Arcus Biosciences, Inc. (NYSE:RCUS) Q1 2024 Earnings Call Transcript

Arcus Biosciences, Inc. (NYSE:RCUS) Q1 2024 Earnings Call Transcript May 8, 2024

Arcus Biosciences, Inc. beats earnings expectations. Reported EPS is $-0.05, expectations were $-0.97. Arcus Biosciences, Inc. isn’t one of the 30 most popular stocks among hedge funds at the end of the third quarter (see the details here).

Operator: Hello, all and welcome to Arcus Biosciences First Quarter 2024 Earnings Call. My name is Lydia, and I’ll be your operator today. [Operator Instructions] I’ll now hand you over to Pia Eaves, Vice President of Investor Relations & Strategy.

Pia Eaves: Hello, everyone and thank you for joining us on today’s conference call to discuss Arcus’s first quarter 2024 financial results and pipeline updates. I’d like to remind you that on this call, management will make forward-looking statements, including statements about our cash runway and our expected clinical development milestones and timelines. All statements other than historical facts reflect the current beliefs and expectations of management and involve risks and uncertainties that may cause our actual results to differ from those expressed. Those risks and uncertainties are described in our annual report on Form 10-K and quarterly report on Form 10-Q, which have been filed with the SEC. We strongly encourage you to review our filings.

Today, you’ll hear from our CEO, Terry Rosen; COO, Jennifer Jarrett; and CFO, Bob Goeltz, will also be joined by our; CMO, Dimitry Nuyten; and President, Juan Jaen for questions after the prepared remarks. For ease of listening, we’ll be referring to abbreviations of our molecule names, domvanalimab as dom, zimberelimab as zim, casdatifan as cas, quemliclustat as quemli, and etrumadenant as etruma. During today’s call, we’ll refer to slides in our corporate deck, which can be found on the Investors section of our website. With that, I’ll turn the call over to our CEO, Terry Rosen.

Terry Rosen: Thanks very much, Pia, and thanks to all of you on the call for listening in today. As you know, 2024 is shaping up to be an incredibly catalyst-rich year for Arcus. By the end of this year, we’ll have data that support all four of our later-stage clinical programs. Dom, zim in lung and upper GI cancers, cas in clear cell RCC, quemli in pancreatic cancer, and etruma in colorectal cancer. We’ll spend most of the quality setting a stage for these upcoming data events with over $1 billion of cash on hand, runway into 2027, partnerships with Gilead, AstraZeneca, Taiho, others, along with a very diversified pipeline, we’re extremely well positioned to capitalize on these datasets, advance our potential first and also best-of-class treatments towards approval and commercialization, quickly and efficiently.

Let me start with ASCO. ASCO is less than a month away, so we’re almost there. We’re thrilled and honored to have two world presentations, both of which will provide strong support for our efforts and programs in the GI cancer field. Importantly, both datasets are in settings where there’s limited competition and huge unmet need. These are genuine opportunities to make a meaningful difference for patients. So first off, on Saturday, June 1st, we’ll have updated data from cohort A1 of the Phase 2 EDGE-Gastric study evaluating dom + zim + chemo in first-line gastric cancer. As you’re aware, dom is the only Fc-silent anti-TIGIT antibody in late-stage clinical development, and we believe that the data presented to-date indicate that dom may potentially have an improved safety profile when combined with chemotherapy relative to that of the Fc-enabled anti-TIGIT antibodies when they’re combined with chemotherapy.

As a reminder, we presented initial data from this cohort of EDGE-Gastric at the ASCO Virtual Plenary Session in November of last year. At the time, Median PFS was immature. However, we did present mature landmark six-month PFS numbers, which you can see on Slide 16 of our corporate deck. What you can see is that six-month landmark PFS was 77% for the overall population and 93% for the PD-L1 high population. So given that the Median PFS for standardized care in this setting ranges from seven to eight months, these data were obviously very, very encouraging. At ASCO, we’re very excited to be presenting mature Median PFS data. We expect the updated data will further support the potential for dom/zim to provide clinically meaningful benefit relative to the standard-of-care in gastric cancer.

