Innoviva, Inc.
Q1 2015 Earnings Call Transcript
Published:
- Operator:
- Ladies and gentlemen, good afternoon. At this time, I would like to welcome everyone to the Theravance First Quarter 2015 Financial Results Webcast and Conference Call. During the presentation, all participants will be in a listen-only mode. A question-and-answer session will follow the Company's formal remarks. [Operator Instructions] Today's conference is being recorded. And now I would like to turn the conference over to Eric D'Esparbes, Chief Financial Officer of Theravance. Please go ahead, sir.
- Eric D'Esparbes:
- Good afternoon, everyone and thank you for joining us. With me on the call today is Mike Aguiar, our Chief Executive Officer. On today's call, Mike will review the highlights from the quarter and I will review our financial results. Following our comments, we will open up the call for questions. Earlier today, Theravance issued a press release announcing recent corporate developments and fourth quarter and full year 2014 financial results. A copy of the press release can be found on our website. Before we get started, we would like to remind you that this conference call contains forward-looking statements regarding future events and the future performance of Theravance. Forward-looking statements include anticipated results and other statements regarding Theravance's goals, plans, objectives, expectations, strategies and beliefs. These statements are based upon the information available to the Company today and Theravance assumes no obligation to update these statements as circumstances change. Future events and actual results could differ materially from those projected in the Company's forward-looking statements. Additional information concerning factors that could cause results to differ materially from our forward-looking statements are described in greater detail in the Company's press release and Form 10-K for the quarter ended March 31, 2015 to be filed with the Securities and Exchange Commission. I would now like to turn the call over to Mike Aguiar, our Chief Executive Officer. Mike.
- Michael W. Aguiar:
- Thank you Eric and good afternoon everybody. This is a very important time at Theravance and we are making good progress towards our 2015 goals. In particular I'm very pleased with last week’s approval by the FDA of BREO for the treatment of patients 18 years and older in the U.S. with asthma which according to IMS represents approximately 92% of total U.S. LABA ICS prescriptions for asthma. This is a significant catalyst for Theravance that provides an important new treatment option for patients and physicians dealing with a serious disease that substantially expands the market opportunity for BREO in the U.S. and it sets Theravance up for a successful 2015. In building Theravance as a standalone company, one of our primary objectives was to create an efficient low cost company with a short path to profitability. I'm pleased to report that in the first quarter of 2015 we have made further progress towards this goal by reducing operating expenses and expanding operating margin versus Q4 last year. Our second important goal of the spin was to return capital to shareholders. As part of this initiative we paid a cash dividend of $0.25 per share on March 31, 2015 and today declared another dividend of $0.25 payable on June 30 to stockholders of record as of the close of businesses on June 12, 2015. Turning now to our programs RELVAR/BREO is our lead respiratory program partnered with GSK for the treatment of patients with chronic obstructive pulmonary disease or COPD and asthma, it is a combination inhaled respiratory medicine consisting of vilanterol, a long-acting beta2 agonist or LABA, and fluticasone furoate, an inhaled corticosteroid, or ICS, both delivered in the ELLIPTA dry powder inhaler. As of March 31, 2015, this medicine has been approved in 58 countries and launched in 36. Total net sales for RELVAR/BREO during the first quarter of 2015 were approximately $60 million. Our second respiratory program with GSK, ANORO, is a combination dual bronchodilator medicine for the treatment of COPD consisting of the LABA vilanterol and the long-acting muscarinic antagonist, or LAMA umeclidinium. As of March 31, 2015, it has been approved in 50 countries and launched in 20. Total net sales for ANORO during the first quarter of 2015, was approximately $18 million. While we are still early in the launch cycle for both products, we're optimistic about the prospects for our portfolio. So far in 2015 we have continued to see further growth in volume and market share for both products. For example, according to IMS total U.S. prescription volumes increased by 35% for BREO and 46% for ANORO in Q1 2015 compared to Q4 2014. In the U.S. a number of positive events and changes are in process, first as we discussed on our last conference call the collaboration plan to grow product volume by making significant commercial investments in higher levels of couponing and gaining additional payer coverage with the cost of these initiatives being a wider growth to net spread. We believe these investments are paying off as total prescriptions for both products increased significantly during Q1 as discussed above. Second, new GSK management and commercial teams in the U.S. are now in place and the salesforce is being reorganized to create dedicated teams for BREO and for ANORO. As GSK mentioned during their call today, the asthma launch event in the U.S. will occur shortly and as part of a new launch