Kymera Therapeutics, Inc.

Good morning and welcome to the Chimera Therapeutics fourth quarter 2023 results call. All participant lines will be in the listen only mode. Should you need assistance, please signal a conference specialist by pressing the star key followed by zero. After today's presentation, there will be an opportunity to ask questions. To ask a question, you may press star then one on your touchtone phone. To withdraw your question, please press star, then two. Please note, this event is being recorded. I now turn the conference over to Justine Phoenixville. Thank you. Please go ahead.

Good morning, and welcome to Chimera's Investor Update. Joining me this morning are Nello Manolfi, President and CEO, Jared Golub, our Chief Medical Officer, and Bruce Jacobs, our Chief Financial Officer. Following our prepared remarks, we will open the call to questions. We ask that you limit your questions to one and a relevant follow-up to allow enough time to address everyone's questions. Before we begin, today's discussion will include forward-looking statements about our future expectations, plans, and prospects. These statements are subject to risks and uncertainties that may cause actual results to differ materially from those projected. A description of these risks can be found in our most recent 10-K filed with the SEC. Any forward-looking statements speak only as of today's date, and we assume no obligation to update any forward-looking statements made on today's call. With that, I will now turn the call over to Nello.

Thank you, Justine. As always, we appreciate everyone joining us for our quarterly call today. This is a particularly exciting call for us in that we're reporting from our new corporate headquarters in Weathertown, Massachusetts, just down the road from our previous office. Our new building provides added space for our growing team, enabling us to maintain a strong on-site presence as we enhance and scale critical capabilities for our R&D organization, especially in areas like CNC as well as other development functions. We look forward to the opportunity to welcome those of you who would like to visit us at our offices in the future. As many of you know, we're on-site five days a week. During our prepared remarks, we'll cover three main topics today. First, I'll provide an update on our strategy to build the best-in-industry oral immunology pipeline. Next, Jared will provide an update on our clinical and newly disclosed immunology programs, as well as our two clinical oncology programs. And before we open the call for questions, Bruce will review our financial results. At our Immunology R&D Day in early January, you heard us discuss our strategy for building a best-in-industry oral immunology pipeline of first-in-class, highly valuable programs. We believe we're uniquely positioned to change existing treatment paradigms for immune-mediated diseases with our innovative and differentiated oral degrader medicines. As we reported this morning, with $745 million in cash and a runway into the first half of 27, were well capitalized to continue to support these very ambitious goals. I thought I'd start with a few comments reflecting on what has led Chimera to our current strategic positioning with an innovative immunology pipeline of oral degraders with biologic-like activity potential. Those of you that have been following us for a long time know we have been driven by our unique target selection strategy. We're focused on first or best-in-class opportunities, and in particular, un-draft or fully-draft targets for which protein degradation is either the best or the only solution. We're also dedicated to pathways that have strong clinical and genetic validation, where there is a clear path to early clinical differentiations. And, of course, our focus is on those indications that represent large clinical and commercial opportunities that create significant value for patients and shareholders. As you all know, we pioneered the first protein-degraded program in immunology with our IREC4 program, which, in addition to STAT3, were the initial targets at Canair when it was founded in 2016. And it was the early clinical results with the IREC4 program, with KT474, the deep and well-tolerated degradation, the early signs of clinical efficacy, which helped us inspire to increase our focus in immunology. Additionally, we believe the activity and fidelity of translation of our TPD platform in the KT474 Phase I trial serves as an important read-through and informs the probability of success of our new STAT6 and TIK2 oral immunology program. One aspect of the current landscape in immunology that is particularly notable and creates a significant opportunity for canaries, the dominance in the market of injectable biologics. These antibody-based therapies have transformed and revolutionized the treatment of immune inflammatory diseases, with what in many cases have been great clinical outcomes for patients. At the same time, monoclonal antibodies, as you know, are injected. They can be costly to manufacture and can be inconvenient for patients. To put this in context, in a recent industry survey, 75% of patients taking biologics said that they would switch to orals with an equivalent profile. We believe this creates a significant opportunity for effective and well-tolerated oral medicines, and in particular, for protein degraders. In fact, while traditional small molecules offer convenience benefits, they frequently cannot match the powerful pharmacology of biologics. as they don't have the ability to block these pathways at the same level. We believe and have shown with preclinical and early clinical data that protein degraders have the potential to provide a unique solution with biologics like specificity and activity, but with the flexibility of oral small molecules. Importantly, because of this profile, we believe that they can potentially reach much broader patient populations, creating significant opportunities for the modality, broadly, and for chimera specifically. So as you think about our immunology pipeline, if we can build a portfolio of molecules that provide comparable pathway inhibition to biologics, as we believe we can, but one with the convenience in oral dosing, we believe the potential is enormous. We have a lot happening across our pipeline, including plenty of activities in our early pipeline that we haven't yet disclosed. We're really at the cutting edge of protein degradation and using this technology to address fundamental clinical, commercial needs and opportunities. I believe our unique approach has resulted in one of the most robust high-value pipeline in the industry. I'm very proud of the continued execution and innovation by our team to support our future growth. I will now pass it to Jared to walk you through in more detail our clinical and soon-to-be clinical pipeline. Jared?

