Trinity Biotech Announces Q3 2022 Financial Results

Trinity Biotech Announces Q3 2022 Financial Results




Trinity Biotech Announces Q3 2022 Financial Results

DUBLIN, Ireland, Dec. 15, 2022 (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 September 30, 2022.

Summary Highlights:

  • Total revenues for Q3 2022 were $19.5m. Excluding our Covid focused PCR Viral Transport Media (“VTM”) products, Q3 2022 revenues of $19.2m were marginally higher by 2% compared to Q3 2021 and were up 6% compared to Q2 2022.
  • A strong YoY 30% increase in revenues attributable to both our Haemoglobins and Fitzgerald Industries Life Sciences businesses offset the timing impact of atypically concentrated sales of UniGold HIV in Q3 2021. In addition, pricing changes and capacity optimisation actions in our Autoimmune product business led to a 30%+ increase compared to the same period in 2021.
  • Quarter over quarter revenue momentum was driven by Fitzgerald Industries at 25%, reflecting actions to optimize demand generation throughout the year, strong demand for UniGold HIV with an increase of over 35% and over 20% Autoimmune product growth
  • We are experiencing particularly strong demand for our Haemoglobins products in AsiaPac and Latin America, with well over 50% YoY revenue growth in AsiaPac and over 40% YoY revenue growth in Latin America. We continue to scale our commercial coverage in these markets where the increase in diabetes and propensity for haemoglobin variants is at some of its highest rates and our boronate affinity technology has a particular competitive advantage.
  • In late August 2022 the Company submitted its 510k submission to the FDA seeking US regulatory approval of its Premier Resolution Haemoglobin Variants instrument and expects to launch the product in the US in Q2 2023.
  • In November 2022, the Company initiated the development of its next generation flagship diabetes HbA1c instrument, the Premier 9210. Expected to launch in Q3 2023, it is planned to feature an improved, backward compatible reagent column system that will feature up to 3x the injection capacity and stability, limited calibration, improved user interface and lab system integration. In addition, this system should underpin the lower cost, mid throughput A1c instrument currently in development.
  • Since World Health Organisation approval in February 2022 of our TrinScreen HIV product, the Kenyan Ministry of Health task force recommended it as the first line screening test for Kenya’s new HIV testing algorithm. We expect to conclude the current pilot program in Kenya by year-end, deliver initial Ministry of Health orders in Q1 2023 and ramp up to approximately 6 million tests per year.
  • The Company is in partnership negotiations with a number of rapid test innovators to leverage its lateral flow biological development and manufacturing capabilities and provide access to its global distribution channels. In addition to capital efficient growth, this strategy provides early access to intellectual property associated with evolving user interface concepts.
  • Improved design for manufacturing, supply chain enhancements and insourcing actions are underway seeking to significantly optimise margins across the portfolio. In Q3, 2022 we focused on streamlining the portfolio with the elimination of loss-making legacy products and inventory. We continue to consolidate multi-product flexible production in our Jamestown facility with the transfer of immunofluorescence and urine tube manufacturing from Buffalo, NY and Burlington, Canada respectively.
  • The Company continues to focus on attracting and developing a world class leadership team with the recent appointments of a Chief Technology Officer, Head of Quality and Regulatory Affairs and Global Supply Chain Leader.
  • Trinity Biotech was recently featured at the 2022 Piper Sandler Healthcare Conference, where Aris Kekedjian, Chairman and Chief Executive Officer, outlined the Company’s strategic growth playbook. A copy of the presentation is available at www.trinitybiotech.com.

Third Quarter Results (Unaudited)

Total revenues for Q3, 2022 were $19.5m which compares to $22.0m in Q3, 2021, a decrease of 11.4% and which were broken down as follows:

  2021
Quarter 3
2022
Quarter 3
(Decrease)
  US$’000 US$’000 %
Clinical Laboratory 17,891 16,966 (5.2%)
Point-of-Care 4,113 2,536 (38.3%)
Total 22,004 19,502 (11.4%)

Clinical Laboratory revenues were $17.0m, compared to $17.9m in Q3, 2021, representing a decrease of $0.9m or 5.2%. This decrease is due to a reduction of approximately $2.9m in revenues from our PCR VTM products compared to Q3, 2021. Sales volumes for PCR VTM products have decreased since 2021 due to a significant scaling down of PCR testing programs for Covid-19.

Excluding VTM products, Clinical Laboratory revenues increased by almost $2.0m or 13.4% to $16.6m compared to $14.6m in Q3, 2021.