for BREO in the U.S. We believe this new indication could provide a significant sales catalyst as asthma affects nearly 19 million adults in the U.S. We are supportive of these actions by GSK and believe they will have significant positive effect on the prospects to our portfolio. Outside the U.S. we continue to see volume growth as well. For example excluding the impact of Q4 stocking associated with the ending of Ryotan restrictions on BREO and currency fluctuations, net sales were up significantly in Q1. Additionally during their call earlier today, GSK forecast up to 16 new market launches with our products this year. As we have discussed before we can expect some lumpiness in reported net sales on a quarter-over-quarter basis as we are still early in the growth phase of our products and new country launches, normal wholesaler inventory fluctuations and currency movements may continue to influence our quarterly results. Looking forward, the next major 2015 catalyst for BREO is the SUMMIT study which evaluates the impact of BREO on all cause mortality in 16,000 patients with preexisting cardiovascular risk factors. We expect SUMMIT to readout in the second half of the year. If the results are positive this could be a significant differentiating feature compared to other LABA ICS products in the treatment of COPD and support the future use of BREO in this patient population. We remain optimistic in the long-term growth drivers for both products, these drivers include the recent approval by the FDA of the asthma indication, the potential for approval and launch of both products in additional countries, further optimization of the ongoing commercial activities especially in the U.S., the results from the SUMMIT mortality study with BREO expected in the second half of the year and results from the Salford Lung Study in 2016. Throughout the rest of the year, we will continue to work closely with our partner GSK as we pursue our goal of optimizing the growth and commercial success of both BREO and ANORO across the globe. I'll now turn the call over to Eric who will review our first quarter 2015 financial results. Eric.
- Eric D'Esparbes:
- Thanks, Mike. Before I present our Q1 financial results, I want to remind you that as a result of the separation of Theravance Biopharma from Theravance, Inc in mid 2014, there have been a number of adjusting entries to prior period that reflect the financial impact as discontinued operation accounting. This will result in limited comparability between Q1 financials, our previously reported results and our future operating results. Total revenues for the first quarter included $10.1 million of royalties earned and $0.2 million of revenues from collaborative arrangements offset by $3.5 million of amortization of capitalized fees from a related party. Royalty revenues earned include $9 million for BREO and $1.1 million for ANORO. As Mike stated earlier, while prescription trends for RELVAR/BREO and ANORO are continuing to show positive weekly growth during the first quarter, this growth was offset during Q1 by a few factors some of which we've discussed in our February call. First we experienced a widening growth to net spread reflective of improved coverage at lower net pricing especially with express script CVS Caremark and an extended coupon program by GSK. Both of which we view as important investments in the success of BREO and ANORO. Second Q4 2014 sales for RELVAR in Japan were higher associated with inventory stocking of one month dosage form due to the end of the Ryotan restrictions. Finally, we experienced foreign exchange headwinds related to the appreciation of the U.S. dollar especially against the euro as the appreciation of the U.S. dollar reached up to 20% in some markets across the globe from the previous quarter. Our operating costs decreased during the first quarter due to the completion of the transaction – transition activities following the separation of Theravance Biopharma. Total operating expense for the first quarter of 2015 were $6.2 million compared to $7.2 million in the fourth quarter of 2014 a decrease of $1 million. Sock based compensation expense was $1.9 million in the first quarter of 2015. We maintain our guidance level for our operating expenses composed of R&D and G&A costs before stock based compensation accruals in the range of between $17 million and $19 million for the full-year 2015. Cash, cash equivalent short-term investments, and marketable securities totaled $255.1 million as of March 31, 2015. For 2015 we will begin reporting adjusted EBITDA as a financial metric, we believe this metric is useful in assessing the contribution to our quarterly liquidity position coming from our operating activities without regards to financing methods, capital structure or non-cash charges. A reconciliation of the metric is included in our earnings press release. For the first quarter of 2015, we generated an adjusted EBITDA of $6.2 million compared to an adjusted EBITDA of $5 million in the fourth quarter of 2014. This increase in a cash generating ability of operations, results from a combination of steady royalty revenues and a continued optimization of our cost structure as a royalty management company. We believe our financial position is strong and remain comfortable with our current level of capital return to our shareholders, which we are maintaining through our second quarter dividend of $0.25 per share payable on June 30, 2015. And now I would like to turn the call over to Mike for final closing comments.
