Vertex Pharmaceuticals Incorporated (VRTX) Q3 2018 Earnings Report, Transcript and Summary

Welcome to the Vertex third quarter 2018 conference call. This is Michael Partridge, Senior Vice President of Investor Relations for Vertex. Tonight, we will review our financial results, our continued progress to develop new medicines for all people with cystic fibrosis and recent advances in our research and development pipeline. Dr. Jeff Leiden, Chairman and CEO; and Ian Smith, Chief Operating Officer, will provide prepared remarks this evening. Stuart Arbuckle, Chief Commercial Officer; and Dr. Reshma Kewalramani, Chief Medical Officer, will join us for Q&A. We recommend that you access the webcast slides on our website as you listen to this call. This conference call is being recorded. A replay will be available on our website. We will make forward-looking statements on this call that are subject to the risks and uncertainties discussed in detail in today's press release and our filings with the Securities and Exchange Commission. These statements including, without limitation, those regarding Vertex's marketed CF medicines, the ongoing development and potential commercialization of our triple-combination regimen for cystic fibrosis, Vertex's other programs and Vertex's future financial performance are based on management's current assumptions. Actual outcomes and events could differ materially. I will now turn the call over to Dr. Jeff Leiden.

Thanks, Michael. Good evening everyone. I'm pleased to say that, we have made tremendous progress across our business in 2018 and are well on track to achieve the key goals that we outlined to start this year. In CF, approximately half of all patients are now eligible for a Vertex CF medicine and we're progressing rapidly toward the development of a single medicine to treat any CF patient with one or more F508del mutations, approximately 90% of all people with the disease. In our development pipeline, we have initiated the first clinical study of CTX001 in beta thalassemia with our partner CRISPR Therapeutics and are progressing VX-150 for the treatment of pain. And in research, we're preparing to advance the first of our potential medicines for alpha-1-antitrypsin deficiency into clinical development by year-end and to move other molecules into development in 2019. First, to our recent progress in cystic fibrosis. CF is a progressive multi organ disease with its presence from birth and a key part of our strategy is to treat patients as early as possible to slow or prevent the progression of disease. To that end, we gained important approvals throughout 2018 that now allow us to treat eligible children as young as one year of age with KALYDECO and as young as two years of age with ORKAMBI. With SYMDEKO demand continues to be strong following the U.S. approval in February. The launch of this medicine in the U.S. has been a significant driver of revenue growth in 2018 as new patients initiate treatment and we also plan to submit a supplemental new drug application to the FDA later this year to gain approval in eligible patients as young as six years of age. In Europe, we anticipate approval of this medicine before the end of this year, which will further increase the number of patients eligible to be treated with the medicine for the underlying cause of their disease. We've also reached multiple important reimbursement agreements across the world, to provide access to ORKAMBI, enabling patients in many countries to treat the underlying cause of the disease for the first time. Many of these agreements, including those recently signed in Denmark and Australia, also provide a pathway to access and rapid reimbursement for certain future CF medicines. Importantly, these portfolio agreements provide certainty to patients that they will have immediate access to future innovations in CF from Vertex. We remain in discussions regarding this type of agreement in other countries, but have yet to reimburse ORKAMBI. We're also rapidly progressing our two Phase 3 programs, evaluating two different triple combination regimens that include a next-generation corrector either VX-659 or VX-445. In September, we completed enrollment of the two Phase 3 studies for the VX-659 triple combination regimen and expect data from these studies in late 2018. We expect to complete enrollment for the VX-445 Phase 3 studies this quarter and to report data from these studies in the first quarter of 2019. We will evaluate data from both programs with the goal of choosing the best regimen to submit for regulatory approval. We remain on track to submit a new drug application for a triple combination regimen no later than mid-2019. In parallel, we've also recently initiated studies of both of our triple combination regimens in patients ages 6 to 11 years of age with the goal of gaining approval for this group of children as quickly as possible. We also continue to innovate in CF to develop even better regimens for the future, including potential once-daily triple combination regimens with our potentiator VX-561 and regimens to contain other next-generation correctors that may have enhanced profiles. We expect to advance one or more of these novel next-generation correctors into early clinical development in the coming months. Beyond CF, our research strategy is well-defined and focused on the development of transformational medicines for serious specialty diseases with large unmet medical need. And we're advancing a portfolio of such potential new medicines into the clinic. The diseases we are targeting all have well understood biology where we can use or create early clinical markers that support the potential for transformative benefit and rapid development timelines. We are establishing proprietary scientific insights into a number of these diseases just as we did in CF and CFTR and we are bringing significant resources to bear to both advance our development stage assets and also to bring other potential new medicines from research into early clinical studies. With our partner CRISPR Therapeutics, we're advancing CTX001 as the first gene-editing treatment for both sickle cell disease and beta thalassemia using the CRISPR/Cas9 technology. This is a cutting-edge transformational technology that holds great promise in the treatment of many diseases and we're pleased with the rapid progress we are making together with CRISPR toward dosing the first patient with the CRISPR/Cas9 gene-editing therapy. Our pain program is another example of Vertex's innovative science translating to the clinic where Phase 2 data generated to date for VX-150 provided the first clinical validation for the sodium channel 1.8 mechanism in the treatment of acute and chronic pain. We expect that Phase 2 results for VX-150 in the third type of pain, neuropathic pain, in early 2019. We now also plan to initiate a Phase 2b dose-ranging study of VX-150 in acute pain following bunionectomy surgery that has the potential to support future pivotal development of this medicine in acute pain. Acute pain represents a multibillion-dollar opportunity where many of the conditions that lead to acute pain are treated by physicians that can be reached with a specialty sales force. Given the significant need for highly efficacious pain medicines that do not have the addiction, tolerability, and abuse issues associated with opioids, acute pain is an opportunity that is well-suited to inhibitors of the NaV1.8 sodium channel and we're also continuing to invest in the discovery of other potential pain molecules including additional NaV1.8 inhibitors as well as medicines targeting other new mechanisms. We're also advancing a portfolio of small molecule correctors for the treatment of alpha-1 antitrypsin deficiency or AAT and I'm pleased to report that we expect to move the first of these compounds into clinical development later this year. There are many similarities between AAT and CF both in the biology of the disease and how we may target its cause and in the potential to establish early clinical proof-of-concept and rapid development pathways for new AAT medicines. Like CF, AAT is a protein folding disorder caused by mutations in a single gene where more than 90% of patients have one common mutation that results in life shortening systemic complications primarily in the lung and also in the liver. We believe our scientific expertise in CFTR protein folding coupled with our development experience position us well to rapidly advance our novel small molecule approach to the treatment of AAT. I look forward to updating you on this program as we enter development later this year and to providing additional insight into our research programs, including those in focal segmental glomerulosclerosis and others as they progress in 2019. As we move our internal R&D pipeline forward, we're also continuously evaluating external opportunities, where our research and business development strategies are fully aligned. With our strong financial profile, we have increased ability to in-license or acquire assets or establish scientific collaborations that provide access to unique product opportunities and technology platforms. We've completed a number of such transactions in recent years and we have expanded our internal team devoted to finding and evaluating potential opportunities for scientific innovation with the goal of further broadening our pipeline and scientific expertise in the future. We believe that it is the combination of our R&D strategy with our business model that truly differentiates Vertex as a biotechnology company with the potential for highly profitable long-term growth based on a portfolio of transformative medicines for multiple serious diseases. This year has been marked by significant progress across research and development and in our efforts to bring our CF medicines to more patients globally, which has led to significant growth in our revenues and earnings, which Ian will now discuss in more detail.

