Standard BioTools Announces First Quarter 2022 Financial Results
Standard BioTools Inc. (Nasdaq:LAB) reported first-quarter 2022 financial results with total revenue of $26.5 million, down from $32.8 million in Q1 2021, primarily due to lower COVID-19 revenue. The GAAP net loss was $76.3 million, significantly higher than a net loss of $18.8 million in Q1 2021, while non-GAAP net loss also increased to $19.5 million from $11.1 million. The company secured a $250 million capital infusion from Casdin Capital and Viking Global, aimed at enhancing operations and growth strategies amidst ongoing sales disruptions and COVID-19 impacts.
- Secured $250 million in capital infusion to strengthen operations.
- New management team appointed to improve operational issues.
- Early adoption of new products like CyTOF XT and Biomark X shows potential for future growth.
- Total revenue decreased by 19% year-over-year, primarily due to lower COVID-19 testing revenue.
- GAAP net loss increased to $76.3 million, significantly impacting financial health.
- Americas revenue dropped 30% year-over-year, driven by lower COVID testing revenue.
SOUTH SAN FRANCISCO, Calif., May 05, 2022 (GLOBE NEWSWIRE) -- Standard BioTools Inc. (Nasdaq:LAB), driven by a bold purpose – unleashing tools to accelerate breakthroughs in human health – today announced financial results for the first quarter ended March 31, 2022.
“The end of first quarter 2022 marked the completion of the company’s strategic evaluation process, which culminated in the closing of a
“During our first few weeks, the new management team has met with numerous key stakeholders, including customers, employees, and partners, and we are highly encouraged and excited by the opportunity before us,” continued Egholm. “Each of these stakeholders sees the opportunity for the now better-capitalized company to better meet the needs of our customers through essential, standardized tools that help them develop breakthrough medicines faster and better.”
Continued Egholm, “Going forward, we will refine our business strategy to build, maintain and strengthen our competitive positions in the markets in which we operate. We will do this by focusing on three areas: First, we will prioritize revenue growth by focusing our efforts to compete in growing market segments where we believe we have or could have a competitive advantage. Specifically, we will focus on servicing more customers in translational and clinical research. Second, we will significantly improve our operating discipline by implementing best-in-class process improvements to manage expenses and increase productivity. Finally, we intend to expand our product offerings for our customers with strategic capital allocation to acquire complementary assets that allow us to leverage our existing infrastructure.
“I believe we now have the resources needed to execute this strategy. I look forward to leading this outstanding team as we embark on this transformation journey and am confident our tool set will indeed accelerate breakthroughs in human health.”
First Quarter 2022 Financial Results
Total revenue was
GAAP net loss for the quarter was
Non-GAAP net loss, which excludes the accounting adjustments for the Series B Preferred Stock and bridge loans, was
Cash and cash equivalents and restricted cash as of March 31, 2022, was
Additional Detail on First Quarter 2022 Financial Results
- Mass cytometry product and service revenue of
$13.5 million for the quarter was down 4 percent over first quarter 2021 driven by lower instrument sales. The launch of our new CyTOF® XT instrument was more than offset by lower sales of our legacy Hyperion™ Imaging System and Helios™ instrument. Going forward, we are seeing encouraging adoption of CyTOF XT™ in the Pharma, Biotech, and CRO segments. Moreover, we expect the recent launch of the Hyperion+™ Imaging System to improve our competitive position in the growing high-plex imaging market. - Base microfluidics product and service revenue, which excludes COVID-19 testing revenue, was
$10.4 million , unchanged year-over-year. COVID-19 testing revenue was$2.3 million , down65% compared with first quarter 2021. Focusing on our base business, we are encouraged by the early adoption of our new Biomark™ X instrument, and our Olink® OEM partnership remains an important growth driver, offsetting weakness in our mature platforms. - Service revenue of
$6.1 million was2% lower year-over-year, following the strong performance for service revenue in fourth quarter 2021.
