Trinity Biotech Announces Q1 2023 Financial Results
- Trinity Biotech reported a 2.0% increase in revenue for Q1 2023 compared to Q1 2022.
- The company experienced growth in Autoimmune, Clinical Chemistry, and diabetes HbA1c consumable products.
- Trinity Biotech's Premier 9210 diabetes HbA1c instrument is on track for a 2024 rollout with improved features and expanded operating margins.
- The company is focused on expanding its market access in China and Brazil.
- Significant orders for Trinity Biotech's TrinScreen HIV test are expected in Kenya.
- The sale of Fitzgerald Industries generated $30 million in proceeds and reduced debt.
- Trinity Biotech will participate in the AACC annual scientific meeting and clinical lab expo in July.
- None.
DUBLIN, Ireland, July 06, 2023 (GLOBE NEWSWIRE) -- Trinity Biotech plc (Nasdaq: TRIB), a leading developer and manufacturer of diagnostic products for the point-of-care and clinical laboratory markets, today announced the Company’s results for the quarter ended March 31, 2023.
Summary Highlights:
Revenue/Margin:
- Total revenue for fiscal Q1, 2023 was
$17.2m . Excluding our Covid focused PCR Viral Transport Media (“VTM”) products and Fitzgerald Industries (which was disposed in April 2023), revenue for the quarter of$14m was2.0% higher than in Q1, 2022. - Our performance in the quarter was led by year over year growth of approximately
35% ,15% and10% respectively for our Autoimmune, Clinical Chemistry and diabetes HbA1c consumable products. Strong demand from key accounts and a focus on clearing order backlogs drove an increase of over80% in revenues for US Autoimmune products compared to Q1, 2022 and an approximately45% increase in deliveries for diabetes consumables in Brazil compared to Q1, 2022. Partly offsetting these revenue gains are lower revenues from low margin diabetes instrument deliveries, compared to Q1 2022. Diabetes instrument placements were up approximately17% in Q1, 2023 vs Q4, 2022. - Gross margin, excluding Fitzgerald Industries, was broadly flat compared to Q1, 2022 but reflected an approximately 4-point improvement over Q4 2022 as we increase prices and stabilize our manufacturing and supply chain processes.
Haemoglobins:
- We continue to work closely with the FDA to gain clearance of our 510(k) submission for the Premier Resolution Haemoglobin Variants instrument. In addition to a US market introduction in the second half of the year, we expect FDA approval will drive significant global order activity.
- The development of the next generation of our flagship diabetes HbA1c instrument, the Premier 9210, is on track for an expected roll-out in 2024. The instrument is expected to feature an improved, backward compatible reagent column system that should feature up to 3 times the injection capacity and stability, limited calibration, improved user interface and lab system integration. This is the first step of a multi-generational product development plan aimed at expanding the target market, driving lower service downtime and cost, while significantly expanding operating margins.
- China and Brazil are markets of particular focus for both product lines as we assess increasing our footprint in both markets to drive cost competitiveness, streamline regulatory pathways and expand market access.
TrinScreen HIV:
- The Company is focused on executing on the launch and distribution of its TrinScreen HIV screening test, following the announcement by the Kenyan Ministry of Health of the adoption of the new HIV rapid testing algorithm. This algorithm establishes Trinity Biotech’s TrinScreen HIV as the standard screening test in Kenya under World Health Organisation (“WHO”) guidelines.
- The Kenyan government is currently addressing legal challenges to the HIV testing algorithm changes and we expect to receive significant orders in the second half of 2023 upon resolution of these legal matters.
- The Kenyan HIV screening program is one of the largest in Africa, with an estimated 7 million to 9 million screening tests annually.
Portfolio Transformation & Capital Structure:
- In April, the Company completed the sale of its Fitzgerald Industries division, generating approximately
$30M of proceeds that were partially used to further reduce debt by approximately$10M . - This exit is the first of several strategic moves aimed at focusing the current portfolio around our core Haemoglobins and HIV franchises, streamlining our cost structure, reducing debt and providing firepower for M&A.
- Our pipeline of attractive M&A opportunities is aimed at disruptive adjacencies with Total Addressable Markets (TAMs) that matter, provide access to next generation diagnostic product platforms and where we can leverage our global manufacturing and distribution footprint.
- In February, the Company secured a
$20 million flexible term-facility specifically to provide the ability to move quickly when opportunistic transactions arise.
Structural & Operational Initiatives:
- Multiple initiatives are underway to significantly reduce cost of goods sold in our core Haemoglobins and HIV franchises. Instrument and consumables design updates, supply chain optimization and outsourced/localized manufacturing are initiatives all aimed at driving significantly higher operating margins for these platforms.
