Trinity Biotech plc (Nasdaq: TRIB), a commercial stage
biotechnology company focused on diabetes management solutions and
human diagnostics, including wearable biosensors, today announced
results for the quarter ended December 31, 2023 and fiscal year
2023 and key business updates.
Business Updates
Comprehensive Transformation
Plan
At the Emerging Growth Investor Conference on
March 7, 2024, our new management team announced a comprehensive
transformation plan to deliver a step change in the financial
performance of our existing business.
Our transformation plan for the existing business
has several key components that we believe are rapidly achievable,
in most cases by mid-2025:
- We are reducing complexity and cost by consolidating our main
manufacturing operations into a considerably smaller number of
sites and also moving to an outsourced model for a significant
amount of our less complex manufacturing activities.
- As part of this initiative, we are today announcing that we
intend to cease manufacturing at our Kansas City manufacturing
plant which currently serves our Haemoglobin business. We expect to
have fully executed this change by the end of 2024 and expect this
will deliver significant annualised savings.
- We are also significantly reducing the cost of goods of many of
our products by changing suppliers and negotiating new deals with
existing suppliers.
- This is an area we have already successfully executed on a
number of cost saving initiatives, which we expect will deliver
multi-million-dollar annualised savings.
- We are simplifying our internal operations, and optimising our
business support function locations:
- Today we are announcing an initiative to move significant
aspects of our business support functions to a lower cost and
centralised location. We plan to complete this activity by Q4, 2024
and it is expected to deliver significant reductions to our
existing SG&A costs, plus provide an efficient scalable
business support platform to facilitate efficient growth in our
wearable biosensor business.
Financial Guidance
The Company is targeting approximately $20 million
of Annualised Run-Rate EBITDASO1 on annualised run-rate revenues of
approximately $75 million by Q2, 2025. This outlook is predicated
solely on growth from the existing businesses including haemoglobin
testing and HIV, and planned improvements to operating margins,
with no contribution from the recently acquired biosensor
business.
Biosensor Technology Acquisition and
Progress Updates
In January 2024, the Company announced the
acquisition of the biosensor assets of Waveform Technologies Inc.
(“Waveform”) for $12.5 million in cash and 1.8 million American
Depositary Shares (“ADS”) plus contingent consideration. We plan to
build a global business in wearable biosensors and are taking the
first steps by using this acquired technology to develop a next
generation version of a continuous glucose monitor (“CGM”). We
believe that our CGM will have a number of game changing benefits
compared to the leading CGMs on the market today, specifically with
respect to affordability, sustainability and enhanced data
capture.
Since the acquisition, we have been building out
our new biosensor team to augment the Waveform team members we
hired, and have made a number of senior appointments across a
number of areas including programme management, R&D, regulatory
& quality and operations. These new team members come from
leading medical device and diabetes management companies such as
Phillips, Johnson & Johnson and Lifescan.
Our team is progressing our plans across a number
of areas including:
- Planning and executing sensor design improvements based on the
existing CGM product design, with the assistance of external
technical & design consultants.
- Initiating enhanced data analysis on Waveform’s large existing
data bank of clinical trial results.
- Progressing discussions and agreements with potential
commercial partners for the launch of CGM products.
- Establishing a scientific and user advisory group for CGM to
support our product development efforts and ensuring that user
needs continue to be at the forefront of our efforts.
We will keep investors appraised on progress in
this business as we advance our plans forward.
Execution On Key Initiatives
- Optimization of our existing Diabetes business:
- Launch of the Improved Column System: Our programme to develop
an improved, backward compatible Diabetes HbA1c column system is
now completed. The results of this development programme have
exceeded expectations, with our new column system now delivering up
to 4 times the number of injections compared to the existing
product. As planned, we are now executing on the commercial launch
of these new products.
- In-house manufacturing process: Our revised in-house
manufacturing process of our key Diabetes HbA1c consumable began in
Q4, 2023 as planned, and in Q1, 2024 we ceased to order any further
product from our outsourced supplier.
- We remain on track to deliver approximately $4 million of
annualised recurring cost savings from this and our ongoing
Diabetes business supply chain optimisation initiatives, based on
expected production volumes, and we believe that these changes will
allow us to deliver an increasingly cost competitive Diabetes HbA1c
solution, putting us in a stronger position to grow market share
over time.
