Good morning, everyone, and welcome to today's conference call. At this time, all participants are on a listen-only mode. After the speaker's presentation, there'll be a question-and-answer session. To ask a question during the session, you will need to press star one one on your telephone. You will then hear an automated message advising your hand is raised. To withdraw your question, please press star one one again. Please note that today's conference call is being recorded. I would now like to turn the call over to Erin Graves, Senior Director of Corporate Communications and Investor Relations at Revolution Medicines. Erin, please go ahead. Thank you, operator. Good morning, everyone. Thank you for joining today's call to discuss Revolution Medicines' acquisition of EQRx and other business updates. On today's call, Mark Goldsmith, Revolution Medicines' Chairman and Chief Executive Officer, will deliver his prepared remarks. Jack Anders, Revolution Medicines' Chief Financial Officer, and Steve Kelsey, Revolution Medicines' President of Research and Development, will join Mark for the question-and-answer session. Before we begin with the prepared remarks, we would like to remind you that Revolution Medicines and EQRx issued a joint press release announcing the proposed acquisition earlier this morning. Revolution Medicines also published a corporate presentation, which is available on the investor relations section of revmed.com. We would also like to remind you that today's presentation will include statements regarding the current beliefs of Revolution Medicines and EQRx with respect to the proposed transaction and the company's business, including the expected timing of the closing of the proposed transaction, the expected benefits of the proposed transaction, the company's pipelines, portfolios, competitive ability, and position, all of which are intended to be covered by the Safe Harbor provisions of the Private Securities Litigation Reform Act of 1995 for forward-looking statements. These statements are subject to a number of assumptions, risks, and uncertainties, and actual results may differ materially from these statements. In addition to any risks highlighted during the call, you should consider the important risk factors and other disclosures that may affect Revolution Medicines and EQRx's future results, as described in their most recent annual report on Form 10-K, quarterly reports on Form 10-Q, and other reports Revolution Medicines or EQRx files with the SEC, and, when available, a registration statement that will include a joint proxy statement and prospectus relating to the proposed transaction. Except as required by law, Revolution Medicines and EQRx undertake no obligation to revise or update any of these forward-looking statements. In connection with the proposed transaction, Revolution Medicines and EQRx intend to file documents with the SEC, including a registration statement on Form S-4, containing a joint proxy statement and prospectus. Investors and security holders are urged to read carefully the joint proxy statement and prospectus when it is filed with the SEC and other documents filed by either company with the SEC relating to the proposed transaction when they are filed, because they will contain important information. With that, I'd like to turn the call over to Mark Goldsmith, Revolution Medicines' Chairman and Chief Executive Officer. Thank you, Erin, and thank you all for joining us on short notice. Today marks a momentous day for Revolution Medicines. Earlier this morning, we announced that Revolution Medicines signed an agreement to gain more than $1 billion in additional capital through the acquisition of EQRx. We are excited to agree to this capital transfer in support of our ongoing efforts to discover, develop, and deliver pioneering RAS(ON) inhibitor drugs on behalf of patients with RAS-addicted cancers. I look forward to walking you through the core financial details of this announcement and what it means for our go-forward portfolio. Before doing so, I'd like to spend a few minutes discussing our strategic rationale behind the transaction. I want to start by emphasizing that this transaction is focused entirely on strengthening our cash position. With additional capital that is supportive of the enormous opportunity created by the scientific advances and clinical momentum we have established to date, this deal will enable us to reinforce and sustain our parallel development approach for our extensive RAS(ON) inhibitor pipeline in multiple RAS-driven cancers by enhancing our balance sheet, thereby increasing our company's financial certainty in a challenging macro environment. Upon closing, which we anticipate to occur in November 2023, we expect to have sufficient operating capital to commit confidently to making investments in late-stage activities and capabilities at scale and sustaining our robust R&D initiatives broadly. These efforts include one or more single-agent pivotal clinical trials, potentially beginning in 2024, which will be focused on our highly differentiated RAS(ON) multi-selective inhibitor, RMC-6236. The planning behind these trials is already underway in view of the encouraging data trends we have seen thus far. Likewise, with encouraging initial clinical experience with our KRAS G12C(ON) inhibitor, RMC-6291, planning is underway for a Phase 1/1b clinical trial to evaluate the combination of RMC-6236 and RMC-6291, potentially to begin in early 2024, while continuing single-agent evaluation of