
    Research and development  10,457   6,104   31,032   19,629 
    Sales and marketing  9,120   7,932   34,459   31,869 
    General and administrative  12,211   11,539   42,653   35,287 
    Change in fair value of acquisition-related contingent consideration  (1,489)  179   (1,099)  (664)
    Gain on sale of business           (10,149)
    Total operating expenses  30,299   25,754   107,045   75,972 
    Operating income (loss)  7,885   4,085   (5,177)  18,611 
    Other income (expense)  (307)  477   1,653   2,720 
    Income (loss) before income taxes  7,578   4,562   (3,524)  21,331 
    Income tax expense  5,718   2,124   11,398   4,675 
    Net income (loss) $1,860  $2,438  $(14,922) $16,656 
    Earnings (loss) per share:                
    Basic $0.03  $0.04  $(0.22) $0.27 
    Diluted $0.03  $0.04  $(0.22) $0.27 
                     
    Weighted average shares:                
    Basic  71,723   61,729   67,505   61,675 
    Diluted  72,817   62,199   67,505   62,170 
                     


      Three Months Ended December 31,  
      Dollars       Percentage of Total Net Revenues  
      2020  2019  %
    Change
       2020   2019  
    Market                       
    Infectious disease testing $17,602  $18,743   (6)%  28 %  38 %
    Risk assessment testing  2,526   2,944   (14)   4    6  
    Molecular solutions  40,281   25,487   58    64    51  
    Net product and service revenues  60,409   47,174   28    96    95  
    Royalty income  1,809   2,160   (16)   3    4  
    Other  637   334   91    1    1  
    Net revenues $62,855  $49,668   27 %  100 %  100 %


      Year Ended December 31,  
      Dollars       Percentage of Total Net Revenues  
      2020  2019  %
    Change
       2020   2019  
    Market                       
    Infectious disease testing $54,227  $58,016   (7)%  32 %  38 %
    Risk assessment testing  9,374   12,189   (23)   5    8  
    Cryosurgical systems     7,054   (100)       5  
    Molecular solutions  102,780   70,814   45    60    45  
    Net product and service revenues  166,381   148,073   12    97    96  
    Royalty income  3,432   5,116   (33)   2    3  
    Other  1,908   1,416   35    1    1  
    Net revenues $171,721  $154,605   11 %  100 %  100 %


      Three Months Ended  Year Ended  
      December 31,  December 31,  
      2020  2019  %
    Change
      2020  2019  %
    Change
      
    OraQuick® Revenues                         
    Domestic HIV $3,861  $4,960   (22)%$15,184  $17,984   (16)%
    International HIV  11,343   9,795   16   29,040   25,108   16  
    Net HIV revenues  15,204   14,755   3   44,224   43,092   3  
    Domestic HCV  1,356   2,202   (38)  4,793   8,108   (41) 
    International HCV  884   1,295   (32)  3,655   4,864   (25) 
    Net HCV revenues  2,240   3,497   (36)  8,448   12,972   (35) 
    Net product revenues $17,444  $18,252   (4)%$52,672  $56,064   (6)%


      Three Months Ended   Year Ended  
      December 31,   December 31,  
      2020  2019  %
    Change
       2020  2019  %
    Change
      
    Molecular Solutions Revenues                          
    Genomics $13,760  $20,761   (34)% $37,141  $56,212   (34)%
    Microbiome  1,898   1,847   3    6,156   7,172   (14) 
    COVID-19  22,494     N/A    49,802     N/A  
    Laboratory services  2,093   2,820   (26)   9,564   6,767   41  
    Other product revenues  36   59   (39)   117   663   (82) 
    Net product and service revenues  40,281   25,487   58    102,780   70,814   45  
    Other  1,866   2,289   (18)   3,701   5,566   (34) 
    Net revenues $42,147  $27,776   52 % $106,481  $76,380   39 %
                               

    Condensed Consolidated Balance Sheets (Unaudited)

      December 31, 2020  December 31, 2019 
    Assets        
    Cash and cash equivalents $160,802  $75,715 
    Short-term investments  48,599   80,623 
    Accounts receivable, net  38,835   36,948 
    Inventories  31,863   23,155 
    Other current assets  8,794   8,109 
    Property, plant and equipment, net  51,860   30,339 
    Intangible assets, net  17,904   14,674 
    Goodwill  40,351   36,201 
    Long-term investments  47,718   33,420 
    Other non-current assets  7,746   10,111 
    Total assets $454,472  $349,295 
             
    Liabilities and Stockholders’ Equity        
    Accounts payable $17,407  $9,567 
    Deferred revenue  4,811   3,713 
    Contingent consideration obligation  402   3,500 
    Other current liabilities  23,869   15,933 
    Non-current contingent consideration obligation  2,049   112 
    Other non-current liabilities  7,363   9,325 
    Stockholders’ equity  398,571   307,145 
    Total liabilities and stockholders’ equity $454,472  $349,295 

    Additional Financial Data (Unaudited)

      Year Ended 
      December 31, 
      2020  2019 
    Capital expenditures $26,674  $9,314 
    Depreciation and amortization $9,714  $7,730 
    Stock-based compensation $7,139  $4,057 
    Cash provided by operating activities $5,807  $9,804 

    Conference Call

    The Company will host a conference call and audio webcast for analysts and investors to discuss the Company’s 2020 full year and fourth quarter results and certain business developments, beginning today at 5:00 p.m. Eastern Time (2:00 p.m. Pacific Time). On the call will be Dr. Stephen S. Tang, President and Chief Executive Officer, and Roberto Cuca, Chief Financial Officer. The call will include prepared remarks by management and a question and answer session.