AACC:
- Trinity Biotech will participate in the American Association of Clinical Chemistry (AACC) annual scientific meeting and clinical lab expo which takes place in Anaheim, CA from July 23 -27.
First Quarter Results (Unaudited)
The results of the Fitzgerald Industries life sciences supply business, which was disposed of on April 27, 2023, have been reported separately as discontinued operations in the Consolidated Income Statements for all periods presented, and the assets and liabilities attributable to Fitzgerald Industries are separately presented within “Assets included in disposal group held for sale” and “Liabilities included in disposal group held for sale”, respectively, in the Consolidated Balance Sheet at March 31, 2023.
Total revenues for Q1, 2023 were
2023 Quarter 1 | 2022 Quarter 1 | Increase/ (decrease) | |
US$’000 | US$’000 | % | |
Clinical Laboratory | 12,669 | 13,511 | ( |
Point-of-Care | 2,160 | 2,164 | ( |
Total | 14,829 | 15,675 | (5.4%) |
Clinical Laboratory revenues were
Partly offsetting the reduction in revenues from our PCR VTM products were solid performances across our autoimmune and clinical chemistry products, which showed over
Point-of-Care revenues for Q1, 2023 were
In Q1, 2023, gross profit was
Research and development expenses declined slightly from
Selling, general and administrative (SG&A) expenses were
- A higher IFRS driven non-cash share-based payments accounting charge, which increased by
$1.2m in Q1, 2023 compared to Q1, 2022, due to options granted since Q1, 2022. - An increase in foreign exchange loss largely related to the accounting driven requirement to mark-to-market Euro-denominated lease liabilities for right-of-use assets. In Q1, 2022, the foreign exchange gain on leases was
$0.1m while in Q1, 2023, a foreign exchange loss of$0.2m was recorded, resulting in an unfavourable quarter-on-quarter variance of$0.3m .
Excluding the impact of the accounting-driven share-based payments expense and the foreign exchange loss on lease liabilities, the remaining increase in SG&A expenses included the following:
- Higher salary costs as a result of senior hires made in late 2022 as part of our continued development of a world class leadership team that can lead the transformation of Trinity Biotech into a high growth, efficient and agile organisation.
- A continued increase in travel costs post COVID-related travel restrictions, as our sales and marketing teams travel to customers and trade shows as we continue to revitalise our sales activities. Similarly, some key functional leaders based in Ireland have resumed visits to our overseas facilities as we seek to drive operational efficiencies. All of this has led to an increase in travel costs in Q1, 2023, compared to Q1, 2022, of approximately
$0.2m . Management believes this is a worthwhile and important investment, but we do not expect the level of travel to stay at this level going forward. - Savings on non-recurring transactional costs incurred in Q1, 2022 of
$0.5m were offset by higher legal and professional fees for due diligence, corporate development and corporate finance activities as we continue to assess strategic opportunities for inorganic growth and balance sheet optimisation.
The SG&A expenses of
Operating loss for the quarter was
Financial income for Q1, 2023 was
Financial expenses in Q1, 2023 were
Q1, 2023 US$’m | Q1, 2022 US$’m | |
Loss on disposal of Exchangeable Notes | – | 9.7 |
Term loan interest | 2.1 | 2.0 |
Convertible note interest | 0.3 | – |
Exchangeable note interest | – | 0.4 |
Notional interest on lease liabilities for Right-of-use assets | 0.2 | 0.2 |
Other | – | – |
2.6 | 12.2 |
Note: table contains rounded numbers.
The comparative period included a loss on disposal of the Exchangeable Notes of
Excluding this non-recurring financial expenses, financial expenses for Q1, 2022, were
The 7 year convertible note had not been drawn down at March 31, 2022 and as such there was no interest expense recorded in the comparative period’s result on that facility.
The loss after tax for continuing operations for the quarter was
Loss before interest, tax, depreciation, amortisation, share option expense, and impairment charges for continuing operations for Q1, 2023 (Adjusted EBITDASO) was
$m | |
Operating loss | (3.9) |
Depreciation | 0.3 |
Amortisation | 0.3 |
Adjusted EBITDA for continuing operations | (3.3) |
Share option expense | 1.4 |
Adjusted EBITDASO for continuing operations | (2.0) |
Note: table contains rounded numbers.
The basic loss per ADS for Q1, 2023 was
Use of Non-IFRS Financial Measures
The attached summary unaudited financial statements were prepared in accordance with International Financial Reporting Standards (IFRS). To supplement the consolidated financial statements presented in accordance with IFRS, the Company presents non-IFRS presentations of, Adjusted EBITDA and Adjusted EBITDASO. The adjustments to the Company's IFRS results are made with the intent of providing both management and investors a more complete understanding of the Company's underlying operational results, trends, and performance. Non-IFRS financial measures mainly exclude, if and when applicable, the effect of share-based payments, significant excess and obsolescence charges related to inventory, depreciation, amortization and impairment charges.