Thanks, Nilo. Starting with our IRAC4 program. In the fourth quarter, our partner, Sanofi, initiated two KT474 Phase II trials, one in hydradenitis suppurativa and one in atopic dermatitis. Enrollment in both trials is ongoing, with top-line data expected to be reported in the first half of 2025. Importantly, with the start of these trials and the dosing of the first HS and AD patients that we disclosed late last year, we collectively earned $55 million in development milestones from Sanofi, which we have already received. We in Sanofi are enthusiastic about the potential for this program. In addition to the two initial indications, we continue to discuss and explore additional potential indications, and we will plan to share more details as we are able in the future. Moving now to our two recently announced preclinical immunology programs, KT621, our once daily oral stat 6 to greater, is slated to enter the clinic later this year. What makes this program particularly exciting is that the IL-4, IL-13 pathway has been exceptionally well validated. CT621 targets STAT6, which is an essential transcription factor to the IL-4, IL-13 signaling pathway, and the central driver of type 2 inflammation in allergic diseases. By degrading STAT6, we believe we can selectively block this pathway fully, and importantly, this pathway only, potentially phenocopying upstream biologics such as dupilumab. At our R&D day, we shared what we believe is a very compelling set of preclinical data that supports the high level of enthusiasm and confidence we have in this program. Specifically, in our preclinical studies, we have demonstrated full inhibition of the IL-4, IL-13 pathway in all relevant human cell contexts with pica molar potency superior to dupilumab and exquisite selectivity. We also demonstrated very high levels of activity in multiple well-established preclinical models that gives us confidence in the potential of KT621 to deliver biologic-like activity as we advance this program into clinical trials later this year. If we are able to replicate our strong preclinical data in the clinical setting, which is something we have accomplished with our clinical stage programs, we believe KT621 would be poised to be a best-in-class therapeutic option for multiple indications. representing a multibillion-dollar opportunity. We are currently in the midst of IND-enabling studies and expect to advance KT621 into Phase I testing in the second half of 2024, with data from that study in 2025. We also recently unveiled KT294, our potential first-in-class oral TIK2 degrader. We believe KT294 also has a potential biologic-like profile creating an opportunity to treat a range of autoimmune and inflammatory diseases. We believe degradation of TIK2 has the potential to overcome the challenges of small molecule TIK2 inhibitors, which have limitations due to lack of selectivity, limited target engagement, and or lack of potent activity against type 1 interferon. Importantly, we believe TIK2 degradation could allow us to recapitulate the human loss-of-function biology of near-full pathway inhibition of type 1 interferon, IL-12, and IL-23, while also sparing IL-10, representing a best-in-class TIK2 agent. Our plan is to move this program into first in human studies in 2025. Across our immunology portfolio, we intend to present preclinical data from the SAT6 and TIK2 programs at multiple scientific and medical meetings this year, starting with the American Academy of Dermatology annual meeting next month. We also expect multiple clinical data readouts from these programs next year. To summarize, In the first half of 2025, we plan to share top-line data from the KT474 Phase II trials, as well as data from the KT621 Phase I study, which, as mentioned, is planned to start later in 2024. So switching gears to our oncology portfolio, we expect additional proof-of-concept data readouts for both KT333 and KT253 this year. Both programs have demonstrated initial encouraging antitumor activity in liquid and solid tumors and are progressing through dose escalation in line with our expectations. For KT333, our stat-free degrader, we shared data at ASH in December, demonstrating early signs of anti-tumor activity at doses that were generally well-tolerated and associated with substantial stat-free knockdown in blood and tumor. Our preclinical to clinical translation showed strong objective responses in both CTCL and in Hodgkin's lymphoma, as well as induction of an interferon gamma response in tumor and blood, that preclinically was shown to enhance the response of solid tumors to anti-PD-1 drugs. We believe this supports KT333's potential to address both hematological malignancies as a single agent and solid tumors as a potential novel combination therapy with anti-PD-1 or other targeted therapies. Our intent is to complete dose escalation in the Phase Ia study in 2024, at which point we will share the trial results and disclose our plans for the next phase of development for the program. And lastly, KT253, our MDM2 degrader. This is another really exciting program. ARM-A of the Phase Ia in solid tumors and lymphomas is ongoing, and in November, we reported clinical data demonstrating evidence of target engagement in P53 pathway activation, as well as initial antitumor activity and a lack of the traditional hematological toxicity seen with small molecule inhibitors. We also announced that we commenced enrollment in arm B for patients with high-grade myeloid malignancies, including AML. For both arms of the study, enrollment is progressing in line with our expectations. Like with stat 3, we expect to complete dose escalation in 2024, at which point we will disclose our plans for the next phase of development for the program. As part of our development plans, later this year, we also expect to present comprehensive preclinical and clinical translational data across liquid and solid tumors that will inform a patient selection strategy for KT253 and ongoing in future clinical studies. I'll now turn the presentation over to Bruce for a review of the Q4 financials.

