Ladies and gentlemen, thank you for standing by. Welcome to Legend Biotech Reports Third Quarter 2024 Financial Results. At this time, all participants are in a listen-only mode. After the speakers' presentation, there will be a question-and-answer session. Please be advised that today's conference is being recorded. I would like now to turn the conference to Jessie Yeung, Vice President of Investor Relations and Finance. Please go ahead.

Good morning. This is Jessie Yeung, VP of Investor Relations and Finance. Thank you for joining our call today to review our third quarter performance. Joining me on today's call are Ying Huang, the company's Chief Executive Officer; and Lori Macomber, the company's Chief Financial Officer. Following the prepared remarks, we will open up the call for Q&A. We have our Chief Medical Officer, Mythili Koneru; and our SVP of Commercial Development, Steven Gavel, joining the Q&A session. During today's call, we will be making forward-looking statements, which are subject to risks and uncertainties that may cause our actual results to differ materially from those expressed or implied herein. These forward-looking statements are discussed in greater detail in our SEC filings, which we encourage you to read and can be found under the Investors section of our company website. Turning to our highlights. In the third quarter, we are pleased that CARVYKTI cells continued their strong momentum, delivering quarter-over-quarter growth of 53% and year-over-year growth of 87%. We are also very excited about the results from the second interim analysis from the CARTITUDE-4 trial, particularly the overall survival benefit that CARVYKTI achieved. These results were announced as a late-breaking presentation at the International Myeloma Society Meeting in Brazil in September, and they received an enthusiastic response from healthcare providers around the world. Now I am pleased to turn the call over to our CEO for his remarks.

Hello, everyone. I'm glad that you're able to join us and hear about our recent accomplishments. As you can see on Slide 5, it's been another eventful quarter for us as we continued to make significant progress against our strategic priorities. I'd like to start by expanding on the importance of CARVYKTI achieving overall survival benefit in the second line plus patient population. To frame this achievement precisely, CARVYKTI is the first and only cell therapy to significantly extend overall survival compared to standard of care in patients with multiple myeloma as early as the second line. Specifically, CARVYKTI reduced the risk of death by 45% versus standard therapies after a three-year follow-up period. Reaching this milestone is monumental for the company, for the marketplace, healthcare providers, and patients. It puts CARVYKTI in the enviable position of providing patients with longer lives, what some call the holy grail of oncology clinical trials. Hand-in-hand with overall survival, CARVYKTI has also maintained significant improvement in progression-free survival compared to standard of care. Also at the International Myeloma Society meeting, a real-world analysis of CARVYKTI efficacy and safety was also presented. The results demonstrated the importance of risk mitigation and the critical learnings from our development program and real-life experience with CARVYKTI. It is noteworthy that with over 4,000 patients treated we see a very low incidence of parkinsonism, and FDA public safety data also suggests that this condition is likely a class effect. As you know, the prior positive interim data from CARTITUDE-4 resulted in FDA and the European Commission approving CARVYKTI use in the second-line study for relapsed and refractory multiple myeloma patients. We along with our collaboration partner, Johnson & Johnson, are planning to submit the CARTITUDE-4 overall survival results to regulatory authorities in the U.S. and Europe in order to update our label with these new paradigm-shifting results. In the third quarter, we also received approval for CARVYKTI from China's National Medical Products Administration for treatment in the fourth-line plus study. We are pleased that CARVYKTI continues to gain recognition from healthcare regulators around the world for the significant clinical benefits our one-time infusion provides. Importantly, for the OUS, rest of the world market, we have expanded our ability to produce CARVYKTI for patients in Europe. In September, we received approval to produce CARVYKTI commercially at our facility called Obelisc in Ghent, Belgium. This is a critical component of our plans for serving patients in Europe and beyond. Congrats to the team in Ghent for securing the approval in what we believe to be record time. It's another demonstration of Legend's commitment to expediting delivery of CARVYKTI to all patients who can benefit from it worldwide. In the third quarter, net trade sales of CARVYKTI were approximately $286 million, which as Jessie highlighted, is an 87.6% increase year-over-year and a 53.2% increase quarter-over-quarter. The robust quarter-over-quarter performance was aligned with our expectations of accelerating growth in the second half of the year and was driven by continued demand, particularly strength in the second-line demand share against continued capacity expansion and manufacturing efficiencies. We are firing on all cylinders, and we expect sequential growth into the fourth quarter. We look forward to treating many more patients in need in the months and years to come. Our OUS sales increased over 100% year-over-year and 35% quarter-over-quarter. Thanks to our increase in capacity and ongoing launch expansion. In the third quarter, CARVYKTI became commercially available in Switzerland and I am pleased to share that Swissmedic just updated label expansion to the third line plus treatment. Switzerland is the fifth country where CARVYKTI is now commercially available to patients along with the United States, Germany, Austria, and Brazil. In the United States, we continue to certify more hospitals as authorized treatment centers. The total number of U.S. hospitals that are approved to treat CARVYKTI patients is now 82. We call it that CARVYKTI has a unique delayed CRS onset profile that allows for extensive outpatient administration. As you can see on Slide 10, outpatient treatment now comprises up to 48% of our volume and is a significant growth opportunity for us to reach even more patients. Usage in the outpatient setting is very important as we expand further into the community setting. This is a key consideration for hospitals as they seek to optimize allocation of limited beds and resources. Patients and their caregivers often prefer to check out of the hospital after treatment. The option for outpatient treatment is a real differentiator for CARVYKTI as the number of patients increases. CARVYKTI has now achieved nearly 90% market share in the BCMA CAR-T class of sales in the U.S. and Germany, and it continues to be the fastest launch CAR-T product on the market. With the explosive growth of CARVYKTI and our evolution as a company, we're excited to announce that recently we appointed a President of the CARVYKTI business unit, Alan Bash. Alan will be responsible for managing the continued growth of CARVYKTI, overseeing Legend's commercial, technical operations, and quality functions of the franchise. Prior to joining us, Alan served as the CEO of two oncology-focused companies, most recently at ZielBio and prior to that at Checkmate Pharmaceuticals. Before that, Alan had a 23-year career with Bristol-Myers Squibb, where he held various leadership positions across all major therapeutic areas, including oncology, where he drove the expansion of products such as Opdivo, Yervoy, and Erbitux. Alan also contributed to several blockbuster products in collaboration with other companies, such as Abilify with Otsuka and Eliquis with Pfizer. We welcome Alan to the Legend family and look forward to introducing him to many of you soon. Turning to midterm growth for CARVYKTI and Legend. We are pleased with the pace of enrollment for our first-line trial CARTITUDE-5 and CARTITUDE-6. As you may know, CARTITUDE-5 is fully enrolled, and we expect to complete enrollment for CARTITUDE-6 next year. The speed of enrollment in these trials is a testament to the benefit-risk profile of CARVYKTI, demonstrated by our growing body of positive clinical trial results. Looking at longer-term growth for Legend. We recently announced a new research facility being built in Philadelphia, which is a growing hub for biotechnology companies. The new site is strategically located among some of the top research institutions in cell therapy and provides potential opportunities for collaborations, which would expedite our innovative cell therapy research. We expect to be up and running in the summer of 2025, and we look forward to updating you on the progress of this exciting project. To summarize the third quarter, it's been another quarter where we executed with excellence, which sets us up for a strong finish to the year. Now it's time to take a closer look at the financials. So let me turn the microphone over to Lori.