Adjusted EBITDA for continuing operations and Adjusted EBITDASO for continuing operations are presented to evaluate the Company's financial and operating results on a consistent basis from period to period. The Company also believes that these measures, when viewed in combination with the Company's financial results prepared in accordance with IFRS, provides useful information to investors to evaluate ongoing operating results and trends. Adjusted EBITDA for continuing operations and Adjusted EBITDASO for continuing operations, however, should not be considered as an alternative to operating income or net income for the period and may not be indicative of the historic operating results of the Company; nor is it meant to be predictive of potential future results. Adjusted EBITDA for continuing operations and Adjusted EBITDASO for continuing operations are not measures of financial performance under IFRS and may not be comparable to other similarly titled measures for other companies. Reconciliation between the Company's operating profit/(loss) and Adjusted EBITDA for continuing operations and Adjusted EBITDASO for continuing operations are presented.
Liquidity
The Group’s cash balance decreased from
Forward-Looking Statements
Certain statements made in this release that are not historical are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. The words “estimate”, “project”, “intend”, “expect”, “believe” and similar expressions are intended to identify forward-looking statements. These forward-looking statements involve known and unknown risks and uncertainties. Many factors could cause the actual results, performance or achievements of Trinity Biotech to be materially different from any future results, performance or achievements that may be expressed or implied by such forward-looking statements, including, but not limited to, the results of research and development efforts, risks associated with the outbreak and global spread of the coronavirus (COVID-19), the effect of regulation by the U.S. Food and Drug Administration and other agencies, the impact of competitive products, product development commercialization and technological difficulties. For additional information regarding these and other risks and uncertainties associated with Trinity Biotech’s business, reference is made to our reports filed from time to time with the U.S. Securities and Exchange Commission. We undertake no obligation to update or revise any forward-looking statements for any reason.
About Trinity Biotech
Trinity Biotech develops, acquires, manufactures and markets diagnostic systems, including both reagents and instrumentation, for the point-of-care and clinical laboratory segments of the diagnostic market. The products are used to detect infectious diseases and to quantify the level of Haemoglobin A1c and other chemistry parameters in serum, plasma and whole blood. Trinity Biotech sells direct in the United States, Germany, France and the U.K. and through a network of international distributors and strategic partners in over 75 countries worldwide. For further information, please see the Company's website: www.trinitybiotech.com
Trinity Biotech plc
Consolidated Income Statements
(US | Three Months Ended March 31, 2023 US (unaudited) | Three Months Ended March 31, 2022 US (unaudited) | ||
Revenues | 14,829 | 15,675 | ||
Cost of sales | (9,256 | ) | (9,693 | ) |
Gross profit | 5,573 | 5,982 | ||
Gross margin % | 37.6 | % | 38.2 | % |
Other operating income | – | 1 | ||
Research & development expenses | (860 | ) | (965 | ) |
Selling, general and administrative expenses | (8,632 | ) | (6,234 | ) |
Operating Loss | (3,919 | ) | (1,216 | ) |
Financial income | 154 | 218 | ||
Financial expenses | (2,551 | ) | (12,222 | ) |
Net financial expense | (2,397 | ) | (12,004 | ) |
Loss before tax | (6,316 | ) | (13,220 | ) |
Income tax credit | 11 | 150 | ||
Loss for the period on continuing operations | (6,305 | ) | (13,070 | ) |
Profit for the period on discontinued operations | 496 | 791 | ||
Loss for the period (all attributable to owners of the parent) | (5,809 | ) | (12,279 | ) |
Loss per ADS (US cents) | (15.2 | ) | (50.0 | ) |
Diluted loss per ADS (US cents) | (15.2 | ) | (50.0 | ) |
Weighted average no. of ADSs used in computing basic earnings per ADS | 38,158,460 | 24,575,333 | ||
Weighted average no. of ADSs used in computing diluted earnings per ADS | 38,158,460 | 24,575,333 |
Trinity Biotech plc
Consolidated Balance Sheets
March 31, 2023 US$ ‘000 (unaudited) | December 31, 2022 US$ ‘000 | |||
