Trinity Biotech PLC (TRIB) CEO Ronan O'Caoimh on Q1 2019 Results - Earnings Call Transcript

|
About: Trinity Biotech plc (TRIB)
by: SA Transcripts
Subscribers Only
Earning Call Audio

Trinity Biotech PLC (NASDAQ:TRIB) Q1 2019 Earnings Conference Call May 7, 2019 11:00 AM ET

Company Participants

Joe Diaz - Lytham Partners

Ronan O'Caoimh - CEO

Kevin Tansley - CFO

Conference Call Participants

Jim Sidoti - Sidoti & Company

Paul Nouri - Noble Equity Funds

Operator

Good morning, and welcome to the Trinity Biotech First Quarter 2019 Financial Results Conference Call. [Operator instructions] Please note this event is being recorded.

I would now like to turn the conference over to Joe Diaz with Lytham Partners. Please go ahead.

Joe Diaz

Thank you, Gary. And thank all of you for joining us to review the financial results of Trinity Biotech for the first quarter of calendar year 2019, which ended March 31, 2019.

With us on the call representing the Company are Ronan O'Caoimh, Chief Executive Officer; and Kevin Tansley, Chief Financial Officer. At the conclusion of today's prepared remarks, we'll open the call for a question-and-answer session.

But before we begin with those prepared remarks, we submit for the record the following statement. Statements made by the management team of Trinity Biotech during the course of this conference call that are not historical facts are considered to be forward-looking statements subject to risks and uncertainties. The Private Securities Litigation Reform Act of 1995 provides a safe harbor for such forward-looking statements.

The word believe, expect, anticipate, estimate, will and other similar statements of expectation identify forward-looking statements. 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 commercialization and technological difficulties; and other risks detailed in the Company's periodic reports filed with the Security and Exchange Commission.

Forward-looking statements reflect management's analysis only as of today. The Company undertakes no obligation to publicly release the results of any revision to these forward-looking statements.

With that said, let me turn the call over to Kevin Tansley, Chief Financial Officer, for a review of the results. After Kevin's remarks, we will hear from Ronan O'Caoimh on his review of the quarter, after which we'll open the call for your questions. Kevin?

Kevin Tansley

Thanks very much, Joe. Today, I'll take you through the results for quarter 1 2019.

Beginning with our revenues, total revenues for the quarter were $22 million, which represents a decrease of approximately $1.8 million versus quarter one last year. Ronan will provide more details in revenues later in call, so I'll then move on and disclose the other aspects of the income statement.

Our gross margin this quarter was 42.4%. Whilst this was a lower than the 43.8% reported on quarter 1 2019, it was stronger than the 42.1% in quarter three and 41.7% in quarter four of last year.

This is not what's done in the fact that revenues were down this quarter. And as I mentioned before, our margins are very sensitive to revenue fluctuations. We were also impacted by the fact that the decreased revenues arose in the more profitable of company's business lines.

And then there was the adverse currency movements mentioned in our release, particularly with regards to the Brazilian real, which were also a drag on margins this quarter. Though we did get at a slight tailwind due to the introduction of new accounting standard on leases, which I will address later on.

Moving next to our indirect costs.

In total, they have fallen by over $600,000 in the quarter to $8.6 million. Within this, you're seeing relatively flat R&D expenses of $1.3 million whilst SG&A expenses decreased by nearly $400,000 to $6.6 million. I will point out that the average SG&A for last year was over $7 million per quarter. And then our share option expense also decreased from $400,000 to $200,000.

The net result of all this there's been a decrease in operating profit from $1.8 million to $1.3 million. Moving on to our financing costs, which includes the impact of our exchangeable notes. Our financial income for the quarter was $140,000 versus $205,000 in the comparative period. This is a primary reflective of the lower levels of cash on deposits.

Financial expenses were $1.2 million for the quarter, and of this, $1 million relates to the cash interest element of the exchangeable notes, for which the equivalent figure in quarter 1 2018 was $1.15 million. The reduction being due to the notes repurchase that we made last year. The remaining $200,000 relates the additional financing charge related to the lease payments of the result of IFRS 16.