The underlying growth in Clinical Laboratory revenues was driven by strong performances from our haemoglobins and Fitzgerald Industries businesses. Haemoglobins revenues continue to grow, with a $1.4m or 30.3% increase in revenues this quarter compared to Q3, 2021. We expect revenues from this business to continue this growth trend driven by a higher instrument installed base and operational and strategic supply chain changes, which we expect will drive margin increase.

Fitzgerald Industries, which is the Group’s distributor of raw materials for the life sciences industry, recorded a revenue increase of $0.9m or 30.2% compared to Q3, 2021 and an increase of 24.6% compared to Q2, 2022.

Lastly, there was a reduction of $0.3m in Clinical Laboratory revenues for our legacy infectious disease range of products compared to Q3, 2021 as continuing COVID-19 lockdowns in Asia hampered demand for these products.

Point-of-Care revenues for Q3, 2022 decreased from $4.1m to $2.5m when compared to Q3, 2021, a decrease of 38.3%. Q3, 2021 marked the highest individual quarter for Point-of-Care revenues in the last three fiscal years and was driven by an unusually high volume of HIV tests sold in Africa. The $2.5m of Point-of-Care revenues recorded for Q3, 2022 represents an increase of 38% compared to Q2, 2022.

  Q3 2022
US$000
Revenues 19,502  
Cost of sales (including significant excess and obsolescence charges related to inventory of $4,697) 17,487  
Gross profit 2,015  
Gross margin % 10.3%  
   
Adjusted Gross profit (excluding significant excess and obsolescence charges related to inventory of $4,697) 6,712  
Adjusted Gross margin % 34.4%  
   

In Q3, 2022, gross profit was $2.0m, equating to a gross margin of 10.3%. This gross profit reflects significant excess inventory and obsolescence charges of $4.7m, consisting of the following:

  1. VTM inventory write down ($3.5m) – as previously disclosed, the situation relating to COVID-19 products was fluid and as such we chose to retain the capability to flex manufacturing volumes should market conditions warrant. As such, we maintained a significant inventory of critical raw materials to allow a ramping up of COVID focused VTM production to meet peak demand as it was important that we were able to fulfil high volume orders at short notice in order to retain existing customers and capture new customers at attractive price points. Unlike in prior years, during Q3 or to date in Q4 2022, we have not seen any evidence of current or future significant peaks in demand. This has led management to revisit our strategy of maintaining significant levels of raw materials inventory to meet demand peaks. We now intend to expedite the sale of the vast majority of this inventory, which given current market conditions, is expected to be at lower prices. Consequently, the value of inventory has been written down to our estimate of its net realisable value.
  2. Other inventory write down ($0.9m) – we have written down the value of certain excess raw materials and work in progress following a review and an update to our relevant quality assurance policy.
  3. Tri-stat inventory write down ($0.3m) – we undertook a strategic review of our Tri-stat instrument line as part of a broader review of our haemoglobins product portfolio. With annual sales of approximately $0.2m, Tri-stat is the least significant product in the portfolio. To rationalise and to simplify the haemoglobins product portfolio and to allow us to focus our resources on the higher growth products within that portfolio, management has decided to limit sales of Tri-stat to certain targeted partnerships. Consequently, management has written down the value of this inventory to reflect the consequent revised outlook.

Excluding the impact of the Q3, 2022 significant inventory excess and obsolescence charges of $4.7m, gross profit for Q3, 2022 decreased from $8.9m to $6.7m when compared to Q3, 2021. The adjusted gross margin of 34.4% for Q3, 2022 is 6.0% lower than the margin achieved in Q3, 2021, with the reduction largely due to sales mix changes, particularly the reduction in higher margin PCR VTM, inflationary increases in the price of raw materials and an under recovery of labour and overhead costs at three of our manufacturing facilities due to reduced production activity, partially driven by limited VTM production. To mitigate the impact of rising input costs, management has implemented sales price increases where appropriate. As part of our ongoing focus on simplification and efficiency and to address the under recovery of labour and overhead costs, management has reduced production headcount at two of our facilities since the end of Q3, 2022. Management is expanding the range of activities at its Jamestown, NY plant to include autoimmune product manufacturing and other activities to increase its output.

Other operating income was lower by $1.0m compared to Q3, 2021. The $1.0m other operating income in Q3, 2021 related to loan funding received under the U.S. government’s Paycheck Protection Program (“PPP”). A PPP loan of $1.0m received by the Company in 2021 was forgiven during Q3, 2021 and was recognised as income in that quarter. No PPP income was recognised in 2022 as all PPP loans were forgiven in previous years.