Thanks, Jeff, and good evening to everyone. I'm pleased to review with you our third quarter 2018 financial results and to discuss our outlook for future financial growth as we approach 2019. Revenues first. Total CF product revenues of $783 million in the third quarter of 2018 represent a 42% increase compared to the $550 million we recorded in the third quarter 2017. We continue to see significant revenue growth as we increase the number of patients treated with our medicines globally. The third quarter included $255 million in revenues from the launch of SYMDEKO in the U.S., which is the primary driver of the rapid growth in our total CF revenues. Demand for SYMDEKO remains strong and we continue to receive positive feedback from patients and physicians and strong coverage for SYMDEKO across both public and private payers. Similar to prior quarters, demand for SYMDEKO has come from all groups of eligible patients, F508del homozygous patients initiating treatment for the first time, patients who discontinued ORKAMBI coming back to initiate therapy with SYMDEKO, and also patients switching from ORKAMBI to SYMDEKO. Our third quarter 2018 non-GAAP combined R&D and SG&A expenses were $379 million compared to $334 million in the third quarter of 2017. This increase was primarily due to the advancement of our portfolio of triple combination regimens for CF and the investment to support the treatment of patients with our medicines globally. Non-GAAP net income for the third quarter of 2018 was $282 million, with an earnings per share of $1.09, compared to non-GAAP net income of $136 million, with an earnings per share of $0.53 for the third quarter of 2017. Our non-GAAP net income and EPS has more than doubled compared to last year, largely driven by strong growth in the total CF product revenues. We ended the quarter with approximately $3.1 billion in cash, cash equivalents, and marketable securities compared to $2.1 billion at the beginning of this year. Today, we also reiterated our guidance for total CF product revenues of $2.9 billion to $3 billion and for combined non-GAAP, R&D, and SG&A expenses of $1.5 billion to $1.55 billion. I will close with a few comments on our expectations for future financial growth and how we anticipate providing revenue guidance next year as well as how we may start to record non-cash tax charges. We have already created a strong financial profile for our business, and we anticipate that our revenues will continue to grow next year. In 2019, revenue growth will be based largely on the impact of SYMDEKO and SYMKEVI launches, the impact of labor expenses across our CF portfolio, and the recent completion of multiple reimbursement agreements. The timing of further revenue growth from countries where we do not currently have reimbursement for ORKAMBI is unpredictable. Therefore, when we provide 2019 guidance for total CF revenues early next year, it will be based only on the geographies where we have established reimbursement agreements at that date. If we gain additional reimbursement agreements in 2019, we will update you on our guidance as appropriate. This is consistent with how we provided guidance at the beginning of 2018. Beyond 2019, continued revenue growth will be driven largely by the potential approval and launch of a triple combination medicine for the large group of patients with one minimal function mutation and one F508del mutation who are not eligible for our currently approved medicines. Now to taxes, I'll note that in 2019 we may begin recording a non-cash tax provision at an effective tax rate in the low to mid-20s as a result of the improving profitability of our business and our future strong financial outlook. The vast majority of our tax provision would be a non-cash expense until we fully utilize our net operating losses. This will be further discussed in our 10-Q filing. The financial profile of our business is strong, and the coming year will be an important period to define our future growth as we obtain Phase 3 data from our triple combination regimens for CF, provide access to each of our CF medicines to more patients globally, progress multiple new medicines in development, and also to advance new approaches for the treatment of serious diseases from research into development. I look forward to updating you on our progress. With that, I will open the line to questions.

And our first question is from Phil Nadeau from Cowen & Company. Your line is now open. Phil Nadeau - Cowen & Co. LLC: Good afternoon. Thanks for taking my question and congrats on the progress. Just two questions for me, one on completion and one on the financial guidance or financial comments that you just made. Ian, in your comments, you talked about 2019 sources of revenue growth. Can you specifically talk about the revenue growth outside the U.S., which I know you said was unpredictable, but which countries could be drivers of growth where you recently got expansions? Which ones are possible for next year and which ones are total wild cards?