Importantly, EDGE-Gastric evaluated the same setting and similar patient population is our ongoing Phase 3 study, STAR-221. So therefore, we expect these data to foreshadow what were our confidence in our STAR-221 study. In that context, enrollment in STAR-221 is expected to complete by midyear. The incredibly rapid enrollment of the study is indicative of the lack of competition in gastric cancer market and the immense need for new therapeutic options, particularly with overall survival in this patient population ranging from only 13 months to 14 months in studies with anti-PD-1 antibodies in chemotherapy. We’d also felt that we actually achieved some tailwinds with our data presentation at the end of last year. So putting this all together, you can infer that there’s a line of sight to data and that dom/zim will have a very substantial head start over potential competitors.

Given there are no other anti-TIGIT antibodies in Phase 3 development for the setting, so we think we’re going to have a clear first-to-market advantage. This creates an exciting opportunity for us to be first in this setting with an addressable patient population of over 25,000 patients in the US alone and 100,000 patients in the G7 countries. So this equates the potential worldwide market of over $3 billion. Now, moving onto our second presentation at ASCO. On Sunday, June 2nd, we’ll be presenting data from our ARC-9 study in third-line colorectal cancer. This will be the first presentation on this study. The data will be from cohort B, which is evaluating etruma in combination with zim, FOLFOX and bev versus regorafenib, one of the standard-of-care treatments for third-line colorectal cancer.

On Slide 41 of our corporate deck, you can see the study design and the conclusion criteria for this portion of the study. Patients in this cohort must have received bev, unless contraindicated, a prior oxaliplatin-based regimen and an irinotecan-based regimen. These are the current standard-of-care therapies for first and second-line CRC. 105 patients were enrolled who were randomized 2:1 between the etruma arm and the regorafenib arm, so this is a relatively large dataset. ARC-9 also include two additional randomized cohorts which evaluated etruma + zim + FOLFOX and bev versus FOLFOX and bev in second-line colorectal cancer. These data are not yet mature and will be presented at a later time. Second-line setting, as you know, has a substantially longer OS.

The ASCO presentation will include mature PFS and OS data with a median follow-up of over 20 months, and our data will include patients with and without liver mets. This is important since patients with liver mets tend to have a poor prognosis and they’re not always included in late-line CRC trials. As many of you know, there are very limited options in third-line + colorectal cancer. Patients are typically treated with regorafenib and more recently with the combination of lonsurf and bev based on the SUNLIGHT study which showed a PFS of 5.6 months and OS of 10.8 months in the third-line patient population, while acknowledging the limitation of cross trial comparisons, but we all do it based on our data which will be shared with you next month.

[Technical difficulty] etruma-based combination regimen may represent a very substantial improvement over current options for patients in the third-line setting. I also want to point out a small dataset of 35 patients that was just presented in a poster at AACR, which actually captured quite a bit of interest and further supports our hypothesis that adenosine blockade enhances the immune activating benefits of chemotherapy. These data were from the MORPHEUS-PDAC study, a randomized, Phase 1b/2 trial operationalized by Roche that evaluated our molecule etruma + Roche’s anti-PD-L1 atezo and chemotherapy versus chemotherapy alone in first-line metastatic pancreatic cancer. We’ve highlighted the design on Slide 37. On slide 38, we’ve shown the spider plots for both the control arm in the etruma-based regimen which showed durable responses.

In this trial, the etruma containing arm demonstrated a meaningful improvement in both PFS and OS and we’ve shown these data on Slides 39 and 40 of the corporate deck. Specifically, the PFS hazard ratio was 0.48 and the OS hazard ratio was 0.67, with the etruma-based regimen yielding an absolute improvement in median over survival of 4.4 months over chemotherapy alone. The median OS for the etruma containing arm was 16.5 months, very similar to what we saw in ARC-8. Before we leave etruma, I want to highlight that now with the ARC-9 data presentation, we’ll have three datasets presented in a very short period of time for our two molecules that inhibit the ATP adenosine pathway, quemli and etruma. Between ARC-8, which evaluated quemli in combination with chemotherapy in first-line pancreatic cancer.