Research and development expenses declined slightly from $1.1m to $1.0m when compared to Q3, 2021 mainly due to lower headcount. Selling, general and administrative (SG&A) expenses were $5.8m in Q3, 2022, a reduction of $0.3m compared to Q3, 2021 partially due to a continued focus on cost control measures. With the lifting of COVID related travel restrictions we have tasked our sales and marketing teams to increase travel to customers and trade shows as we continue to revitalise our sales activities. This has led to an increase in travel and marketing costs in Q3, 2022, however management believes this is a worthwhile and important investment. The strengthening of the US Dollar against the Euro this year has aided cost reductions in our Euro-denominated SG&A expenses.

Impairment charges for Q3, 2022 were $2.3m, compared to zero in Q3, 2021. Under IFRS accounting standards, companies are required to assess at the end of each reporting period whether there is any indication that an asset may be impaired. If any such indication exists, the entity is required to estimate the recoverable amount of the asset. For the period ended September 30, 2022, we determined that two internally developed products, the autoimmune smart reader and the Tri-stat instrument, which had a combined carrying value of $2.3m within intangible assets, had a recoverable amount of zero.

The development project for the autoimmune smart reader was paused earlier in 2022 as management reviewed other options, including the potential to proceed with a third-party reader instead of our own internally developed reader. Following this review, we determined that there were likely greater opportunities to capture more market share in a more capital efficient manner through partnering with a third-party reader manufacturer rather than pursuing an independent strategy. At this point in time there is significant uncertainty if we will complete the project to develop our own in-house autoimmune smart reader and thus while we may re-visit this decision in the future, in the interests of prudence we have impaired the project’s carrying value. As described above, we undertook a strategic review of our Tri-stat instrument as part of a broader review of our haemoglobins product portfolio. In order to rationalise the haemoglobins product portfolio and to allow us to focus our resources on the higher growth products within that portfolio, management decided that Tri-stat sales would be restricted to only certain targeted partnerships, and this has led to an impairment in the carrying value of the Tri-stat intangible asset.

Operating loss for the quarter was $7.1m, which represents a decrease in profitability of $9.9m compared to Q3, 2021 and was attributable to a lower gross profit (including the impact of the Q3, 2022 significant excess and obsolescence charges related to inventory), lower other operating income and higher impairment charges recorded this quarter. These effects were partly offset by lower R&D and SG&A expenses.

Financial income for Q3, 2022 was $0.3m compared to $0.2m for Q3, 2021. In Q3, 2022, financial income mainly related to a fair value adjustment for the derivative liability related to warrants granted to the Group’s principal lender. The financial income in Q3, 2021 was due to a fair value adjustment for the embedded derivatives in the exchangeable notes. There is no equivalent adjustment in Q3, 2022 because 99.7% of the exchangeable notes were retired in January 2022.

Financial expenses in Q3, 2022 were $2.2m compared to $1.4m in Q3, 2021, an increase of $0.8m. The interest expense relating to the senior secured term loan and the 7-year convertible note were $1.8m and $0.3m respectively in Q3, 2022. These amounts consist of both cash interest and non-cash accretion interest. As both of these borrowings are new in 2022, there was no interest expense recorded in the comparative period’s results in respect of these facilities. In Q3, 2021 the cash and non-cash interest expense for the exchangeable notes was $1.2m, which was reduced to almost zero in Q3, 2022 due to the debt re-financing earlier this year. The remainder of the financial expense in Q3, 2022 and Q3, 2021 consists of notional interest on lease liabilities for right-of-use assets, which has remained broadly stable at between $0.1m and $0.2m.

The loss after tax for continuing operations for the quarter was $8.9m in comparison to a profit of $1.3m for the equivalent period last year. This decrease in profitability is primarily due to lower gross profit, lower other operating income, higher impairment charges and higher financial expenses this quarter.

Earnings before interest, tax, depreciation, amortisation, share option expense, impairment charges and significant excess and obsolescence charges related to inventory for Q3, 2022 (Adjusted EBITDASO) was $0.8m. This is made up as follows:

  $m
Operating loss (7.1)
Depreciation 0.5
Amortisation 0.3
Impairment charges 2.3
Significant excess and obsolescence charges related to inventory 4.7
   
Adjusted EBITDA 0.7
Share option expense 0.1
   
Adjusted EBITDASO 0.8

The basic loss per ADS for Q3, 2022 was 23.5 cents compared to a basic profit per ADS of 6.3 cents in Q3, 2021. The diluted loss per ADS for Q3, 2022 was 23.5 cents compared to a diluted profit per ADS of 6.1 cents in Q3, 2021.