Thank you, Ying, and good morning, everyone. As Ying mentioned, we generated approximately $286 million in total net sales for CARVYKTI during the third quarter, an increase of 87.6% year-over-year. As a reminder, we share equally in all profits and losses of CARVYKTI ex-China with our partner, Janssen. As you can see on Slide 12, total revenues for the third quarter were $160 million, consisting of $143 million in collaboration revenue from the sale of CARVYKTI and license revenue of $17 million from the recognition of deferred revenue in connection with our agreement with Novartis to develop, manufacture, and commercialize LB2102 and other potential CAR-T therapy selectively targeting DL3. The net loss for the quarter ended September 30, 2024, was $125 million or a loss of $0.34 per share compared to a net loss of $62 million or a loss of $0.17 per share for the same period. For the quarter, unrealized foreign exchange losses of $63 million were incurred primarily due to intercompany transactions and balances between the U.S. and non-U.S. legal entities. For the same period last year, $16 million in unrealized foreign exchange gain was reported. Moving on to expenses on Slide 13. Collaboration cost of revenue for the third quarter of 2024 was $52 million compared to $43 million for the same period last year. These are Legend's portions of collaboration cost of sales in connection with the collaboration revenue under the Janssen agreement, along with expenditures to support the manufacturing capacity expansion. Additionally, cost of license and other revenue for the third quarter of 2024 was $3 million compared to no cost of license and other revenue for the third quarter of 2023. These costs are connected with our agreement with Novartis to develop, manufacture, and commercialize LB2102 and other potential CAR-T therapies selectively targeting DL3. Research and development expenses for the third quarter of 2024 were $96 million, similar to the same period last year. These expenses are primarily due to research and development activities in cilta-cel, including startup costs for clinical production in Belgium as well as continued investment in our solid tumor program. Administrative expenses for the three months ended September 30, 2024, were $35 million compared to $28 million for the same period last year. The increase of $7 million year-over-year was primarily due to the expansion of administrative functions and infrastructure to increase manufacturing capacity. Selling and distribution expense for the three months ended September 30, 2024, was $44 million compared to $21 million for the same period last year. The increase of $23 million year-over-year was due to costs associated with the commercial activities for CARVYKTI, including the expansion of the sales force and support for the second-line indication launch. Other expenses were $62 million for the three months ended September 30, 2024, compared to $0.1 million for the same period last year. This increase was almost entirely driven by unrealized foreign exchange losses for the three months ended September 30, 2024. In the same period last year, there were no unrealized foreign exchange losses. The unrealized foreign exchange losses were primarily driven by intercompany transactions and balances between the U.S. and non-U.S. legal entities related to research and development activities. To summarize, our spending remains on track, and we continue to maintain a strong balance sheet. As of September 30th, we had $1.2 billion in cash and equivalents and time deposits. Thus, we believe we have sufficient capital to fund our operating and capital expenditures into 2026 when we expect to begin to achieve an operating profit. Thank you. I will now pass it back to Ying for closing remarks.