MORPHEUS-PDAC very similar, which evaluated etruma with chemo in first-line pancreatic cancer. And now ARC-9, we have three independent, but similar datasets which together provide compelling evidence demonstrating that mitigating the immunosuppressive action of adenosine combined with immunogenic chemotherapy may prolong survival relative to that associated with chemotherapy alone. For those of you who have been following us for a long time, keep in mind, this was the original hypothesis which drove us to the adenosine access in the first place. So we’re getting to the point where the data are matching the hypothesis. Importantly, two of these studies showed meaningful improvement in OS versus the standard-of-care control, and all three showed substantial improvement above historical benchmarks when adenosine blockade was combined with immunogenic chemotherapy.

Now that we’ve covered with what we’ll be sharing at ASCO, I’d like to turn it over to Jen to discuss expectations for our HIF-2alpha inhibitor program later this year.

Jennifer Jarrett: Thanks, Terry. I’ll now turn to our data events for the second half of 2024 and specifically for cas, our HIF-2alpha inhibitor, which we are developing in clear cell renal cell carcinoma or ccRCC. As a reminder, HIF-2alpha is a validated mechanism with belzutifan recently approved as monotherapy for late-line clear cell RCC patients. Cas has PK and PD advantages over belz, which should enable it to hit the target harder with the goal of achieving greater clinical efficacy than that of belzutifan. As we talked about on our last earnings call, there are multiple opportunities to improve upon the profile of belzutifan, a lower rate of primary progressive disease, a higher overall response rate, and more prolonged responses, any of which could translate into a higher PFS and ultimately longer OS for cas relative to that of belzutifan.

Our Phase 1b study for cas are 20 now has enrolled over 80 patients, 8-0. It was designed to answer numerous questions, so I want to spend a minute describing the various components of this multi-cohort study, which is summarized on Slide 27 of our corporate deck. First, for the dose escalation. As of our last earnings call in February, we had completed enrollment of the 20 mg, 50 mg and 100 mg dose cohorts with no dose-limiting toxicities observed. We have now completed enrollment of the 150 mg cohort, and again, we did not observe any DLTs and we just cleared that dose. Additionally, we continue to see linear dose proportional PK for cas even at the 150 mg dose. The dose expansion portion of ARC-20 was designed to serve a few purposes. First and foremost, to generate data for a proposed Phase 3 dose of 100 mg of cas.

These data will be used to support initiation of our first Phase 3 study, which is an advanced stages of planning for cas. The monotherapy dose expansion portion is enrolling patients that have received at least one prior anti-PD-1 therapy, and at least one TKI. In the 100 mg dose cohort, approximately one-third of patients have received four or more prior lines of therapy, so these patients were relatively advanced. On our last earnings call, we disclosed that while the majority of patients in this cohort had only received one or two scans, we were already seeing a response rate, including responses pending confirmation in line with LITESPARK-005, the Phase 3 study for belzutifan. We also mentioned that we observed a lower rate of primary progressive disease or the percent of patients that progressed prior to their first scan that was reported for LITESPARK-005.

This is important. As one weakness in the LITESPARK-005 dataset as we’ve heard consistently from clinicians is the high rate of primary progressive disease. Bringing this rate down should result in more patients benefiting from treatment and prolonged PFS and survival. We are very excited to present detailed data from this cohort at a medical conference in the second half of this year. We also designed the dose expansion portion to satisfy the dose optimization work required for regulatory submissions. Specifically, we included two additional monotherapy cohorts in ARC-20, which are evaluating a 50 mg dose and 150 mg dose. We have now completed enrollment of the 50 mg cohort and we just initiated enrollment of the 150 mg cohort. So, in addition to enabling us to complete the dose optimization work required for Project Optimus, these cohorts will also generate a lot of additional data that will further elucidate the clinical profile of cas.

