NASDAQ:LKFT Lakefront Biotherapeutics American Depositary Shares Q1 2026 Earnings Report $29.84 +0.46 (+1.57%) As of 04:00 PM Eastern ProfileEarnings HistoryForecast Lakefront Biotherapeutics American Depositary Shares EPS ResultsActual EPS$0.25Consensus EPS -$1.27Beat/MissBeat by +$1.52One Year Ago EPSN/ALakefront Biotherapeutics American Depositary Shares Revenue ResultsActual Revenue$8.75 millionExpected Revenue$11.26 millionBeat/MissMissed by -$2.50 millionYoY Revenue GrowthN/ALakefront Biotherapeutics American Depositary Shares Announcement DetailsQuarterQ1 2026Date5/6/2026TimeAfter Market ClosesConference Call DateThursday, May 7, 2026Conference Call Time8:00AM ETConference Call ResourcesConference Call AudioConference Call TranscriptSlide DeckPress Release (6-K)Interim ReportEarnings HistoryCompany ProfileSlide DeckFull Screen Slide DeckPowered by Lakefront Biotherapeutics American Depositary Shares Q1 2026 Earnings Call TranscriptProvided by QuartrMay 7, 2026ShareShareShare This ReportLink copied to clipboard.Key Takeaways Positive Sentiment: Galapagos signed a binding deal with Gilead for Ouro's lead BCMA/CD3 T‑cell engager gamgertamig, which the company describes as potentially first‑/best‑in‑class with registrational trials possible as early as 2027 and Fast Track/Orphan designations for ITP and AHA. Positive Sentiment: A partial waiver/modification of the legacy OLCA with Gilead unlocked €500 million of capital for independent use (with up to €150 million optionally available for return of capital) and shareholder approval for a buyback gives the company meaningful financial flexibility. Neutral Sentiment: Q1 results showed revenues of €6.5 million (down vs. prior year due to prior OLCA revenue recognition) but an improved operating loss (~€63.7M), a net profit of €14.5M (driven by fair value and FX gains), and cash/investments of ~€2,982.2M at quarter‑end. Neutral Sentiment: Management announced a corporate rebrand to Lakefront Biotherapeutics and an expected ticker change to LKFT on Euronext and Nasdaq effective May 8, 2026. Negative Sentiment: Key execution and clinical risks remain — dose/schedule must balance deep B‑cell depletion with minimized CRS/infection risk, and 2026 will include sizable near‑term cash outlays for the Ouro transaction (~€775M–€790M) plus cell‑therapy wind‑down costs (~€125M–€175M), which will materially draw on the cash balance despite management saying funding remains robust. AI Generated. May Contain Errors.Conference Call Audio Live Call not available Earnings Conference CallLakefront Biotherapeutics American Depositary Shares Q1 202600:00 / 00:00Speed:1x1.25x1.5x2xTranscript SectionsPresentationParticipantsPresentationSkip to Participants Operator00:00:00Good day. Thank you for standing by. Welcome to Galapagos Q1 2026 financial results conference call. At this time, all participants are in a listen-only mode. After the speaker's presentation, there will be a question-and-answer session. To ask a question during the session, you will need to press star one one on your telephone. You will hear an automated message advising your hand is raised. To withdraw your question, please press star one and one again. Please be advised that today's conference is being recorded. I would now like to hand the conference over to your speaker today, Sherri Spear. Please go ahead. Sherri SpearHead of Investor Relations at Galapagos00:00:42Hello again from Belgium. Thank you for joining us today as we report Galapagos first quarter 2026 financial results and business update. Last evening, we issued a press release outlining these results. This release, along with today's presentation, can be found on the Galapagos investor website at www.glpg.com. Before we begin, I would like to remind everyone that we will be making forward-looking statements. These forward-looking statements include remarks concerning future developments of our company and our pipeline and possible changes in the industry and competitive environment. These forward-looking statements reflect our current views about our plans, intentions, expectations, strategies, and prospects, which are based on the information currently available to us and on assumptions we have made. Actual results may differ materially from those indicated by these statements and are accurate only as of the date of this recording, May 7, 2026. Sherri SpearHead of Investor Relations at Galapagos00:01:40Galapagos is not under any obligation to update statements regarding the future or to conform to these statements in relation to actual results unless required by law. You are cautioned not to place any undue reliance on these statements. Joining us on today's call from the executive team are Henry Gosebruch, Chief Executive Officer, and Aaron Cox, Chief Financial Officer. Eric