Thanks for the question, Phil, and thanks for the comment on the good quarter. I do want to replay some of the comments I just made, which is that when we think about 2019, first of all, we see 2019 as being a continued growth year for our revenues. When we look over the previous years and we look over future years, I think what we're seeing here is we're treating more patients or treating more patients globally, and therefore, that's driving our revenue line year on year and into the future, and so it's a really nice profile. As we think about more proximately in time and we think about going from 2018 into 2019, we should continue to see growth even without reimbursement outside the U.S., and that growth would be driven by the continued launch of SYMDEKO in the U.S. and getting a full year's contribution for patients that are on drug. But then also outside of the U.S., SYMDEKO, which is known as SYMKEVI outside the U.S., is also launching into certain markets where it is already reimbursed. So we see baseline growth from already approved geographies. More specifically to your question, as in where the geographies that we could anticipate or possibly attain reimbursement approval, to have an impact in terms of growth on our revenues, it would have to be those larger markets. And principally, those would be either the UK, France, or Canada. I do want to replay, though, that this is unpredictable in terms of timing, and in particular, in the UK, which is probably the – it is the second largest CF market. If we are to obtain reimbursements over there, then we are launching the drug from anew, so we're in a launch curve in the UK. It's not that we're just switching on a large pause of revenue. We have to launch the drugs in the UK. We continue to make good progress with discussions with all three of those countries. However, resolution, whether it is in 2019 or whether it's in 2020, we'll update you as we progress. Phil Nadeau - Cowen & Co. LLC: That's really helpful. And then second on competition, after the close today, Galapagos NV had a couple announcements, some new data as well as a change to the collaboration, and Proteostasis recently announced some data for their programs. I'm curious to get the team's updated thoughts on competition from those two parties. How real was it? What do you see as the strengths and weaknesses?

So this is Jeff. Thanks for the question. As you know, we don't typically comment individual competitors or data. I think actually the data sort of speaks for itself. But what I would like to comment on is sort of how we view our competitive position and our data and sort of where we are in the process. And I think we've learned a lot over the last year. In fact, I think our competitive position has improved over the last year significantly. One of the things we've learned is that it's going to be a world of triples, and it's going to be a world of triples pretty quickly. And the reason for that is that in order to really get to all patients, particularly to have men patients who are so difficult to treat and to maximize benefit for the homozygous patients, it's pretty clear now that you need a triple, any company needs a triple. And that doesn't only mean you have three components. It means you have three medicines that can be combined, co-formulated, that have the right PK that can provide really superior efficacy, and I think the bar in efficacy has gone up very significantly and we'll talk about that in a minute. And also important is that they're tolerable and safe. These are medicines that kids are going to take for the rest of their lives. And we learned a lot about our regimens in that regard in the last year. We know that we have two different triple regimens that are now have been in hundreds of patients. They are co-formulatable, they do have the right PK, they raised the bar in efficacy very significantly into the double digits for -- to have men patients and into the mid double digits for the homozygous patients, that's going to be the bar, I think, for the future. And most importantly to us, we're well into our Phase 3 trials, which are enrolling ahead of schedule to the point where we're very confident we'll be able to file one of those regimens no later than mid next year, which would allow us to launch those drugs and get patients on them pretty quickly in the coming years. And so I think from our perspective, we like where we are, we have multiple options and most importantly, we have clinical data both on efficacy and on safety with these drugs, which is a high bar, frankly. Phil Nadeau - Cowen & Co. LLC: That's helpful, thank you.

Thank you. Our next question is from Geoff Meacham from Barclays. Your line is now open.

Good afternoon. Thanks for the question, guys. I just have a couple. The first one is on the triple selection process, just for the NDA, when you guys think about it, you likely won't have much in the way of mature data on exacerbation benefit on BMI when you pick the regimen so – and that may matter, actually, over the long-term. So, is it just about safety, tolerability in FEV1 or are there other parts of the profile that you think will be impactful that you're looking for?

Geoff, this is Jeff Leiden. You're right. I think that at the point we can pick these triples, the primary data that we'll base that on is FEV1 data and safety and tolerability data as well as the whole profile of these drugs. Remember, we have a lot of preclinical and early clinical data as well. I think the good thing is, is there hasn't been enormous disparity between many of those long-term outcomes and short-term outcomes, and what I mean by that is that, at least, in our experience so far, drugs that have a very positive acute effect on FEV1 and a lowering sweat chloride is significant, acutely have also turned out to have these very profound, long-term effects. And, in fact, as you know, one of the interesting things is that KALYDECO and, say, ORKAMBI, which have a bit different acute profiles, ORKAMBI being less potent acutely, actually have very similar long-term profiles, which suggest that if you can really hit CFTR effectively in these patients, you will get the long-term benefit. So, I think the risk of a disconnect between an acute effect and a long-term effect is rather small. Now, obviously, we will have the long-term effects of both of these drugs within a relatively short period of time, but you're right. Probably not by the time we decide which one to file.

Okay. And just a follow-up for Ian and I know you haven't given a 2019 outlook, but when you plan for OpEx spend, you'll have the triple launch pending the data obviously and then a bunch of new programs and R&D. So, how are you guys thinking about that in the context of also showing some operating leverage?