- TrinScreen HIV update:
- Earlier this week we received a purchase order for an
additional 2 million TrinScreen HIV tests for the Kenya market and
expect to deliver these in Q2, 2024.
- Additionally, in Q1, 2024 we successfully scaled manufacturing
of our new rapid HIV screening test, TrinScreen HIV and have
manufactured all 2.5 million tests from the initial Kenya purchase
order.
- The ability to deliver such a significant increase in
production capacity was an important demonstration to our
stakeholders of our execution capabilities and our commitment to
the new HIV testing algorithm adopted by the Kenyan Ministry of
Health that established TrinScreen HIV as the screening test under
World Health Organisation guidelines.
- The Kenyan HIV screening programme is one of the largest in
Africa, with up to an estimated 10 million screening tests
annually.
_______________________
1 Earnings before interest, tax, depreciation, amortisation,
share based payments – also excludes impairment charges and one-off
items
Fourth Quarter Results
The results of the Fitzgerald Industries life
sciences supply business, which was sold as of April 27, 2023, have
been reported separately as discontinued operations in the
Consolidated Income Statements for all periods presented. The
assets and liabilities attributable to Fitzgerald Industries have
been removed from our Consolidated Balance Sheet as of December 31,
2023.
Total revenues for Q4, 2023 were $13.4m which
compares to $15.7m in Q4, 2022, a decrease of 14.6% and which were
broken down as follows:
|
2023 Quarter 4 |
2022 Quarter 4 |
Decrease |
|
US$’000 |
US$’000 |
% |
Clinical laboratory |
11,279 |
13,050 |
13.6% |
Point-of-Care |
2,149 |
2,675 |
19.7% |
Total |
13,428 |
15,725 |
14.6% |
Clinical laboratory revenues for the quarter
were $11.3m, compared to $13.1m in Q4, 2022, representing a
decrease of $1.8m or 13.6%. This decrease in clinical laboratory
revenues was driven by lower revenues for haemoglobins, autoimmune
and COVID-19 related products. Haemoglobins revenues in Q4, 2023
were $1.0 million lower than in Q4, 2022. As announced in our
business update two months ago, our haemoglobins revenues were
reduced in Q4, 2023 by the deferral of shipments of products at
sub-optimal pricing as we renegotiated contract terms with a key
customer in line with the new management team’s focus on
profitability. As of Q1, 2024, these revised terms have been agreed
upon.
Autoimmune lab services and product revenue in
Q4, 2023 were $0.6 million lower than in Q4 2022 primarily because
we ceased transplant testing activity at our New York laboratory in
early 2023. Lastly, there was a reduction of $0.2 million in
revenues from our COVID-19 VTM products. Partly offsetting these
decreases was an increase in revenues for clinical chemistry
products of $0.2m in Q4, 2023 compared to Q4, 2022.
Point-of-Care revenues for Q4, 2023 decreased
from $2.7m to $2.2m when compared to Q4, 2022, a decrease of 19.7%.
Lower revenues from our HIV confirmatory test, Uni-Gold caused the
decrease which was attributed to the irregular quarter on quarter
ordering patterns that characterise the HIV testing market in
Africa. This decrease was partly offset by $0.4m of revenues for
our new HIV screening test, TrinScreen HIV, following our first
shipments to Kenya in December 2023.
Gross Profit
In Q4, 2023, gross profit was $4.6m, equating to
a gross margin of 34.0%. In Q4, 2022, gross profit amounted to
$5.4m equating to a gross margin of 34.2%.
Other operating income
Other operating income decreased from $0.3m in
Q4, 2022 to zero in Q4, 2023. Other operating income in Q4, 2022
was comprised of government grants in relation to R&D
activities and there were no equivalent grants in Q4, 2023.
R&D and SG&A
Research and development expenses were $1.1m in
Q4, 2023, which is broadly flat compared to Q4, 2022.
Selling, general and administrative expenses
(“SG&A”) were $6.9m in Q4, 2023, compared to $9.7m in Q4, 2022.