Hedrick, Chief Clinical Advisor, Sooin Kwon, Chief Business Officer, and Dan Grossman, Chief Strategy Officer, will be joining us for the Q&A session. With all of that, let me now turn the call over to Henry Gosebruch, CEO. Henry? Henry GosebruchCEO at Galapagos00:02:20Thank you, Sherri, and thank you all for joining us today. It is truly an exciting time to be here. This call marks my one-year anniversary as CEO, and I couldn't be more proud of what we've accomplished together in the first year of our journey. We have transformed our management team and board, repositioned our portfolio, added an exciting set of new pipeline programs, and we are changing our name to Lakefront Biotherapeutics. This is not a story of small adjustments. It's a story of real transformation. A transformation like this requires the right people. At Galapagos, we've assembled a management team with world-class business development expertise and a shared mission of leveraging our unique position to develop new medicines for patients and to create significant value for our shareholders. Our executives bring world-class deal-making experience, and each has an enviable track record. Henry GosebruchCEO at Galapagos00:03:18This is a team built for this new phase of our company. We are focused on disciplined decision-making, careful capital allocation, reshaping our pipeline through business development, and focused execution that can create long-term sustainable value. As Galapagos transforms, it's also important that the board brings the right mix of capabilities and background. We are very pleased with the talented group that has joined us. The board's expertise and background brings the skills and experience that are needed to provide effective oversight of our strategy and the company. Our previous board chair, Jérôme Contamine, retired from the board following the 2026 AGM/EGM. I am extraordinarily grateful for Jérôme's service. He has been a great partner and provided valuable insights that have positioned us for this next phase of growth. I'm excited to work with Gino Santini as our new board chair going forward. Henry GosebruchCEO at Galapagos00:04:19Gino is a seasoned pharmaceutical professional with a 27-year career at Eli Lilly, where he served as Senior Vice President of Corporate Strategy and Business Development and led major acquisitions and partnerships. He has advised and directed numerous pharmaceutical, biotech, and venture-backed organizations and has relevant experience in M&A, commercial partnerships, and board governance. Gino's extensive operational, strategic, and business development expertise, shaped by decades of global leadership in our sector, will be invaluable as we execute on our strategy to deliver meaningful patient impact and sustainable shareholder returns. Just a few weeks ago, we announced that we have entered into a binding agreement with Gilead regarding the portfolio created by Ouro Medicines. This did not happen overnight. Henry GosebruchCEO at Galapagos00:05:10It was the result of a structured process, early relationship building, confidential reviews, negotiations, and ultimately successful agreement on a partnership with Gilead that has the potential to drive significant value for our shareholders. The transaction centers on Ouro's lead program, gamgertamig, a BCMA/CD3 T-cell engager for autoimmune diseases with multi-billion-dollar revenue potential. Currently in Phase 1b dose-ranging studies and expected to enter registrational studies as early as 2027. Gamgertamig, Ouro's lead molecule, is, in our view, a potential first and best-in-class T-cell engager that has demonstrated a compelling profile in clinical studies. The collaboration brings a meaningfully clinically differentiated high-potential asset into our portfolio. The proof of concept initial indications are orphan indications, where the clinical trials are manageable in size and scope, with significant potential for expansion into additional indications. Henry GosebruchCEO at Galapagos00:06:15We've seen compelling data from over 60 patients treated with gamgertamig across five distinct autoimmune indications. This clinical experience has highlighted the differentiated profile of gamgertamig, characterized by rapid induction of durable complete responses, minimal cytokine release syndrome with the current schedule of administration, and remarkable consistency in these findings across studies and disease indications. We look forward to sharing data with investors over the coming months in a series of publication and presentations at medical meetings. We believe that gamgertamig has a clear speed to market advantage. The initial focus on the treatment of rare autoimmune diseases has provided rapid proof of concept, enabling initiation of registrational trials as