In addition to the three monotherapy expansion cohorts in ARC-20, we are about to initiate enrollment of a cohort to evaluate cas in combination with cabo, the most commonly used TKI in clear cell RCC. Data generated from this cohort, in addition to the data generated from STELLAR-009, our Phase 2 study being operationalized by Exelixis will be used to support the planned initiation of at least one Phase 3 study for cas in combination with the TKI. Given the enthusiasm for cas and the rapid enrollment of ARC-20, we expect our 100 mg dose expansion cohort data presentation later this year to be followed quickly by data from the various other cohorts. We are aggressively advancing cas towards the initiation of our first Phase 3 trial early next year.

Importantly, we are taking a strategic approach to our development plan to maximize the value of what we believe is a best-in-class HIF-2alpha inhibitor. For example, the STELLAR-009 study is evaluating cas for the next-generation and potentially best-in-class TKI, zanzalintinib. We believe that both zanza and cabo could have advantages over belzutifan’s TKI partner, lenvatinib, with a better tolerated AE profile. And therefore, we expect our cas-TKI combination could be differentiated from both an efficacy and safety and tolerability perspective relative to belzutifan + lenvatinib. I’d like to end by spending a few moments on the RCC market, for which, approximately 80% of patients, 8-0% of patients have the clear cell histology. The annual addressable patient population for first-line clear cell RCC includes over 12,000 incident patients in the US and approximately 30,000 in the G7 countries.

Around two-thirds of these patients progressed on first-line treatment and are addressable in the second-line, resulting in more than 8,000 patients in the US and approximately 20,000 across the G7 countries. The ccRCC market is fragmented, but cabo is the most frequently used TKI. Cabo sales in 2023 in the US alone were over $1.6 billion, driven almost entirely by RCC and with only one quarter of market share in first-line and under 50% market share in the second-line setting. In terms of the treatment paradigm for first-line RCC, patients are typically treated with anti-PD-1 + a TKI or a combination of nivolumab + zimberelimab. When patients experience tumor progression on front-line therapy, they cycle through different TKIs frequently for a few years or more.

With few options beyond TKIs, the clinician community has been eagerly waiting for the introduction of HIF-2alpha inhibitors, particularly given the relatively benign safety profile relative to TKIs. And so not surprisingly, the positive Phase 3 data for belzutifan resulted in an immediate and steep inflection in script trajectory. Monthly scripts are now at twofold since top line data for belz and clear cell RCC was released in August 2023, and up 50% in just the first four months after belzutifan’s approval in the setting. Based on just large scripts, belzutifan is now at an approximately $400 million run rate in the US alone and growing. As we’ve discussed, we believe that cas may improve clinical outcomes relative to belzutifan, and we plan on developing cas in differentiated combinations, all of which support a very meaningful market opportunity for cas, which we believe is north of $2 billion.

Before we conclude, I’ll now turn the call over to Bob to review our quarterly financials.

Bob Goeltz: Thanks, Jen. Arcus continues to be in a strong financial position. Our cash as of March 31st, 2024, was $1.1 billion, as compared to $866 million as of December 31st, 2023. Turning to our P&L, we recognized GAAP revenue for the first quarter of $145 million, which compares to $31 million in the fourth quarter of 2023. Our revenues primarily driven by our collaborations with Gilead and Taiho, and in the first quarter, included a cumulative catch up of $107 million resulting from the Gilead amendment we executed in January. We expect to recognize GAAP revenue of approximately $30 million per quarter for the remainder of 2024. Our R&D expenses for the first quarter are stated net of reimbursements from Gilead and were $109 million as compared to $93 million in the fourth quarter of 2023.