Bruce? Thanks, Jared. I'll quickly review the fourth quarter financial results, and you can certainly reference the tables in the back of the press release today. As Nello mentioned, with the advancement of 474 into the Phase II trials in HS and AD, we earned $55 million in milestones from Sanofi. We received $40 million of that in the fourth quarter. The other $15 million, which was recorded as receivable at year end, that payment was received in the early part of 2024. These milestones were added to the total consideration received under the Santa Fe collaboration, with a portion recognized as revenue in the fourth quarter and the remaining in deferred revenue. At the end of the quarter, our deferred revenue balance total on the balance sheet was approximately $54.7 million. That reflects partnership revenue that we expect to receive over the next several years, excluding the receipt of any potential future milestones. And then quickly with respect to operating expenses, R&D for the quarter totaled $53 million. Of that, about $5.3 million was non-cash stock-based compensation. The adjusted cash R&D spend of $47.7 million, excluding that stock-based comp, was up 13% from the comparable quarter a year ago. On the G&A side, our spending for the quarter was $14.2 million, of which $5.6 million was non-cash stock-based comp. And that adjusted G&A spend of $8.6 million, again, excluding stock-based comp, is a 5% increase year over year. And then finishing up with our cash balance, as stated earlier, at the end of 2023, it was $436 million, including the $300 million of net proceeds from our equity offering last month. and the $15 million that I referenced from Sanofi that was received early this year. That brought our unaudited cash and equivalent balance as of January 9th to approximately $745 million. That is expected to provide a runway into the first half of 2027, and it will enable us to deliver the next stage of growth in data readouts, including, as Jared mentioned, the KT474 Phase II data, our oncology proof-of-concept results this year, and then several critical and clinical inflection points for our STAT6 and TIK2 programs. So that's what we had for you today in terms of prepared remarks, and now we'd be happy to answer any questions. Operator?

Thank you. We will now begin the question and answer session. To ask a question, you may press star then one on your touchtone phone. If you are using a speakerphone, please pick up your handset before pressing the keys. To withdraw your question, please press star then two. At this time, we will pause momentarily to assemble our roster. The first question comes from Vikram P. Hutt from Morgan Stanley. Please go ahead.

Hi, good morning. Thanks for taking our questions. We had two, both on immunology. First, so you alluded to in your prepared remarks potential pipeline expansion for 474. To the extent possible, I was wondering if you could speak a bit about what's going to feed into that decision and how the datasets we get in the first half of next year for HS and AD might be related to how you think about, with Sanofi, where to go next with this molecule. And then a similar question for 621 and 294. What will you be assessing from the initial clinical data we're going to be getting next year to help prioritize indications for subsequent development in INI indications. Thank you.