    In order to listen to the conference call, please dial 844-831-3030 (Domestic) or 315-625-6887 (International) and reference Conference ID # 8168847 or go to OraSure Technologies’ web site, www.orasure.com, and click on the Investor Relations page. Please click on the webcast link and follow the prompts for registration and access 10 minutes prior to the call. A replay of the call will be archived on OraSure Technologies’ web site shortly after the call has ended and will be available for seven days. A replay of the call can also be accessed until midnight, March 15, 2021, by dialing 855-859-2056 (Domestic) or (404) 537-3406 (International) and entering the Conference ID #9459222.

    It is recommended to dial-in at most 15 to 20 minutes prior to the call start to reduce waiting times. If a participant will be listen-only, they are encouraged to listen via the webcast on OraSure’s Investor Relations page.

    About OraSure Technologies

    OraSure Technologies empowers the global community to improve health and wellness by providing access to accurate, essential information. Together with its wholly-owned subsidiaries, DNA Genotek, Diversigen and Novosanis, OraSure provides its customers with end-to-end solutions that encompass tools, services and diagnostics. The OraSure family of companies is a leader in the development, manufacture, and distribution of rapid diagnostic tests, sample collection and stabilization devices, and molecular services solutions designed to discover and detect critical medical conditions. OraSure’s portfolio of products is sold globally to clinical laboratories, hospitals, physician’s offices, clinics, public health and community-based organizations, research institutions, government agencies, pharma, commercial entities and direct to consumers. For more information on OraSure Technologies, please visit www.orasure.com.

    Important Information

    This press release contains certain forward-looking statements, including with respect to expected revenues, products, product development activities, regulatory submissions and authorizations and other matters. Forward-looking statements are not guarantees of future performance or results. Known and unknown factors that could cause actual performance or results to be materially different from those expressed or implied in these statements include, but are not limited to: ability to successfully manage and integrate acquisitions of other companies in a manner that complements or leverages our existing business, or otherwise expands or enhances our portfolio of products and our end-to-end service offerings, and the diversion of management’s attention from our ongoing business and regular business responsibilities to effect such integration; the expected economic benefits of acquisitions (and increased returns for our stockholders), including that the anticipated synergies, revenue enhancement strategies and other benefits from the acquisitions may not be fully realized or may take longer to realize than expected and our actual integration costs may exceed our estimates; impact of increased or different risks arising from the acquisition of companies located in foreign countries; ability to market and sell products, whether through our internal, direct sales force or third parties; impact of significant customer concentration in the genomics business; failure of distributors or other customers to meet purchase forecasts, historic purchase levels or minimum purchase requirements for our products; ability to manufacture products in accordance with applicable specifications, performance standards and quality requirements; ability to obtain, and timing and cost of obtaining, necessary regulatory approvals for new products or new indications or applications for existing products; ability to comply with applicable regulatory requirements; ability to effectively resolve warning letters, audit observations and other findings or comments from the U.S. Food and Drug Administration (“FDA”) or other regulators; the impact of the novel coronavirus (“COVID-19”) pandemic on our business and our ability to successfully develop new products, validate the expanded use of existing collector products, receive necessary regulatory approvals and authorizations and commercialize such products for COVID-19 testing; changes in relationships, including disputes or disagreements, with strategic partners or other parties and reliance on strategic partners for the performance of critical activities under collaborative arrangements; ability to meet increased demand for the Company’s products; impact of replacing distributors; inventory levels at distributors and other customers; ability of the Company to achieve its financial and strategic objectives and continue to increase its revenues, including the ability to expand international sales; ability to identify, complete, integrate and realize the full benefits of future acquisitions; impact of competitors, competing products and technology changes; reduction or deferral of public funding available to customers; competition from new or better technology or lower cost products; ability to develop, commercialize and market new products; market acceptance of oral fluid or urine testing, collection or other products; market acceptance and uptake of microbiome informatics, microbial genetics technology and related analytics services; changes in market acceptance of products based on product performance or other factors, including changes in testing guidelines, algorithms or other recommendations by the Centers for Disease Control and Prevention (“CDC”) or other agencies; ability to fund research and development and other products and operations; ability to obtain and maintain new or existing product distribution channels; reliance on sole supply sources for critical products and components; availability of related products produced by third parties or products required for use of our products; impact of contracting with the U.S. government; impact of negative economic conditions; ability to maintain sustained profitability; ability to utilize net operating loss carry forwards or other deferred tax assets; volatility of the Company’s stock price; uncertainty relating to patent protection and potential patent infringement claims; uncertainty and costs of litigation relating to patents and other intellectual property; availability of licenses to patents or other technology; ability to enter into international manufacturing agreements; obstacles to international marketing and manufacturing of products; ability to sell products internationally, including the impact of changes in international funding sources and testing algorithms; adverse movements in foreign currency exchange rates; loss or impairment of sources of capital; ability to attract and retain qualified personnel; exposure to product liability and other types of litigation; changes in international, federal or state laws and regulations; customer consolidations and inventory practices; equipment failures and ability to obtain needed raw materials and components; the impact of terrorist attacks and civil unrest; and general political, business and economic conditions. These and other factors that could affect our results are discussed more fully in our SEC filings, including our registration statements, Annual Report on Form 10-K for the year ended December 31, 2020, Quarterly Reports on Form 10-Q, and other filings with the SEC. Although forward-looking statements help to provide information about future prospects, readers should keep in mind that forward-looking statements may not be reliable. Readers are cautioned not to place undue reliance on the forward-looking statements. The forward-looking statements are made as of the date of this press release and OraSure Technologies undertakes no duty to update these statements.

    Investor contact:Media contact:
    Sam MartinJeanne Mell
    Argot PartnersOraSure Technologies
    212-600-1902484-353-1575
    orasure@argotpartners.commedia@orasure.com

    Primary Logo

شارك على،