In the first quarter, non-cash stock compensation represented $10 million of our R&D expenses. The increase in the first quarter was related to higher clinical manufacturing, clinical trial and headcount-related costs associated with our late-stage programs. We continue to expect modest increases in R&D expenses as our Phase 3 studies mature and spend will fluctuate primarily based on the timing of clinical manufacturing activities and the purchase of standard-of-care therapeutics for our clinical trials. G&A expenses were $32 million for the first quarter, compared to $29 million in the fourth quarter of 2023. Non-cash stock compensation represented $10 million of our G&A expenses for the first quarter, and we expect G&A to remain stable for 2024.

Total operating expenses in the first quarter were impacted by a $20 million non-cash impairment charge resulting from the intended sublease of a portion of our office space. Finally, we continue to expect our cash balance at the end of 2024 to be between $870 million and $920 million and to fund operations into 2027. This guidance includes a $100 million partnership continuation payment from Gilead in the third quarter and excludes potential opt in payments and approval milestones from our partners. For more details regarding our financial results, please refer to our earnings release from earlier today and our 10-Q. I’ll now turn it back over to Terry for concluding remarks.

Terry Rosen: Thanks, Bob. As you’ve heard from us today, we are genuinely at a significant inflection in the evolution markets. With completion of enrollment of STAR-221 in first-line gastric cancer expected by midyear, we’re turning our attention to our first Phase 3 readout. Behind this, we’ll have Phase 3 data from our second registrational study for dom/zim, STAR-121 in first-line non-small cell lung cancer, with enrollment for this trial also expected to complete this year. In addition, we’ll be starting at least two additional Phase 3 trials by early next year for cas and clear cell RCC and quemli in first-line pancreatic cancer. And as we talked about today, we have several important near-term datasets which may provide further validation and meaningful de-risking of several of our programs.

This will all kick off shortly at ASCO with two oral presentations for dom/zim and etruma/zim, and together they’ll showcase our emerging GI cancer franchise. And we’re of course looking forward to sharing much more on our HIF-2alpha program later this year from the dose expansion cohorts of ARC-20. I want to highlight how unusual it is for an early-stage company to be executing multiple Phase 3 studies for several different molecules, all targeting massive opportunities and doing so in parallel. This is obviously all enabled by our current cash position and our partners that include Gilead, AstraZeneca, Exelixis and Taiho. These partnerships have and will continue to provide a combination of development funding through the receipt of opt in fees, milestones and cost sharing to reduce our overall development expenses.

I want to conclude by thanking all of you for your continued and ongoing support of Arcus and our mission to bring innovative therapies to patients in need. We’ll now open the call for questions.

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Q&A Session

Operator: Thank you. [Operator Instructions] Our first question comes from Kaveri Pohlman of BTIG. Your line is open. Please go ahead.

Kaveri Pohlman: Yeah, good evening. Thanks for taking my question. For HIF-2alpha, some of the literature suggests that HIF-2alpha is upstream of VEGF, and it leads to its production, so they’re basically in the same pathway. Do you think that could make cabo responsive patients more sensitive to 521? And because of the same biology, do you expect to see any overlapping toxicities with zanza, which also target VEGF?

Terry Rosen: Yeah. So they are in the same pathway. We do believe that HIF-2 on the other hand, though, since it controls probably 100 genes, there are other effects ongoing in cancer. We don’t really expect. And, in fact, we know what the side effect in AE profiles are. So we do not expect that you would see overlapping toxicities. And I would just say that with HIF-2alpha, those toxicities in AEs have already been well defined by belzutifan. What you primarily see is very manageable anemia. We’ve seen similar, and even though, we believe and know, in fact, that we’re hitting the target harder, essentially, nature’s built in a break because only so much HIF-2 mediated EPO expression is happening in the kidney. And there’s other sources of EPO, and we’ve seen a safety profile that continues to look very similar to what has been reported for belzutifan.

As Jen noted, we’ve actually even completed a 150 milligram cohort. Again, we have not seen any DLTs to-date.