early as 2027. The program has also received Fast Track and Orphan Drug Designation in the U.S. for ITP and AHA, further supporting an accelerated development path. Henry GosebruchCEO at Galapagos00:07:16Finally, the spectrum of diseases that may be addressable by gamgertamig encompasses over 20 separate indications, giving us a pipeline and a product opportunity. In conclusion, we believe gamgertamig could represent a very important new type of treatment approach for immune reset therapy for patients across a large number of conditions. It has shown compelling clinical data so far, and it may have both a first-in-class advantage and best-in-class potential. Our partnership also includes three exciting preclinical programs, which we will look to progress with urgency. We look forward to sharing more about these programs in the future. Now, I'll turn the call over to Aaron to talk about financials. Aaron? Aaron CoxCFO at Galapagos00:08:01Thanks, Henry, and hello, everyone. As you heard from Henry, we are really excited about the Ouro transaction. Another major benefit is that it includes a partial waiver and modification of terms of our legacy Option, License and Collaboration Agreement, or OLCA, with Gilead, marking a meaningful step forward in our strategic and financial flexibility. This slide details the benefits of this transaction relative to our legacy relationship. In short, the participation of Gilead was far above the $150 million expected with the legacy agreement. I'm really proud of our team for negotiating far better terms and proving that we are able to work together with Gilead to achieve our common goals. Aaron CoxCFO at Galapagos00:08:44As noted in our transaction announcement, under the revised terms and subject to the closing of the transaction, $500 million is now unlocked for broader use beyond the Ouro Medicines investment, enabling Galapagos to pursue new opportunities and transactions independently of Gilead and expanding the universe of potential strategic targets. Up to $150 million of this $500 million may be used for return of capital to shareholders, subject to certain limitations, providing us with additional optionality to drive shareholder value. This partial waiver and modification to terms of the OLCA further strengthen our ability to deploy capital strategically and to pursue additional value-accretive opportunities. Last week, we also received approval from our shareholders to complete a share repurchase. We will provide an update regarding a potential share repurchase following the close of the Ouro Medicines transaction. Aaron CoxCFO at Galapagos00:09:40Turning now to our Q1 2026 financial results, as outlined in the press release issued last night, our total net revenues were EUR 6.5 million compared to EUR 75 million in Q1 2025. This decrease is mainly driven by the prior year comparison, which included EUR 57.6 million related to the OLCA revenue recognition. As noted with our full year 2025 results, the remaining deferred income balance related to the OLCA was fully released at year-end 2025. In Q1 2026, revenues were primarily driven by EUR 4.9 million in supply revenues from Jyseleca inventory sales to Alfasigma, and EUR 1.6 million in collaboration revenues, reflecting royalties from Gilead. On the cost side, we continue to see significant reduction in our operating expenses. R&D expenses decreased to EUR 31 million, contributing to an overall improvement in our cost base. Aaron CoxCFO at Galapagos00:10:40This reduction is driven by lower severance expenses as well as the absence of restructuring-related charges that impacted Q1 2025. As a result, operating loss improved to EUR 63.7 million compared to EUR 158.7 million last year, which included EUR 111 million in restructuring costs. Moving below operating income, we've reported net financial income of EUR 77.7 million, mainly driven by positive fair value adjustments and favorable unrealized currency exchange gains on our US dollar-denominated cash and investments of EUR 64.3 million. This led to a net profit of EUR 14.5 million for the quarter, compared to a net loss of EUR 153.4 million for the first three months of 2025. Aaron CoxCFO at Galapagos00:11:31Financial investments and cash and cash equivalents totaled EUR 2,982.2 million on March 31, 2026, as compared to EUR 3,297 million on March 31, 2025. The quarter-end cash balance meaningfully benefited from a decrease in the U.S. dollar to euro exchange rate, which moved from 1.175 at year-end 2025 to approximately 1.15 at the end of the quarter. Turning now to our guidance for 2026. With the closing of the Ouro transaction expected in the second quarter, we expect to spend EUR 60 million-EUR 75 million on Ouro-related cash expenditures, including operating costs and transaction expenses in 