The reduction in SG&A expenses is mainly due to lower
share-based payments expenses, which decreased by $2.3m in Q4, 2023
compared to Q4, 2022. This decrease is primarily due to the
reversal of the cumulative share-based payment expense for unvested
options related to the former CEO due to his resignation in Q4,
2023. Included within our SG&A spend this quarter were
professional advisory and consulting fees of $1.8m, which we would
consider to be higher than normal. The main driver of this were
costs associated with the acquisition of the biosensor assets of
Waveform (which closed in January 2024). These expenses related to
the Waveform acquisition are non-recurring in nature, and we expect
our go forward quarterly non-product development professional
advisory, audit and consulting fees to be approximately a quarter
of what was incurred in Q4, 2023, unless we engage in additional
transactions.
Impairment Charges
The Company recognised an impairment charge of
$0.3m in Q4, 2023, compared to an impairment charge of $3.0m in Q4,
2022. The charge in Q4, 2023 was driven by an impairment loss in
two cash generating units, namely Trinity Biotech Do Brasil ($0.2m)
and Immco Diagnostics Inc. (“Immco”) ($0.1m).
Operating Loss
Operating loss decreased from $8.2m in Q4, 2022,
to $3.8m in Q4, 2023 and was mainly attributable to lower
impairment charges and SG&A expenses in Q4, 2023.
Financial income and expenses
Financial income for Q4, 2023 was $0.6m compared
to $0.1m for Q4, 2022. In both quarters the financial income
related to a fair value adjustment for the derivative liability
related to warrants granted to the Group’s principal lender,
Perceptive Advisors. The liability reduced by $0.6m in Q4, 2023
mainly due to a decrease in the price per ADS, leading to a gain of
that amount.
Financial expenses in Q4, 2023 were $2.3m
compared to $2.4m in Q4, 2022, a decrease of $0.1m. The decrease is
mainly due to lower cash interest expense for the senior secured
term loan due to the reduced principal amount outstanding during Q4
2023, compared to the equivalent quarter in 2022 partly offset by a
higher interest rate in Q4, 2023.
Other Items
The loss after tax for continuing operations for
the quarter was $5.5m in comparison to a loss of $10.4m for the
equivalent period last year. This decrease is primarily due to
lower impairment charges and SG&A expenses and higher financial
income, offset by lower gross profit and other operating
income.
Loss before interest, tax, depreciation,
amortisation, share based payments credit and impairment charges
for Q4, 2023 (Adjusted EBITDASO) was $4.0m. This is made up as
follows:
|
US$’M |
Operating loss |
(3.8) |
Depreciation & Amortisation |
0.5 |
Impairment charges |
0.3 |
|
|
Adjusted EBITDA |
(3.0) |
Credit for share based payments |
(1.0) |
|
|
Adjusted EBITDASO |
(4.0) |
Liquidity
The Group’s cash balance decreased from $6.3m at
the end of Q3, 2023 to $3.7m at the end of Q4, 2023, a decrease of
$2.6m. Cash generated from operations for Q4, 2023 was $0.3m, a
decrease of $2.0m compared to Q4, 2022. During Q4, 2023 the Company
had capital expenditure cash outflows of $0.9m (Q4, 2022: $1.1m)
and payments for property leases of $0.6m (Q4, 2022: $0.6m).
Interest payments in the quarter were $1.2m (Q4, 2022: $1.2m).
In January 2024, the Company entered into an
amended credit agreement (the “Amended Term Loan”) with its
existing main lender, Perceptive Advisors. Under the Amended Term
Loan, an additional $22 million of funding was made available to
the Company, with $12.5 million being used to acquire the Waveform
assets. The remaining $9.5 million is available for general
corporate purposes including for the further development of the CGM
and biosensor technologies. In addition, the Amended Term Loan
provides for additional liquidity of up to $6.5 million, that may
be drawn down by the Company between April and December 2024, and
can be used for general corporate purposes, thereby providing
further liquidity to fund the development of the CGM and biosensor
technologies. The Amended Term Loan also immediately reduced the
annual rate of interest on the loan by 2.5% to 8.75% (the “Base
Rate”) plus the greater of (a) Term Secured Overnight Financing
Rate (SOFR) or (b) 4.0% per annum, and allows for a further 2.5%
reduction in the Base Rate to 6.25% once the outstanding principal
under the Amended Term Loan falls below $35 million. Additionally,
the Amended Term Loan reduced the early repayment penalty from a
range of 8% to 7% to 4.0% to 3.5%, dependent on timing of early
repayment, and also reduced the revenue covenants. The Amended Term
Loan matures in January 2026.