Kaveri Pohlman: Got it, that’s helpful. And maybe a quick one regarding STAR-121 trial for first-line non-small cell lung cancer. It has primary endpoints of PFS and OS. Do you have to win on both? And what are the expectations from the ARM C? How much variation from the control arm and/or TIGIT arm is acceptable? Thank you.

Terry Rosen: Dimitry, do you want to handle that question?

Dimitry Nuyten: Sure, Terry. So the first question is relatively simple. So, statistically speaking, the way it’s set up, it’s a dual primary endpoint, meaning that, either PFS or OS, if either one of those is statistically significant, it would be a positive trial. I think we’ve been very clear in previous calls as well, in lots of interactions that are in the public domain, that from a regulatory perspective, OS is really the registrational endpoint. PFS is supportive. And your second question, can you repeat it, please? I didn’t get the entire question.

Kaveri Pohlman: Sure. And I just wanted to get some. So the PFS and OS are really comparing arm A and B, C is, I believe, Keytruda combination, but there is an arm C for them. I was just wondering how much variation from that arm versus control arm, Keytruda arm is acceptable?

Dimitry Nuyten: Yeah, that’s a hard question, as the FDA would say it’s a review issue. That arm, I think, is clear from, let’s say, the public domain is a 4:4:1 randomization. So very limited number of patients is going on to zim and chemotherapy to establish contribution of components. Based on FDA guidance I can share that contribution of components mostly is established by looking at the response rate. And, of course, in a randomized session, a time to event endpoint could also be assessed. There’s no absolute guidance on what the variability can be. That’s a review issue. I can summarize. I’m very confident with the data we’ve generated for zim that a positive trial, meaning that dom and zim combined with chemotherapy clearly beat Keytruda, that the contribution of components, let’s say discussion, is a modest part of the discussion, and I’m confident that we will be able to achieve that successfully with the study design.

Kaveri Pohlman: That’s very helpful and thanks for taking my questions.

Terry Rosen: Thank you, Kaveri.

Operator: The next question comes from Peter Lawson of Barclays. Your line is open.

Peter Lawson: Great. Thanks so much. Thanks for taking the question. Just around HIF-2alpha. For the second half data what defines success for you for that dataset? And could you remind us what Gilead or what the trigger points are for Gilead to potentially opt in? Thank you.

Terry Rosen: Sure. Thanks, Peter. So on the what defines success, as we’ve articulated, there’s a number of variables and opportunities for differentiation from belzutifan. So starting with response rate, rate of primary progression, depth of response, even if we have PFS by that point. So we want to do better than belzutifan. I’ll remind you, in thinking about our overall program, though, based upon what we’ve already seen, the data look good and we’re full speed ahead to registrational trial. And keep in mind that we are not going to be developing this, at least in the near-term, as a monotherapy. We also believe, as Jen was discussing, that will be combining with a better TKI than levatinib. So that will give us another opportunity for differentiation.

So there’s multiple places and we think that we have an opportunity to beat belz on more than one of those. In terms of the Gilead opt in, that’s something that we would expect. We’ve converged on what would define that opt in and we would expect a decision either towards the end of this year or early into next year.

Peter Lawson: Great. Thanks so much.

Operator: The next question comes from Yigal Nochomovitz of Citi. Please go ahead.

Ashiq Mubarack: Hi guys, this is Ashiq Mubarack on for Yigal. Thanks for taking my questions. I have a few on the EDGE-Gastric update at ASCO. Obviously, based on the data you’ve already shared, it looks like the capital Minot curves on PFS are obviously trending well beyond the seven to eight months hurdle. I think you cited, but naturally with a small end. So I’m just curious how much greater do you think the PFS benefit really needs to be to de-risk STAR-221? And a more theoretical question, I guess. How well do you think PFS correlates with OS benefit in this setting, given that’s the primary endpoint in STAR-221?