2026. Aaron CoxCFO at Galapagos00:12:17Along with the upfront payment of approximately EUR 713 million, this results in total Ouro-related cash expenditures of EUR 775 million-EUR 790 million for 2026. We continue to expect one-time cash costs of EUR 125 million-EUR 175 million related to the wind down of cell therapy activities. Inclusive of the Ouro-related expenditures and continued wind down of cell therapy, we now expect to end the year with EUR 1.975 billion-EUR 2.05 billion of cash and cash equivalents. Importantly, the company remains robustly funded. Following this transaction and including estimated R&D spend associated with gamgertamig until first approval, the company will continue to have a majority of its current cash remaining for additional strategic transactions and other capital allocation priorities. Aaron CoxCFO at Galapagos00:13:12Now, let me turn it back to Henry to wrap up. Henry GosebruchCEO at Galapagos00:13:14Thank you, Aaron. In closing, I'm just thrilled to introduce you to the new Lakefront Biotherapeutics. To us, Lakefront symbolizes the attractive opportunity in front of us and the new beginning we are creating. My most reflective moments often occur when I'm out exercising on Chicago's lakefront. Our new name captures what we aspire to achieve for patients, enhance quality of life, meaningful, positive impact, and more time for what matters most. It represents helping patients move toward a better future with greater hope and possibility. As of tomorrow, May 8th, we expect to be listed as LKFT on Euronext and Nasdaq, symbolizing another pivotal step in our transformation. With that, thank you all for your attention, and we will now open it up for your questions. Operator. Operator00:14:11Thank you. As a reminder, to ask a question, please press star one one on your telephone and wait for your name to be announced. To withdraw your question, please press star one and one again. We will now take the first question from the line of Brian Abrahams from RBC Capital Markets. Please go ahead. Brian AbrahamsAnalyst at RBC Capital Markets00:14:36Hey, good morning, guys. Thanks for taking my question and congrats on all the transformation over there. I was wondering if you could give us maybe your latest thoughts on what the dose ranging gamgertamig data will need to show specifically just in terms of B-cell depletion depth and durability, the CRS rate reductions to move forward in registrationals. How you're gonna be picking which registrational trials to begin first, and just any more thoughts on the potential size and complexity of these trials that could start next year? Thanks. Henry GosebruchCEO at Galapagos00:15:17Hey, Brian, it's Henry. Good morning. Thanks for the question. I'll start, and then I'll have Eric supplement. First of all, look, we, as we said on the prior discussion, we had a chance to really thoroughly diligence not only gamgertamig, but other programs out there with other T-cell engagers. We've seen really compelling data from over 60 patients that showed very rapid onset, very deep depletion and very good durability. Again, as we've talked about, that will come out here in the next couple of quarters in terms of individual releases at medical meetings and other publications. Henry GosebruchCEO at Galapagos00:16:10Just for context, I'll have Eric go through the specifics on the three points you raised. Eric. Analyst00:16:17Yeah. Thanks, Henry. Hi, Brian. Thanks for the question. You know, sort of expanding on what Henry just said, I think the team at Ouro has done really good work on, you know, exploring dose ranging here. I would say that the profile that, you know, would be an optimal profile for going into late-stage development would be one where you get profound B-cell depletion, but a dose duration schedule that minimizes CRS risk. I think at the current dose and schedule, you know, we've re-referred to this previously, it really does seem like alterations in the dose and the duration of therapy can really minimize the CRS risk. Analyst00:17:09I think the other aspect here that's important will be, you know, having a dose that results in a period of B-cell depletion that is deep but relatively short, right? That you can minimize the infectious risk, the need for supplemental intravenous immunoglobulin. Again, I think the team at Ouro is well on your way to identifying that dose. You know, we fully expect that, you know, by 2027, you know, we'll be comfortable with the doses that we take forward into phase III programs. Operator00:17:53Thank you. We will now take the next question from the line of Judah Frommer from Morgan Stanley. Please go ahead. Judah FrommerAnalyst at Morgan Stanley00:18:04Yeah. Hi, guys. Thanks for the update, and thanks for taking the question. You know, I think we saw