- Michael W. Aguiar:
- Thank you Eric. In summary I'm pleased with the progress of our programs and on increasing volume and getting approval for Asthma in the U.S., our primary focus for the remainder of 2015 will remain on maximizing the value of our base businesses collaboration with GSK. This includes working with GSK to optimize the commercial success of both BREO and ANORO and continuing the global rollout of both products. We're encouraged by the approval of BREO for asthma in the U.S. the recent commercial trends of both products and remain optimistic about the future prospects of Theravance. I would now like to turn the call over to the conference facilitator and open up the call for questions.
- Operator:
- Thank you sir. [Operator Instructions] And our first question comes from Tyler Van Buren of Cowen and Company. Your line is open.
- Tyler Van Buren:
- Hi. Thanks for taking my question. I guess, just on the strategic front, in terms of the various strategic potential options that you are considering in terms of bringing in additional royalty streams, clearly that seems like a long term opportunity, but at what point in time, in the inflection of these launch curves from a financial stand point, do you all become comfortable enough to start examining those opportunities, if you are not already, and is the potential redomiciling still in the works? Are those two related, as well as potential other royalties in the future, heard an update from Glaxo this morning on the Close Triple we’re just hoping you could confirm timing on that program, as well as the vilanterol monotherapy program. Thanks so much.
- Michael W. Aguiar:
- Great. And thanks for the question, Tyler. There is few things to talk about here. So no updates on the Closed Triple or on vilanterol, Closed Triple, as I think everybody knows is in the middle of the Phase III program, there are a number of studies underway, the results from the totality of that probably are not due here for a couple of years yet at this point. So no updates on either of those. With regard to our prioritization, what we working on, again the most important thing we can do right now, is continue to make progress with GSK on our base business. I think in one of the calls, when we first completed the separation, I laid out the priorities, number one was to get the company set up for public company status, I think that is done; number two was to work to optimize the value of the base assets we have with GSK. I think there is a lot of progress that’s been made as we reported today, as GSK reported, lots of changes whether they are increasing volumes, changes in the U.S. organization et cetera. So a lot of progresses has been made there. The third priority in the list of priorities we have was looking at additional assets. There are certainly things we have looked at, we’re being more opportunistic than anything, but that is really to one third of our priorities at this point in time. So if the right opportunity came up tomorrow, we will certainly look at it. I would say that the hurdle is pretty high for us, we certainly are not looking to do a deal just to do a deal. Anything that we ever do, would have to be really a terrific opportunity. The last question you had asked about was redomiciling ultimately comes now to tax rates. So as everybody knows we are a U.S. corporation, we are subject to U.S. taxes, not California taxes, but U.S. taxes, and today we have approximately $1.1 billion dollars of NOLs, that would be used to shelter those over time. So if again, the right opportunity came up we are always looking to optimize the overall cost structure of the business so we will certainly consider things if it came up. There is nothing that’s in the works at this moment in time and we are not in any imminent danger of paying taxes due to the substantial NOL balances out there today. So I think I have hit on all the points, is there any other thing, Tyler, I missed in your question asked?
- Tyler Van Buren:
- No, that was great. Thanks so much.
- Michael W. Aguiar:
- Great. Thanks, Tyler.
- Operator:
- Our next question comes from Ronny Gal with Bernstein. Your line is open.
- Aaron Gal:
- Good afternoon. And thank you for taking my question. I got two. First one is regarding Advair detailing, can you just, I don’t know what GSK said on the call today, do we know if GSK will continue to detail Advair in parallel to BREO as essentially the focus is shifting essentially completely or near to detailing BREO. And second, higher gross to net adjustment still don’t speak very clearly to what you might want to call just realized profit or net profit. So if you kind of look at the projection going forward couple of years that you’re working on with GSK, should we think about the realized price of BREO and ANORO as being flat, increasing or decreasing.