RMC-6291. It's important to note that our proposed acquisition of EQRx reflects both companies' confidence in our ability to build on scientific advances in clinical momentum and to deploy this amount of capital effectively. With the additional capital, we will be positioned to maximize the potential clinical impact of our targeted drug pipeline, all while retaining strategic control of our RAS(ON) inhibitor pipeline. In view of the considerable impact that this additional financial strength will have on our capacity to advance our own pipeline, at this time, we do not anticipate taking on a development or marketing partnership that would affect our rights in the U.S., and we can be especially discerning about timing in terms of potential partnerships we might consider outside the U.S. Moving on to the details of the transaction. As discussed earlier, this acquisition is all about enhancing our cash position in a way that takes into account our shareholders' interests and is designed to limit the dilutive impact to them. Through this all-stock transaction, we expect to receive more than $1 billion of additional capital from EQRx. The stock exchange ratio formula in the merger agreement that will determine the rate of exchange of Revolution Medicines shares for EQRx shares, uses a blended average from stock price determinations at two time points to account for developments in our ongoing business and potential movement in our stock price. In recognition of the forward-looking commitment by EQRx to support this transaction on behalf of its shareholders, approximately 20% of the exchange ratio is based on a determined $26 price per share of Revolution Medicines' common stock. The number of Revolution Medicines shares contributing to this portion of the exchange ratio was calculated as $200 million divided by $26, or 7,692,308 shares. Approximately 80% of the stock exchange ratio will be determined by a formula based on the price per share of Revolution Medicines stock, using a five-day volume-weighted average price measured during a period in close proximity to the EQRx stockholder vote, to which a 6% discount will be applied. The number of Revolution Medicines shares contributing to this portion of the exchange ratio will be calculated as $870 million, divided by the determined price per share. We agreed to this share price discount on this portion of the calculation as part of the overall transaction terms, in part because of our assessment of precedent, public biotech equity offering discounts, and conventional underwriting fees that are avoided in this transaction. We expect the transaction to close in November 2023, subject to the satisfaction of customary closing conditions, including regulatory review and approval by stockholders of Revolution Medicines and EQRX. I am pleased to say that holders representing more than 40% of voting common shares of EQRX have already entered into support and voting agreements to vote their shares in favor of the transaction. Before we wrap up today, given that our investors expect visibility into an updated data set on RMC-6236 safety and activity in the coming months based on guidance we've previously provided, we expect to provide this visibility as planned and believe it is important for all investors to have the opportunity to learn and understand these planned updates in order to appreciate a key component of the strategic rationale underlying this innovative transaction. An update on the clinical antitumor activity by our RAS multi-on inhibitor, RMC-6236, in patients with non-small cell lung cancer or pancreatic cancer, will be presented as a proffered paper oral presentation during the Developmental Therapeutics session on Sunday, October 22nd, at the 2023 ESMO Congress. Supporting clinical data will be presented at the 2023 AACR-NCI-EORTC or Triple Meeting, also in October. We are pleased to be an invited speaker in a plenary session at the Triple Meeting, delivering a presentation entitled "Targeting RAS-addicted Cancers with Investigational RAS(ON) Inhibitors." Furthermore, a first report on initial clinical findings with our KRAS G12C inhibitor, RMC-6291, which will include preliminary evidence of differentiation from KRAS G12C(OFF) inhibitors, will also be presented at the Triple Meeting. Further details on each of these upcoming presentations will be provided when available. Finally, we are pleased to announce that study site activation is ongoing under an Investigational New Drug application for a Phase 1/1b trial of our KRAS G12D inhibitor, RMC-9805. We continue to be energized by the trajectory of our late-stage development of RAS(ON) inhibitor drug candidates, and we look forward to sharing more with you in the coming months. In line with our continued prioritization and focus of our resources on novel drug mechanisms of action targeting RAS-addicted cancers, we do not intend to advance EQRx's research and development portfolio. EQRx will commence a process to wind down these programs, and we will work with EQRx to help ensure the well-being of patients and respectful treatment of any affected EQRx employees. Finally, I want to give a special thank you to our Revolution Medicines employees, who are the heartbeat of our organization and the key to our success. We are very proud that these efforts by our employees and collaborators have led to significant scientific advances that may help shape the future of oncology, and I know that we are only getting started. Today's announcement is a major step in