Use of Non-IFRS Financial Measures
The Company reports financial results in accordance with IFRS. To supplement the consolidated financial statements presented in accordance with IFRS, the Company presents the non-IFRS presentation of Adjusted Gross Profit, Adjusted Gross Margin, Adjusted EBITDA, Adjusted EBITDASO. The Company uses these non-IFRS measures to evaluate and manage the Company’s operations internally. The Company is also providing this information to assist investors in performing additional financial analysis. Reconciliation between the Company’s results on an IFRS and non-IFRS basis is provided in a table above.

Liquidity
The Group’s cash balance decreased from $10.5m at the end of Q2, 2022 to $7.3m at the end of Q3, 2022, a decrease of $3.2m. Cash generated from operations for Q3, 2022 was $0.7m, an increase of $0.1m compared to Q3, 2021. During Q3, 2022 the Company had capital expenditure cash outflows of $1.3m (Q3, 2021: $2.0m) and payments for property leases of $0.7m (Q3, 2021: $0.7m). Interest payments in the quarter were $1.7m (Q3, 2021: $0.0m).

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$000’s except share data) Three Months Ended
September 30, 2022
US$000

(unaudited)
  Three Months Ended
September 30, 2021
US$000

(unaudited)
  Nine Months Ended
September 30, 2022
US$000

(unaudited)
  Nine Months Ended
September 30, 2021
US$000

(unaudited)
 
         
Revenues 19,502   22,004   56,742   73,441  
Cost of sales (including Q3, 2022 significant excess and obsolescence charges related to inventory of $4,697; 2021: $Nil) (17,487 ) (13,104 ) (40,930 ) (42,601 )
Gross profit 2,015   8,900   15,812   30,840  
Gross margin % 10.3 % 40.4 % 27.9 % 42.0 %
         
         
Other operating income 1   1,043   2   3,950  
Research & development expenses (1,023 ) (1,063 ) (2,972 ) (3,556 )
Selling, general and administrative expenses (5,791 ) (6,112 ) (18,979 ) (19,102 )
Impairment charges (2,288 ) 0   (2,808 ) (6,068 )
         
Operating (Loss)/Profit (7,086 ) 2,768   (8,945 ) 6,064  
         
Financial income 329   194   329   1,213  
Financial expenses (2,184 ) (1,361 ) (22,488 ) (4,097 )
Net financial expense (1,855 ) (1,167 ) (22,159 ) (2,884 )
         
(Loss)/Profit before tax (8,941 ) 1,601   (31,104 ) 3,180  
         
Income tax (expense)/credit (3 ) (251 ) 177   (1,011 )
(Loss)/Profit for the period on continuing operations (8,944 ) 1,350   (30,927 ) 2,169  
         
Loss for the period on discontinued operations (1 ) (29 ) (3 ) (29 )
(Loss)/Profit for the period (all attributable to owners of the parent) (8,945 ) 1,321   (30,930 ) 2,140  
         
(Loss)/ Earnings per ADS (US cents) (23.5 ) 6.3   (95.9 ) 10.2  
         
Diluted (loss)/ Earnings per ADS (US cents) (23.5 ) 6.1   (95.9 ) 9.6  
         
Weighted average no. of ADSs used in computing basic earnings per ADS 38,107,571   20,901,703   32,261,235   20,901,703  
         
Weighted average no. of ADSs used in computing diluted earnings per ADS 38,107,571   21,831,978   32,261,235   22,262,325  

Trinity Biotech plc
Consolidated Balance Sheets

  September 30,
2022
US$ ‘000
(unaudited)
  June 30,
2022
US$ ‘000
(unaudited)
  March 31,
2022
US$ ‘000
(unaudited)
  December 31,
2021
US$ ‘000

 
ASSETS        
Non-current assets        
Property, plant and equipment 6,082   6,261   5,634   5,918  
Goodwill and intangible assets 37,144   38,743   37,320   35,981  
Deferred tax assets 4,533   4,553   4,478   4,101  
Derivative financial asset 147   140   219    
Other assets 155   207   175   207  
Total non-current assets 48,061   49,904   47,826   46,207  
         
Current assets        
Inventories 23,553   29,109   29,627   29,123  
Trade and other receivables 17,265   15,913   16,898   16,116  
Income tax receivable 1,762   1,762   1,734   1,539  
Cash, cash equivalents and deposits 7,254   10,453   10,012   25,910  
Total current assets 49,834   57,237   58,271   72,688  
         