- Michael W. Aguiar:
- Thanks, Ronny. So on the Advair question, there are changes that are happening here but I really would like to punt that back over to GSK, since that’s an Advair question as opposed to a BREO question. The important announcement today was the creation of these separate groups, particular, a BREO salesforce and an ANORO sales force, which obviously is something we’re pretty supportive of; if you have a rep with a relatively short time with a doctor and there is a question in your mind about what’s the priority or what the messaging, right, this clears that up a lot. So I would just say we are quite pleased with the changes we’re aware of, I really wouldn’t want go into much more detail beyond that particularly for something like Advair and would have to punt that one back to GSK. So on the second question, higher gross to net again there is a fairly complex answer to this. As I think a lot of folks in the call we had talked about this last quarter where there was an increased level of couponing that was going out and this was really targeted at dealing with a physician perspective that coverage was not as good as the actual reality of coverage was and this was an investment we chose to make to close that loop. And I do think based upon the market research we’ve done that that has been pretty successful and it is not a major barrier today that we perceive in terms of prescribing BREO. So when you think about couponing programs obviously that increases gross to net for a period of time when the couponing program is over one would expect the gross to net to close relative to that piece there, so I don’t view this today as a permanent program, but we will continue to monitor that one and see how that goes along. On the longer term I really wouldn’t want to get in front of predicting where prices go; there was clearly some price movement that happened last year in particular with regard to the two that we’ve called out, Express Scripts, CVS Caremark, probably the majority of that worked its way through at this point into the first quarter here, we will see where things go. It has been a little tougher pricing environment here in the U.S., we talked about that a couple of quarters ago, but I would just say we internally adjusted our models more than a year ago at Theravance here that things would be a little bit tougher and I think we have really changed much in our internal models since that time because we did anticipate that it will be a little bit tougher. So we will see where things go out there. I think I'm pretty comfortable with our models regarding that and even regarding assumptions around generics, I know there was some level of discussion on that today on the GSK call, but again Theravance has been pretty, pretty consistent over the last five or six years that our thought was it was more likely not going to be a generic here in the 2016 timeframe and again we've had that in our model for a long time. So we are not adjusting anything at this point in time relative to future pricing or relative to generics.
- Aaron Gal:
- Okay. So I'm going to ask you one more question about projections. So GSK have given long term projections for the respiratory franchise saying that they will globally in 2020 equal the 6 billion pounds that came in 2014, but that will be spread across more products, so essentially nine products contributing as opposed to being primarily Advair. The question that I have for you is primarily are BREO and ANORO still the hallmarks of that GSK 6 billion pounds or should we think about them being equal in size to the other seven products in that portfolio?
- Michael W. Aguiar:
- Again I couldn’t make comments on every product in that portfolio, I think our view here at Theravance has been in the spaces where we play and I am very distinctly not including something like single agents steroids because we don’t have a product in that particular mix and I wouldn’t know how GSK has reflected that in their mix or not. But in the space that we play with GSK which is largely the LABA ICS space and again in the bronchodilator space, I think that the three programs that we have that are either approved today or that are in Phase 3 so you would add to that the close triple, those probably occupy the disproportionate amount of what we see as the opportunity set, today as you think about guidelines, as you think about treatment paradigms et cetera those are really the three combinations that have more likely not the potential to be disproportionate contributors. So I wouldn’t be able to make a comment around the entirety of their nine fit products that we would not even be playing in that space but our view here for quite a while has been the combination products rather than single products are going to ultimately be the biggest players in these spaces and if you look at something like guidelines it would really point towards one of those three products or all three of those products has been the likely contributors to that. So we will see where things go certainly in the short term here and the short term on the finance before the triple potentially comes to market which is several years down the road, I think our view is that BREO and ANORO have the highest probability of being the biggest contributors in that group.
- Aaron Gal:
- Okay. Thank you very much.
- Michael W. Aguiar:
- Thanks Ronny.
- Operator:
- Thank you. Our next question comes from Gena Wang of Leerink Partners. Your line is open.
- Gena Wang:
- Thank you for taking my question. So for both BREO and ANORO U.S. sales its seems like the reporting number much less than what that implied sales, so just wondering in addition to widening gross to that with their significant inventory destocking in 1Q?