Revenue by geographic area:
- Americas revenue was
$12.9 million , down30% year-over-year, driven almost entirely by lower COVID testing revenue, NRE and grant revenues. The base business in Americas was unchanged year over year. - EMEA revenue was at
$8.6 million , down6% year-over-year. Changes in foreign exchange rates reduced the year-over-year growth by approximately 4 percentage points. COVID-19 continues to negatively impact our business, particularly with new waves in March, as many labs are operating below capacity. Negative impact from the conflict in Ukraine on the European economy together with COVID-19 related expenses on public healthcare systems remain operating headwinds for growth. - Asia-Pacific revenue decreased
3% to$5.0 million . The year-over-year decline was driven by continued COVID-19 related disruptions, particularly in China and Japan.
Recent Highlights
Innovation:
- Launched the Hyperion+ Imaging System, the new standard in spatial imaging with superior phenotyping, up to 10x cost savings compared with immunohistochemistry, and the most proven high-plex proteomics approach for scanning eight to 40-plus targets in a single run with easy scaling to 100-plus targets.
- Sold 7 CyTOF XT systems in Q1 2022 for a total of 29 since launch.
- Sold 9 of our recently launched Biomark X instruments, which shipped in Q1 2022.
Partnerships:
- Shipped 18 Olink Signature Q100 benchtop instrument systems, designed and manufactured by Standard BioTools, in Q1 2022.
- On February 17, 2022, we announced a collaboration agreement with the Abu Dhabi Stem Cells Center (ADSCC) for development of targeted stem cell therapies and research applications utilizing two Standard BioTools mass cytometry and tissue imaging technologies: Imaging Mass Cytometry™ (IMC™) and the Maxpar® Direct™ Immune Profiling Assay™.
Beachheads:
- At quarter end, 200 clinical trials were underway using CyTOF technology.
- Total publications and preprints involving CyTOF technology exceeded 2,000, including over 200 publications and preprints for Imaging Mass Cytometry, as of the end of Q1 2022.
Conference Call Information
The Company’s management will host a conference call and webcast today at 2:00 p.m. PT, 5:00 p.m. ET, to discuss first quarter 2022 financial results and operational progress.
Individuals interested in listening to the conference call may do so by dialing:
US domestic callers: (877) 344-8082
Outside US callers: (213) 992-4618
Live audio of the webcast will be available online from the Investor Relations page of the Company’s website at Events & Presentations. The webcast will be archived on Standard BioTools Investor Relations page at investors.fluidigm.com and will be available until May 12.
Due to the appointment in April of new management team members who are focused on completing a 90-day assessment following the closing of a
A reconciliation of GAAP to non-GAAP financial measures can be found in the tables of this release.
Our investor presentation including Supplemental Financial Information has been posted on our website concurrent with this release.
Statement Regarding Use of Non-GAAP Financial Information
Standard BioTools has presented certain financial information in accordance with U.S. GAAP and also on a non-GAAP basis for the three-month periods ended March 31, 2022, and March 31, 2021. Management believes that non-GAAP financial measures, taken in conjunction with GAAP financial measures, provide useful information for both management and investors by excluding certain non-cash and other expenses that are not indicative of the company’s core operating results. Management uses non-GAAP measures to compare the company’s performance relative to forecasts and strategic plans and to benchmark the company’s performance externally against competitors. The time and amount of certain material items needed to estimate non-GAAP financial measures are inherently unpredictable or outside of our control. Material changes to any of these items could have a significant effect on guidance and future GAAP results. Non-GAAP information is not prepared under a comprehensive set of accounting rules and should only be used to supplement an understanding of the company’s operating results as reported under U.S. GAAP. Standard BioTools encourages investors to carefully consider its results under GAAP, as well as its supplemental non-GAAP information and the reconciliation between these presentations, to more fully understand its business. Reconciliations between GAAP and non-GAAP operating results are presented in the accompanying tables of this release.