Then there is the noncash financial expense of $300,000, which is disclosed further down the income statement, and that relates to our exchangeable notes with noncash interest of approximately $200,000 and a loss of over $100,000 recorded for the change in the fair value of the derivatives embedded in the notes, which is the same as this time last year.

Our tax charge for the quarter was under $105,000, and this represents an effective tax rate of 8% of operating profit, which is a broadly in line with last year.

The net results for the loss for the quarter of $200,000. However, excluding the noncash items that was a profit for the quarter of over $100,000 versus an equivalent figure of $700,000 last year, the basic EPS for the quarter excluding noncash items was $0.05 compared to $0.34 last year. Meanwhile, fully diluted EPS was $0.044 compared to $0.071.

Finally, on the income statement, earnings before income, interest, tax, depreciation, amortization and share option expense for the quarter was $3.1 million versus $3.3 million in quarter 1 2018.

In advance of discussing the balance sheet movements, I will now talk about IFRS 16 as this the statement that is most impacted by the new standard. But before talking about the impact on our financial statements this quarter, I will remind you of what the standard is about following the remarks that would have made is this, on last quarter's call.

The standard deals with lease payments such as rent paid on our manufacturing and other premises which are subject to leases, which are over 1 year in duration or had more than 1 year left to run from the end of 2018. From January 1, 2019, such payments will no longer be expensed to the income statement evenly over the lease period, instead such leases are now essentially be treated as financing instruments whereby assets even though not legally owned will be treated as fixed assets on the balance sheet and then depreciated through the income statement over the life of the lease.

In addition to this, and this is the depreciation that will be an interest charge which will reflect, an effect of financing charge and which will appear in the financing section of the income statement.

So in essence, lease rental charges are now being replaced by a combination of depreciation and interest.

I had flagged last time that from an income statement point of view, that this would have, overall, a slightly adverse impact, which you can see from the release is about $100,000 this quarter. This is because at the moment, the combined new depreciation and interest charges are slightly higher than the amounts of the payments made. So this will even out over time.

However, the income on the, the impact on the balance sheet is much more significant, as the inclusion of the leased assets has increased our fixed assets by $21.2 million as accumulated depreciation for the quarter of $600,000. And this is the deemed value of the leased assets for the remaining period of the leases from the end of March. And you are seeing then a broadly corresponding increase in payables in terms of both current and greater than one year of payables, which in effect, relates to the discounted value of the remaining lease payments.

In this case, the increase is $2.1 million in relation to trade and other payables less than one year and $18.6 million to other payables -- payable greater than one year. And then in the statement of cash flows, the lease payments are $800,000 and these are separately disclosed. Bearing all that in mind, I will now move on and talk about the significant balance sheet movements since the end of December 2018.

The overall increase in property plans and equipments, as you'll see, is over $21.2 million. However, when we exclude the IFRS movement in this caption, the remaining movement is negligible as the additions in the quarter of $1 million perversely offset by depreciation of $900,000. In the same period, our intangible assets increased by $1.4 million, and this was made up of additions of $2.1 million offset by amortization charge of $700,000.

Moving on to inventories. You will see that these have increased by $600,000 to $30.9 million. This is partly due to timing factors, which resulted in higher instruments-related inventory and also increased Lyme-related inventory in advance of the Lyme season.

Trade and other receivables have decreased by $900,000 to $23.4 million. Most of this increase was due to a decrease in trade efforts due to improved cash collections during the quarter. This decrease was slightly offset by an increase of prepayments due, in this case, the renewal of certain annual contracts, such as insurance and IT support, which tend to occur at the beginning of the year.

Meanwhile, our trade and other payables, including both current and noncurrent, have increased from $17.9 million to $38.6 million, which is largely the IFRS 16 effect that I mentioned earlier. But it also includes an additional quarter of accrued interest of a $1 million in relation to the exchangeable notes. The remaining movement is quite modest is due to the timing of raw material purchases and vendor payments.

Finally, I will disclose our cash flows for the quarter. Cash generated from operations for the quarter was $2.7 million compared to only $600,000 during the equivalent period last year, though contained within this are negative working capital movements of $500,000.