Thank you, Lori. Moving to Slide 14. We are excited that we had so much good news to share from this past quarter, and we could not have done it without the dedication of our 2,400 team members globally. Their commitment inspires me every single day, but we continue to have lots of work ahead of us, and we strive to execute our strategic priorities. Before we take your questions, I'd like to share context on the recent development. After our Annual General Shareholder Meeting in October, GenScript announced that they will deconsolidate Legend from their financial statements as they are no longer a majority shareholder of the company. This has no material impact on our operations as Legend has operated as a separate company since our spin-off and IPO in 2020. Now it's time to take your questions. Operator, we're ready for the first question, please.

Thank you. Our first question will come from Gena Wang with Barclays. Your line is now open.

Thank you for taking my questions. I have two questions related to the upcoming data update that investors are focused on regarding the CARTITUDE-1 comparison to Imaging 1 ahead of the ASH update. With the ASH abstract released, we are looking forward to the full data presentation at ASH in three weeks. What key data points should investors pay attention to in terms of efficacy and safety? Additionally, regarding the overall survival benefit we presented for CARTITUDE-4, when can we expect this benefit to be incorporated into the NCCN guidelines and labeling, and what is the current status of that process?

Hey, good morning, Gena. Thank you for the questions. I'll take the first one. So we already saw the baseline from the IMAGINE-1 trial. And you can tell that from every metric we look at, including the number of prior lines of therapy, the percentage of only three prior lines of therapy, the triple refractory patient population, the penta-refractory population, I think we can conclude that clearly, the patient population in IMAGINE-1 is less sick than the patients we enrolled in CARTITUDE-1. Now we don't know, for example, some other metrics, including the percentage of EMD patients, but that might be another metric that could tell us more, right? But even compared to their own Phase 1 trial, this is an easier-to-treat patient population, suffice to say. Now secondly, if you look at efficacy, we did present CARTITUDE-1 with about a 12-month follow-up at ASH 2020. And again, if you look at the ORR rate, which is 97%, and then the CR rate, it's 67%. But I want to mention that all every CR we observed is a stringent CR. Again, we would like to see whether the other party breaks down the percentage of CR versus stringent CR. However, as you may know, in myeloma treatment, it's always about durability. For that, unfortunately, we will not get much data from the other party. And we stand behind the consistent results we have seen from CARTITUDE-1, CARTITUDE-2, CARTITUDE-4, and all trials across all the settings. So I think it's all about durability, it's about PFS. And we have nearly three years PFS in the last time patient population as demonstrated in CARTITUDE-1. So regarding your second question, I'm going to ask Steve to comment on maybe NCCN.

Yes. It's hard to predict the guidelines in terms of when they will be updating them in terms of new data that we would be expecting an update sometime by the end of the fourth quarter.

Sorry. Sorry, Ying. also regarding safety. Can you comment?

Sure. I mean, we do understand that if you use a proactive management strategy in terms of selecting patients and also managing patients with both IL-6 and steroids, it can be very effective. In fact, if you look at the history of CD19 CAR-Ts, right? If you recall almost 10 years ago, there was a perception that maybe the June of CD19 was not as safe as the credit CAR-T. Yet in real life, I don't think it's been that case, right? If you look at the real-world CRS and also neurotox. So clearly, a lot of that has to do with the patient selection and also management. And we are already starting to institute those and we're talking to KOLs about this. You will see more data at ASH as well.

Yes. Hi, it's Steven. What I was saying is that it's hard to predict the guidelines in terms of when they will be updating them in terms of new data that we would be expecting an update sometime by the end of the fourth quarter.

And Gena, just to supplement, we and our partner, Johnson & Johnson, are planning to submit the overall survival data in a supplement to both FDA and EMA in the near future. So we do expect that will be reflected in the label in both U.S. and Europe by end of next year.

And our next question comes from Yaron Werber with TD Cowen. Your line is open.

All right. This is Dana on for Yaron. Congrats on your quarter. And thanks for taking our question. I have two. Obviously, for the first one, you had a strong Q3, but I'm curious how we should think about quarter-over-quarter growth going into Q4? Should we expect the same kind of cadence or is most of kind of the growth driven from the additional manufacturing already realized in Q3? And then secondly, I think you've noted in the past that key limiting factor for BCMA CAR-T supply is the FDA cap on CAR-T production? Is this just for BCMA CAR-T because we're hearing that Gilead was never limited in their volumes for YESCARTA and TECARTUS. So what do you think that might be? Thank you.