Thanks, Vikram. So maybe I'll start. So with 474, it's just a bit more challenging because, as you know, this is in collaboration with Sanofi, so we're not in the liberty to disclose several things around decision-making and timing. But as we said in the past, The reason why we built this program several years ago, actually, we said today that IREC4 and STAT3 were the first programs in 2016-17. So the idea around IREC4 degradation is the opportunity to generate and develop a broad anti-inflammatory drug with a good tolerability profile. So in our goal, there's always been the possibility and high probability to move beyond skin indications. And, you know, we've disclosed some of the other potential indications that one could go after. It could be respiratory. It could be rheumatology. It could be GI. So I think when we're ready with our partner Sanofi to disclose the path forward, you know, we'll be happy to do so. Obviously, personally, I don't believe that, you know, a... a skin indication will inform necessarily the probability of success of this drug in other types of diseases. But obviously, confirming the safety and activity in longer-term phase two studies will bolster confidence to then move into other indication. Maybe that's high level how I would characterize it today. For STAT6 and TIK2, I think it's early for us to comment on decision-making beyond early clinical studies. I mean, these are, you know, we could spend hours talking about your question, maybe just high level. You know, with STAT6 that we've been saying now for a few months, it feels like two months, but it's actually two months, the value proposition is the oral degrader that can match the biologics-like activity of upstream monoclonal antibodies such as dupilumab, we've shown with our preclinical data that we can match that type of phenotype. You know, some would argue we're more potent than it in some contexts, but maybe we don't have to go there. So we have a pretty exciting blueprint of development plans in front of us. I think we as we've done with all the other programs, for us it's imperative that we go into humans and demonstrate this beautiful translation that we've seen with other programs of target knockdown, predictable safety, predictable PKPD. And then we have this, I think, very elegant biomarker strategy that we'll be talking about later in the year that I think will allow us to validate the ability to match the type of pathway inhibition that upstream biologics do. And for TIK2, briefly, again, this is a well-characterized mechanism. We know what other TIK2 inhibitors are missing, which I would say are several things. Some are selectivity, all are target engagement tests, and some are ability to block all the other scaffolding functions. And so what good looks like for us is a loss of function-like phenotype. And we know what that looks like based on human genetics, and that's what we want to confirm in phase one. And then once we're there, you know, Jared and his team will be happy, I'm sure, to share more details about the late development plan.

Got it. Thank you. Thank you.

The next question is from the line of Michael Schmidt.

This is Paul. I'm for Michael. Thanks for taking our questions. Mine are on KT333. So, the first one is on your bar for pursuing a development in solid tumors. I believe the ASH data had about a third of the patients with stable disease. So, you know, would higher rates of stable disease and biomarker data be sufficient to advance the program? into combinations, or would you really need to see some objective responses to sort of commit to evaluation in solid tumors? And then second is just, you know, how does your thinking now for SAT3 and autoimmune fit into your current pipeline, and are you waiting for 333 data to evolve further before making further commitments? Thank you.

So maybe, Jerry, you want to take the first one, and then I'll make comments on the second one.

Sure. I think with regarding your question on the bar for solid tumors, as you noted, we have had some patients who have had prolonged stable disease, and that, of course, is of interest to us, and we continue, as we enroll patients onto the study and continue to dose escalate, look for opportunities for bringing on solid tumor patients that can give us a better idea as to what our activity will be as a monotherapy in solid tumors. I think all along, you know, we've been guiding that we expect that ultimately we're if we move this into solid tumors, it would be as a combination approach, especially anti-PD-1 combination is something we're very interested in based on our promising preclinical data and based on what we've shown with our biomarkers that we can induce this interferon gamma response in tumor and blood, which can actually facilitate responses to anti-PD-1. We're also looking at additional targeted agent combinations preclinically. So I think what will inform moving forward with solid tumors will be a combination of what we continue to learn preclinically with combination studies and whether we do see continued signals of some sort of activity as a monotherapy, either stable disease or even preferably major responses. With regard to major responses, we are seeing those in hematologic malignancies, including Hodgkin's lymphoma and cutaneous T-cell lymphoma, and that continues to be of interest to us and will continue to bring on patients onto the ongoing phase when they study to further explore activity there as well.

Yes, thanks, Jerry. That's great. And on the SAT-3, maybe I just want to go back to our strategy, which is something that we've talked about at the R&D Day. We believe we exist to bring together the power of the technology and unmet needs that are both clinical, commercial, and I would say also the opportunity to do with this technology things that cannot be done with other technologies. So I guess another type of unmet need, the technological one. And only, I think, when we marry those three together, we're going to go all in. And as you've seen with IRAC4, with STAT6, and TIK2, I think we have a very, very easy-to-articulate value proposition. I hope you guys also feel that way. And these are, you know, complete degradation of targets that lead to exceptional anti-inflammatory profiles that are well-tolerated, at least in our hands so far. And so with STAT3, it's obviously a program that we know, I would argue, better than anybody at this point. We've been working on this target for several years. And the reason why you haven't seen us disclosing more details on STAT3 I&Is is because we feel that at this point we don't have all the information in hand to being able to say that we'll fit the profile of the type of programs that we've articulated so far. When we do, when it does, it will be would be able to do so, we'll disclose more.

Okay, thank you. Thank you.

The next question comes from Ellie Moll from UBS. Please go ahead.

Hi, this is Jasmine on for Ellie. Thanks so much for taking our question. Hi, this is Jasmine on for Ellie. Thanks so much for taking our question. What's your latest thinking on whether you would take both STAT3 and MDM2 into Phase II, or is the thinking that you'll prioritize one over the other, given your focus on immunology? And what would your threshold for success be for each program in thinking about the go and no-go decisions?