our sustained strategic journey to advance our compelling RAS(ON) inhibitor drug candidates into late-stage development ... and to continue advancing our deep pipeline of mutant selective RAS(ON) inhibitors. With the additional capital, we are highly encouraged that we will be even better positioned to advance these high-performing oncology assets for patients and create even greater value for our shareholders. We are highly motivated by the progress to date and eagerly anticipate the next steps. Thank you all for your support. With that, I'd like to open up the call for questions. Operator? Thank you, sir. As a reminder, to ask a question, you will need to press star one one on your telephone. To withdraw your question, please press star one one again. We ask that you keep your questions to no more than one question and one follow-up, please feel free to go back into the queue, and if time permits, we'll be more than happy to take your follow-up questions at that time. Please stand by while we compile the Q&A roster. I show our first question comes from the line of Marc Frahm from TD Cowen. Please go ahead. Hey, congrats on the deal, and thanks for taking my question. Maybe just to dig in a little bit on 636, just can you kind of give an update on where dose escalation is right now and kind of how much are we likely to see at ESMO? You know, is this still going to be a population that's very weighted to G12D, just given the epidemiology and the early activity you showed? You know, should we be thinking about this being a pretty meaningful update in patient populations outside of that mutation? Thanks, Marc. Let me answer part of that, and then Steve can comment on the dosing. Well, given that KRAS G12D is the single most common RAS mutant driver of human cancer, I think that any emphasis on KRAS G12D would, would be, by definition, fairly broad. The fact is that what enrolls in this study is reflective of that epidemiology. There are KRAS G12D patients, KRAS G12V, and other G12X patients. We'll represent the story as we have it from the data that we've collected, but it will, of course, be heavily weighted towards the top two mutants that are represented in human cancers, KRAS G12D and G12V. Steve, do you want to comment on dosing for RMC-6236? Yes. We, we just made a decision to dose escalate from 300 mg daily to 400 mg daily, and those patients are currently being enrolled in the, in the study. As soon as that dose escalation cohort is fully enrolled, we will backfill the 300 mg dose level to make sure that there's 20 patients minimum in, at that dose level. It's not clear at this stage how much of that data we'll be able to get into the presentation at ESMO because of the internal guidelines that we set ourselves for data cut-off, et cetera. I think it'll be a substantive update on the one we gave in February, that's for sure. Okay, that, that's very helpful. Maybe just given amount of cash and then, you know, if something still closes, the, the amount of cash that goes in, it seems like you have a lot of firepower to go after a variety of combinations with RMC-6236. Can you just kind of walk through some of the priority list there, of combinations and, and different settings that you, that you really want to go, after quickly? I think we'll tag team this one, too, but let me just start by saying, as we announced, we will continue developing RMC-6236 as monotherapy, and in fact, we expect to launch one or more pivotal trials on RMC-6236 as a single agent beginning as early as 2024, and that'll be based on the data set that we're able to present in October. The trends that we've seen so far are supportive of that plan. Secondly, we also announced that planning is underway now for a first combination, which is with RMC-6236, combined with RMC-6291. That study should begin also in early 2024. That, that's the kind of two important foundational points. Then maybe Steve, you comment more broadly on RMC-6236 and combinations. Yeah, I mean, as we've said before, you know, we, we perceive RMC-6236 in two, in two ways. One is as a mutant, a RAS mutation inhibitor, for RAS mutations, for which there isn't a specific inhibitor, which right now is pretty much everything outside G12C, even though we and others have G12D inhibitors in, in development. But I mean, there are many patients, as we just discussed, with G12D, G12V, and other G12 mutations, for which 6236 could be used as a RAS mutation inhibitor. In, and in those indications, you know, with the first thing we would be looking to is combinations with existing standard of care, which could include chemotherapy and, and, and checkpoint inhibitors. The second, you know, high-priority utility-... six is leveraging the ability to inhibit mutations that may not be the one that the mutant selective inhibitor inhibits, but also inhibiting wild-type RAS. We would combine it with our mutant selective inhibitor, like RMC-6291. Both of those are, both of those are either being, are being planned to start as really as soon as possible. I think we've provided some guidance on the approximate timing of those studies. But they're high priority combinations and they, and we're planning to start them really, you know, pretty soon. Thank you very much. Thanks, Marc. Thank you. I show our next question comes from the line of Jonathan Chang from Leerink Partners. Please go ahead. Good morning, thanks for taking my question. Just one. Can you provide your thoughts on the timing of this acquisition? I guess, why now, versus waiting