- Michael W. Aguiar:
- Hi, Gena, it’s Mike. I wouldn’t want to make any specific comments that are too direct on that one. There clearly as always some level of inventory movement. The [Indiscernible] of course IMA is on place among all the major players which limits the movement around but there is always something that is going on at some levels just, normal inventory fluctuation. So there was probably something there. I think that as we described here you would expect normal, kind of year-over-year, quarter-over-quarter inventory fluctuates, going to be some small portion of it to date early in launch has the potential to be perhaps little bit larger then later in the launch. And the addition to that there was a couponing program, that was started here and my opinion is pretty successful so far, that was certainly a measurable contributor to that an then you have some of the recent changes that have happen with the additional coverage that kicked I mean for example, the BREO coverage is kicked on January 1 and typically what you do when you have new coverage as you have to adjust your estimates for sales throughout in the channel things like that. So there were number of moving pieces, I’m not sure I would in any one particular went down on all of those and the end of the day what we really view as the most important metric is scripts. We had talked about the growth from the widening for period of time as some of this working through and you seen that happen now. I think our expectation is looking forward that will start to narrow back up again particular the couponing program works its way through.
- Gena Wang:
- Okay, and just one to confirm, I think coupon will not be captured by on as right.
- Michael W. Aguiar:
- No, it would be captured by them. So my belief is that IMS is capturing all the prescriptions that are written in a coupon is used to pay for a prescription, was not captured our samples and we talked before samples are significant portion of volume is out there today but those are not captured volume IMS.
- Gena Wang:
- Okay, so for the ex-U.S sales BREO revenue in Europe, it seems to have big increase from 9 million pounds last quarter to 16 million was the increase mainly due to geographic expansion were due to inventory stocking.
- Michael W. Aguiar:
- Yeah, I’m not aware of any particular inventory stocking is out there, what is happening of course is we are continuing to roll out and to what you tend to see is country ex as they initially that will be in a initial inventory stocking and that’s a very typical. I talked about another up to16 country rolls ups certainly happening later this year, obviously you are getting smaller and smaller counties, each one of those have initial stocking associated with it. I think probably the bigger piece just was continued growth and expansion in the markets over, so that is one piece of what’s happening and then of course you saw a decrease happening in Japan and that really was reflective of the initial stocking that happened in Q4 related to into the [Indiscernible] restrictions, so what the channel had to do was to put enough of 28 day supply out in the market to meet the new demand and the Japanese subsidiary is doing a pretty good job. They’ve got a very nice business over there and so there was some initial stocking with there and that’s why you saw sales little bit here and this quarter was just clearly reflective of stocking that went in place and then a very nice business and is continued to do well over there, as based business.
- Gena Wang:
- Thank you. And I have two more questions for Eric. So may be instead of asking you will you maintain current dividend policy, want to ask you what condition will make you reduce current $0.25 to quarter dividend.
- Michael W. Aguiar:
- Yes so I will probably refer to something that I had mentioned in the prior quarter earnings call and if I recall I think Gena, what probably one of the questions you had asked as well is we’ve set up a dividend policy on the basis of a forecast, we call it dividend forecast that we had established early last year and as long as our sales trajectory remains above that forecast, we think to the math works that we are in a position to maintain the capital return level that we currently have. So currently we are above that forecast, we feel comfortable with where we are and again we are really pushing for volume increase initially which will ultimately translate into earnings to cover those [indiscernible] obligations. So right now we feel comfortable.
- Eric D'Esparbes:
- I would add is, of course if we saw those two slops converging at some point in time, then, of course we would have conversation around it. So I don’t think it would be case that we will get down to the last nickel before it dawned on us to something was going on. So we feel pretty comfortable today. Obviously, we watch that closely because it is important to us, but it is a relatively early warning signal that you would theoretically see these slops converging and see that ahead of time before there was a big issue.
- Gena Wang:
- Okay. So my last question is the stock option for SG&A. This quarter seems a little bit high versus last quarter, would this be the benchmark we should think of for the remaining of 2015.
- Michael W. Aguiar:
- Is the question about total effects or a stock based compensation?
- Gena Wang:
- It’s stock base compensation.
- Michael W. Aguiar:
- Right. It really is a function of grants and accruals, we’ve viewed a stock based compass of non-cash OpEx, so at the end of the day, it really follows the cycle of grants and accruals. So from that perspective, we can’t make any specific forecast on this one, which is why we gave guidance for OpEx for the year before stock based comp especially for that reason.
- Gena Wang:
- Okay. So maybe I will ask like, is that 1Q usually the time you would issue the stock option?
- Eric D'Esparbes:
- So yes, when you have new issuance, you have additional accruals that add up. But then it is spread out over divesting period. So that’s the – if you wanted the basic mechanic of those accruals.