Sure. So let me address the first question about sequential growth in the fourth quarter. I think you have heard from both the Legend and Johnson & Johnson teams, reiterating that we confirm we will expect sequential growth in the fourth quarter. Now it is our policy not to comment or provide guidance. So I'm not able to give you any quantitative guidance. But yes, we are reaffirming sequential growth. Even though we have a fantastic growth rate in the third quarter already, but we still expect to see a higher revenue number in the fourth quarter. So regarding your second question, I guess what we can tell is that from the BCMA class in both experience for ABECMA from Bristol and also for CARVYKTI from J&J and Legend. Yes, in both cases, FDA did regulate the capacity. Now I would refer you to ask Kite about their capacity for CD19. But our understanding is that FDA does regulate all CAR-T manufactured facility capacity. It's not just even for franchise but also for each individual facility that produces CAR-T. You can also download the FDA review documents on the FDA website of the process and also how FDA determines the capacity. Sorry. I also want to add that if you look at the performance of all commercial CAR-T brands in the market, 10 quarters in since FDA approval of CARVYKTI in February of 2022, we have been able to supply the market with the highest number in terms of revenue and also slots.

And our next question comes from Kelly Shi with Jefferies. Your line is open.

Congratulations on the progress and thank you for addressing the questions. Regarding the launch of the second line, could you provide more details on the ramp-up schedule? How should we compare this to the baseline launch, especially with two quarters having passed since the approval for the early line? Additionally, do you anticipate that the majority of CARVYKTI usage will transition from the main line to the early line in the near future? Thank you.

Yes, why don't I take that question. It's Steve. Thanks for asking. Why don't I start with the second question first and the question, I think had to do with a percentage of patients in our CARTITUDE-1 versus CARTITUDE-4 indications. We expect to be exiting next year, for example, with the overwhelming majority of our patients treated to be in the CARTITUDE-4 population, something in terms of a ratio of two-thirds to one-third. In terms of where we are right now for this particular year, we are well ahead of where we thought we would be in terms of early line adoption. I think that's built off a number of different things, most notably, the most recent overall survival data that we're coming out with now. So we expect that trend to continue and accelerate to where we would expect to be next year. But in terms of where we're pacing right now for the year, we're outpacing where we thought we would be in terms of our CARTITUDE-4 launch. I don't think there was any other follow-up questions to that. Let me look here. I think that's it.

Thank you.

You're welcome.

And our next question comes from Jessica Fye with JPMorgan. Your line is open.

Hey guys. Good morning. Thanks for taking my question. My question is on just how we should think about the evolution of the mix of inpatient versus outpatient use. Specifically, is the shift that we're seeing driven by the conversion of existing treatment sites to more outpatient use? Or is that more a function of the new sites coming online as outpatient sites? And can you also just remind me where you think that proportion of inpatient versus outpatient could be looking out, say, 12 months from now? Thank you.

I'm happy to take that question. It's an important one. We've been monitoring this since we launched CARTITUDE-1. To give you some context, when we launched our initial indication, we were already focused on the second indication, anticipating that the increase in volume for second line and beyond would be significant. This would represent an unprecedented number of CAR-T eligible patients entering our hospitals. This is why we've seen rapid adoption, approaching 50%, and in some instances reaching 50% at specific sites. The primary driver of this adoption is that sites recognize the volume impact they need to prepare for, and as a strategy, many are moving towards outpatient usage whenever appropriate. Inpatient usage is observed in sites that have embraced the outpatient model, particularly for higher-risk populations, where patients are often admitted for treatment. I hope this clarifies what's driving outpatient adoption. Regarding who is adopting, we're seeing widespread uptake, mainly from the larger academic sites in the United States, particularly our top 18 locations that account for a significant portion of our volume. As new sites come online, it generally takes time for them to ramp up in the outpatient setting. This is because providers need to treat enough patients to understand how they respond to the product and gain real-world experience compared to our label, leading to a slower adoption rate, which has been consistently observed with any new site we've integrated into our commercial footprint in the U.S.

Thank you.

And our next question comes from Umer Raffat with Evercore. Your line is open.

Hi, guys. This is Jon on for Umer. Congrats on the quarter and thanks for taking my question. I'd love to start with one on the drivers of neurotox evolution across your trials. Obviously, Ying you mentioned management patient selection being very important there. But where do you think the tolerability profile could go in the future for CARVYKTI, is it possible to control this even further going forward and to eventually get a better safety profile in the label? And then secondly, maybe since nobody has asked about it, I'd love to get the latest update on your autoimmune progress. I know you're in Phase 1 there, but what are you seeing from a patient enrollment perspective? And when could we see potential data? Thanks so much.

So Jon, I am going to ask our Chief Medical Officer, Mythili to answer the first question.

Thank you for your question. Regarding the neurotoxicity profile, we have observed a significant decrease in delayed neurotoxicity, including Parkinsonism, compared to the CARTITUDE-1 and CARTITUDE-4 data. This improvement reflects better management of these patients, including decreased tumor burden and more accurate patient identification. Notably, in CARTITUDE-4, this rate is currently less than 1%, which is crucial to highlight. Furthermore, we have identified additional factors that may help to reduce this rate even further. We’ve consulted with various key opinion leaders who are using this treatment in commercial settings. Additionally, as Ying mentioned earlier, competitors are actively employing steroid use in their studies. We have discovered that absolute lymphocyte count (ALC) is a promising early indicator of potential rapid expansion, and the application of steroids may help mitigate delayed neurotoxicity. KOLs have shared that they are actively implementing this in the commercial setting. Thus, effective bridging therapy and close monitoring of ALC are essential strategies we are focusing on to help reduce potential neurotoxicity.