ASSETS | ||||
Non-current assets | ||||
Property, plant and equipment | 5,496 | 5,682 | ||
Goodwill and intangible assets | 21,330 | 35,269 | ||
Financial asset1 | 1,500 | – | ||
Deferred tax assets | 4,297 | 4,218 | ||
Derivative financial asset | 152 | 128 | ||
Other assets | 120 | 139 | ||
Total non-current assets | 32,895 | 45,436 | ||
Current assets | ||||
Assets included in disposal group held for sale | 17,746 | – | ||
Inventories | 21,532 | 22,503 | ||
Trade and other receivables | 13,594 | 15,753 | ||
Income tax receivable | 1,858 | 1,834 | ||
Cash, cash equivalents and deposits | 3,532 | 6,578 | ||
Total current assets | 58,262 | 46,668 | ||
TOTAL ASSETS | 91,157 | 92,104 | ||
EQUITY AND LIABILITIES | ||||
Equity attributable to the equity holders of the parent | ||||
Share capital | 1,967 | 1,963 | ||
Share premium | 46,532 | 46,458 | ||
Treasury shares | (24,922 | ) | (24,922 | ) |
Accumulated deficit | (31,140 | ) | (26,695 | ) |
Translation reserve | (5,787 | ) | (5,775 | ) |
Equity component of convertible note | 6,709 | 6,709 | ||
Other reserves | 23 | 86 | ||
Total deficit | (6,618 | ) | (2,176 | ) |
Current liabilities | ||||
Liabilities included in disposal group held for sale | 1,386 | – | ||
Income tax payable | 33 | 28 | ||
Trade and other payables | 12,910 | 15,375 | ||
Exchangeable senior note payable | 210 | 210 | ||
Provisions | 50 | 50 | ||
Lease liabilities | 1,561 | 1,676 | ||
Total current liabilities | 16,150 | 17,339 | ||
Non-current liabilities | ||||
Senior secured term loan | 49,199 | 44,301 | ||
Derivative financial liability | 1,517 | 1,569 | ||
Convertible note | 13,936 | 13,746 | ||
Lease liabilities | 12,026 | 12,267 | ||
Deferred tax liabilities | 4,947 | 5,058 | ||
Total non-current liabilities | 81,625 | 76,941 | ||
TOTAL LIABILITIES | 97,775 | 94,280 | ||
TOTAL EQUITY AND LIABILITIES | 91,157 | 92,104 |
1 The Group’s investment commitment of
Trinity Biotech plc
Consolidated Statement of Cash Flows
Three Months Ended March 31, 2023 US (unaudited) | Three Months Ended March 31, 2022 US (unaudited) | |||
Cash flows from operating activities | ||||
Loss for the period | (5,809 | ) | (12,279 | ) |
Adjustments to reconcile loss to cash used in operating activities: | ||||
Depreciation | 351 | 432 | ||
Amortisation | 251 | 228 | ||
Income tax credit | (11 | ) | (150 | ) |
Financial income | (154 | ) | (218 | ) |
Financial expense | 2,551 | 12,222 | ||
Share-based payments | 1,364 | 197 | ||
Foreign exchange (gains)/losses on operating cash flows | (89 | ) | 42 | |
Other non-cash items | 195 | (691 | ) | |
Operating cash outflows before changes in working capital | (1,351 | ) | (217 | ) |
Net movement on working capital | (1,364 | ) | (1,263 | ) |
Cash used in operations before income taxes | (2,715 | ) | (1,480 | ) |
Income taxes paid | (3 | ) | (13 | ) |
Net cash used in operating activities | (2,718 | ) | (1,493 | ) |
Cash flows from investing activities | ||||
Payments to acquire intangible assets | (355 | ) | (1,553 | ) |
Payments to acquire financial assets | (700 | ) | – | |
Acquisition of property, plant and equipment | (274 | ) | (162 | ) |
Net cash used in investing activities | (1,329 | ) | (1,715 | ) |
Cash flows from financing activities | ||||
Net proceeds from new senior secured term loan | 4,853 | 80,015 | ||
Expenses paid in connection with debt financing | - | (2,316 | ) | |
Purchase of exchangeable notes | - | (86,730 | ) | |
Interest paid on senior secured term loan | (2,567 | ) | (1,786 | ) |
Interest paid on convertible note | (75 | ) | - | |
Interest payment on exchangeable notes | (4 | ) | (1,285 | ) |
Payment of lease liabilities | (599 | ) | (770 | ) |
Net cash provided by/(used in) financing activities | 1,608 | (12,872 | ) | |
Decrease in cash and cash equivalents | (2,439 | ) | (16,080 | ) |
Effects of exchange rate movements on cash held | 14 | 182 | ||
Cash and cash equivalents at beginning of period | 6,578 | 25,910 | ||
Cash and cash equivalents at end of period | 4,153 | 10,012 | ||
The above financial statements have been prepared in accordance with the principles of International Financial Reporting Standards and the Company’s accounting policies but do not constitute an interim financial report as defined in IAS 34 (Interim Financial Reporting).
Contact:
Trinity Biotech plc
John Gillard
(353)-1-2769800
Lytham Partners, LLC
Joe Diaz
(1)-602-889-9700
investorrelations@trinitybiotech.com
FAQ
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