TOTAL ASSETS 97,895   107,141   106,097   118,895  
         
EQUITY AND LIABILITIES        
Equity attributable to the equity holders of the parent        
Share capital 1,963   1,963   1,445   1,213  
Share premium 53,297   53,297   21,874   16,187  
Treasury shares (24,922 ) (24,922 ) (24,922 ) (24,922 )
Accumulated (deficit)/surplus (17,929 ) (9,103 ) 481   12,559  
Translation reserve (5,799 ) (5,439 ) (5,186 ) (5,379 )
Other reserves 23   23   23   23  
Total equity/(deficit) 6,633   15,819   (6,285 ) (319 )
         
Current liabilities        
Trade and other payables 14,447   13,600   15,637   17,107  
Income tax payable 21   21   40   22  
Exchangeable note payable 210   210   210   83,312  
Provisions 50   50   50   50  
Total current liabilities 14,728   13,881   15,937   100,491  
         
Non-current liabilities        
Senior secured term loan 44,143   43,990   76,246    
Derivative financial liability 1,681   2,002   1,671    
Convertible note 13,557   13,372      
Other payables 11,818   12,723   13,279   13,865  
Deferred tax liabilities 5,335   5,354   5,249   4,858  
Total non-current liabilities 76,534   77,441   96,445   18,723  
         
TOTAL LIABILITIES 91,262   91,322   112,382   119,214  
         
TOTAL EQUITY AND LIABILITIES 97,895   107,141   106,097   118,895  

Trinity Biotech plc
Consolidated Statement of Cash Flows

  Three Months Ended
September 30, 2022
US$000
(unaudited)
    Three Months Ended
September 30, 2021
US$000
(unaudited)
    Nine Months Ended
September 30, 2022
US$000
(unaudited)
    Nine Months Ended
September 30, 2021
US$000
(unaudited)
 
Cash flows from operating activities                      
(Loss)/profit for the period (8,945 )   1,321     (30,930 )   2,140  
Adjustments to reconcile net profit/(loss) to cash provided by operating activities:                      
Depreciation 478     545     957     1,681  
Amortisation 266     231     708     689  
Income tax expense/(credit) 3     251     (177 )   1,011  
Financial income (329 )   (194 )   (329 )   (1,213 )
Financial expense 2,184     1,361     22,488     4,097  
Share-based payments 119     253     438     946  
Foreign exchange gains on operating cash flows 164     101     15     34  
Impairment charges 2,288         2,808     6,068  
Excess and obsolescence charges related to inventory 4,697         4,697      
Other non-cash items (399 )   (1,487 )   (96 )   (4,631 )
                       
Operating cash flows before changes in working capital 526     2,382     579     10,822  
Net movement on working capital 153     (1,777 )   (3,328 )   (3,103 )
                       
Cash generated/(used) from operations 679     605             (2,749 )   7,719  
Interest paid (1 )   (13 )   (4 )   (38 )
Interest received 0     1     2     3  
Income taxes (paid)/received (2 )   1,104     (1 )   1,224  
                       
Net cash generated/(used) by operating activities 676     1,697             (2,752 )   8,908  
                       
Cash flows from investing activities                      
Payments to acquire intangible assets (1,003 )   (1,686 )   (4,214 )   (4,974 )
Acquisition of property, plant and equipment (321 )   (273 )   (626 )   (1,242 )
                       
Net cash used in investing activities (1,324 )   (1,959 )   (4,840 )   (6,216 )
                       
Cash flows from financing activities                      
Issue of ordinary share capital including share premium (net of issuance costs)         25,019      
Net proceeds from new senior secured term loan         80,014      
Proceeds for convertible note issued         20,000      
Expenses paid in connection with debt financing         (2,356 )    
Repayment of senior secured term loan         (34,500 )    
Penalty for early settlement of term loan         (3,450 )    
Purchase of exchangeable notes         (86,730 )    
Interest paid on senior secured term loan (1,609 )       (5,315 )    
Interest paid on convertible note (75 )       (124 )    
Proceeds from Paycheck Protection loans             1,764  
Interest payment on exchangeable notes (4 )       (1,293 )   (1,998 )
Payment of lease liabilities (684 )   (726 )   (2,184 )   (2,198 )
                       
Net cash generated/(used) in financing activities (2,372 )   (726 )   (10,919 )   (2,432 )
                       
(Decrease)/increase in cash and cash equivalents and short-term investments (3,020 )   (988 )   (18,511 )   260  
Effects of exchange rate movements on cash held (179 )   (154 )   (145 )   (112 )
Cash and cash equivalents and short-term investments at beginning of period 10,453     28,617     25,910     27,327  
                       
Cash and cash equivalents and short-term investments at end of period 7,254     27,475     7,254     27,475  


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
E-mail: investorrelations@trinitybiotech.com