Capital expenditure in the quarter was $3.1 million, which represents a decrease of approximately $1 million on the corresponding quarter last year. And then we have the lease payments of $800,000 to which I mentioned earlier. And then the net result is thus that we had a decrease in cash for the quarter of approximately $900,000, bringing the quarter-end balance to $29.4 million.

I'll now hand over to Ronan.

Ronan O'Caoimh

Thanks, Kevin. I'm going to review our revenues for quarter 1 before opening the call to a question-and-answer session. Our revenues for quarter 1 were $22 million compared with $23.8 million in the corresponding quarter last year, which is a decrease of 7%. Point-of-Care revenues were $3.2 million compared with $3.8 million in the corresponding quarter last year, which is a decrease of 15%. Clinical Laboratory revenues were $18.8 million compared with $20 million in the corresponding quarter last year, which is a decrease of 6%.

And moving back to Point-of-Care, our revenues decreased this quarter by 6% when compared with the corresponding quarter. Our U.S. HIV revenues decreased 9%, and this is explained by the fact that public health spending in the U.S. on HIV testing continues to decrease.

Moving on to Africa, our HIV sales decreased 3% when compared with the corresponding quarter. However, we do not believe that either the market or indeed our market share have diminished.

We believe that this movement is consistent with the haphazard nature of NGO purchasing. For the past 15 years, we have held approximately 90% of the African confirmatory market, and we believe that we will continue to do so given the status of our products as gold standard.

However, as previously indicated, we have developed a HIV screening product, which we anticipate will be launched on the African market around the end of this year.

Given the quality of the product and given that the price at which we can manufacture this product in our new automated plant in Ireland and given our long reparation as manufacturer of gold standard, we believe that we can take significant market share in the screening segment of the African HIV market, which comprises 170 million tests annually, and is many times greater than the confirmatory market.

Our new HIV Trin-Screen product is currently undergoing independent trials in Africa to support the WHO submission. And it is anticipated that the product will be submitted to the WHO by the end of September this year. Given that we now have a high-volume, low-cost automated HIV manufacturing capability in Dublin, we believe that this new product will transform our HIV business into a strong growth engine in the future.

Moving on to our Clinical Laboratory business. Our revenues for the quarter were $18.8 million, which is a decrease of 6% over the corresponding quarter last year. During the quarter, we suffered a currency headwind, which amounted to $300,000, and the biggest component of this is explained by the weakening of the Brazilian real, which moved from BRL 325 last year to BRL 375 on average this year.

Our infectious disease business decreased 16% year-on-year. Our mainline infectious disease business decreased 6% when compared with the prior quarter. And as we have signaled in the past, this is in line with our expectations given the ongoing migration by laboratories from ELISA onto random-access platforms in the USA.

However, additionally, during the year, we also suffered a loss of a significant Lyme confirmatory contract with one of the major clinical laboratory service providers in the U.S.

And this loss, which approximates $2.1 million annually, gave rise to a 10% decrease in our infectious disease revenues in this quarter when compared with the corresponding quarter last year.

On an ongoing basis, we expect shrinkage of our infectious disease business to be approximately 5% annually, given that other segments of the business have performed well, particularly in China.

Our Diabetes and Hemoglobin variant business, which are served by the premier and premier resolution instruments, grew 2% during the quarter compared with the corresponding quarter last year, although growth in the 12-month period to the end of March '19 was 8%. The slower growth of 2% experienced during the quarter is probably larger explained by the fact that instrument placements were so strong last quarter at 96 units and came in this quarter as a more modest 61 units.

However, we believe that for 2019 we will achieve similar placements to last year's level, which was 317 units.

It's important to bear in mind that every instrument we place is new business and we are never replacing an existing Trinity instrument as we are in the middle years of the placement cycle.

Meanwhile, our premier resolution instruments, which serves the hemoglobin variant market for sickle cell anemia and thalassemia, performed well in Europe, while we submitted the premier resolution instrument to the FDA recently and expect approval within the next couple of months.