Thank you. I think I felt like there were two people, but anyway, I think we got the question. I'm sure there were similar questions. So... So, great question. So, maybe I will start with saying that as everything that we've done at Chimera, you know, for the past almost eight years, all our decisions are going to be data-driven. So, and, you know, for example, decisions even that we've made for programs that we discontinued, for example, 413, even though the molecule was behaving well and was well-tolerated, was driven by plethora of data, obviously clinical, commercial data, landscape and, you know, to a large extent also MPV analysis that we did. So we'll apply the same rigor to all programs that are pipeline, whether these are in immunology or in oncology. As we said, in order for us to invest in, let's say, in these two oncology programs, we need to be able to see in front of us opportunities to impact broad patient populations. So I think our goal criteria for both programs will be driven by opportunities that are both in heme and solid tumors generally at this level. And I think we should probably wait for when we disclose more data later in the year on what exactly the strategy will be. What I will say is that For STAT3, we've shown something that has not been shown before, which is this is an active target, and we have an active drive. We've shown, you know, a small data set in December, and us, we'll show more later in the year. And in MDM2, we also have an active drug. We've shown really few patients' data. In November, we'll show much more later in the year. So I think only when we're able together to look at the totality of the data, it will be much clearer what the decision-making process is going to look like.

Great. Thanks so much.

Thank you. The next question is from the line of Jeff Meacham from Bank of America. Please go ahead.

Hi, good morning. This is Susan on for Jeff. Thanks for taking our question. Can you walk us through what the strategy is for indication selection for the immunology program, the STAT6 and the TIK2 and the IL-4? And just commenting specifically on maybe competitive landscape or maybe what kind of data you're going to look at prior to initiating first in human studies.

Okay, so I'm going to take this really high level just because I want to be consistent with our message, which has been that as we get into the clinic in our healthy volunteer studies, at least for SET6 and for TIC2, I think at that point we will feel more comfortable talking about later development for several reasons. One, You know, we don't have to talk about it now. And two, you know, the landscape, as you said, is competitive, and I don't believe at this point it's necessary to disclose information that are not needed. So at the high level, what I want to say is, you know, high level for step six, I don't believe that there are well-tolerated oral drugs in indications in which dupilumab has been approved. that have, as I say, the well-tolerated, strong activity. So we have a huge potential in a variety of indications. I don't have to name them because they're all well-established, you know, from AD, asthma, hopefully soon COPD, chronic rhinitis, and others, COE. There is actually white space in that area for oral drugs with a good safety profile. So, while obviously all of those indications are going to get more and more competitive given large investments that biopharma is putting into immunology, we're actually in a really unique position right now going forward. And once we disclose our development plans, you'll see how actually we would be able, we believe, to be really competitive in terms of timing of our trials as well as the design of our trials. With regards to TIK2, it's obviously a different landscape. But I would say that there, while there are several TIK2 small molecule inhibitors, we've seen also recently data from an AL23 peptide from Protagonist slash J&J. There is still room to match AL23 type 1 interferon biologics. especially in a single oral molecule that is well-tolerated and active. And so I think that is the gap that we're going to fill with our programs. So just patience on the design, but they will come, you know, as we get into the phase one studies.

Thank you. The next question comes from

Thomas Smith from Clearink. Please go ahead.

Hi, this is Will on for Thomas. Thanks for taking our questions. A couple on the ZEN and ADVANTA trials. If you could give us a sense of how enrollment is progressing thus far and any color on what the patient enthusiasm and willingness to enroll has looked like. And when enrollment is complete for those trials, Are you planning to share that information or just wait until the data release? And then I have a follow up.

Great, thanks for the question. As you know, Sanofi is running both of those phase two trials. If you look on clintrials.gov, you can see the publicly stated timelines for estimated primary completion for both of those studies, which is in the first half of next year. And to our knowledge, both studies are still on track to meet those timelines. You know, that's pretty much all we can really say right now with regard to how those are staying on track. You know, our understanding is that there is significant enthusiasm on behalf of the various sites who are being engaged. You know, these are both sort of global studies, and so I think that's been very encouraging in terms of what we've heard from Sanofi in terms of site engagement. And so I think, again, you know, we're still expecting that both of those studies would read out on the publicly stated timelines. In terms of you know, sharing, you know, data, I think that will be something that, you know, Sanofi and Chimera will need to sort of work out in terms of exactly how that will look next year, you know, in the first half of next year when those readouts are expected to occur.

Okay. That sounds cool. And then I'll just do the follow-up as well. Thank you.

The next question comes from Kelly Shee from Jefferies. Please go ahead.