another transaction recently for a BCMA/CD3. You know, there's several assets in this space. I'm just curious how you think this space might evolve and how you're thinking about development plans. Do you see room for multiple assets targeting the same mechanism within the same large indications? Do you think this is gonna be an area where various assets are going to kind of carve up sub-indications, maybe stick to smaller indications as opposed to necessarily all going after the same large ones? Thank you. Henry GosebruchCEO at Galapagos00:18:45Thanks, Judah. It's Henry. Again, just for context, we were able to diligence multiple opportunities in some depth. We're quite pleased that our top choice, i.e., gamgertamig, was the one that we were ultimately able to transact with. We continue to believe that gamgertamig is the best alternative out there and has the potential to be first in class. That being said, look, we're very encouraged by the fact that we're not the only ones excited about the space, that there's a lot of investment going into it. I think that's that is good to see and ultimately good for patients. Henry GosebruchCEO at Galapagos00:19:32The Ouro team has been really, really savvy in terms of picking very interesting indications that we believe are, you know, quite sizable, you know, multi-billion EUR potential easily. Where they have a clear timing advantage. I think in those places, we're in a really favorable position. That being said, we don't view gamgertamig behind in any other indication as well, and those are being very actively explored. To your question, whether ultimately, you know, the best drug takes all of it or the market gets split up in some way, I think, you know, we'll defer that when we go a little bit further. Again, we're based on our diligence of multiple programs. Henry GosebruchCEO at Galapagos00:20:17We think we got the first and best in class alternative here with us. Operator00:20:28We will now take the next question from the line of Phil Nadeau from TD Cowen. Please go ahead. Phil NadeauAnalyst at TD Cowen00:20:38Good morning. Thanks for taking our questions, congrats on the progress. Two from us. First on gamgertamig, you've mentioned that it's perhaps best in class. Can you go into a little bit more detail about how it is differentiated structurally or otherwise from the other BCMA CD3s? That's first. Then a follow-on to Brian's question. In terms of moving into pivotal development, can you talk about the framework with which you're evaluating the different indications and opportunities, and how you prioritize the first one or several to move forward into pivotal development? Thank you. Henry GosebruchCEO at Galapagos00:21:15Eric, why don't you, take the first one, and then perhaps, Dan can, take the second one. Analyst00:21:22Yeah, sure, Phil, thanks for your question. I think in terms of, you know, differentiation amongst these BCMA-directed T-cell engagers, one of the things that was attractive about the Ouro molecule, I guess there was two aspects. One is the detuning of the CD3 binding arm, which, you know, we think goes a long way in addition to dosing and, you know, significantly reducing the CRS risk. That was important. The BCMA binding arm is very potent, right? We're comfortable that, you know, from the data we've seen so far is, you know, is sort of resulting in very deep B-cell depletion and, you know, the sort of response in disease that you would associate with profound B-cell depletion. Analyst00:22:19I think those were the main aspects of the molecule that were attractive to us. Again, you know, the Ouro Medicines team has really advanced this very well in the clinic, and I think you're seeing the clinical representations of those molecular features. Maybe Dan, if you wanna comment as well. Dan GrossmanChief Strategy Officer at Galapagos00:22:38Yeah. Sure. I'm happy to talk about indication selection. You know, first I'll echo what Henry said in terms of appreciation for the Ouro team's strategic judgment in choosing initial indications in which you could get a very rapid and very clear signal of the actual clinical potency of the molecule, and particularly in those in the, you know, the benign hematologic indications. You know, beyond that, I mean, we kind of see gamgertamig as the vanguard of, you know, TCE T-cell engager therapy for autoimmune disease broadly, which could really be revolutionary over the next 10 years. Dan GrossmanChief Strategy Officer at Galapagos00:23:09We anticipate that There's a high likelihood that in 10 years, it'll be hard to imagine there was a time when this was not, you know, this kind of technology was not part of standard of care across, you know, across these B-cell mediated autoimmune disease. You know, we are really looking for quite a bit