Hey, Geoff. Thanks for the question. I really appreciate you pointing out that we've got this continued investment and commitment to CF. I just want to cover that because we do sometimes get asked the question whether when we deliver on these Phase 3 trials, are we declining our investment in CF? And I actually we want to maintain the position that we're not. We continue to invest in CF. In fact, those patients that were in our Phase 3 studies roll over to open-label studies. Those open-label studies we have found to be incredibly important because we gather longitudinal data to show the benefit of these medicines longer term. We're also doing studies in the younger patients and so we're able to treat these children at much younger ages of their lives. And so our commitment and investment to CF into these medicines that we believe will be hugely beneficial to them is maintained. So, if you could think about that as a steady state part of our R&D investment and then as we think about advancing our pipeline in other disease areas beyond cystic fibrosis, we are happy to be letting you -- we'll bring you more up-to-date with how we're advancing new medicines into the clinic in these new disease areas that Jeff just referred to earlier. The investment in these disease areas is smaller in magnitude, it's earlier stage, but it is additional investments and therefore, when you compare a 2018 operating expense profile to a 2019 operating expense profile, you should see a relatively small increase compared to the increase we anticipate on the revenue line. So yeah, we do like to anticipate operating to increase. And then one last thing I would say is that you got to remember, we're also launching medicines globally, not just where it's been in the U.S. and therefore, there are launch costs that are being incurred outside of the U.S., not significant because of the nature of the disease and how we can reach these patients with our medicines, but there is investments there as well. So, you should expect to see operating expense margin increase in 2019 compared to 2018, but the key will be the revenue growth which will allow us to continue to generate more cash flow.

Okay, that's helpful. Thanks, guys.

Thank you. Our next question is from Michael Yee from Jefferies. Your line is now open.

Thanks for the question. Congrats on a great quarter as well. On the once-daily, you made a comment that you've had some positive feedback and are moving that forward. Can you just, I guess, clarify the process going forward and why you're choosing gaining mutations as sort of the first move forward and not maybe a broader population? How should we think about that? And then second question was more of a modeling finance question which is that obviously, the triples are advancing forward like you said, but ORKAMBI and SYMDEKO are pretty big franchises. Over some period of time, is that expected conceptually to have those doublet drugs go away and the triple is basically the single line item? How do you think about that? Were there patients that actually would stay on doubles? Thanks.

This is Reshma. Let me start by taking the first part of the question with regard to VX-561. As you know and we've talked about this on previous calls, the FDA had asked us to do additional dose-ranging before proceeding to Phase 3 and part of that request was to study VX-561 across these dose ranges in gaining patients and we've had productive discussions with the agency and we're now at the point where we've designed our study, we've selected our doses, and I expect that this study will get started next year, probably in the first half or so. Stuart?

Yeah, Mike, and on the question of what do we think the triple combinations might do to the doublets, certainly, if we see the sort of results in Phase 3 that we saw in Phase 2 in the homozygous population where, as you know, we saw the triple combinations deliver very, very substantial increases in clinical benefit over and above a baseline of tezacaftor and ivacaftor. If those results hold true, then our expectation would be that the vast majority of patients would be transferred to a triple combination rather than staying on a doublet just given the significant benefit risk improvement that we saw in those Phase 2 studies.

Okay. And just to clarify on VX-561, you have to test it in gaining patients first, but the full plan certainly is to move it into a broader population after that? Is that fair?

You got that right.

Okay. Thanks so much.

Thank you. Our next question is from Robyn Karnauskas from Citi. Your line is now open.

Hi, thanks for taking my question and also congratulations. So I guess let me ask about VX-150. So you mentioned that you're doing a dose-ranging study. Things are already done – some trials and execute. I was curious if this is to get a drug that may be superior to Vicodin since the other doses were just trying to be equivalent.\ And another question on that is like you talked about the acute market, some checks we've done suggest that reimbursement might be challenging there because doctors may just give a cheap generic drug. What has your market told you what has to happen for a more expensive, non-addictive drug to have uptake in that setting?

Thanks for the questions, both good questions. Let me start with maybe your second one and I'll come back to the dose-ranging study, which is pretty straightforward. With respect to reimbursement, you're correct. A large part of the acute market has been genericized and as you know, a large part of that market is actually opioids for acute post-surgical pain, post-dental pain, et cetera. Obviously, we're sitting in the middle of an opioid epidemic and the number one objective that I think patients, physicians, and the government has is to find medicines that have essentially equivalent efficacy with opioids without the abuse potential and the side effects of opioids. We believe that VX-150, based on the data we have so far, has potential to hit that profile. You saw that in the comparative trial that we did. If that's true, we feel that VX-150 is a very, very competitive drug to a generic opioid and with just reasonable pricing, that market is a multibillion-dollar opportunity even if you only capture a portion of it. You may know in the U.S. last year, there were over 200 million opioid prescriptions written, which is a truly astounding number. Obviously, not all of them for acute pain, but a lot of them. So does that answer the question in terms of reimbursement?

Yes, that's very helpful.

Okay. Then in terms of VX-150 -- I'm sorry, go ahead. Did you have another question on it?

No, go ahead. I was just asking about the dose-ranging...

Yeah.

If your does range is higher to maybe sell a superior profile in the acute setting, which may make reimbursement even easier.

Yeah, yeah. So you may remember, the study that we did in acute bunionectomy, it's actually I would call it a proof-of-mechanism study because it was the first time anybody had shown that a NaV1.8 inhibitor could work in acute pain. And so we actually used a fairly high dose there just to make sure that we were getting up to a reasonable exposure. You also know that before you can move into Phase 3, regulators will require you to do a dose-ranging study really to understand two things: one, what is the PK/PD profile of the drug; and frankly, two, what is the lowest effective dose because you always want to give the lowest fully effective dose. And so think of this as just a standard part of the Phase 2 regulatory process where we need to identify the PK/PD profile of the lowest effective dose, and that would then enable us to go to the agency with a plan for a pivotal trial, again, assuming that it's successful.