Receipt of FDA approval for the resolution instrument will enable us to enter the U.S. market, but it will also enable us -- will also enable the commencement of the Chinese regulatory process. And these are high-value markets with few competitors. And we believe that with our best-in-class instrument and reagent, that we can take significant market share.

Meanwhile, the launch of our new hemoglobin Point-of-Care instrument and test, the TRIstat, adds a significant new business opportunity to our hemoglobins business. Having received FDA approval for the product and instrument, we are now pursuing Chinese approval.

During the quarter, we also received Brazilian approval for this product. During the current quarter, we placed 150 TRIstat instruments around the world, and we anticipate significant success with this product, which we believe, will quickly grow to constitute a significant percentage of our overall hemoglobin revenue base.

Meanwhile, our Autoimmune business, which grew 7% last year had a quieter quarter with growth of 3% this quarter when compared with corresponding quarter of last year. However, we have consistently grown this business since its acquisition with the reference laboratory business being the best-performing component with significant coming from our Sjogren test range and from the growth of our business with the two U.S. mega labs.

On the product revenue side of our Autoimmune business, our strategies is to grow our best-in-class immunofluorescence product revenues while also growing our enzyme immunoassay product revenues around the world, but particularly in the emerging markets, while meanwhile developing our new automated, integrated immunofluorescence processor and reader, which will eliminate the requirement for the use of microscopes with our immunofluorescence product range. This strategy is working successfully for us, and we have had significant success in China with our IFA product range.

At this point today, please pass back and commence our question-and-answer session.

Question-and-Answer Session

Operator

[Operator instructions] Our first question comes from Jim Sidoti with Sidoti & Company.

Jim Sidoti

Great. Can you give us a little more color on the new HIV screening test and the process with the WHO. Have you had any communication with them since the last call? What makes you confident you still get that in the market at some point in 2019?

Ronan O'Caoimh

Well, so we are conducting trials in three different countries. In Kenya, Ivory Coast and South Africa. So those trials are ongoing. And we believe that we will -- so we're broad -- we're most of the way through. So we're kind of waiting for some outliers. For example, we're waiting for more walk-ins with HIV-2 and with subtype O. So we have -- I think we've all got our HIV-1s done.

So to that extent -- to some extent, we're talking about less prevalent samples and this an element of -- it's difficult to estimate when you are going to actually get the numbers when we need. But the balance we believe that we will have got everything together and collated everything and sometime in September, submit it to WHO at that point in time. And then really it's difficult to determine when the actual approval would occur. It could probably, on balanced, be anytime between December and early next year. There's an element of luck attaching there.

Jim Sidoti

Okay. And then in the U.S. you said you have one instrument approved and then another one before the FDA. Can you just remind me what they are?

Ronan O'Caoimh

Would you repeat that, please, Jim?

Jim Sidoti

You mentioned that you have an instrument before the FDA for approval. I believe it was the hemoglobin variant. Can you just remind me what that's used for?

Kevin Tansley

Oh, yes. Okay. So the hemoglobin variant would be for variants which for example, would be sickle cell anemia, thalassemia. So basically, mutations are the hemoglobin gene. Nothing to do with diabetes, right? And basically, so it's a very spacious market with really only one other significant participant. And we are as well as the new kids on the block here with an excellent instrument. Average prices are higher. So this constitutes for us a significant market opportunity whether that be U.S.A. or Brazil or indeed, China.

And I think, sorry, the estimated value of the market for variants worldwide, including neonatals, all new born babies maybe is like $150 million, that kind of size.

Jim Sidoti

Okay. And did you say that, that application has been submitted, or is that something you're still working on?

Kevin Tansley

No, it's submitted. So we have approval in Europe and we have submitted to the FDA about two months ago in the U.S.A. And of course that has dual importance for us because not only will it open up the U.S.A. for us, but it also enables us to commence our regulatory process in China. So we need to have home approval before we can go for Chinese approval. The Chinese market in particular is largest, the higher instances of variance. And also they are very committed to coming to grips with it. And meanwhile in Brazil, we're in the regulatory process as we speak.

Jim Sidoti

So what's your thought for revenue growth?