Use of Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including, among others, statements regarding operational and strategic plans, revenue growth and business transformation expectations, potential acquisitions, customer adoption of and demand for new products, improvements in competitive position based on introductions of new products, plans with respect to third party relationships and the positive impact of such relationships on growth, and demand trends, including the anticipated impact of geopolitical dynamics and the COVID pandemic. Forward-looking statements are subject to numerous risks and uncertainties that could cause actual results to differ materially from currently anticipated results, including but not limited to risks relating to the potential adverse effects of the coronavirus pandemic on our business and operating results; possible transition-related disruption, including through the loss of customers, suppliers and employees; changes in Standard BioTools’ business or external market conditions; customers and prospective customers continuing to curtail or suspend activities utilizing our products; our ability and/or the ability of the research institutions utilizing our products and technology to obtain and maintain Emergency Use Authorization from the FDA and any other requisite authorizations or approvals to use our products and technology for diagnostic testing purposes; challenges inherent in developing, manufacturing, launching, marketing, and selling new products; interruptions or delays in the supply of components or materials for, or manufacturing of, Standard BioTools products; reliance on sales of capital equipment for a significant proportion of revenues in each quarter; seasonal variations in customer operations; unanticipated increases in costs or expenses; uncertainties in contractual relationships; reductions in research and development spending or changes in budget priorities by customers; Standard BioTools research and development and distribution plans and capabilities; interruptions or delays in the supply of components or materials for, or manufacturing of, Standard BioTools products; potential product performance and quality issues; risks associated with international operations; intellectual property risks; and competition. Information on these and additional risks and uncertainties and other information affecting Standard BioTools’ business and operating results is contained in its Annual Report on Form 10-K for the year ended December 31, 2021, and in its other filings with the Securities and Exchange Commission. These forward-looking statements speak only as of the date hereof. Standard BioTools disclaims any obligation to update these forward-looking statements except as may be required by law.
About Standard BioTools Inc.
Standard BioTools Inc. (Nasdaq:LAB), previously known as Fluidigm Corporation, is driven by a bold purpose – unleashing tools to accelerate breakthroughs in human health. Standard BioTools has an established portfolio of essential, standardized next-generation technologies that help biomedical researchers develop medicines faster and better. As a leading solutions provider, the Company provides reliable and repeatable insights in health and disease using its proprietary mass cytometry and microfluidics technologies, which help transform scientific discoveries into better patient outcomes. Standard BioTools works with leading academic, government, pharmaceutical, biotechnology, plant and animal research, and clinical laboratories worldwide, focusing on the most pressing needs in translational and clinical research, including oncology, immunology, and immunotherapy. Learn more at www.standardbiotools.com or connect with us on Twitter®, Facebook®, LinkedIn, and YouTube™. Standard BioTools, the Standard BioTools logo, Fluidigm, and the Fluidigm logo are trademarks and/or registered trademarks of Standard BioTools Inc. or its affiliates in the United States and/or other countries. Standard BioTools products are provided for Research Use Only. Not for use in diagnostic procedures.
Available Information
Standard BioTools uses its website (standardbiotools.com), investor site (investors.standardbiotools.com), corporate Twitter account (@fluidigm), Facebook page (facebook.com/fluidigm), and LinkedIn page (linkedin.com/company/fluidigm-corporation) as channels of distribution of information about its products, its planned financial and other announcements, its attendance at upcoming investor and industry conferences, and other matters. Such information may be deemed material information, and Standard BioTools may use these channels to comply with its disclosure obligations under Regulation FD. Therefore, investors should monitor Standard BioTools’ website and its social media accounts in addition to following its press releases, SEC filings, public conference calls, and webcasts.