Right. And second question on alpha or antitrypsin. You mentioned (30:24) efficacy but I do have flashbacks for ORKAMBI I think not correlating with FEV. In this indication, is it more straightforward that if you see a reduction, you're going to see an improvement in efficacy? Help us understand a little bit the disease.

Sure. Sure. Yeah, let me maybe give you a little context on the disease, if you don't mind. It might take me a minute. One of the remarkable things about AAT is how similar – it smells and looks a lot like CF in many, many different ways. It's a genetic disease. It affects somewhere between 60,000 and 100,000 people in the U.S. and probably about another 50,000 to 60,000 outside the U.S. It's caused by one major mutation in more than 90% of people, and it's a protein folding disorder as it turns out, just like CF is, which is a remarkable similarity. In this case, the normal protein, AAT, is made in the liver and is normally secreted into the blood, where it travels to the lung and it protects the lung against autodigestion essentially by endogenous enzymes. So in the disease, the mutant protein has two problems. One, it doesn't fold correctly and accumulates in the liver, and so it causes significant liver disease actually in up to 30% of all the patients. And two, obviously it's not secreted into the blood, so it's unable to go to the lungs and protect the lung. And so if the lung gets autodigested, that means patients suffer from early-onset emphysema. So, that's the disease. The challenge is, for us, was could we make a corrector, a small molecule corrector of AAT just as we had for CFTR that would essentially refill the protein in the liver so it would be secreted from the liver and therefore presumably help treat the liver disease, and more importantly, that would secrete functionally into the blood where it would go to the lung and protect the lung. That was the challenge. It's a very hard problem, I could tell you, biological problem. I think we've cracked that problem now. We've made a series of small molecule correctors that clearly do both of those things. They refold the protein so it's secreted, and it's secreted in a functional form so that it could protect the lung. One of the really nice things in this disease is that there is both a cell or several cell models. And there's also, in this case, an animal model which we didn't have in CF of which the human mutation has been engineered into the animal. And so we've been able to test these molecules both in the cells and in the animals, and they do what we thought they would do. They refold the protein. It's secreted from the cells. In the animals, they produce secreted AAT at levels that would be sufficient to essentially be preventative or curative in the disease. And then the other thing that's very similar to CF is this is a nice biomarker, which is simply the circulating levels of AAT in the serum. You can treat the patients for several weeks and just measure both levels and function of the AAT in the serum. And we know from human experiments of nature essentially that if you have a certain level of AAT in the serum, you don't get the disease. And so we know exactly what we're shooting for here and we can measure it very easily. And so the plan is take this into normal healthies by the end of this year, the first of these molecules, and we have a whole series of them just like we did the CFTR correctors. And that if they are safe and more tolerable, (33:43) once we understand the PK, take them into patients. And again, with relatively small numbers of patients treated for relatively short periods of time, you simply measure AAT in the serum and you know exactly where you are.

All right, thanks a lot. That's helpful.

Thanks, Robyn.

Thank you. Our next question is from Geoffrey Porges from Leerink. Your line is now open.

Thank you very much. I appreciate taking the questions. First, Jeff, you mentioned a mid-teens FEV1 improvement now being the hurdle for triples for competition. Could you give us your sense of what the bar is, the sweat chloride relative and absolute for homozygous and het/mins, so we know how to appraise all these competitors coming along? And then just wondering, Stuart, if you could give us a sense of where you are in the eligible F508del penetration in the U.S. between SYMDEKO and ORKAMBI. You've mentioned that you had quite a few discontinuations in patients who never started on ORKAMBI. And have you caught all those patients up yet, or are you still substantially below the penetration you've achieved with KALYDECO in the eligible population sector?

Geoff, thanks. I'll answer the first part, and Stuart then, of course, will answer the second part. On the first part, I do want to just correct what may have been a misimpression of what I said or maybe I said the wrong thing, but I want to be very clear. I don't think mid-teens is the bar, for instance, for het/min patients. I think the bar that we've set, as you know from the data, is somewhere between 9.8% and 13.8% in our Phase 2 data for het/mins. And for homozygous patients who already have an effect from doubles that we believe (35:33) was around 4%, we showed an additional 9.6% or 10% improvement, which is how I get to that mid-teens. So I just want to be clear that I'm not suggesting 15% is the bar that you need for het/mins to get to be successful. With respect to sweat chloride, I think these are approximate numbers. But I think when you reach sweat chloride that approaches carrier levels, which is our goal, let's say 40 to 50, that's probably the goal that you know you're there with a triple. And so I think those are the two numbers we look at. In most cases but not in all cases, they correlate pretty well. And at the end of the day, as you know, the regulatory endpoint is going to be the FEV1.

Great, thanks.

Geoff, it's Stuart here. Just commenting on the SYMDEKO launch in the U.S., so as you suggested, one of the most important things for us, for SYMDEKO is the ability to get patients who were not being treated by ORKAMBI onto a CFTR modulator, and that was really two populations. One was those who were completely naïve, had never been exposed to ORKAMBI, and we've seen good uptake in that population. And the second population was those who had discontinued ORKAMBI, often because of the respiratory adverse events, and we've also seen good uptake in that patient population as well. We've also seen a number of patients switch from ORKAMBI to SYMDEKO. So we've seen strong uptake in all those patient populations. We're certainly not done with the launch whilst we've seen good uptake, Geoff. We're certainly not done. We haven't flattened out on SYMDEKO uptake in the U.S. yet so we still have some ways to go, but we're certainly pleased with how the launch has gone so far.

Okay, thanks very much.

