Full Press Release Details
T2 Biosystems Announces Fourth Quarter and Full Year 2022 Financial Results
Achieved record sepsis product revenue and sepsis-driven T2Dx Instrument placements in 2022
LEXINGTON, Mass., March 13, 2023 (GLOBE NEWSWIRE) T2 Biosystems, Inc. (NASDAQ:TTOO) (the Company ), a leader in the rapid
detection of sepsis-causing pathogens and antibiotic resistance genes, today announced financial results for the fourth quarter and full year ended December 31, 2022.
Recent Commercial and Financial Highlights
Recent Pipeline and Clinical Highlights
Throughout 2022, the T2 Biosystems team generated record sepsis and related product revenue and expanded the installed base of T2Dx Instruments through
record sepsis-driven instrument contracts. We also advanced our product pipeline, positioning T2 Biosystems to expand our test menu in 2023, stated John Sperzel, Chairman and CEO of T2 Biosystems. We look forward to continuing this
momentum to advance our three corporate priorities accelerating our sales, enhancing our operations, and advancing our pipeline to support long term growth.
Fourth Quarter 2022 Financial Results
the fourth quarter of 2022 was $5.5 million, a decrease of 21% compared to the prior year period. Product revenue for the fourth quarter of 2022 was $2.2 million, a decrease of 45% compared to the prior year period, driven by an 89%
decline in COVID-19 test sales and partially offset by increased sepsis test sales. Research contribution revenues were $3.3 million, an increase of 10% compared to the prior year period driven by the
timing of enrollments in the T2Resistance clinical trial.
Product costs for the fourth quarter of 2022 were $3.8 million, a decrease of 30% compared
to the prior year period, driven by decreased COVID-19 test sales. Research and development expenses were $4.9 million, a decrease of 9% compared to the prior year period driven by decreased development
expenses during the clinical trial phases of the BARDA contract. Selling, general and administrative expenses were $6.7 million, an increase of $2% compared to the prior year period driven by increased selling activity.
Net loss for the fourth quarter of 2022 was $10.4 million, $1.41 per share, compared to a net loss of
$12.1 million, $3.65 per share, in the prior year period.
Full Year 2022 Financial Results
Total revenue for 2022 was $22.3 million, a decrease of 21%, compared to the prior year. Product revenue for 2022 was $11.3 million, a decrease of
32% compared to the prior year, driven by decreased Covid-19 test panel sales and partially offset by increased sepsis test panel sales. Research and contribution revenue for 2022 was $11.0 million, a
decrease of 3% compared to the prior year.
Operating expenses for 2022 were $56.7 million, an increase of 13% million compared to the prior year
driven by increased BARDA contract research and development and U.S. clinical trials activity.
Net loss for 2022 was $62.3 million, $12.28 per
share, compared to a net loss of $49.2 million, $15.50 per share, in 2021.
Cash, equivalents, and restricted cash were $11.9 million as of
December 31, 2022. In February 2023, we raised $12.0 million through a common stock and warrants sale.
2023 Financial Outlook
The Company expects full year 2023 total sepsis and related product revenue of $11.0 million to $13.0 million, representing growth of 31% to 55%,
compared to $8.4 million in 2022. Given the focus on product revenue, the Company is not providing guidance on research and contribution revenue.
Webcast and Conference Call Information
Company s management team will host a conference call today, March 13, 2023, beginning at 4:30 pm ET. Investors interested in listening to the call may do so by dialing
877-545-0523 for domestic callers or 973-528-0016 for International callers and using
conference ID 411579 approximately five minutes prior to the start time. A live and recorded webcast of the call will be available on the Investors section of the Company s website at www.t2biosystems.com.
T2 Biosystems, a leader in the rapid
detection of sepsis-causing pathogens and antibiotic resistance genes, is dedicated to improving patient care and reducing the cost of care by helping clinicians effectively treat patients faster than ever before. T2 Biosystems products
include the T2Dx Instrument, the T2Bacteria Panel, the T2Candida Panel, the
T2Resistance Panel, and the T2SARS-CoV-2 Panel and
are powered by the proprietary T2 Magnetic Resonance (T2MR ) technology. T2 Biosystems has an active pipeline of future products, including the T2Biothreat Panel, the T2Cauris Panel, and T2Lyme Panel, as well as next-generation
products for the detection of bacterial and fungal pathogens and associated antimicrobial resistance markers.