until after the upcoming data presentations at ESMO and Triple Meeting to consider your options? Thank you. Yeah, thanks, Jonathan. We think that this is really the opportune time to do this for a number of reasons. On a practical level, this is when it was available from EQRx. They had a process underway in which they were looking at their strategic alternatives in the context of a revised strategy. From our point of view, we see significant momentum in the development of data. We have expectations around what we'll be able to disclose in October, and you've just heard important development plans that are already, you know, underway and in the relatively near future, you know, to quote Steve, "As soon as possible." That will require significantly increased resources and commitments that we wanna be in the strongest financial position to be able to make those decisions. I'd also point out, though, that the structure of the deal is, is really critical to understand. It is designed such that 80% of the stock exchange rate will be determined in close proximity to the shareholder votes. Those shareholder votes won't occur until after the data are disclosed, the next data update, or updates, plural, are disclosed in October. What we've effectively done in this deal is we've secured access to $1 billion by achieving a commitment by EQRx to participate in this transaction. We've secured it now, it largely gets priced later. From our perspective, we get the benefits of, of both, securing the access to an unusually large amount of capital that's rarely available in the marketplace today, but to do so, at a price that reflects people's understanding and view of RevMed after those very important clinical updates. Understood. Thank you. Thank you. I show our next question comes from the line of Michael Schmidt from Guggenheim. Please go ahead. Hey, Mark and Steve, thanks for taking my questions, and congrats on the deal today. I had a question on six two nine one, where you're saying, in the press release that you have, preliminary evidence of differentiation. I was just wondering, you know, what are some of those measures? I guess, how do you determine differentiation in this, in this data update? Then also, how do you think about sort of the single agent development opportunity for six two nine one, perhaps relative to some of the combination work that you're planning? Thanks, Michael. Good to hear from you. Steve's going to answer that. Let me just provide one, one comment, though. Obviously, we can't pre-disclose the information that we, we'll be reporting in October, so we can only talk in generalities here, but I think Steve can, can give you a framework. Well, yeah. I mean, I can, I can only reiterate the framework that we've provided previously, which is, we, we have thought about RMC 6291 really has to be demonstrably better. I mean, it has to be better than KRAS G12C inhibitors, otherwise, it's probably not something that Revolution Medicines are gonna spend an enormous amount of human capital and, and cash developing. We've thought about it really in two ways. It's gotta-- it's either gotta be demonstrably superior in the context of efficacy in some situation, and you are well versed with that field, so you are aware that, lung cancer and colorectal cancer make up the vast majority of the tumors harboring the G12C mutation. It's gotta be demonstrably superior in terms of tolerability, such that it can be combined with things like pembrolizumab, that some of the other G12C inhibitors cannot be combined with. That's the data set that we've been looking to collect, and we will provide more specifics on that at the presentation that we will be giving in October. Single agent opportunities for G12C inhibitors are few and far between. Again, you know, unless the single agent activity has to be demonstrably superior to something that's already in clinical development or on the market in order for it to really have a shot. And it's, and it's, it's tough to infer superiority in a, in single agent efficacy from, from, from studies where the endpoint that's reading out soonest is overall response rate. Nevertheless, there are still some opportunities there. And again, I think we have a chance to collate the data and discuss it, actually show it and discuss it, it'll be a lot easier to have this conversation. Yeah. If I could add to that, we're excited about RMC-6291, and we have been since its discovery and preclinical development and as you know, we've disclosed quite a lot of preclinical data that very strongly bolster the case that it is differentiated and acts in a superior way in preclinical models to comparators. That's certainly part of what we're evaluating in the clinic. We're quite excited about it. We think that we've made a lot of progress. We're really looking forward to sharing that with you in October. As Steve pointed out, that will make it a lot easier to have the discussion, but we can't go beyond that framework today. All I can say is stay tuned, and we're excited about it. Great. Thank you. Thank you. I show our next question comes from the line of Ami Fadia from Needham. Please go ahead. Hi, good morning. Thanks for taking my question. I have two quick questions. Firstly, on RMC-6236, you mentioned that you've started to enroll the 400 mg dose. Can you talk about how that correlates with the doses you tested in the preclinical setting? Secondly, just with regard to RMC-6291, if it does not show meaningfully better overall response rate compared