And, Geoff, maybe just to add one thing that I know you are aware of is we talked about the efficacy side of these triples, but clearly, tolerability and safety is the other side of the equation and long-term tolerability and safety, not one week or two weeks and so I think that's going to be an important thing that we'll all look at as well as these trials progress.

Great, thanks.

Thank you. Our next question is from Terence Flynn from Goldman Sachs. Your line is now open. Terence Flynn - Goldman Sachs & Co. LLC: Hi, thanks for taking the question. Congrats on all the progress. Was just wondering, first, you might not comment on this yet at this point, but just with respect to the triple combo, can you maybe just give us an update on the different inputs you're thinking about with respect to pricing? And then just love your way of thoughts on capital allocation here. I know, Jeff, you made some comments in your opening remarks but could you have $3 billion on the balance sheet? That might be the most you guys have ever had so just curious how you're thinking about that as that continues to grow here into next year. Thank you.

Terence, Stuart here. On pricing for the triples, obviously, much too early to make any specific comments, but we'll be taking into account the same factors that we always do and that will be the magnitude of the clinical benefit that we're able to deliver for patients. It will be the label that we get approved for and that obviously leads into what's the eligible patient population. So those are really going to be the inputs that we take into consideration and obviously, we'll get more information on those in the coming months.

And as far as capital allocation is concerned, it's really interesting. I can tell you that being in the company has invested mainly and it's been about capital preservation for a long period of time in the last three years. We're now a cash accumulator and creator and it's about capital allocation. It is an interesting philosophical change for the company. But I'd like to start by saying that revenue line is the main source of cash and because after that, we then allocate inside the company on our internal programs. That's often not thought about until the capital allocation, but the main source of capital is our revenue line and then we allocate that internally. And as you can hear, in terms of the questions we were asked on operating expense earlier, we still allocate significant amount of capital towards cystic fibrosis medicines, but also now, we're starting to allocate capital to diseases that are beyond cystic fibrosis and we're really happy about that. Some of those opportunities that are beyond cystic fibrosis are our next order of priority, which is we're allocating capital outside the company towards collaborations and towards medicines that we can accelerate into developments and some of the opportunities we have with beta thalassemia and also sickle cell have been a product of a very successful, a nice collaboration with CRISPR Therapeutics and we're really excited to be going into the clinic very shortly with these medicines, both sickle cell and beta thalassemia. And we anticipate that there will be others to follow. The medicines for FSGS, for example, was something that we in-licensed from a very early stage a couple years ago and -- but what it allowed us to do is to really reignite a research effort in that area is now providing the opportunity to go into the clinic in a very short period of time, a very important medicine. So that -- it's a high order priority for us to allocate capital outside the company to do collaborations to give us opportunity with more modalities and more medicines for diseases that we would be interested in. But I would say there is also a consideration for how we may also limit the increase of our share count. Our share count – outstanding shares, does increase year by year based on the issuance and exercise of options and restricted stock. And so we like to think of ways that we may limit that creep in outstanding shares and we've been doing that throughout this year. We did announce earlier this year that we entered in a $500 million share buyback program and we have been buying shares back throughout this year and that's been very successful for us as well and therefore has limited the creep in the outstanding shares, which obviously helps us with a small amount on the dilution. And so that's how we think about capital allocation. It's very important, very close to us, and we're happy that we have the opportunity to prioritize it in this way. Terence Flynn - Goldman Sachs & Co. LLC: Great. Thank you.

Thank you. Our next question is from Alethia Young from Cantor Fitzgerald. Your line is now open.

Hey, guys. This is Ellie on for Alethia. Thanks for taking the question. Just on the earlier status income on the R&D side, you've recently did a deal with Genomics. So could you talk a little bit more about this and sort of how having this particular discovery engine will sort of enhance your R&D efforts?

Yeah. Thanks for the question. We were actually quite excited about that collaboration. As you know, one of the principles of our research effort is to really, I mean, work on what we call highly validated targets. There's really two major ways you validate targets. One is pharmacologically with medicines. That's actually the minority, by the way, and the second is human genetics where mutations either gain a function or loss of function will tell you a lot about the role-specific targets. A beautiful example of that is NaV1.7 and NaV1.8, which were validated by human genetics, obviously, CFTR, et cetera. The collaboration of Genomics, who we believe is the leading small company in the world working on this kind of high throughput human genetics, will allow us to screen for new targets on the one hand through large scale data analysis of human genetic databases. But also, it will allow us to ask questions, for instance, about the potential side effects of hitting a specific target because we can screen the human population for mutation from that the target, which is a loss of function, for example, and ask are those people normal or not until they suffer from any mechanism-based side effects. That's a far a very important thing to know as we begin to pick targets and develop small molecules. So think about it as a way of tapping into the human genetic data resource that both help pick targets and help screen for safety and that collaboration is off to a very nice start in a number of different diseases.

Got you, thanks. And then just another one in terms of early phase development. Can you just talk a little bit more about the preclinical models for AAT? I mean, obviously, with CF, you guys are very successful on optimizing these preclinical models. But could you tell us a little bit sort of about your thoughts on what you think the best preclinical model for AAT and also part of your thoughts on how predictive these models might be? Thanks

Thanks for the question. There's two kinds of models that are generally used. These are not by the way necessarily proprietary to us. One is the set of cell-based models in which either derived from patients or derived from engineered cells with the human gene mutation in them which is the major AAT mutation. And in those cells, the mutant protein is made, it's misfolded, it's not secreted and so one can test molecules on those cells as to do they help refold protein secreted as a function, et cetera. The other one is there is a transgenic model which is actually expresses the human mutant protein. Again that protein is not secreted well. It accumulates in the liver of those mice and one can dose those mice with medicine and then ask if the protein's secreted as a function or what levels do you reach, et cetera. So two very nice models which we feel actually will be highly predictive because they do to actually study the human mutation not some mouse mutation.