And also, Jon, I'd like to also mention that for our potential competitor, it's not fair for them to compare our data from four years ago when they compare efficacy. But then when they talk about safety, again, why don't they compare to our current data, right, where we do see a dramatically lower incidence of Parkinsonism in the CARTITUDE-4 trial and also in the real world, the physicians have been gaining experience in terms of how to manage that, and it is lower again than what we observed in CARTITUDE-1. Now on to your second question about our autoimmune program. Yes, we have officially kicked off our first-in-human study for the trispecific CD19, CD20, CD22 targeting CAR-T for autoimmune indications. And we have already opened our first site. Enrollment is ongoing now. But besides that, we also are working on a couple of other programs that are allogeneic again, targeting autoimmune indications. So that should go into first-in-human study sometime in 2025. With regard to data. Again, we're not guiding, but we do expect some sort of clinical data to emerge in the year of 2025 for the first program. Thank you.

And our next question comes from Kostas Biliouris with BMO Capital. Your line is open.

Good morning everyone. Thanks for taking our question. And congrats on the progress. One question from us on the competitive dynamics, although you already alluded to that, but given that the competitor CARTITUDE product will be entering the market, potentially in the late lines in about a year or so. How should we be thinking about the competitive dynamics there? Are you focusing on protecting your market share in late lines or just focusing on getting as much market share as possible in any lines? Thank you.

Sure, Kostas. Let me start by mentioning a fact, which is in the case of the registration program for late-line multiple myeloma, the first assessment of efficacy is at day 28 or a month after the last patient was enrolled. And then after that, the FDA requires a 12-month minimum follow-up. So if you do the math, that is 13 months after the last patient in. And of course, following that, the sponsor needs to clean up the data, lock up the database, get all the filing into the FDA-acceptable format and the FDA will review. So we're not expecting anything to come into the market next year or maybe even the year after that, honestly, it depends on how fast the regulatory review goes, right? And that's just a fact. If you look at the regulatory history for CARVYKTI for ABECMA. I don't understand why the agency FDA would take any special treatment for others. And then I'll ask Steve to comment on the question.

Yes. Thanks, Ying. In terms of promotional focus, the fact that we are now clearly differentiating ourselves in terms of the only CAR-T therapy in earlier lines today, which is the second line plus. We will continue to promote in those earlier lines and that will remain our focus for the foreseeable future. One thing to keep in mind, and I think it's an important comment here as it relates to any downstream competitors in the United States, when a CAR-T therapy is used right now, at least in the private sector, and this is consistent with Medicare, the payers are not paying to go from a CAR-T drug to another CAR-T therapy. It's denied. So it's the primary reason, one of the reasons why we'll be driving our promotional efforts in the earlier lines, not to mention that's where the majority of the benefit is for our patients. But that will be consistent in terms of our promotional focus, again, for the foreseeable future.

And Kostas, maybe I would also add another two comments here. First of all, I think outpatient administration is very, very important today. And that is why compared to all the other brands, we have the highest revenue mix coming from outpatient use close to 50% of our revenue is coming from outpatient use. And that is a distinct important commercial advantage. Secondly, as you probably know, every hospital and every insurance plan has a preferred provider and has a formulary. And as a third or fourth entry into the market, that increases the degree of difficulty in terms of launching into the commercial space as well.

Yes. Maybe before we jump off that question, I think it's important because we never get the question why, right? I mean, we get it once in a while. We got it early in terms of why, this is one of the only CAR-T therapies that have been used so frequently in the outpatient setting. And it will continue to be the case in the foreseeable future, including this competitor, I think people are referring to. The reason behind the why is around the onset of CRS that you're seeing with CARVYKTI. It's the only CAR-T therapy today, where you see a prolonged timeframe passed before the actual onset hits, which does allow or enable our sites to dose, monitor remotely, and then have these patients being brought in at a later date. My understanding with the competitor that we're referring to, their onset is relatively acute. So that's going to be very, very difficult to, in essence, utilize outpatient-type guidelines for a competitive product that has that type of acute onset. It makes it very difficult for physicians to discharge if patients are experiencing short-term toxicity. So I did want to highlight that for you because I keep hearing about outpatient use in other particular CAR-T products. It's one of the distinct clinical differences with this program, which enables us to, in essence, take our patients outside the hospital.

And our next question comes from James Shin with DB. Your line is open.

Hey everyone. Thank you for taking my question. I have another inquiry for Alan and Ying regarding the outpatient setting. We have a real-world example of how short onset CRS behaves with ide-cel, and it doesn’t perform well in outpatient scenarios. So how could a different product perform better in outpatient settings? That’s my question. Thanks.

From a medical perspective, the update will focus on the onset of actions or the onset?