of breadth and to get the product out, you know, into the clinic and then into the hands of physicians to see what it can do across not just different diseases, but different therapeutic areas. Of course, the first filter is always going to be a mechanistic hypothesis that deep B-cell depletion will result in meaningful clinical benefit to patients. You know, that's sort of effectively a proxy for PTRS. Dan GrossmanChief Strategy Officer at Galapagos00:23:50You know, within that, we see, you know, a range of disease states in which the standard of care today and anticipated over the next couple of years is woefully inadequate. There's the room to, you know, do the most good for patients, where there are material size patient populations, and where, you know, the feasibility of running clinical trials and bringing the product to the commercial market is most feasible. We're gonna be balancing those factors, but really looking to show the broad potential of this kind of technology. Henry GosebruchCEO at Galapagos00:24:24Yeah. Phil, it's Henry. Just to add to Dan's answer. You know, one thing that again, really attracted us in our, in our diligence is that given how profound the impact is on patients that we've been able to see, you really need just pretty small numbers of patients in these diseases to really figure out. Dan GrossmanChief Strategy Officer at Galapagos00:24:43Yeah Henry GosebruchCEO at Galapagos00:24:44You get the right dosing scheme to take it forward into larger studies. We quite like the fact that this is very capital efficient. Again, in due time, we'll provide a little bit more on sort of our R&D spend, et cetera. Aaron gave it for this year, of course. But that's another very important feature that there's really relatively modestly sized studies needed. You can go into pivotals, which are also quite modest, given again, this profound impact on patients we've seen. Dan GrossmanChief Strategy Officer at Galapagos00:25:17We can do a lot with a little at this effect size. Phil NadeauAnalyst at TD Cowen00:25:20That's very helpful. Thank you. Operator00:25:22Thank you. We will now take the next question from the line of Sean McCutcheon from Raymond James. Please go ahead. Yang HongAnalyst at Raymond James00:25:32Hi. Good morning, team. This is Yang on for Sean. I have two questions. Maybe the first one is, could you speak to the optionality on continued BD activities and the prioritization, for instance, targets or indications driven that may have a clear strategy to have a synergism with gamgertamig in autoimmune disease? I have a follow-up. Henry GosebruchCEO at Galapagos00:26:02Yeah, thanks for the question. It's Henry. A couple things. Again, we've said that the majority of our capital is available for other strategic initiatives and future BD. Aaron walked through the EUR 500 million bucket we now have that we can do deals independent from Gilead, and we can take a portion of that for return of capital as well. We're very excited about that flexibility and the substantial capital we have left to look for other BD. That being said, we're very excited about Ouro and the potential that we just in the prior question outlined, and the three preclinical assets we have that could also be a meaningful opportunity. Henry GosebruchCEO at Galapagos00:26:44I would say, the hurdle for the next BD deal is very, very high. Just, you know, the hurdle for the first one was also high, but the next one is very, very high because we've got a really, really nice portfolio. We do have increased capability now, and we of course have a set of, you know, diseases that it could make sense to build on, as you say, to introduce some, you know, development or even commercial synergy down the road. I think the message right now is, look, we're excited about what we have. We're gonna be very, very busy executing these programs, and we're in no rush to do a second BD deal here, given how much we have in our plate. Yang HongAnalyst at Raymond James00:27:29Great. Thanks. Could you also please comment on the infection risk hematology event associated with gamgertamig and all the BCMA TCE class in general, and the company's view on the differences it may be associated with CD19 TCE for autoimmune disease? Thanks. Henry GosebruchCEO at Galapagos00:27:55Eric, why don't you take that one? Analyst00:27:58Yeah, thanks for the question. You know, I would say that, you know, the, you know, sort of in relation to the comment I made previously, you know, the infectious risk here really has to do with the duration of B-cell depletion and plasma cell depletion, right. You know, when we're giving, you know, when team at Ouro is giving this drug, you know, in the current dose and schedule, we're comfortable that we're getting to the point where the period of B-cell