Got you. Thanks very much. That's helpful.

Thank you. Our next question is from Ying Huang from Bank of America Merrill Lynch. Your line is now open.

Hi. Thanks for taking my question. First one maybe on, again, competition, we have seen some data from Proteostasis. I was wondering, if you guys have done any work in the lab about the role of amplifier? Do you have any view on that or not? And then second maybe for Stu. Can you tell us by when you might see SYMDEKO pretty much reaching a full penetration in the U.S. market given where you're seeing the market today?

This is Jeff. I'll take the first one in terms of the amplifier. Again, we really don't comment on other people's specific molecules. One of the things that we like about our triple and our correctors are we know that they're quite specific for the CFTR protein which is I think one of the reasons – they're quite selective, if you will, they don't hit other proteins, one of the reasons why they've been so tolerated and so I think as we look at – as you look at other molecules, that issue of specificity and potency is a very important thing to look at.

And then in terms of the SYMDEKO uptaking, obviously, we're very pleased with how it's gone to date. Predicting exactly where it's going to reach full penetration is hard to do, but you can rest assured that when we get the point of giving 2019 guidance, we'll be including our expectations in that how SYMDEKO is going to perform in the U.S. and then also hopefully by then we'll have the approval of SYMKEVI in Europe as well and we'll incorporate all that in our 2019 guidance.

Thank you.

Thank you. Our next question is from Brian Abrahams from RBC Capital Markets. Your line is now open.

Hi, there. Thanks very much for taking my questions. And congrats on all the progress. In NACF data we saw more specifics on the rate of cough for the triple combo. I know these weren't classified as bronchoconstrictions. I was wondering if you can give us any more details on the quality, severity, and duration, and remind us, should we think about this as related to the initial mucus clearance and how it might compare to ORKAMBI? And then just a follow-up on the pain program, obviously, some really interesting Phase 2 data. Wondering if there are ways you might be able to further improve upon the bioavailability and potency of VX-150? And should we assume VX-128 is no longer being pursued? Thanks.

Yeah. Maybe I'll take both of those real quickly. I think the question you're trying to get at with the triple, but correct me if I'm wrong is are we seeing bronchoconstriction as we saw with ORKAMBI, the answer is no. We actually measured that specifically not only in terms of cough or anything else. So we do not see bronchoconstriction with the triple and we did not see it with tez/iva, as you remember. But I think the more important point, Brian, is just looking at the total tolerability and safety profile of these drugs now in a couple hundred patients. What we're seeing is they're quite clean. They look a lot like the earlier drugs. ORKAMBI excepted, they don't have the bronchoconstriction and they've been very well-tolerated and very safe so far. Does that answer your question? I just want to make sure that was the question you're asking.

That's very helpful. I just wanted to contextualize that, yeah.

Yes. And then the other question was about VX-150 and VX-128?

Yes.

So maybe just again, let me take a step back and remind you that the approach that we're taking in pain, actually not unlike the approach we've taken in CF and the approach we're taking in AAT is to create a portfolio of molecules, not one, not single rifle shots, but multiple molecules that have different properties, both with respect to things like potency but also with respect to things like PK biodistribution, drug-drug interactions, et cetera, and then take those molecules forward into early-stage clinical development to understand their profiles more fully. Obviously, VX-150 we have the most data on. We know that it's well-tolerated. We know that it has efficacy, at least at these higher doses, in acute pain and in osteoarthritis, and we'll get a readout on the third kind of pain, neuropathic pain, early next year. VX-128 was a follow-on molecule, if you will, with some different properties than VX-150. We discontinued development of VX-128 in Phase 1 healthy volunteers because it didn't have the PK profile and tolerability improvement that we were hoping to see over VX-150. We have multiple additional 1.8 inhibitors coming behind that, and so you should expect to see us bring other inhibitors into early clinical development, the same way trying to optimize these molecules. Remember, in acute pain, you're going to need molecules that are highly efficacious and also highly safe and highly tolerable. We don't want to create molecules that have liabilities like opioids.

That's really helpful. Thanks so much, Jeff.

Operator, we have time for two more questions.

Thank you. Our next question is from Paul Matteis from Stifel. Your line is now open. Benjamin Burnett - Stifel, Nicolaus & Co., Inc.: Hey, thank you so much. This is Ben Burnett on for Paul. I wanted to ask another question about VX-150. I wonder if you could provide a little bit more color on the Phase 2b study in acute pain. I guess specifically what are you looking for and what is the efficacy hurdle that you need to advance this pivotal program? And then the second question just more at a high level, I guess across these different pain indications, the acute, I know neuropathy is ongoing as well as osteoarthritis-related pain, you have some data there. What is the ultimate vision for this program? And I guess under what scenarios would you want to commercialize this yourself? And is there a scenario where a partner might be involved in that aspect of it? Thank you.