to the RAS(OFF) G12Cs, what, you know, what would be the takeaway in terms of the value of RAS(ON) versus RAS(OFF)? Should we not almost expect the response rate to be higher? Thank you. Yeah. I, I'd like to just comment on that second question. That sort of stands out to me. I don't think Steve said that we would or wouldn't show a, a, a difference. I think his comment was with response rates, because there is essentially a range around the current compounds that are out there, coming to the conclusion definitively that one has a superior response rate, just takes a very large study to do that. That requires a large enough N, which is just not the sort of thing that one obtains in a dose response, dose escalation study. We've made that point previously, but that's not to say... He's not trying to signal what we're seeing or not seeing. He's just making the point that for us to make the definitive statement about superiority is just hard. People shouldn't expect us to be able to take that position on the basis of, of, of the first dataset. There are other parameters that go beyond response rate, like durability. Also keep in mind that there isn't a single response rate, response rates in a particular subset of patients, and response rates in another subset of patients, and so on. You have to look at tumor type, condition, pretreatment versus not pretreatment, etc. There are multiple response rates, and there are multiple PFS values, if you will, or durability, signals as-associated with each of those. We can't-- we shouldn't really just blend them all together. Again, without actually speaking to the specific data, it's hard for us to, to give you the kind of, definitive answer you want, but there's a lot of opportunity for that compound to show why it could be beneficial to patients and beneficial in a way that is distinguished from the RAS(OFF) inhibitors. Maybe I'll put it this way: I think we stand by our belief that inhibiting the on or active form of RAS with our tri-complex inhibitors provides a meaningful biological pharmacologic benefit that we believe will translate, for patients. That's the second question, and now I've forgotten the first. The first was RMC-6236, and how high, how high are we? Maybe I'll answer that one. We're higher than we were before. In the... You know, when we got to 80 mg, we disclosed that we now felt that we were in the exposure range in humans. That synced up with kind of the exposure range, the lower end of the exposure range in mice, that drove regressions. So, while we're, we're not going to take a position today in the absence of sharing all of the PK data on exactly what that exposure level is for a given dose level, we'd rather, you know, do that in the context of showing you all of the PK. What we can say is that we've continued to see dose-dependent increases in exposure as, as we've advanced from on dose level to the next. So today we're dosing at 5 times the total dose that-... We've already shown you, antitumor activity for, and for which, we saw strong antitumor activity in preclinical, species. That doesn't quite get to a precise answer for you, but I think it gives you, gives you the concept. Thank you. That's helpful. Thank you. As a reminder, to ask a question, you will need to press star one one on your telephone. To withdraw your question, please press star one one again. I show our next question comes from the line of Ben Burnett from Stifel. Please go ahead. Hey, great. Thanks so much. I just want to ask one point of clarification on the shareholder vote timing. I appreciate the commentary earlier, but if I heard you right, that shareholder vote is expected to happen after both ESMO and the Triple Meeting in October. Is that correct? Correct. We expect the shareholder vote to happen in early November or in November, and those meetings will be completed in October. I think shareholders will have, all investors will have plenty of opportunity to understand the data sets. That's really critical for us. We made a commitment earlier this year to provide data specifically on RMC-6236 in that time frame. We're really excited about our chance to do that. We're excited about the trends that we're seeing, and we want to share that in a fulsome way, and the combination of the Triple meeting and the ESMO meeting will enable that. In addition to that, although we had never guided to anything specific about RMC-6291, we're now laying out for you a commitment to disclose the first data set on clinical behavior of RMC-6291 at the Triple meeting. There's gonna be a lot of information, and we can't wait to get there. Okay, that's wonderful. If I could just slip one more in, just around the status of the RMC-9805 G12D, as in dog, phase 1. Anything you can say just in terms of whether this has begun enrolling and, and when we might expect an initial update on the clinical results? Yes. Well, we have an active IND, we're, we're activating clinical sites. I can assure you there is enormous enthusiasm for this. Quite a lot of interest among investigators, so I, I think that's moving swiftly. We'll disclose when we've begun dosing patients. It's too early to give you a timeline for when we'll be able to disclose data around that. I, I certainly would, would not want to set expectations that in October, that we'll be presenting early data from RMC-9805, but, you know, let's just see how it goes, and, it's a tremendously exciting time for us to have our third compound entering clinical development. Today, effectively, we