So I think that CARVYKTI being given outpatient is something that we actually recently did an advisory board on. And there are several institutions that are actually doing this quite successfully and able to completely monitor remotely and they're actually working on a publication to kind of continue to kind of promote this outpatient model, which is very easy to do because of what Steve mentioned earlier about the delayed CRS onset. Other competitors tend to have very early effects. And so what that does is it creates a setting where right after administration, you have to kind of monitor these patients closely. It's not to say that you can't give it to outpatient, but it tends to be a higher hurdle to do so. And that, I think, is a significant advantage given that these hospitals are extremely burdened by doing all of these things in patients, keeping the patients in the hospital for prolonged periods of time. So it's a significant advantage, as Steve mentioned.

Yes. Let me add one thing to My's comments, you're all spot on. The best proxy to look at and to ask yourself the question is, why has the market if outpatient administration is so relevant, why hasn't the market successfully moved to outpatient treatment with ABECMA? And the reason for that is, it also has a very acute onset of CRS. It's that simple or you would have seen that migration outside of the hospital there. So again, it's a benefit that, like I said earlier, it's a very unique toxicity attributed to this program that is unique not only to the BCMA therapies but also CD19. And it's the first time that you're seeing this type of outpatient adoption across the class of CAR-T, and it was something that we were hoping to have happened, quite frankly, and it was something that our investigators predicted back when we were launching back in CARTITUDE-1. So anyway, I'll stop with that.

And our next question comes from Leonid Timashev with RBC Capital Markets. Your line is open.

Hey, this is Joe on for Leo. Thanks for taking our question. What are your expectations for Europe now that you have commercial capacity up and running? And what are some differences between European and U.S. physicians in selecting CAR-T over other options? Thank you.

Yes. So it's Steve. So I do want to take a crack at that one. So Europe has a very different model. So we just had a long discussion here, I think, around outpatient administration. So that model is not available for most sites in Europe. So this whole outpatient conversation. I don't think you're going to hear a whole lot about with CAR-T therapies in general. So in terms of the CAR-T adoption within Pan Europe, whether it be BCMA or CD19, it's been relatively slow and unfortunately, it's been mostly a product of coming to an agreement around pricing. It's unfortunate, but that is a situation in Europe. As I believe you know, our partner is driving CARVYKTI in the European markets today. And I won't reiterate the countries that we are launched into today, because Ying already did that in the opening. But right now, the key driver for this brand in Europe is Germany, and we'll continue to ramp up into next year and beyond. So that will continue to be our major market in Europe.

This is Ying. I also want to add that you probably know that in Europe, where pretty much every country has a single payer system. The survival data is utmost important because those government agencies, they do care a lot about the outcome, right? So it's not about response rates or even just stringent CR. It is about durability. It is about PFS. And most importantly, they do ask questions about survival. So we're very pleased to be armed with this survival benefit we have observed in CARTITUDE-4. In fact, we're already talking to different countries and agencies in Europe, including Germany, about the latest survival benefit we observed. And I want to emphasize again, to date, CARVYKTI is the only and also the first CAR-T targeting BCMA or any BCMA-targeting modalities in the treatment of myeloma that has demonstrated both clinical and meaningful and also a statistically significant survival benefit with a hazard ratio of 0.55. That is probably the lowest hazard ratio you have seen in any major myeloma trial to date.

I'll also add that the clinical trial enrollment, as Ying mentioned in his opening. The CARTITUDE-5 and CARTITUDE-6 had significant or is having significant enrollment in Europe. So clearly, the treating physicians are very interested and being able to provide this therapy for their patients.

And the next question will come from Vikram Purohit with Morgan Stanley. Your line is open.

Hi, good morning. Thank you for taking the questions. We had two on CARVYKTI pipeline efforts. First, for the CARTITUDE-2 study, we just wanted to see what you think the timeline could be for an update from cohorts E and F and your guidance on the best way to interpret that data when it's available? And then second, apologies if you mentioned this and we missed it, but I wanted to see what the status was on your and J&J's plan to discuss the MRD negativity as a potential endpoint for CARTITUDE-6 and when we could receive an update here? Thanks.

Sure. Thank you for your questions. Regarding CARTITUDE-2 cohorts E and F, which are the frontline newly diagnosed multiple myeloma, we ultimately need longer follow-up. So we will continue to monitor those cohorts very closely. And when we're able to have more follow-ups, we'll be able to report that externally. Regarding your second question regarding the CARTITUDE-5 and CARTITUDE-6 and some with MRD negative, this is obviously with the recent ODAC discussion, the FDA is more open to using MRD negative DCR as potentially as an endpoint, particularly in these frontline studies where these endpoints tend to be extremely long in terms of PFS and OS. Therefore, we hope to get in front of the FDA and have some interactions with them on using this as an endpoint. So more to come.

And the next question comes from Mitchell Kapoor with H.C. Wainright. Your line is open.

Hey, thanks for taking the questions. I want to build on a question from earlier. When KOLs are successfully using steroids to manage some of the safety events such as CRS to neurotox, could you just talk about, is there a way to follow that formally and potentially include that in the label at some point? And then separately, could you talk about if there's any significant work that remains on the payer side for getting them up to speed with the second line label? Thank you.

