Trinity Biotech Announces Quarter 1 Financial Results

EPS of 19.4 Cents Per ADR - An Increase of 11%


DUBLIN, April 19, 2012 (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 results for the quarter ended March 31, 2012.

Quarter 1 Results

Total revenues for Q1, 2012 were $20.0m which compares to $18.7m in Q1, 2011, an increase of 7.4%.

Point-Of-Care revenues for Q1, 2012 increased by 13.3% when compared to Q1, 2011. This increase was mainly attributable to increased HIV sales in Africa.

Clinical Laboratory revenues increased from $14.1m to $14.9m, which represents an increase of 5.5% compared to Q1, 2011. This included increased revenues from sales of the new Premier instrument, including the first placements in the USA.

Revenues for Q1, 2012 by key product area were as follows:

 
  2011
Quarter 1
2012
Quarter 1
 
Increase
  US$'000 US$'000 %
Point-of-Care 4,521 5,121 13.3%
Clinical Laboratory 14,133 14,905 5.5%
Total 18,654 20,026 7.4%

Gross profit for Q1, 2012 amounted to $10.3m, representing a gross margin of 51.6% which represents an improvement from the 51.2% for the same period in 2011. This improvement was due to increased Point-Of-Care sales, which traditionally have higher gross margins. However, this was partially offset by lower margins on increased sales of Premier instruments.

Research and Development expenses increased from $0.7m to $0.8m, representing an increase of 23%. Meanwhile Selling, General and Administrative (SG&A) expenses increased from $5.0m to $5.2m compared to Q1, 2011. This was mainly due to professional fees related to the acquisition of Fiomi Diagnostics AB during the quarter.

Operating Profit increased from $3.7m to over $4.1m for Q1, 2012 which was an increase of 11.7%.  In the same period, operating margin increased from 19.8% to 20.6%.

Net financial income decreased slightly from $0.6m in Q1, 2011 to $0.5m this quarter.

Profit After Tax increased by almost 10% to $4.1m from $3.8m in the comparative period last year. Meanwhile, EPS for Q1, 2012 increased by 11% from 17.5 cents to 19.4 cents. The tax charge for Q1, 2012 was in line with the comparative period and represented an effective tax rate of 12.1%.

Free Cash Flows for the quarter were $1.4m and were impacted by the timing of revenue receipts and the anticipated increased working capital associated with moving to full production of the Premier instrument. Other significant cash movements in the quarter included cash payments of $5.6m related to the acquisition of Fiomi Diagnostics and share repurchases of $1m. The total cash balance at the end of the quarter was $65.5m and this will be increased by a further $11.25m following the receipt of the final deferred consideration payment from the Stago Group on April 30, 2012.

Recent Developments

  • The Company continued to sell its new Premier instrument, with sales during the quarter in Europe, Turkey, South America as well as the first placements in the USA. Overall, the launch of Premier is now gathering significant momentum. Having shipped 12 instruments in Q4, 2011, this increased to 31 instruments this quarter. With the increasing pace of sales in Europe and the USA, the number of instruments sold in Q2 can be expected to increase substantially. Further increases will be achieved when Chinese registration is obtained in Q4, 2012.     
  • The Company announced it had obtained CE Marking and filed for FDA approval for its new point-of-care Uni-Gold™ Giardia test. This is the first of a range of new point-of-care tests to be developed at the Company's San Diego facility and will be followed by tests for C Difficile, Cryptosporidium, Syphilis, Strep pneumonia and Herpes by the end of 2012.
  • The Company continued its share buyback program during the quarter, repurchasing 97,000 ADRs at a cost of $1m.
  • During the quarter, Trinity completed the acquisition of Fiomi Diagnostics AB for $13.1m. This consisted of an upfront cash payment of $5.6m, 408,000 ADRs in Trinity Biotech and contingent consideration of $3.4m. Fiomi is at an advanced stage of developing a point-of-care test for Troponin I and other cardiac markers. The technology, which uses a micro-pillar flow technique, is capable of providing extremely sensitive, highly reproducible, quantitative, multiplexed results which give more accurate results than the current established point-of-care tests in the $900m cardiac market. 

Comments

Commenting on the results, Kevin Tansley, Chief Financial Officer, said, "This quarter we have continued our growth trajectory in terms of both revenues and earnings. Revenues grew by 7% largely driven by increased HIV revenues and sales of our new A1c analyzer, the Premier. Meanwhile, profit after tax for the quarter increased to over $4m, thus resulting in an improvement of 11% in EPS to 19.4 cents." 

Ronan O'Caoimh, CEO, stated, "We have had an extremely strong start to 2012. From a financial perspective we have continued to perform very well with the main highlights being the 13% growth in HIV revenues and the placement of our first Premier instruments in the USA. 