have three RAS(ON) inhibitors, in the clinic, and the first two of which are generating exciting data. Okay, great. That makes sense. Thank you so much. Thank you. Thank you. I show our next question comes from the line of Eric Joseph from JPMorgan. Please go ahead. Hi, good morning. Thanks for taking the question. Yeah, I just had a follow-up on the 9805 phase 1, and really whether... Well, actually, just given the sort of the overlapping patient population with that of, I guess, the majority of patients coming into the trial for 6236, I guess, are you thinking any differently about the design of phase 1, of the, of the 9805 phase 1 and perhaps some patient prioritization there, or will it be similarly broad? I guess when might be the earliest opportunities to potentially look at combinations with the rationality? Thank you. Yeah. Hi, Eric. Thanks for your question. Well, the KRAS G12D bearing cancer population is enormous, and the needs are very deep, as you know. And so the demand to evaluate an investigational new drug, particularly, compounds like RMC-6236 and RMC-9805, that have clearly shown very compelling preclinical profiles, is very high and enthusiasm for continuing to enroll patients for RMC-6236 remains extremely high among investigators, and we can't provide the number of slots that people want. That's just the reality. We've tried to communicate that over the last number of months, but it continues to be the case, that there's just very high demand, and we can't meet that demand really during a dose escalation study. There's a large number of patients, an enormous number of patients, who just aren't even having the opportunity right now to, you know, evaluate for themselves the, the, the potential impact of RMC-6236. I don't think we're gonna need to do anything special in the clinical trial. We'll open it up as a, as a typical phase I dose escalation with, you know, the sorts of bells and whistles we typically include in that sort of thing. We'll get to that information as quickly as possible. I think our development organization has been extraordinarily effective at accessing quality clinical sites, patients, serving them well, and generating data. I think that's going to go just as swiftly as it's gone for RMC-6236 and RMC-6291. Okay, great. Thanks for taking my question. Thank you. I show our next question comes from the line of Jonathan Chang from Leerink Partners. Please go ahead. Hi, guys. Thanks for taking the follow-up. What data has EQRx seen? Yeah, Jonathan, that's, that's not an unexpected question. You know, we can't, we can't give you the detail of that, but I can assure you that neither company would have entered into this transaction, committed to this transaction, without doing full and proper confidential diligence on the other party. That happened. It was bilateral diligence on multiple levels between the two companies and under confidentiality. Clearly, the EQRx management team and board of directors feel compelled about the opportunity that they see, and likewise, we feel compelled about the opportunity that we see to enhance our programs. I think that's, that's sort of the best, the best way I can put it. Got it. Thank you. Thank you. As a reminder, if you have a question at this time, please press star one one on your touchtone telephone. If you have a question at this time, please press star one one. I think I show a question from Mr. Ben Burnett from Stifel. Hey, great. Thank you. I just want to ask a follow-up question. Is there any color you can give around the types of data that's meant by supporting clinical data at, at the Triple, relative to what we should expect at the ESMO update, which I think you gave a lot of color on? I guess, what's, what's kind of meant by the sort of supporting clinical data? It's mainly the nuts and bolts of the dose escalation, the safety, tolerability, PK, ctDNA data. We will almost certainly attempt to answer the question that was already been asked once today, that we declined to answer on this conference call, which is: How is the exposure in the patients at the higher doses correlate with the 25 mg per gram daily in mind? It's not, not a simple thing to answer, but I think we can do it in the context of a scientific presentation. The follow-up, the presentation at ESMO the following week, focuses largely on efficacy, and the, the sheer might of the data forced us to split those presentations into each two presentations rather than attempt to cram it all into, into one. It's purely a pragmatic solution to the, the, the weight of data that we've accumulated. Yeah. Okay. That's very helpful. I appreciate it. Thank you. Thank you. I show no further questions at this time. I'll now turn the call to Mark for a few closing remarks. Well, thank you again for joining us today. In summary, the deal we announced today represents a unique opportunity for Revolution Medicines to acquire a sizable quantum of capital in a single transaction at a competitive cost. It will further empower the advancement of an important set of oncology assets and help us realize our vision as a self-sufficient organization with the fortitude to discover and develop pioneering, high-impact, targeted medicines, with the goal of delivering these on behalf of cancer patients. All of us at Revolution Medicines are excited about our future, and we look forward to providing you with updates on our progress. Thank you very much. This concludes today's conference call. Thank you for participating. You may now disconnect.