Kevin Tansley

Jim, just to give you a flavor for, we would supply the 2 U.S. mega labs with virtually all of their requirements in this area, for example. So we have an existing presence here.

Jim Sidoti

So do still think if you can get this product approved this year and still grow revenues in 2019, or do you think because of the headwinds with the Lyme disease test and the lower public health spending that you think you'll be down again in 2018?

Ronan O'Caoimh

Well. I mean, I think that premier resolution that Lyme has no effect whatsoever on it. It's an independent opportunity. But in terms of just if you're looking at overall revenues and I would make the point that quarter 1, historically, has always been our weakest quarter. This particular quarter we have, I think, for the third we've had, just this quarter, we've had the weakest growth in our hemoglobin A1c business that we've had for a number of years.

But I think that's generally a blip just a more reflective probably for higher placements, as I mentioned, of instruments last quarter than this quarter, so it kind of went from 96 down to 61. But I could see us being right up there next quarter. So we are -- I mean you've put out a paper in terms of your revenue expectations for us for the year and we would be confident of achieving those numbers.

Jim Sidoti

Okay. So what I was asking, so despite the headwind you have with the Lyme disease, you still think you will grow revenue this year because of the diabetes business and then getting some these new products launched?

Ronan O'Caoimh

Yes. I mean just to quantify, just to look at the Lyme, we lost a Lyme contractor worth $2.1 million and we, of course, we lost it last May. So from comparability point of view post perspective, it hit quarter one like -- because they were just buying their last products almost virtually last year and they were probably stocking up a bit in context of looking to transition to a different technology. And therefore, the sales of that product in quarter one last year were like approximately $600,000. And so from a comparability point of view, it makes this quarter look weak. But just to bear in mind that the loss of that business it had virtually no impact next quarter from a comparability point of view. So I think that just in overall terms, what we need to realize is that the quarter 1 has always been our weakest quarter. I mean we still have a very substantial Lyme business worth in excess of $6 million and there's virtually no sales in quarter one. Lyme, ticks is a kind of summer time problem. People don't buy much Lyme testing in January, February, March and some other factors as well. So the point is that our HIV -- sorry, is that our quarter 1 revenues it's our lowest quarter.

Jim Sidoti

Okay. So do you still think you can grow revenue this year, and I assume you still think that you'll be cash flow neutral or better?

Ronan O'Caoimh

Yes. We've indicated that we want to maintain a cash balance of $30 million, and we believe we will do that.

Kevin Tansley

Maintain or strengthen.

Operator

The next question comes from Paul Nouri with Noble Equity Funds.

Paul Nouri

Hey, just wondering if you expect growth to pick up in the autoimmune business throughout the year?

Ronan O'Caoimh

Paul, yes, hi. Yes, we do. I mean we bought this business 4.5 years years ago, it was doing $12.5 million and it did $20 million last year and hoping it will do $22 million this year. So we had a soft enough quarter, quarter 1. But our quarter -- we expect quarter two is looking quite good, and we are very optimistic about our autoimmune business. We think it's a real opportunity for us. It's a very nice niche market for us. We have the next in the range of product, and we have very positive about growing it.

Paul Nouri

And where are you with the expansion? I know you're expanding the current location or moving to a new one out in Buffalo?

Ronan O'Caoimh

Yes. That expansion is now complete. So basically, we didn't have enough production capacity. I mean bear in mind the business we bought was doing $12 million, $12.5 million. So we have opened -- we've opened a second location in Buffalo. Well, in fact, we had two locations in Buffalo. We had a lab in the city center and then we have a factory. And so we've moved the lab out of the city center into a new facility and expanded our production capability within in addition. So basically, we have two locations within Buffalo now up and running.

Operator

This concludes our question-and-answer session. I would like to turn the conference back over to Ronan O'Caoimh for any closing remarks.

Ronan O'Caoimh

Alright. Well, thank you very much indeed for attention, your support, and your interest. And we look forward to speaking to you in a couple of months on quarter 2. Bye-bye.

Operator

The conference is now concluded. Thank you for attending today's presentation. You may now disconnect.