- Michael W. Aguiar:
- Yes Gena, I would just add one of those things, so Eric, exactly correct, if you could spread out over period of time but there is some lumpiness to it and portions of that related to the separation. So that’s why we are being a little bit increased size in this because there will be some lumpiness this year and if not because our stock option are down, it’s due to some corks of win we did the separation here. So again, I would just expect a little bit of lumpiness here and it’s not going to be anything other than again non-cash compensations.
- Gena Wang:
- Okay. Thank you.
- Michael W. Aguiar:
- Thanks.
- Operator:
- Thank you. Our next question comes from Brian Skorney of Robert W. Baird. Your line is open.
- Brian Skorney:
- Hey, good afternoon, guys. Thanks for taking my question. I guess just when we start thinking about modeling out the launch in the asthma indication for BREO. How we should think about formulary restrictions given other some segmentation in the asthma market between kids and adults and the label is only adults. Could you just walk through kind of your expectation of how access to formulary can still be negotiated despite the divergence between your label and as say Adware [indiscernible] on the courts.
- Michael W. Aguiar:
- Thanks, Brian. I don’t expect to have any particular issues on reimbursement, we’ve got the existing reimbursements in place, reimbursement typically as a product – by products reimbursement as opposed to an indication or an age category or whatever. So I don’t expect to see anything on that. That being said, of course, we are clearly not going to be out promoting this for in the age category that’s not in the label or anything like that. But I just don’t expect that that’s going to result in restriction, we have the coverage we’ve got, and the coverage is in place today so the good news is unlike when we launch in COPD we are not starting from 0. We are starting from the mid-70s and up for BREO for example so I think we are feeling pretty good about the overall coverage is out there. And then last point again is the age group that we have covered is greater than 90% of the total volume of LABA ICS prescription that are written for asthma in the United States anyways. So we’ve covered the vast majority of patients with our label. So I don’t expect to see any particularly hiccups on that I suppose something could happen somewhere. But we are just not expecting any big drama around that.
- Brian Skorney:
- And I guess just to jump off from the share announce mode, do you have a feel for what the breakdown in terms of patients new to all therapies, what were percentage of adults versus kids?
- Michael W. Aguiar:
- I don’t have at the top of my head, we share a good number for you, I don’t have that information in front of me.
- Brian Skorney:
- Thanks guys.
- Michael W. Aguiar:
- Thanks Brian.
- Operator:
- Thank you. [Operator Instructions] Our next question comes from Stephen Willey of Stifel. Your line is open.
- Stephen Willey:
- Yes thanks for taking the question. Just kind of wondering I guess if you look at where commercial BREO reimbursement is at this point I think CSK was around 65% as of the end of the quarter just kind of wondering if maybe kind of look at those plans whereby you made still not be covered or covered with kind of non preferred I am just wondering if those plans are expected to conduct reviews either on the buy annual kind of June, July timeframe or towards the end of the year, and I guess does that having label now somehow facilitates that process in terms of either care jumping or getting coverage, thanks.
- Michael W. Aguiar:
- Yes I don’t have any specific forward-looking statements on where we are going to be with coverage and you are correct about the numbers that you had noted around 55% commercial, this is really gave me the hard one the items we talked about a little bit earlier which was couponing because of that program I don’t expect to see a significant impact on coverage meaning patients who are getting rejected because again, patients should be able to get in with these coupons so where we continue to work on improving coverage improving tearing all that’s the year, yes, I don’t think I have a singular answer of what are all these other companies are that we haven’t got coverage lift whether they are on a middle of June, July cycle or something else I think again answers are all over the place. But I don’t really expect to see any big issues around coverage on a commercial at a Part D again in deed we have done some market research area, at Theravance and that issue is cropping far, far frequently today and then it was before and so I think we are feeling pretty good about the overall coverage status of the products at this point in time.
- Stephen Willey:
- Okay. Thanks.
- Michael W. Aguiar:
- Great. Thanks, Steve.
- Operator:
- Thank you. It appears we have no further question on the phone. I’d like to turn the conference back over to Mr. D'Esparbes for closing remarks.
- Eric D'Esparbes:
- All right. Thank you very much, operator. And thanks everyone for participating. Just to mention we will be participating at the BOMA Healthcare Conference next week and Mike will be presenting so hopefully we look forward to see some of you over there. Have a great day.
- Operator:
- This does conclude the conference for today. We thank you for participating. You may now disconnect.
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