Fiscal Year 2023 Results
Total revenues for continuing operations for
fiscal year 2023 were $56.8m compared to $62.5m in 2022, a decrease
of 9.1% year on year and were broken down as follows:
|
Full Year 2023 |
Full Year 2022 |
Decrease |
|
US$’000 |
US$’000 |
% |
Clinical laboratory |
47,741 |
53,308 |
10.4% |
Point-of-Care |
9,091 |
9,213 |
1.3% |
Total |
56,832 |
62,521 |
9.1% |
Clinical laboratory product revenues decreased
by $5.6m from $53.3m for the year ended December 31, 2022 to $47.7m
for year ended December 31, 2023, which represents a decrease of
10.4%. This decrease in clinical laboratory revenues was driven by
i) lower revenues for our COVID-19 related products of $1.8m year
on year as COVID-19 testing programs scaled down, ii) lower
autoimmune lab services revenue of $1.8m, primarily due to the loss
of our transplant testing service contract with a local healthcare
provider which ended in Q1, 2023 and iii) declines in our
haemoglobin business, with revenues 8% lower year on year due to a)
the predicted decrease in revenues for our legacy
haemoglobinopathies product, the Ultra II instrument, and b) due to
the deferral of shipments in Q4, 2023 of products at sub-optimal
pricing as we renegotiated contract terms with a key customer in
line with the new management team’s focus on profitability. As of
Q1, 2024, these revised terms have been agreed upon.
Point-of-Care revenues for the year 2023 were
broadly flat (-1.3%) compared to 2022. Included in our HIV
point-of-care revenues is $0.4m in relation to our TrinScreen HIV
test, which commenced its first shipments in the month of December
2023.
Gross profit for the year ended December 31,
2023 amounted to $19.5m, representing a gross margin of 34.2%. This
is 6.6% higher than fiscal year 2022. The increase in margin
percentage year on year was primarily due to an inventory
obsolescence charge of $4.7million in Q3, 2022. In 2023, we also
had some inventory obsolescence charges in relation to our VTM
products and the Tri-stat instrument but these charges were
significantly lower than the amount recorded in Q3, 2022.
Other operating income decreased from $0.3m for
the year ended December 31, 2022 to $0.1m for the year ended
December 31, 2023. The income for 2023 relates to a transition
services agreement with the acquirers of Fitzgerald Industries. The
income for 2022 was comprised of government grants in relation to
R&D activities and there were no equivalent grants in 2023.
R&D and SG&A
Research and development expenses increased from
$4.1 million to $4.4 million when compared to the year ended
December 31, 2022, an increase of 5.8% mainly due to lower
capitalisation of product payroll costs into product development
intangible assets.
Selling, General and Administrative (“SG&A”)
expenses increased by $4.2m to $31.2m when compared to the year
ended December 31, 2022, representing an increase of 15.5%. A
significant element of the $4.2m increase relates to i) an
increase in technical advisory, legal and professional fees of
$1.6 million, primarily due to the acquisition of the
biosensor assets of Waveform (which closed in January 2024)
together with other corporate development and corporate finance
activities as we continue to assess strategic opportunities and
balance sheet optimization initiatives and ii) an increase of $1.5m
in foreign exchange losses largely relating to the accounting
revaluation of euro-denominated lease liabilities for right-of-use
assets.
Impairment Charges
Impairment charges increased from $5.8m for the
year ended December 31, 2022 to $11.1m for the year ended December
31, 2023. The impairment charges for the year ended December 31,
2023 relate to Immco ($10.8m) and Trinity Biotech Do Brasil
($0.3m). The impairment in Immco was driven by i) lost revenues as
a local healthcare provider transferred its requirement for
transplant testing services to a different service provider, ii)
the expected level of laboratory services revenue arising from its
partnership with imaware, Inc (“imaware”) have not materialised and
iii) a full impairment of the financial assets associated with the
Group’s investment in imaware.