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements contained in
this press release that do not relate to matters of historical fact should be considered forward-looking statements, including, without limitation, statements regarding our revenue results and cash balance, financial outlook, instrument contracts,
timing of completing clinical trials and filing of an FDA submission, impact of operating expense reductions, anticipated strategic priorities, product demand, commitments or opportunities, and
growth expectations or targets, as well as statements that include the words expect, may, should, anticipate, and similar statements of a future or forward looking nature. These forward-looking
statements are based on management s current expectations. These statements are neither promises nor guarantees, but involve known and unknown risks, uncertainties and other important factors that may cause actual results, performance or
achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements, including, but not limited to, (i) any inability to (a) realize anticipated benefits from
commitments, contracts or products; (b) successfully execute strategic priorities; (c) bring products to market; (d) expand product usage or adoption; (e) obtain customer testimonials; (f) accurately predict growth
assumptions; (g) realize anticipated revenues; (h) incur expected levels of operating expenses; or (i) increase the number of high-risk patients at customer facilities; (ii) failure of early data to predict eventual outcomes;
(iii) failure to make or obtain anticipated FDA filings or clearances within expected time frames or at all; or (iv) the factors discussed under Item 1A. Risk Factors in the Company s Annual Report on Form 10-K for the year ended December 31, 2021, filed with the U.S. Securities and Exchange Commission, or SEC, on March 23, 2022, and other filings the Company makes with the SEC from time to time, including
our Quarterly Reports on Form 10-Q and Current Reports on Form 8-K. These and other important factors could cause actual results to differ materially from those
indicated by the forward-looking statements made in this press release. Any such forward-looking statements represent management s estimates as of the date of this press release. While the Company may elect to update such forward-looking
statements at some point in the future, unless required by law, it disclaims any obligation to do so, even if subsequent events cause its views to change. Thus, no one should assume that the Company s silence over time means that actual events
are bearing out as expressed or implied in such forward-looking statements. These forward-looking statements should not be relied upon as representing the Company s views as of any date subsequent to the date of this press release.
Philip Trip Taylor, Gilmartin Group
Consolidated Balance Sheets
(In thousands, except share and per share data)
| December 31, | December 31, | |||||||
| 2022 | 2021 | |||||||
| Assets | ||||||||
| Current assets: | ||||||||
| Cash and cash equivalents | $ | 10,329 | $ | 22,245 | ||||
| Marketable securities | 9,996 | |||||||
| Accounts receivable | 2,163 | 5,134 | ||||||
| Inventories | 4,349 | 3,909 | ||||||
| Prepaid expenses and other current assets | 2,582 | 3,110 | ||||||
| Total current assets | 19,423 | 44,394 | ||||||
| Property and equipment, net | 4,533 | 4,675 | ||||||
| Operating lease right-of-use assets | 8,741 | 9,766 | ||||||
| Restricted cash | 1,551 | 1,551 | ||||||
| Other assets | 143 | 153 | ||||||
| Total assets | $ | 34,391 | $ | 60,539 | ||||
| Liabilities and stockholders deficit | ||||||||
| Current liabilities: | ||||||||
| Accounts payable | $ | 1,296 | $ | 2,832 | ||||
| Accrued expenses and other current liabilities | 7,647 | 8,338 | ||||||
| Operating Lease Liability | 1,352 | |||||||
| Warrant Liability | 39 | |||||||
| Deferred revenue | 172 | 518 | ||||||
| Total current liabilities | 10,506 | 11,688 | ||||||
| Notes payable | 49,651 | 47,790 | ||||||
| Operating lease liabilities, net of current portion | 8,214 | 9,359 | ||||||
| Deferred revenue, net of current portion | 52 | 28 | ||||||
| Derivative liability | 1,088 | |||||||
| Other liabilities | 4,849 | 4,577 | ||||||
| Total liabilities | 74,360 | 73,442 | ||||||
| Commitments and contingencies | ||||||||
| Stockholders deficit: | ||||||||