depletion will be such that the infectious risk should be manageable. That will be a key point in sort of determining the dose to go forward. Analyst00:28:44Again, I think, you know, the key point is that you can dose this drug in such a way that you can have an impact on the period of B-cell depletion, and then the infectious risk should really go along with the durability of B-cell depletion. Again, the team at Ouro has done a really nice job at dose ranging and trying to like, you know, optimize that period. Yang HongAnalyst at Raymond James00:29:14Got it. Thanks. Operator00:29:17Thank you. We will now take the next question from the line of [Matthias] from KBCS. Please go ahead. Analyst at KBCS00:29:28Hi. Yeah, Matthias coming in for Jacob. I had a question on the Galapagos 36,667 program. What are the strategic options you are currently considering? Could one of the potential outcomes be that you choose to develop the program in collaboration with Gilead, or how do you look at that program at the moment? Thanks. Henry GosebruchCEO at Galapagos00:29:56Yeah, thanks for the question. It's Henry. As we said previously, we're analyzing various alternatives relating to 3667. That process continues, although it's quite well advanced at this point. We're coming close to the end of that process and making a decision which way to go, and we're assessing kind of a broad range of options. More to come on that in the not too distant future, but it's inappropriate at this point to comment further on it. Analyst at KBCS00:30:27Great. Thanks. Operator00:30:29Thank you. I would now like to turn the conference back to Henry Gosebruch for closing remarks. Henry GosebruchCEO at Galapagos00:30:37Very good. Well, thank you for your time today. We look forward to closing the Ouro transaction here in the second quarter and welcoming the team from Ouro to join us here. More broadly reflecting on the last year, it's just really been a fantastic year, and I'm super proud of what we've accomplished together. I'm also super excited about the year ahead for Lakefront Biotherapeutics. Thank you, and we hope you have a great day. Operator00:31:07This concludes today's conference call. Thank you for participating. You may now disconnect.Read moreParticipantsAnalystsAaron CoxCFO at GalapagosBrian AbrahamsAnalyst at RBC Capital MarketsDan GrossmanChief Strategy Officer at GalapagosHenry GosebruchCEO at GalapagosJudah FrommerAnalyst at Morgan StanleyPhil NadeauAnalyst at TD CowenSherri SpearHead of Investor Relations at GalapagosYang HongAnalyst at Raymond JamesAnalystAnalyst at KBCSPowered by Earnings DocumentsSlide DeckPress Release(6-K)Interim report Lakefront Biotherapeutics American Depositary Shares Earnings HeadlinesContrasting Lakefront Biotherapeutics American Depositary Shares (NASDAQ:LKFT) and X4 Pharmaceuticals (NASDAQ:XFOR)September 28 at 4:44 AM | americanbankingnews.comLakefront Biotherapeutics American Depositary Shares (NASDAQ:LKFT) Raised to "Outperform" at Royal Bank Of CanadaSeptember 25 at 2:12 AM | americanbankingnews.comAnalyst nicknamed “The Prophet” issues new warning for AmericaWhitney Tilson exposed a major company on 60 Minutes in an Emmy-winning investigation - the stock lost nearly 80% afterward. He also called the housing crisis and the collapse of Bear Stearns and Lehman Brothers before they happened. Now Tilson says the day after this year's midterm elections, America enters a period of economic change unlike anything seen in decades - and most investors are unprepared.September 28 at 1:00 AM | Stansberry Research (Ad)Lakefront Biotherapeutics American Depositary Shares (NASDAQ:LKFT) Shares Gap Up Following Analyst UpgradeSeptember 25 at 1:21 AM | americanbankingnews.comLakefront Biotherapeutics Stock Rises 4% After Share Repurchase UpdateSeptember 24, 2026 | rttnews.comLakefront Biotherapeutics' Gamgertamig Has Meaningful Opportunity in Rare Autoimmune Diseases, RBC SaysSeptember 23, 2026 | marketscreener.comMSee More Lakefront Biotherapeutics American Depositary Shares Headlines Get Earnings Announcements in your inboxWant to stay updated on the latest earnings announcements and upcoming reports for companies like Lakefront Biotherapeutics American Depositary Shares? Sign up for Earnings360's daily newsletter to receive timely earnings updates on Lakefront Biotherapeutics American Depositary Shares and other key companies, straight to your email. Email Address About Lakefront Biotherapeutics American Depositary SharesLakefront is a clinical-stage biotechnology company developing therapies in immunology and inflammation. Its clinical-stage portfolio includes lead asset gamgertamig, a BCMAxCD3 T-cell engager being developed for the treatment of autoimmune diseases. The company identifies, acquires, and advances therapeutic assets through