Operating Loss
Operating loss for the year ended December 31,
2023 was $27.0m, compared to an operating loss of $19.3m in the
year ended December 31, 2022. The higher loss was mainly
attributable to decreased revenues, lower other operating income,
higher impairment charges and higher indirect costs, partly offset
by a higher gross margin.
Financial expenses
Financial expenses in the year ended December
31, 2023 were $11.1m compared to $24.7m in the year ended December
31, 2022, a decrease of $13.6m, broken down as follows:
|
Full Year 2023 |
Full Year 2022 |
|
US$’M |
US$’M |
Interest on senior secured term loan |
8.4 |
9.8 |
Interest on convertible note |
1.1 |
0.7 |
Penalty for early partial settlement of term loan |
0.9 |
3.5 |
Lease interest |
0.6 |
0.7 |
Loss on disposal of exchangeable notes |
0.0 |
9.7 |
Interest on exchangeable notes |
0.0 |
0.4 |
Other non-cash financial expense |
0.0 |
0.1 |
Total |
11.1 |
24.7 |
Note: table above contains rounded numbers
The year-on-year decrease is mainly due to two
material expenses incurred in 2022, which were a loss of $9.7m on
the disposal of the exchangeable notes and an early repayment
penalty of $3.5m, compared to $0.9m in 2023.
Interest on the senior secured term loan,
comprising cash and non-cash interest, decreased from $9.8m in 2022
to $8.4m for 2023 as the principal amount outstanding was lower
across the 2023 financial year, although this was partly offset by
the impact of higher prevailing interest rates during 2023.
Interest on the convertible note, comprising cash and non-cash
interest, increased from $0.7m in 2022 to $1.1m in 2023 due to the
full year effect (the convertible note was issued in Q2, 2022). An
early repayment penalty of $0.9m was incurred in Q2, 2023 because
of an early partial settlement of the term loan of $10.1m. Interest
on exchangeable notes decreased from $0.4m in 2022 to $8,000 in
2023 because 99.7% of the exchangeable notes were retired during
Q1, 2022.
Other Items
Financial income for the year ended December 31,
2023 was $1.2m compared to $0.3m for the year ended December 31,
2022. In both years the financial income related to a fair value
adjustment for the derivative liability related to warrants granted
to the Group’s principal lender.
The loss before tax for continuing operations
for the year ended December 31, 2023 was $36.9m, in comparison to
$43.8m for the year ended December 31, 2022.
Profit for the period from discontinued
operations totalled $12.9 million, largely attributable to the gain
of $12.7m on the divesture of Fitzgerald Industries. The gain
consisted of proceeds of approximately $30.0m offset by transaction
costs of $1.3m with net assets eliminated on disposal of $16.0
million.
Loss before interest, tax, depreciation,
amortisation, share based payments and impairment charges for 2023
(Adjusted EBITDASO) was $12.1m. This is made up as follows:
|
$m |
Operating loss |
(27.0) |
Depreciation & Amortisation |
1.7 |
Impairment charges |
11.1 |
|
|
Adjusted EBITDA |
(14.2) |
Share option expense |
2.1 |
|
|
Adjusted EBITDASO |
(12.1) |
Non-GAAP 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
compensation, significant excess and obsolescence charges related
to inventory, depreciation, amortization and impairment
charges.
Adjusted EBITDA and Adjusted EBITDASO 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 and adjusted
EBITDASO, 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 and adjusted EBITDASO 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 and Adjusted
EBITDASO are presented.
Forward-Looking Statements
This release includes statements that constitute
“forward-looking statements” within the meaning of the Private
Securities Litigation Reform Act of 1995 (the “Reform Act”),
including but not limited to statements related to Trinity
Biotech’s cash position, financial resources and potential for
future growth, market acceptance and penetration of new or planned
product offerings, and future recurring revenues and results of
operations. Trinity Biotech claims the protection of the
safe-harbor for forward-looking statements contained in the Reform
Act. These forward-looking statements are often characterised by
the terms “may,” “believes,” “projects,” “expects,” “anticipates,”
or words of similar import, and do not reflect historical facts.