Ben, thank you. I'll take the second part actually first, I'm sorry, because it's a little more strategic. Maybe we'll give you some context and then Reshma will take the first part, which is about the VX-150 Phase 2b trial. I said this before but maybe just to give you some context. We think about pain both from a commercial standpoint and from a scientific standpoint not as one disease but as actually multiple diseases. So an easy way to divide it, for instance, is acute pain. That's the kind of postsurgical pain or dental pain when you have an acute injury. That's one segment. The second segment is chronic inflammatory pain, things like osteoarthritis, lower back pain. A third segment is neuropathic pain. That's pain like diabetic neuropathy. They have different commercial channels obviously, but they also potentially have different pain mechanisms. And so it's important to study them separately because some drugs will work in one and some drugs will work in two, and frankly, some drugs might work in all three. So that's the approach that we've taken with our portfolio. We've done separate trials in acute pain using bunionectomy as the model. We've done separate trials in chronic inflammatory pain using OA as the model, osteoarthritis, and we're doing a third set of trials in neuropathic pain using small fiber neuropathy as the model. And as you know, what we've seen so far, just to remind you, is a high level of efficacy in acute pain, a high level of efficacy in osteoarthritis chronic pain, and we're still waiting to see the data from the neuropathic trial, which is due early next year. So that's where things sort of stand from a scientific standpoint. Now again, if I take a step back, remember that there is a very large need for a new class of pain medicines. There really hasn't been a new class for over 50 years. And the reason is that we have opioids on the one hand, which have high efficacy but are burdened with all of the addictive and other side effects, and then we have drugs like Aspirin, Tylenol, and NSAIDs, which have lower efficacy and also, by the way, have some of their own side effects which are not trivial. And so the target for us is really can we find a new mechanism of pain that approaches opioid-like efficacy without the liabilities, addictive and other liabilities of opioids. And so far, based on Phase 2 data, what we're seeing is yes, NaV1.8 looks like such a target. VX-150 is the first medicine that does look like it hits in both of those two pain indications, and the third one we're waiting to see. And the final part of your question is what about commercializing that. It turns out acute pain, as I said, is a multibillion-dollar opportunity. And at least many, not all necessarily, but many of the channels in the acute pain market can be addressed by a specialty sales force. That's something that we would develop and commercialize ourselves. Contrast that with, say, OA pain or lower back pain, that's clearly not a specialty disease. That's like a community disease that requires a primary care sales force. And while we may take the science in Phase 2 trials forward, we would certainly not develop our own primary care sales force and commercialize that. That would be done with a partner. Nevertheless, we think if we have such a molecule, it's a very valuable asset for us to partner. And then neuropathic pain lies somewhere in between. It can be covered by a rather large specialty sales force, meaning 100 to 150 reps probably in this country, so it is seen mostly by a specialist. And it really depends on the quality of data that we're going to see then in the first part of the year in terms of deciding what we would do with respect to further development and commercialization. Does that give you the lay of the land of how we're thinking about it? Benjamin Burnett - Stifel, Nicolaus & Co., Inc.: Absolutely makes sense. I appreciate it.

Okay, Reshma?

This is Reshma. With regards to VX-150 Phase 2 study that we are going to be initiating shortly, it's a fairly standard Phase 2 dose-ranging study. This is going to be in the bunionectomy acute pain model. And in essence, it's going to be several doses that we study to get a full dose exposure range. You'll remember that the bunionectomy study that had the positive results from early in the year was a high-dose study because we were really testing proof-of-mechanism in that one. The endpoint is going to be SPID24, SPID48. This is a pretty standard endpoint for the bunionectomy model. And with regard to the treatment effect, we were very pleased with the treatment effect we saw in the bunionectomy study. And now we need to explore the full dose range and exposure to see what the lowest effective dose is going to be and that's really what we're studying here. Benjamin Burnett - Stifel, Nicolaus & Co., Inc.: Got it. Okay, thank you very much.

Thank you. Our next question is from Cory Kasimov from JPMorgan. Your line is now open.

Hey, thanks for squeezing me in. Two for me as well. In your prepared remarks, you mentioned you'll have some enhanced next-gen correctors moving into the clinic in the coming months. I'm wondering if there's any additional information you could provide about these in terms of how they might be further differentiated from what you already have. And then my second question is with regard to the clinical hold for CTX001 in sickle cell not being listed in initial trials slated to begin. How much data do you ideally want to accumulate before you're potentially comfortable providing an update? And will this be something that's your responsibility or your partners?

Cory, this is Jeff. Maybe I'll take part one and Ian will talk about disclosure in part two of the question. With respect to the enhanced next-gen correctors, I would say what we're looking for here is two things. One, I think we've showed you the chart before that as we've gone through the last four years, it's really remarkable to see how we've been able to improve the potency and efficacy of these next-gen correctors. With the current molecules VX-59 and VX-445, we're close to getting all patients to carrier levels, but not quite there. And so the goal would be to find a next-gen corrector that could get all patients, meaning het/mins in particular, as well as homozygous patients, the carrier levels of chloride transport because we believe if you can get there, particularly, in young patients, you'll either prevent or greatly, greatly lessen the severity of the disease. The other goal of that program is to continue to diversify the chemotypes. We always like to have multiple chemotypes of any medicine that we're making. And so we've been able to explore alternative chemotypes and we're working on those as well. So, those are the two kinds of molecules that you can expect to see entry to clinic. We already have examples of both. And so the first ones of those, I do expect going into the clinic early next year and you can probably see some more as the year goes along as well. Does that answer your question about the enhanced next-gen correctors?

Yes, perfect.

Okay.

And, Cory, to your disclosure question, well, we've just started recruiting patients of these studies and I think the next disclosure we'll provide you would be kind of an update of where we are on the recruitment. We'd anticipate dosing first patient probably around towards the end of this year, early next year. And then once we have a number of patients in the study, we'd anticipate a disclosure of data from the study later on next year. But that would probably be timed with multiple patients in both studies and – so being on therapy or, let's say, have had the procedure for a certain duration of time.

Okay, great. Thanks for taking the questions.

Thank you.

Well, that will conclude the call. The Investor Relations team is in the office tonight to answer any further follow-up questions. Thank you very much for joining the call and have a good evening.

Ladies and gentlemen, thank you for your participation in today's conference. This concludes the program. You may now disconnect.