Hi, good morning. This is Yun for Kelly. Thanks very much for taking the questions. Are you able to share the status of dose escalation in STAT3 and also the MDM2 program? And also, are you able to disclose, have you reached the targeted 90% degradation that you thought could be required for clinical efficacy? And also for INI indications, is there a specific threshold like the 90% in oncology indication that you think you will have to achieve? And based on your experience with oncology indications, how confident are you that the preclinical degradation data will translate into human data? Thank you.

All right. These were, I think, three questions. I even lost track of them. So let's start with... the oncology program. So we generally do not provide updates in these quarterly calls on how recruitment is going. We provide updates when we disclose data, obviously, and we try to target medical meetings. So you should just look out for, you know, meetings later in the year where a full update on each of those two programs will be provided. Now, you know, we love to share but because, as you know, there is abstract admission and we need to hear from the conferences, you know, we're not able to now confidently say exactly where, but just know that there is a plan in place, and we believe this will be both presented at high-impact medical meetings within 2024. If you look at what we've disclosed so far, obviously we have reached, for Stat III, the targeted degradation And really here, we continue dose escalation because we're getting through, we're targeting to reach an MTD, which, as we've seen preclinically, seems to be above our targeted degradation. And that's really a testament to the design of the molecule, the design of the study, that the translation has happened in a very predictable and positive manner. For MDM2, it's earlier, I think it's hard for us to comment based on you know, three, four patients' worth of data that we shared in November. So just stay tuned for our next update where it will be clearer where we are with regards to target engagement. You know, I think if you look at all our programs, if you look at our R&D data, or actually on our corporate deck today, you will see that each one of our programs, whether in college or immunology, we have reached targeted degradation in the clinics. with a good safety profile. With RX4, we reached complete degradation in blood. With STAT3, we've reached more than 90%, around 90% or more, depending on patients in both blood and tumors. With even 413, we reached that targeted degradation. So we know really well how to design our molecule and translate those profiles in the clinic, so we expect that for STAT6 and TIK2, that should happen just the same way. Like, that is one thing that we're not concerned about here at Chimera. With regards to what is the profile in immunology, the profile in immunology is what you've seen in our preclinical data. You've seen that if you degrade, for example, STAT6 anywhere between 80% and 90%, you can match dupilumab activity in those preclinical, for example, asthma models or even AD models. So it doesn't look like you need complete target removal, but we will, as we've done in the past, target complete stat6 degradation and then know that we can obviously do dose exploration in the clinic. Similarly with TIK2. So, you know, once we generate data, we can talk more about what is our late-stage design. But the Phase I design will look a lot like the IREC-IV program for immunology.

Thank you very much.

Thank you. The next question comes from Adam Vogel with Wells Fargo. Please go ahead.

Hey, thank you for taking my call today. I'm on for Derek. So maybe just a few quick questions from us on oncology pipeline. Can you walk us through further what data you expect to share from KT253? Will you be reading out data from both ARMS A and B? And then perhaps, given your deepening focus and efforts in I&I, will you be looking to partner either with KT253 or KT253 in the future?

Thank you.

All right, so, Jared, maybe you take the first one. I just want to take the second one first. So, you know, I think we need to think about, for us, our decision to invest in programs is driven by a philosophy of opportunities and return on investment and patient impact. It turns out that based on our analysis, If you look at our current immunology pipeline, we believe that, you know, these are all extremely valuable programs at the outset. I think for our oncology pipeline, we believe that if the program translates in the way that we hope based on preclinical data, those could be also really valuable programs. MDM2, if we can unlock it, that biology, that is going to be another really large program for SETRI, if we're able to also unlock the solid tumor opportunity, I think that would be the case too. So I think the partnering discussion comes with the conversation around what type of expertise we want to build in terms of late-stage clinical and commercial, given that we're still an early company. I think at some point, hopefully, we won't be asked anymore. You know, you can only... you know, do one versus the other because we're trying to build a large commercial stage company. And as you've seen, all the successful ones can navigate multiple disease areas. But we also are not naive. And so we understand that at this stage, in terms of late stage capabilities, it probably makes much more sense to invest in one area. We've said already clearly that we're committed heavily in immunology. And so I think with oncology, the question is, what are the key value drivers that Chimera wants to drive this program through? And then if we feel that these programs are best positioned in a collaboration for maximum value creation, we can do that, but we also reserve the right to being able to advance this program or one of these programs on our own if we believe that the value proposition fits the philosophy of the company right now. Jared, maybe you can comment on the type of data in 253.