Specific forward-looking statements contained in this presentation
may be affected by risks and uncertainties, including, but not
limited to, our ability to capitalize on our purchase of the assets
of Waveform, our continued listing on the Nasdaq Stock Market, our
ability to achieve profitable operations in the future, the impact
of the spread of COVID-19 and its variants, potential excess
inventory levels and inventory imbalances at the company’s
distributors, losses or system failures with respect to Trinity
Biotech’s facilities or manufacturing operations, the effect of
exchange rate fluctuations on international operations,
fluctuations in quarterly operating results, dependence on
suppliers, the market acceptance of Trinity Biotech’s products and
services, the continuing development of its products, required
government approvals, risks associated with manufacturing and
distributing its products on a commercial scale free of defects,
risks related to the introduction of new instruments manufactured
by third parties, risks associated with competing in the human
diagnostic market, risks related to the protection of Trinity
Biotech’s intellectual property or claims of infringement of
intellectual property asserted by third parties and risks related
to condition of the United States economy and other risks detailed
under “Risk Factors” in Trinity Biotech’s annual report on Form
20-F for the fiscal year ended December 31, 2022 and Trinity
Biotech’s other periodic reports filed from time to time with the
United States Securities and Exchange Commission. Forward-looking
statements speak only as of the date the statements were made.
Trinity Biotech does not undertake and specifically disclaims any
obligation to update any forward-looking statements.
About Trinity Biotech
Trinity Biotech is a commercial stage
biotechnology company focused on diabetes management solutions and
human diagnostics, including wearable biosensors. The Company
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 and has
recently entered the wearable biosensor industry, with the
acquisition of the biosensor assets of Waveform Technologies Inc.
and intends to develop a range of biosensor devices and related
services, starting with a continuous glucose monitoring product.
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 December 31,
2023 (unaudited) |
Three Months Ended December 31,
2022(unaudited) |
Twelve Months Ended December 31,
2023 (unaudited) |
Twelve Months Ended December 31,
2022 |
|
|
|
|
|
Revenues |
13,428 |
15,725 |
56,832 |
62,521 |
|
|
|
|
|
Cost of
sales |
(8,861) |
(10,350) |
(37,382) |
(45,253) |
|
|
|
|
|
Gross profit |
4,567 |
5,375 |
19,450 |
17,268 |
Gross margin
% |
34.0% |
34.2% |
34.2% |
27.6% |
|
|
|
|
|
Other
operating income |
- |
341 |
141 |
343 |
|
|
|
|
|
Research
& development expenses |
(1,117) |
(1,166) |
(4,379) |
(4,138) |
Selling,
general and administrative expenses |
(6,939) |
(9,675) |
(31,152) |
(26,983) |
Impairment
charges |
(290) |
(3,032) |
(11,105) |
(5,839) |
|
|
|
|
|
Operating Loss |
(3,779) |
(8,157) |
(27,045) |
(19,349) |
|
|
|
|
|
Financial
income |
611 |
112 |
1,171 |
303 |
Financial
expenses |
(2,337) |
(2,384) |
(11,053) |
(24,734) |
Net
financing expense |
(1,726) |
(2,272) |
(9,882) |
(24,431) |
|
|
|
|
|
Loss
before tax |
(5,505) |
(10,429) |
(36,927) |
(43,780) |
|
|
|
|
|
Income tax
credit |
3 |
13 |
59 |
194 |
Loss
for the period on continuing operations |
(5,502) |
(10,416) |
(36,868) |
(43,586) |
|
|
|
|
|
Profit for
the period on discontinued operations |
- |
336 |
12,850 |
2,577 |
Loss
for the period (all attributable to owners of the
parent) |
(5,502) |
(10,080) |
(24,018) |
(41,009) |
|
|
|
|
|
Loss per ADS
(US cents) |
(71.8) |
(132.3) |
(313.8) |
(607.8) |
|
|
|
|
|
Diluted loss
per ADS (US cents) |
(71.8) |
(132.3) |
(313.8) |
(607.8) |
|
|
|
|
|
Weighted
average no. of ADSs used in computing basic earnings per ADS* |
7,665,514 |
7,621,514 |
7,654,970 |
6,746,966 |
|
|
|
|
|
Weighted
average no. of ADSs used in computing diluted earnings per
ADS* |
7,665,514 |
7,621,514 |
7,654,970 |
6,746,966 |
|
|
|
|
|
*As of February 23, 2024, Trinity Biotech changed
the ratio of its American Depositary Shares (“ADS”) from one (1)
ADS representing four (4) ‘A’ ordinary shares to one (1) ADS
representing twenty (20) ‘A’ ordinary shares. The above loss per
ADS calculations reflects this change.