Yes. So regarding the steroid question, we hope to incorporate something like that in the CARTITUDE-6 protocol so that we can look at using ALC as an early surrogate marker for extension and treat with steroids accordingly. Therefore, if we're able to incorporate that, we hope that that can also potentially go into the label. And we do have precedence for this. If we look at YESCARTA's label, they do have recommendations on steroid use. So we think that this is a good management tool moving forward.

I will address the second part of your question regarding payer coverage. I'm pleased to inform you that there are no payment barriers with our commercial plans for the CARTITUDE-4 indication. In fact, with the significant overall survival benefits we're witnessing, private insurers are very supportive of CARVYKTI due to the cost savings it creates in the long run. Additionally, insurers appreciate the potential for CAR-T therapies to be administered in outpatient settings, which significantly lowers inpatient costs when managed effectively and safely.

Thank you.

And our next question comes from Justin Zelin with BTIG. Your line is open.

Hey, good morning. This is Jed on for Justin. Thanks for taking our questions. So you've talked about lymphocyte monitoring and steroid use to manage the delayed neurotox. But in your experience, are there still a fraction of clinicians that are hesitant to use CARVYKTI due to the neurotoxicity and parkinsonism in the second-line setting? And due to concerns the gain will wait as they look to the frontline setting? And my second question was just with the China approval now in place, how should we think about that launch trajectory moving forward? Thank you.

You want to take a crack at that?

Clinical piece, and I'll do the commercial state.

Yes. So regarding the ALC and the steroid use, this is something that some clinicians have actively adopted and we are potentially working on more publications on an attempt to create more awareness on this. That being said, clearly, I think this is going to be an important factor as we move into earlier lines of therapy. And that's why I think it's so critical to make sure that we inform treating physicians that there are ways to mitigate it appropriately.

Yes, I can share some research that has remained consistent over the years. You're completely right. In the earlier line setting, the issue of toxicity is increasingly important for treating physicians. This has been evident from our CARTITUDE-4 launch research. It's one of the main reasons we have increased our promotional efforts in the outpatient setting. As Lori mentioned earlier, there were some expenses this quarter to expand our sales organization. This expansion was largely to address the need for educating physicians who may not be as familiar with CAR-T therapies. Many of these physicians work in community settings, and we are now actively educating them alongside our partner about the features and benefits of CARVYKTI, including its toxicity profile. One of the key differentiators for us now is the overall survival benefit, which is extremely significant. This conversation becomes particularly important in areas where there may be concerns about neurotoxicity in earlier lines.

So Jed, on your second question about China launch. So we're actually in discussion with our partner, Johnson & Johnson about this. But given the supply trend and also the availability of Lentiviral vector, we are obviously prioritizing markets such as U.S. and Europe, where we already launched CARVYKTI. So that is an ongoing discussion with Johnson & Johnson. And then regarding China, I do hear some questions from investors and analysts about the topic. So I may just want to add another layer of the comment here. That is with President-elect Trump coming into the White House in January and also all the discussions about tariffs. Is there any impact on Legend at all? So I can confirm that we use no raw material or starting material from China in the production of CARVYKTI in U.S. and Europe. If you look at our supply chain operation to supply CARVYKTI in U.S. and Europe, 100% of all raw materials and starting materials are coming from U.S. or Europe. So that is a very clear cut answer to the tariff question. We don't see any impact at all whatsoever. Thank you.

And our next question comes from Rick Bienkowski with Cantor Fitzgerald. Your line is open.

Hi, good morning. Congrats on the progress and thanks for taking the questions. I have two. So about a week ago, there were reports that Peter Marks and the FDA were reconsidering the black box warnings on CAR-T products based on having better information about the background rate of secondary malignancies. So I think could get a little color on what this means from the perspective of CARVYKTI? And also if there's been any recent communications with the FDA about this issue? And the second question, just looking at the clinical pipeline, there are quite a few Phase 1 trials being conducted in parallel. Could you just remind us which of these trials are in later stages and which of these programs are likely to see clinical updates from in 2025?

Yes. Thank you for your questions. Regarding the secondary primary malignancy, despite the comments by Dr. Marks, it still remains something that's seen across many different CAR-T therapies. We have not had any specific discussions with the FDA on this as of yet. Regarding your second question regarding our pipeline, we do have two U.S. studies in Phase 1, one involving DLL3 in small cell lung cancer, which we are in collaboration with Novartis on and a second Claudin 18.2 in gastric and pancreatic cancer. Both of these studies have been enrolling, I think, well this year, and we look forward to some publications next year on the Phase 1a dose escalation, both in terms of some safety and efficacy as well.

And Rick, I would like to add that if you see some recent literature, which actually suggest that if you look at the background rate. So for patients who have been treated with multiple myeloma that are on standard of care versus the SPM rate in patients treated with CAR-T, there's really no difference in terms of the incidence rate of SPM or second primary malignancy. So really, we're not seeing additional or higher rate of SPM in the CAR-T-treated patients versus patients treated with other methods of therapies for myeloma. And then also on the pipeline, we do have eight ongoing Phase 1 IT programs in China. I would say maybe we can focus more on allogeneic modalities, including our commonality programs and also our autoimmune programs. So those are probably two focuses for the research effort.