Sure. So our plan for this year is to complete dose escalation across both studies, the 333 and 253 phase 1A trials, and to establish an MTD, and then to present those data at a medical meeting later in the year. That would include, of course, update on enrollment, the types of patients that we're including, And for 253, as you mentioned, yes, we're enrolling in both the solid tumor lymphoma arm A as well as in the high-grade myeloid malignancy AML arm B. So to show what types of patients have we enrolled, what does the safety profile look like, and what is PD, and what kind of clinical efficacy are we seeing to start to give us insights into where we want to go in terms of the next stage of development for both of these programs. As I mentioned earlier in the presentation up front, for 253, we've also been doing a lot of work on preclinical work and clinical work to really understand, you know, patient selection, you know, both for the remainder of Phase Ia but also for the next steps in development. And so I think we're also looking for an opportunity potentially at a medical meeting to present those data sometime this year as well to give further insights into how we think about patient selection for either liquid and or solid tumors with 253.

Great. Thank you. Thank you.

The next question comes from Mark Fram. from DD Corwin, please go ahead.

Hi, thanks for taking my questions. Maybe, Nello, with IREC 4, when we get the data next year and, you know, Sanofi will make their own decision of going forward or not, but you guys will also have, well, if Sanofi chooses to move forward, you guys will have an opt-in decision. So how are you kind of approaching the opt-in? What do you want to see that, you know, you would commit Chimera's resources early on and how important is kind of the phase one data from stat six and tick two and seeing kind of the exposures you want to making that decision for IRAC4?

That's a great question and probably requires a very nuanced answer. So I'll try and do my best in the short time we have. So first, as I just said earlier, we are extremely bullish on IRAC4. Our value propositions has only grown with more data. This has the potential to be one of the largest drugs in inflammatory diseases. We have early positive data, but I think we are all here recognizing that we just don't know how active this drug is until we run a well-powered randomized study, which is what we're doing with Sanofi. Actually, we're doing two of them. The value proposition for this drug, in our view, is As I said earlier, it's an active oral drug with a good safety profile in indications that, to be honest, go well beyond HS and AD. I think these are obviously intriguing, exciting early indications, but by no means our view is that this is where the drug should go only. I think if the drug fulfills that profile and we believe, that the company is positioned to support the growth of the company the way we see it today, for us would be a no-brainer to opt in when the time is right. Again, if the drug fulfills that profile. And the reasons are varied. Not only the value that can be created downstream, but the way that our collaboration is built we've done all sorts of analyses and all the analyses that we've done financially, even though it might be a bit more expensive early on in the opt-in phase while we're doing co-development, the value creation at the back end is so vast that that decision would be so easy. Yes, If we have successful programs with phase one, which we believe we will, for phase six and phase two, I mean, I suppose that our cost of capital will be different, that we can continue to sustain the growth of this company to support the pipeline. So hopefully that answers the question, but that's how we're viewing it at this point.

Okay, thanks. Very helpful.

Thank you. The next question comes from Brad Canino from Stifle. Please go ahead.

Good morning. This is Brad. Perhaps an expansion of the prior questions really for MDM2 and the data this year. It'd be great to get just more of a scope of the disclosure that you expect to present in terms of patients, disease types, and would you flag any key data elements to watch? And then just maybe to be clear on the decision-making process at this disclosure, will you be in a position to outline the broader development thesis? Thank you.

So maybe just eye level, and then I'll let Jared comment on some more specifics if we're willing to do so. But I think the totality of our data, of our disclosure plans, which hopefully was clear enough from our press release and from comments from Jared earlier. So what is the totality of the data? The totality of the data is a large, hopefully close to complete data set from the dose escalation in both solid lymphomas and leukemias, married with the patient stratification work that we're doing that should enable us to build a development program extremely differentiated from others in the space. I think if those things come together, And we believe we should be able for those things to come together in 2024. And if all of those are suggesting that we both have activity and also we have a, let's call it a smart way to develop this drug, I think that decision of continuing investment will be a no-brainer. Obviously, then depending on you know, nuances there. The decisions could be different. But I think that's high level of the expectation. I think this year, you know, while I hear obviously a lot of excitement around the immunology programs and we share those, but those would be 2025 data sets, many data sets, impactful data sets. But I also want to make sure we're also paying attention to 24 data releases around these programs because We believe there is an opportunity here to change how we think about this target. Jared, what about patients? I don't know what we can say at this point.