Investors:
Peter DeNardo
415 389 6400
ir@fluidigm.com
| STANDARD BIOTOOLS INC. | ||||||||
| (formerly known as FLUIDIGM CORPORATION) | ||||||||
| CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS | ||||||||
| (In thousands, except per share amounts) | ||||||||
| (Unaudited) | ||||||||
| Three Months Ended March 31, | ||||||||
| 2022 | 2021 | |||||||
| Revenue: | ||||||||
| Product revenue | $ | 20,004 | $ | 24,728 | ||||
| Service revenue | 6,144 | 6,286 | ||||||
| Product and service revenue | 26,148 | 31,014 | ||||||
| Other revenue (1) | 356 | 1,780 | ||||||
| Total revenue | 26,504 | 32,794 | ||||||
| Costs and expenses: | ||||||||
| Cost of product revenue | 12,339 | 11,663 | ||||||
| Cost of service revenue | 1,928 | 2,090 | ||||||
| Cost of product and service revenue | 14,267 | 13,753 | ||||||
| Research and development | 8,865 | 10,753 | ||||||
| Selling, general and administrative | 30,875 | 27,608 | ||||||
| Total costs and expenses | 54,007 | 52,114 | ||||||
| Loss from operations | (27,503 | ) | (19,320 | ) | ||||
| Interest expense | (1,030 | ) | (887 | ) | ||||
| Loss on forward sale of Series B Preferred Stock | (37,792 | ) | — | |||||
| Unrealized loss on bridge loans | (10,655 | ) | — | |||||
| Other expense, net | 118 | (285 | ) | |||||
| Loss before income taxes | (76,862 | ) | (20,492 | ) | ||||
| Income tax benefit | 574 | 1,671 | ||||||
| Net loss | $ | (76,288 | ) | $ | (18,821 | ) | ||
| Net loss per share, basic and diluted | $ | (0.99 | ) | $ | (0.25 | ) | ||
| Shares used to compute net loss per share, basic and diluted | 77,031 | 74,707 | ||||||
| Note: (1) Other revenue includes product development, license, and grant revenue. | ||||||||
| STANDARD BIOTOOLS INC. | ||||||
| (formerly known as FLUIDIGM CORPORATION) | ||||||
| CONDENSED CONSOLIDATED BALANCE SHEETS | ||||||
| (In thousands) | ||||||
| (Unaudited) | ||||||
| March 31, 2022 | December 31, 2021 (1) | |||||
| ASSETS | ||||||
| Current assets: | ||||||
| Cash and cash equivalents (2) | $ | 29,983 | $ | 28,451 | ||
| Accounts receivable, net | 15,422 | 18,320 | ||||
| Inventories, net | 23,245 | 20,825 | ||||
| Prepaid expenses and other current assets (2) | 4,547 | 4,470 | ||||
| Total current assets | 73,197 | 72,066 | ||||
| Property and equipment, net | 27,699 | 28,034 | ||||
| Operating lease right-of-use assets, net | 36,389 | 37,119 | ||||
| Other non-current assets (2) | 3,445 | 3,689 | ||||
| Developed technology, net | 24,875 | 27,927 | ||||
| Goodwill | 106,333 | 106,379 | ||||
| Total assets | $ | 271,938 | $ | 275,214 | ||
| LIABILITIES AND STOCKHOLDERS' EQUITY | ||||||
| Current liabilities: | ||||||
| Accounts payable | $ | 12,517 | $ | 10,602 | ||
| Accrued compensation and related benefits | 7,964 | 4,920 | ||||
| Operating lease liabilities, current | 3,209 | 3,053 | ||||
| Deferred revenue, current | 12,291 | 11,947 | ||||
| Deferred grant income, current | 3,603 | 3,535 | ||||
| Other accrued liabilities | 7,589 | 8,673 | ||||
| Advances under revolving credit agreement, current | — | 6,838 | ||||
| Total current liabilities | 47,173 | 49,568 | ||||
| Bridge loans | 35,655 | — | ||||
| Convertible notes, net | 54,271 | 54,160 | ||||
| Term loan, net | 10,106 | 10,049 | ||||
| Deferred tax liability | 3,544 | 4,329 | ||||