Trinity
Biotech plc Consolidated Balance
Sheets |
|
|
December 31, 2023 US$
‘000 (unaudited) |
September 30, 2023 US$
‘000 (unaudited) |
December 31, 2022 US$
‘000 |
ASSETS |
|
|
|
Non-current assets |
|
|
|
Property,
plant and equipment |
1,892 |
1,804 |
5,682 |
Goodwill and
intangible assets |
16,270 |
16,164 |
35,269 |
Deferred tax
assets |
1,975 |
1,507 |
4,218 |
Derivative
financial asset |
178 |
196 |
128 |
Other
assets |
79 |
98 |
139 |
Total non-current assets |
20,394 |
19,769 |
45,436 |
|
|
|
|
Current assets |
|
|
|
Inventories |
19,933 |
20,880 |
22,503 |
Trade and
other receivables |
13,901 |
15,095 |
15,753 |
Income tax
receivable |
1,516 |
1,592 |
1,834 |
Cash, cash
equivalents and deposits |
3,691 |
6,261 |
6,578 |
Total current assets |
39,041 |
43,828 |
46,668 |
|
|
|
|
TOTAL ASSETS |
59,435 |
63,597 |
92,104 |
|
|
|
|
EQUITY AND LIABILITIES |
|
|
|
Equity attributable to the equity holders of the
parent |
|
|
|
Share
capital |
1,972 |
1,972 |
1,963 |
Share
premium |
46,619 |
46,619 |
46,458 |
Treasury
shares |
(24,922) |
(24,922) |
(24,922) |
Accumulated
deficit |
(48,644) |
(42,135) |
(26,695) |
Translation
reserve |
(5,706) |
(5,753) |
(5,775) |
Equity
component of convertible note |
6,709 |
6,709 |
6,709 |
Other
reserves |
23 |
23 |
86 |
Total deficit |
(23,949) |
(17,487) |
(2,176) |
|
|
|
|
Current liabilities |
|
|
|
Income tax
payable |
279 |
252 |
28 |
Trade and
other payables |
14,496 |
12,226 |
17,051 |
Exchangeable
senior note payable |
210 |
210 |
210 |
Provisions |
50 |
50 |
50 |
Total current liabilities |
15,035 |
12,738 |
17,339 |
|
|
|
|
Non-current liabilities |
|
|
|
Senior
secured term loan |
40,109 |
39,947 |
44,301 |
Derivative
financial liability |
526 |
1,138 |
1,569 |
Convertible
note |
14,542 |
14,337 |
13,746 |
Other
payables |
10,872 |
10,921 |
12,267 |
Deferred tax
liabilities |
2,300 |
2,003 |
5,058 |
Total non-current liabilities |
68,349 |
68,346 |
76,941 |
|
|
|
|
TOTAL LIABILITIES |
83,384 |
81,084 |
94,280 |
|
|
|
|
TOTAL EQUITY AND LIABILITIES |
59,435 |
63,597 |
92,104 |
Trinity
Biotech plc Consolidated Statements of Cash
Flows |
|
|
Three Months
Ended December 31, 2023
US$ ‘000
(unaudited) |
Three Months Ended December 31,
2022 US$ ‘000
(unaudited) |
Twelve Months Ended December 31,
2023 US$ ‘000
(unaudited) |
Twelve Months Ended December 31,
2022 US$ ‘000 |
Cash
flows from operating activities |
|
|
|
|
Loss for the
period |
(5,502) |
(10,080) |
(24,018) |
(41,009) |
Adjustments
to reconcile loss to cash generated by/(used in) operating
activities: |
|
|
|
|
Depreciation |
2 |
453 |
831 |
1,410 |
Amortisation |
460 |
215 |
946 |
923 |
Income tax
credit |
(3) |
(16) |
(59) |
(192) |
Financial
income |
(611) |
(112) |
(1,171) |
(303) |
Financial
expense |
2,337 |
2,395 |
11,053 |
24,744 |
Share-based