Terry Rosen: So thanks for the question. You’re right on the sample size and I think you’ll be able to make your own call on that. As you suggested, it’s known and actually the data being pretty tight. So, in addition to CheckMate-649, there’s been two other registrational studies with anti-PD-1 and chemo, and they both come in and they have roughly just under seven to eight months PFS. So that’s pretty firm number. We think our data will be quite meaningful. I think one other thing to keep in mind, when you compare our datasets, interestingly enough, CheckMate-649 had 60:40 high PD-L1, low PD-L1, and we’re actually 40:60. So pretty substantial difference. And as you saw, even our numbers in the all-comer population look pretty good.

So, we’re three weeks away, we’re excited about the data. You’ll make your own call on how much you think they’ve de-risked the site. Interestingly enough, as we also mentioned, we’re on the cusp of that registrational study being completed. So, you’ll see those data in a couple of weeks. In terms of the correlation, as you know, in general, PFS and OS, particularly in the context of immunotherapy, are certainly qualitatively correlative. But I wouldn’t necessarily think that you can plot a line for them. But given our dataset, I think you’ll clearly be able to form some speculation as to what might happen on the OS, just like you formed some speculation on the six month landmark numbers what might happen. I think those dots are going to connect at least qualitatively in a direction that will be confidence enhancing.

Jennifer Jarrett: And if you look at the CheckMate-649 dataset, I think you could say that the PFS and OS benefit was pretty correlative and pretty similar, if you look at the hazard ratios. So that’s at least one data point that I think shows that the correlation should be pretty strong between PFS and OS in this disease.

Ashiq Mubarack: Got it. Got another one more. Correct me if I’m wrong, but I think you said the data, the EDGE-Gastric data at ASCO will only be from cohort A1. So I’m curious. I know where things stand with the other cohort, especially cohort A2, which is I think zim + FOLFOX arm. And obviously that one will be important to help you understand the contribution of dom if that cohort varies from the seven to eight month number you’re talking about. So I’m just curious where thing stand there?

Terry Rosen: Sure. So that cohort actually enrolled sequentially to the first one. So, the final patient actually just was enrolled a few weeks ago. Keep in mind, not only was it sequential, but since it’s essentially a single-arm study, the fact that you don’t have an experimental arm is another thing that probably slowed its enrollment. So it’s probably trending a year behind the initial cohort. I’ll also mention that as you’ve probably seen on clinicaltrials.gov, we have two additional arms that are probably more designed to take on their contribution of components that will be run in a randomized fashion and with a larger end. The other thing that may be important about that cohort that you just referenced, that we recognize it’s another opportunity, albeit a single-arm, non-randomized dataset that will give people another look at how zim + chemo compares to historical numbers for other anti-PD-1 such as Keytruda or nivo + chemo.

So we think it will be an interesting dataset as well, but it’s at least a year behind this cohort.

Ashiq Mubarack: Got it. Thanks very much.

Terry Rosen: Thank you.

Operator: Our next question comes from Jonathan Miller with Evercore ISI. Your line is open.

Jonathan Miller: Thanks, guys. A couple on HIF-2 for me. Obviously, we’re very excited to see the 100 milligram cohort release and get a better sense for HIF-2 efficacy here versus the competitor. But I’m wondering why, well, specifically, there’s 50 milligram cohort isn’t going to be part of that same release that was enrolled before 100 milligrams. No. So I understand 150 just got finished, but why not include 50 in your end of year release? Secondly, this quarter, as well as last quarter, you highlighted that you’re already –

Terry Rosen: Hey, Jon, let me answer the –

Jonathan Miller: Sure, sure.

Terry Rosen: I was going to answer that, because I forget what you said. Your brain is younger and faster than mine, so I’ll forget the first question. Let me just answer the first one and then I’ll take your second question. So the 50 milligram cohort was actually enrolled after the 100 milligram cohort. And it was basically, we added both the 50 and then we wanted to go with the higher in the context of Optimus. So the 50 milligram cohort just very recently was fully enrolled. And, in fact, it won’t be part of the medical conference presentation, because clearly it won’t be mature. But whatever we know about it, you’ll be able to get that out of me without much inducing. So we’ll share whatever we know about it.