Yeah, I mean, I think maybe just to briefly elaborate, you know, I mean, obviously for this program, you know, we do plan on providing a pretty comprehensive update, you know, later in the year. As I mentioned earlier, our hope is to be through dose escalation, you know, in both arms, you know, the solid tumor lymphoma arm and the heme malignancy arm. to really provide a comprehensive update on safety, PD, and efficacy. You know, keeping in mind, again, that one of the important premises here is that this is going to be very differentiated from MDM2 small molecule inhibitors. We want to show that we have a therapeutic index that is superior to MDM2 small molecule inhibitors, so that takes into account both superior safety as well as potentially superior efficacy. And so I think our aim is to be able to show a data set that will hopefully establish, you know, that we are well differentiated from MDM2 is for this drug in both solid tumors and in liquid tumors. And to marry that sort of presentation potentially with a separate presentation on our patient selection strategy, which is also going to be a very important part of what we do moving forward after phase one.

Thank you.

The next question comes from R. Patel with B. Reilly Securities. Please go ahead.

Yeah, hey, good morning, and thanks for taking the question. One, for the STAT6 and TIK2 program, you've shown data from the proteome study to confirm the selectivity and maybe rule out the off-target effects. Can you share how many proteins were identified in those studies and what the coverage rate was in those proteome studies? Thank you.

So we're not going to share any more data today on that program, and we're going to be, to be honest, quite sensitive about what else we're going to share just based on we want to maintain our competitive advantage here. But that doesn't mean I'm not going to answer your question. So we have high proteome coverage in these studies. We usually can detect north of 11,000 proteins in every study. proteomics study. And what we do at Chimera, we actually look across several cell types. So what we've shown, I believe, were PBMCs because we believe are, you know, one of the more relevant for the diseases we're going after. But in order for us to actually cover the whole proteome, which as you know, it's in the 20,000 proteins roughly, hopefully I didn't We didn't get a wrong number here. So we actually go across many cell types so that we actually cover 100% of the proteome. And the picture that you've seen in our slides is consistent. We only really degrade STAT6. And I would say we only really bind to STAT6.

And that's true also for the TIK2 program and for the RF4 program and for the STAT3 program. Okay, thank you. All right, I can keep going. Yeah, thanks, Kapit. Thank you.

Thank you. We have another question. Okay. It comes from Andy Chen with Wolf Research. Please go ahead.

Hi, this is Emma Ahn for Andy. Thanks for taking our question. I guess just focusing on TIC-2, We're curious where you see weaknesses with current TIK2 inhibitors on the market and just how much headroom there is for improvement with a potential degrader entrant like KT294 into the market. Thank you.

I think that's weakness. Differentiation is of the original. Ah, the weakness. Sorry, I didn't hear it well. So, I mean, as we said before, there are several layers of differentiation. So there is first that small molecule inhibitors These are allosteric inhibitors that actually block also the kinase function and some of the scaffold function, but not the full scaffolding function. And so the actual phenotype of small molecule, even allosteric inhibitor, is closer to kinase inhibitor than to the loss of function profile. We have a slide in our deck that shows you with the pluses and pluses. and shows where is the kinase dead versus loss of function versus wild type. And only a degrader matches the loss of function profile, which basically means we block IL-23, IL-12, type 1 interferon, and spare IL-10. So the compound that is approved, the drug that is approved right now, which is an allosteric inhibitor that actually is not as selective. It actually impacts also JAK1 and so also impacts IL-10, which is a big detriment for GI indication. It's also not very selective, so they have to play around with the doses in order to hit the targets at a reasonable target engagement. Other molecules in the clinic have more, I would say, maybe a higher selectivity profile, but they're not able to block all the scaffolding function and match the loss of function profile. And we believe that by blocking the pathway fully, We should be able, again, as we've shown with STAT6, we've shown with Rx4, once you find the mode of full pathway blockade, you should be able to match the upstream biologics. So the R23 biologics, the type 1 interferon biologics in a single oral molecule. So what is that going to translate in the clinic? You know, we don't have a number, right? So if you look at biologics in psoriasis, they reach close to 90%. of positive 75, for example. Small molecules don't get there. They get into the 60s, 70s, maybe pushing into the mid-70s. So maybe that is a gap that we can fill. But I think that the actual extent of of gas that we're going to be filling with our degrader, we have a goal of biologics, but we actually don't know. It might be even superior or it might be slightly inferior. I think that is a clinical experiment that we have to run. All we're saying here is that biologically, we have a differentiated profile, and we have confidence that that will clinically result in a meaningfully differentiated drug.

Thank you. Thank you.

This concludes our question and answer session. I would like to turn the conference back over to Justine Koenigsberg for any closing remarks.

Thank you. And on behalf of the Chimera team, we'd like to thank everyone for joining us this morning and look forward to keeping you updated on our progress. In the meantime, please don't hesitate to reach out if there are any additional questions following today's call. Thank you.

thank you the conference has now concluded thank you for attending today's presentation