"During the quarter, we acquired Fiomi Diagnostics AB, a Swedish company which is at an advanced stage in the development of a highly sensitive Troponin I test. This marks Trinity's entry into the highly lucrative and growing $900m cardiac market. We expect to be selling this product in Europe in the second half of 2013 and in the USA by the end of Q2, 2014, once FDA approval has been obtained. This Troponin I test will be followed by a test for BNP and a multiplex cardiac panel, thus giving a complete suite of cardiac products. The technology also has a broad range of non-cardiac applications.

"Also in the first quarter, we successfully launched the first of our new point-of-care products, a test for Giardia. This test was developed at our San Diego facility and will be followed by the launch of tests for C Difficile, Cryptosporidium, Syphilis, Strep pneumonia and Herpes by the end of the year."  

Litigation Reform Act of 1995. Investors are cautioned that such forward-looking statements involve risks and uncertainties including, but not limited to, the results of research and development efforts, the effect of regulation by the United States Food and Drug Administration and other agencies, the impact of competitive products, product development commercialisation and technological difficulties, and other risks detailed in the Company's periodic reports filed with the Securities and Exchange Commission.

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.

The Trinity Biotech plc logo is available at http://www.globenewswire.com/newsroom/prs/?pkgid=10602

Trinity Biotech plc
Consolidated Income Statements
     
(US$000's except share data)
     
  Three Months Ended
March 31, 2012
Three Months Ended
March 31, 2011
  (unaudited) (unaudited)
     
Revenues 20,026 18,654
     
Cost of sales   (9,683)  (9,097)
     
Gross profit  10,343 9,557
Gross profit %  51.6% 51.2%
     
Other operating income  175  297
     
Research & development expenses  (845)  (687)
Selling, general and administrative expenses  (5,204)  (5,046)
Indirect share based payments  (337)  (422)
     
Operating profit   4,132  3,699
     
Financial income  546  642
Financial expenses  (1)  (4)
Net financing income  545  638
     
Profit before tax   4,677  4,337
     
Income tax expense   (567)  (585)
     
Profit for the period  4,110  3,752
     
Earnings per ADR (US cents)  19.4 17.5
     
Diluted earnings per ADR (US cents) 18.6 16.9
     
Weighted average no. of ADRs used in computing basic earnings per ADR 21,217,683 21,388,026
Weighted average no. of ADRs used in computing diluted earnings per ADR 22,154,641 22,191,689
     
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). 
     
Trinity Biotech plc    
Consolidated Balance Sheets    
     
  March 31,
2012
US$ '000
(unaudited)
Dec 31,
2011
US$ '000
(audited)
ASSETS    
Non-current assets    
Property, plant and equipment 7,823 7,626
Goodwill and intangible assets 59,832 45,390
Deferred tax assets 3,034 2,977
Other assets 528 493
Total non-current assets 71,217 56,486
     
Current assets    
Inventories 19,301 19,838
Trade and other receivables 25,677 23,973
Income tax receivable 271 117
Cash and cash equivalents 65,499 71,085
Total current assets 110,748 115,013
     
TOTAL ASSETS 181,965 171,499
     
EQUITY AND LIABILITIES    
Equity attributable to the equity holders of the parent    
Share capital 1,109 1,106
Share premium 3,086 2,736
Accumulated surplus 151,082 143,482
Other reserves 4,021 4,008
Total equity 159,298 151,332
     
Current liabilities    
Interest-bearing loans and borrowings 70 108
Income tax payable 1,879 1,582
Trade and other payables 10,104 11,589
Provisions 50 50
Total current liabilities 12,103 13,329
     
Non-current liabilities    
Other payables 3,273 10
Deferred tax liabilities 7,291 6,828
Total non-current liabilities 10,564 6,838
     
TOTAL LIABILITIES 22,667 20,167
     
TOTAL EQUITY AND LIABILITIES 181,965 171,499
 
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).
Trinity Biotech plc    
Consolidated Statement of Cash Flows    
     
(US$000's) Three Months Ended March 31, 2012
(unaudited)
Three Months Ended March 31, 2011
(unaudited)
     
Cash and cash equivalents at beginning of period 71,085 58,002
     
Operating cash flows before changes in working capital 5,115 4,773
Changes in working capital (1,821) 980
Cash generated from operations 3,294 5,753
     
Net Interest and Income taxes received 475 238
     
Capital Expenditure & Financing (net) (2,387) (2,105)
     
Free cash flow 1,382 3,886
     
Cash paid to acquire Phoenix Bio-tech (333) (1,000)
     
Cash paid to acquire Fiomi Diagnostics (5,624) --
     
Repurchase of own company shares (1,011) (1,070)
     
Cash and cash equivalents at end of period 65,499 59,818
 
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).
     


            

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