All right, great. Thank you.

And the next question comes from Sean McCutcheon with Raymond James. Your line is open.

Hey guys, good morning and thanks for taking the question. Just one quick follow-up and then another question. The follow-up is, is there a specific reason you need additional follow-up for CARTITUDE-2 for E and F? Are you waiting for any specific metrics that would have a read-through to the frontline pivotal, say, 12-month MRD-negative CR, for example? And then the second question is any additional color on the out-of-spec rate and where you see that moving in the near term with more distance between the widening of the release specs in April and presumably more fit patients entering the top of the funnel with earlier line approval? Thanks.

Thank you for your question. So regarding the CARTITUDE-2 cohort E and F, just to remind you, these are both frontline newly diagnosed multiple myeloma patients. And as such, these patients typically have very prolonged courses, including extensive PFS. So even for MRD-negative CR, we still need quite a bit of follow-up in these patients, and that's why we won't be able to give you an exact timeframe when we anticipate this at this moment, unfortunately.

Yes. Sean, also, just as a reminder, if you look at the data from the PERSEUS trial, conducted by our partner for the RVd regimen. You're looking at a 4-year PFS rate of 85%. So that is why it's really not meaningful to release data with, let's say, even one-year follow-up. That's the reason behind it. And then regarding our out of spec rate, in general, we are seeing quarter-over-quarter improvement and without giving any specific numbers, I can tell you, our OS in general is the range of low teens. And one interesting observation so far since the secular approval by the FDA is that, if we look at the preliminary out-of-spec data from the old indication based on CARTITUDE-1 and then versus the patients who are under indication of CARTITUDE-4, second to fourth line, we did notice that between the two groups of patients in our commercial mix here that the CARTITUDE-4 patients are coming in with a lower out-of-spec rate. I thought this is early. This is preliminary, but that is an interesting observation we are seeing already in the manufacturing operation.

And our next question comes from George Farmer with Scotiabank. Your line is open.

Hi, good morning. This is Chloe on for George. Thanks for taking in my questions. We have two. I was wondering if you could speak a little bit more to the drivers of this accelerated approval for commercial production at the Obelisc site in Belgium. And we admitted some of the regulatory requirements around that? And can we expect more stepwise issues going forward kind of similar to the U.S. or now that you have obtained kind of like a bolus approval for a bunch of commercial slots you need to go back to that before further approval? And the second question is if you could walk us through your current assumptions for penetration of the frontline market?

Thanks, Chloe. Thank you for the questions. I'll address the first one. So yes, we're very pleased with the approval from EMA on commercial production at our Obelisc facility in Ghent, Belgium, that happened on September 19. And on the second day, September 20, we already started our first commercial batch production in that facility. So this is, again, a testament to the quality of our manufacturing operation in the Obelisc facility. And because Obelisc right now is only producing for commercial patients in the European Union, we don't need any cash or regulation because you probably know, EMA actually does not regulate CAR-T manufacturing capacity. This is different from the FDA policy in the U.S. And next year, when we do expect our much larger facility in Belgium called Tech Lane to be online, and that will be the same case again. So right now, we do expect clinical production to be approved in Tech Lane in probably the first half of next year, followed by the official EMA approval of commercial production in that facility by the end of next year. And then I may also want to add that Novartis already won FDA approval to start clinical production in the summer. And I'm very pleased to announce that Novartis has already submitted the application to the FDA. So right now, we do expect FDA approval in the first half of next year for the Novartis facility in New Jersey to start commercial production. So everything is on track, and we reiterate that we do expect to have combined in-network capacity of more than 10,000 doses per year by the end of 2025. That is on track. And then I'll ask Steve to talk about maybe frontline.

Thank you. I'd like to discuss CARTITUDE-4, as it connects to our strategies for CARTITUDE-5 and 6. With the launch of CARTITUDE-4, we've made significant changes to our go-to-market model. When we launched CARTITUDE-1 for fifth-line plus treatment, our primary focus, along with our partners, was in U.S. hospitals, which is consistent globally. As we’ve noted, patients are becoming healthier, so our focus has expanded beyond hospitals in the U.S. to include outpatient settings. This broader reach means we will engage a larger group of providers who will be diagnosing and treating these patients. This approach is crucial as it sets the stage for CARTITUDE-5 and 6. By establishing a presence in outpatient settings, we can ensure that the same providers diagnosing these patients will hopefully refer them for our frontline therapy as soon as possible. It's also worth mentioning that we haven't yet activated patient engagement or efficacy largely due to supply issues. However, we are now actively working with patient and advocacy groups in community settings, which is a significant advancement. Looking ahead, in the coming years, we aim to collaborate with larger retail or outpatient community DPOs, such as the U.S. Oncologies and Florida Cancers, to explore ways to bring our product closer to more mobile patients. While this is still in development, we are actively engaged with our partners, which is very exciting and represents a major step for CAR-T therapies as we prepare for the CARTITUDE-5 launch. I'll conclude with that.

Thanks so much.

This does conclude today's conference call. Thank you for participating, and you may now disconnect.