| Preferred stock, $0.001 par value; 10,000,000 shares authorized; no shares issued and outstanding | ||||||||
| Common stock, $0.001 par value; 400,000,000 shares authorized; 7,716,519 and 3,328,017 shares issued and outstanding at December 31, 2022 and December 31, 2021, respectively | 8 | 166 | ||||||
| Additional paid-in capital | 494,556 | 459,151 | ||||||
| Accumulated other comprehensive (loss) income | (4 | ) | ||||||
| Accumulated deficit | (534,533 | ) | (472,216 | ) | ||||
| Total stockholders deficit | (39,969 | ) | (12,903 | ) | ||||
| Total liabilities and stockholders deficit | $ | 34,391 | $ | 60,539 |
Consolidated Statements of Operations and Comprehensive Loss
(In thousands, except share and per share data)
| Year ended | ||||||||
| December 31, | ||||||||
| 2022 | 2021 | |||||||
| Revenue: | ||||||||
| Product revenue | $ | 11,259 | $ | 16,646 | ||||
| Contribution revenue | 11,046 | 11,412 | ||||||
| Total revenue | 22,305 | 28,058 | ||||||
| Costs and expenses: | ||||||||
| Cost of product revenue | 21,139 | 20,703 | ||||||
| Research and development | 25,932 | 21,801 | ||||||
| Selling, general and administrative | 30,744 | 28,527 | ||||||
| Total costs and expenses | 77,815 | 71,031 | ||||||
| Loss from operations | (55,510 | ) | (42,973 | ) | ||||
| Other income (expense): | ||||||||
| Interest income | 8 | 112 | ||||||
| Interest expense | (6,084 | ) | (7,596 | ) | ||||
| Change in fair value of derivative instrument | (1,088 | ) | 1,010 | |||||
| Change in fair value of warrant liability | 326 | |||||||
| Other income | 125 | 218 | ||||||
| Other expense | (15 | ) | ||||||
| Other gains/losses | (79 | ) | (12 | ) | ||||
| Total other expense | (6,807 | ) | (6,268 | ) | ||||
| Net loss | $ | (62,317 | ) | $ | (49,241 | ) | ||
| Deemed dividend on Series A redeemable convertible preferred stock | $ | (330 | ) | $ | ||||
| Net loss attributable to common stockholders | $ | (62,647 | ) | $ | (49,241 | ) | ||
| Net loss per share basic and diluted | $ | (12.28 | ) | $ | (15.50 | ) | ||
| Weighted-average number of common shares used in computing net loss per share basic and diluted | 5,100,395 | 3,177,228 | ||||||
| Other comprehensive loss: | ||||||||
| Net loss | $ | (62,317 | ) | $ | (49,241 | ) | ||
| Net unrealized (loss) gain on marketable securities arising during the period | 2 | (4 | ) | |||||
| Less: net realized (gain) loss on marketable securities included in net loss | 2 | (9 | ) | |||||
| Total other comprehensive (loss) gain, net of taxes | 4 | (13 | ) | |||||
| Comprehensive loss | $ | (62,313 | ) | $ | (49,254 | ) |
Consolidated Statements of Operations and Comprehensive Loss
(In thousands, except share and per share data)
| Three Months ended | ||||||||
| December 31, | ||||||||
| 2022 | 2021 | |||||||
| Revenue: | ||||||||
| Product revenue | $ | 2,215 | $ | 4,012 | ||||
| Contribution revenue | 3,268 | 2,968 | ||||||
| Total revenue | 5,483 | 6,980 | ||||||
| Costs and expenses: | ||||||||
| Cost of product revenue | 3,768 | 5,362 | ||||||
| Research and development | 4,876 | 5,353 | ||||||
| Selling, general and administrative | 6,673 | 6,544 | ||||||
| Total costs and expenses | 15,317 | 17,259 | ||||||
| Loss from operations | (9,834 | ) | (10,279 | ) | ||||
| Other income (expense): | ||||||||
| Interest income | 2 | 94 | ||||||
| Interest expense | (1,528 | ) | (944 | ) | ||||
| Change in fair value of derivative instrument | 704 | (1,010 | ) | |||||
| Change in fair value of warrant liability | 147 | |||||||
| Other income | 100 | (5 | ) | |||||
| Other gains/losses | (4 | ) | ||||||
| Total other expense | (579 | ) | (1,865 | ) | ||||
| Net loss | $ | (10,413 | ) | $ | (12,144 | ) | ||
| Deemed dividend on Series A redeemable convertible preferred stock | ||||||||
| Net loss attributable to common stockholders | $ | (10,413 | ) | $ | (12,144 | ) | ||
| Net loss per share basic and diluted | $ | (1.41 | ) | $ | (3.65 | ) | ||
| Weighted-average number of common shares used in computing net loss per share basic and diluted | 7,405,889 | 3,323,451 | ||||||
| Other comprehensive loss: | ||||||||
| Net loss | $ | (10,413 | ) | $ | (12,144 | ) | ||
| Net unrealized (loss) gain on marketable securities arising during the period | (13 | ) | ||||||
| Less: net realized (gain) loss on marketable securities included in net loss | 5 | |||||||
| Total other comprehensive (loss) gain, net of taxes | (8 | ) | ||||||
| Comprehensive loss | $ | (10,413 | ) | $ | (12,152 | ) |