payments |
(1,009) |
1,318 |
2,069 |
1,756 |
Foreign
exchange gains on operating cash flows |
385 |
(91) |
238 |
(76) |
Impairment
charge |
290 |
3,032 |
11,105 |
5,839 |
Gain on sale
of business |
- |
- |
(12,718) |
- |
Other
non-cash items |
2,602 |
3,061 |
2,548 |
7,662 |
|
|
|
|
|
Operating cash inflows/(outflows) before changes in working
capital |
(1,049) |
175 |
(9,176) |
754 |
Net movement
on working capital |
1,359 |
2,112 |
(2,693) |
(1,662) |
|
|
|
|
|
Cash
generated by/(used in) operations |
310 |
2,287 |
(11,869) |
(908) |
Interest
received |
- |
- |
- |
2 |
Income taxes
(paid)/received |
(65) |
(12) |
312 |
(15) |
|
|
|
|
|
Net
cash generated by/(used in) operating activities |
245 |
2,275 |
(11,557) |
(921) |
|
|
|
|
|
Cash
flows from investing activities |
|
|
|
|
Payments to
acquire intangible assets |
(641) |
(663) |
(1,901) |
(4,876) |
Acquisition
of property, plant and equipment |
(250) |
(475) |
(803) |
(1,101) |
Payments to
acquire financial asset |
- |
- |
(700) |
- |
Proceeds
from sale of business (net of transaction costs) |
- |
- |
28,160 |
- |
|
|
|
|
|
|
|
|
|
|
Net
cash generated by/(used in) investing activities |
(891) |
(1,138) |
24,756 |
(5,977) |
|
|
|
|
|
Cash
flows from financing activities |
|
|
|
|
Issue of
ordinary share capital including share premium (net of issuance
costs) |
- |
(130) |
- |
25,336 |
Proceeds
from shares to be issued |
|
63 |
- |
63 |
Net proceeds
from new senior secured term loan |
- |
- |
5,000 |
80,015 |
Proceeds for
convertible note issued |
- |
- |
- |
20,000 |
Expenses
paid in connection with debt financing |
- |
- |
(147) |
(2,356) |
Purchase of
exchangeable notes |
- |
- |
- |
(86,730) |
Repayment of
senior secured term loan |
- |
- |
(10,050) |
(34,500) |
Penalty for
early settlement of term loan |
- |
- |
(905) |
(3,450) |
Repayment of
other loan |
- |
(23) |
- |
(23) |
Interest
paid on senior secured term loan |
(1,129) |
(1,103) |
(7,314) |
(6,424) |
Interest
paid on convertible note |
(75) |
(75) |
(300) |
(199) |
Interest
paid on exchangeable notes |
(4) |
- |
(8) |
(1,293) |
Payment of
lease liabilities |
(558) |
(577) |
(2,318) |
(2,761) |
|
|
|
|
|
Net
cash used in financing activities |
(1,766) |
(1,845) |
(16,042) |
(12,322) |
|
|
|
|
|
Decrease in
cash and cash equivalents |
(2,412) |
(708) |
(2,843) |
(19,220) |
Effects of
exchange rate movements on cash held |
(158) |
32 |
(44) |
(112) |
Cash and
cash equivalents at beginning of period |
6,261 |
7,254 |
6,578 |
25,910 |
|
|
|
|
|
Cash
and cash equivalents at end of period |
3,691 |
6,578 |
3,691 |
6,578 |
|
|
|
|
|
Contact:
Trinity Biotech plc
Des Fitzgerald
(353)-1-2769800
LifeSci Partners, LLC
Eric Ribner
(1)-646-751-4363
E-mail: investorrelations@trinitybiotech.com
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