| Operating lease liabilities, non-current | 36,760 | 37,548 | ||||
| Deferred revenue, non-current | 5,793 | 5,966 | ||||
| Deferred grant income, non-current | 17,237 | 18,116 | ||||
| Obligation for Series B Preferred Stock | 37,792 | — | ||||
| Other non-current liabilities | 1,494 | 882 | ||||
| Total liabilities | 249,825 | 180,618 | ||||
| Total stockholders' equity | 22,113 | 94,596 | ||||
| Total liabilities and stockholders' equity | $ | 271,938 | $ | 275,214 | ||
| Notes: | ||||||
| (1) Derived from audited consolidated financial statements | ||||||
| (2) Cash, cash equivalents and restricted cash consist of: | ||||||
| Cash and cash equivalents | $ | 29,983 | $ | 28,451 | ||
| Restricted cash (included in other current assets, and other non-current assets) | 1,016 | 1,016 | ||||
| Total cash, cash equivalents and restricted cash | $ | 30,999 | $ | 29,467 | ||
| STANDARD BIOTOOLS INC. | ||||||||
| (formerly known as FLUIDIGM CORPORATION) | ||||||||
| CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS | ||||||||
| (In thousands) | ||||||||
| (Unaudited) | ||||||||
| Three Months Ended March 31, | ||||||||
| 2022 | 2021 | |||||||
| OPERATING ACTIVITIES | ||||||||
| Net loss | $ | (76,288 | ) | $ | (18,821 | ) | ||
| Loss on forward sale of Series B Preferred Stock | 37,792 | — | ||||||
| Unrealized loss on bridge loans | 10,655 | — | ||||||
| Stock-based compensation expense | 4,042 | 3,677 | ||||||
| Amortization of developed technology | 2,968 | 2,983 | ||||||
| Depreciation and amortization | 1,003 | 934 | ||||||
| Other non-cash items | 1,166 | 610 | ||||||
| Changes in assets and liabilities, net | 3,072 | (2,284 | ) | |||||
| Net cash used in operating activities | (15,590 | ) | (12,901 | ) | ||||
| INVESTING ACTIVITIES | ||||||||
| Proceeds from NIH Contract | — | 2,000 | ||||||
| Purchases of property and equipment | (868 | ) | (6,923 | ) | ||||
| Net cash used in investing activities | (868 | ) | (4,923 | ) | ||||
| FINANCING ACTIVITIES | ||||||||
| Proceeds from bridge loans | 25,000 | — | ||||||
| Repayment of advances under credit agreement | (6,838 | ) | — | |||||
| Repayment of long-term debt | — | (501 | ) | |||||
| Payments for employee equity programs, net | (87 | ) | (525 | ) | ||||
| Net cash provided by (used in) financing activities | 18,075 | (1,026 | ) | |||||
| Effect of foreign exchange rate fluctuations on cash and cash equivalents | (85 | ) | 74 | |||||
| Net increase (decrease) in cash, cash equivalents and restricted cash | 1,532 | (18,776 | ) | |||||
| Cash, cash equivalents and restricted cash at beginning of period | 29,467 | 69,536 | ||||||
| Cash, cash equivalents and restricted cash at end of period | $ | 30,999 | $ | 50,760 | ||||
| Cash, cash equivalents and restricted cash consist of: | ||||||||
| Cash and cash equivalents | $ | 29,983 | $ | 49,744 | ||||
| Restricted cash (included in prepaid and other current assets, and other non-current assets) | 1,016 | 1,016 | ||||||
| Total cash, cash equivalents and restricted cash | $ | 30,999 | $ | 50,760 | ||||
| STANDARD BIOTOOLS INC. | ||||||||
| (formerly known as FLUIDIGM CORPORATION) | ||||||||
| RECONCILIATION OF GAAP TO NON-GAAP FINANCIAL INFORMATION | ||||||||
| (In thousands, except per share amounts) | ||||||||
| (Unaudited) | ||||||||
| ITEMIZED RECONCILIATION BETWEEN GAAP AND NON-GAAP NET LOSS | ||||||||
| Three Months Ended March 31, | ||||||||
| 2022 | 2021 | |||||||
| Net loss (GAAP) | $ | (76,288 | ) | $ | (18,821 | ) | ||
| Loss on forward sale of Series B Preferred Stock | 37,792 | — | ||||||
| Unrealized loss on bridge loans | 10,655 | — | ||||||
| Stock-based compensation expense | 4,042 | 3,677 | ||||||
| Amortization of developed technology (a) | 2,967 | 2,983 | ||||||
| Depreciation and amortization | 1,003 | 934 | ||||||
| Interest expense (b) | 1,030 | 887 | ||||||
| Loss on disposal of property and equipment | 9 | — | ||||||
| Loss on extinguishment of debt | — | 9 | ||||||
| Benefit from acquisition related income taxes (c) | (742 | ) | (742 | ) | ||||
| Net loss (Non-GAAP) | $ | (19,532 | ) | $ | (11,073 | ) | ||
| Shares used in net loss per share calculation - | ||||||||
| basic and diluted (GAAP and Non-GAAP) | 77,031 | 74,707 | ||||||
| Net loss per share - basic and diluted (GAAP) | $ | (0.99 | ) | $ | (0.25 | ) | ||
| Net loss per share - basic and diluted (Non-GAAP) | $ | (0.25 | ) | $ | (0.15 | ) | ||
| ITEMIZED RECONCILIATION BETWEEN GAAP AND NON-GAAP PRODUCT AND SERVICE MARGIN | ||||||||
| Three Months Ended March 31, | ||||||||
| 2022 | 2021 | |||||||
| Product and service gross profit (GAAP) | $ | 11,881 | $ | 17,261 | ||||
| Amortization of developed technology (a) | 2,967 | 2,800 | ||||||
| Depreciation and amortization (d) | 315 | 420 | ||||||
| Stock-based compensation expense (d) | 141 | 98 | ||||||
| Product and service gross profit (Non-GAAP) | $ | 15,304 | $ | 20,579 | ||||
| Product and service margin percentage (GAAP) | 45.4 | % | 55.7 | % | ||||
| Product and service margin percentage (Non-GAAP) | 58.5 | % | 66.4 | % | ||||
| ITEMIZED RECONCILIATION BETWEEN GAAP AND NON-GAAP OPERATING EXPENSES | ||||||||
| Three Months Ended March 31, | ||||||||
| 2022 | 2021 | |||||||
| Operating expenses (GAAP) | $ | 39,740 | $ | 38,361 | ||||
| Stock-based compensation expense (e) | (3,901 | ) | (3,579 | ) | ||||
| Depreciation and amortization (e) | (688 | ) | (697 | ) | ||||
| Loss on disposal of property and equipment (e) | (9 | ) | — | |||||
| Operating expenses (Non-GAAP) | $ | 35,142 | $ | 34,085 | ||||
| ITEMIZED RECONCILIATION BETWEEN GAAP AND NON-GAAP LOSS FROM OPERATIONS | ||||||||
| Three Months Ended March 31, | ||||||||
| 2022 | 2021 | |||||||
| Loss from operations (GAAP) | $ | (27,503 | ) | $ | (19,320 | ) | ||
| Stock-based compensation expense | 4,042 | 3,677 | ||||||
| Amortization of developed technology (a) | 2,967 | 2,983 | ||||||
| Depreciation and amortization (e) | 1,003 | 934 | ||||||
| Loss on disposal of property and equipment (e) | 9 | — | ||||||
| Loss from operations (Non-GAAP) | $ | (19,482 | ) | $ | (11,726 | ) | ||
| (a) Represents amortization of developed technology in connection with the DVS and InstruNor acquisitions | ||||||||
| (b) Represents interest expense, primarily on convertible debt and the term loan | ||||||||
| (c) Represents the tax impact on the purchase of intangible assets in connection with the DVS acquisition | ||||||||
| (d) Represents expense associated with cost of product revenue | ||||||||
| (e) Represents expense associated with research and development, and selling, general and administrative activities | ||||||||
FAQ
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