business development and clinical development activities. Lakefront evaluates opportunities for portfolio expansion based on their scientific, clinical, and commercial potential. Lakefront focuses on developing medicines for diseases with unmet medical needs and advancing its product candidates through clinical development.View Lakefront Biotherapeutics American Depositary Shares ProfileRead more More Earnings Resources from MarketBeat Earnings Tools Today's Earnings Tomorrow's Earnings Next Week's Earnings Upcoming Earnings Calls Earnings Newsletter Earnings Call Transcripts Earnings Beats & Misses Corporate Guidance Earnings Screener Latest Articles Brewing Trouble? Starbucks Spills the Beans on 250 Store ClosuresMarketBeat Week in Review – 09/21 - 09/25Analyst Rating Boosts May Signal More Upside for These 3 Stocks3 Stocks Under the Microscope After Large Insider Sales3 Healthcare Stocks Showing Why the Sector Still Has Momentum2 Cybersecurity Stocks Breaking Out as AI Continues to Be a TailwindFertilizer Prices Keep Climbing: 3 Stocks Still Trading at a Discount Upcoming Earnings Micron Technology (9/30/2026)NIKE (10/1/2026)Accenture (10/1/2026)PepsiCo (10/8/2026)Delta Air Lines (10/9/2026)America Movil (10/13/2026)BlackRock (10/13/2026)Citigroup (10/13/2026)The Goldman Sachs Group (10/13/2026)JPMorgan Chase & Co. (10/13/2026) Unlock superior investment research and tools. Sign up for MarketBeat All Access to gain access to MarketBeat's full suite of research tools and reports. Get MarketBeat All Access MarketBeat All Access Features Best-in-Class Portfolio Monitoring Get personalized stock ideas. Compare portfolio to indices. Check stock news, ratings, SEC filings, and more. Stock Ideas and Recommendations See daily stock ideas from top analysts. Receive short-term trading ideas from MarketBeat. Identify trending stocks on social media. Advanced Stock Screeners and Research Tools Use our seven stock screeners to find suitable stocks. Stay informed with MarketBeat's real-time news. Export data to Excel for personal analysis. Sign in to your free account to enjoy these benefits In-depth profiles and analysis for 20,000 public companies. Real-time analyst ratings, insider transactions, earnings data, and more. Our daily ratings and market update email newsletter. Sign in to your free account to enjoy all that MarketBeat has to offer. Sign In Create Account Your Email Address: Email Address Required Your Password: Password Required Log In Email Me a Login Link or Sign in with Facebook Sign in with Google Forgot your password? Your Email Address: Please enter your email address. Please enter a valid email address Choose a Password: Please enter your password. Your password must be at least 8 characters long and contain at least 1 number, 1 letter, and 1 special character. Create My Account (Free) or Sign in with Facebook Sign in with Google By creating a free account, you agree to our terms of service. This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
PresentationSkip to Participants Operator00:00:00Good day. Thank you for standing by. Welcome to Galapagos Q1 2026 financial results conference call. At this time, all participants are in a listen-only mode. After the speaker's presentation, there will be a question-and-answer session. To ask a question during the session, you will need to press star one one on your telephone. You will hear an automated message advising your hand is raised. To withdraw your question, please press star one and one again. Please be advised that today's conference is being recorded. I would now like to hand the conference over to your speaker today, Sherri Spear. Please go ahead. Sherri SpearHead of Investor Relations at Galapagos00:00:42Hello again from Belgium. Thank you for joining us today as we report Galapagos first quarter 2026 financial results and business update. Last evening, we issued a press release outlining these results. This release, along with today's presentation, can be found on the Galapagos investor website at www.glpg.com. Before we begin, I would like to remind everyone that we will be making forward-looking statements. These forward-looking statements include remarks concerning future developments of our company and our pipeline and possible changes in the industry and competitive environment. These forward-looking statements reflect our current views about our plans, intentions, expectations, strategies, and prospects, which are based on the information currently available to us and on assumptions we have made. Actual results may differ materially from those indicated by these statements and are accurate only as of the date of this recording, May 7, 2026. Sherri SpearHead of Investor Relations at Galapagos00:01:40Galapagos is not under any obligation to update statements regarding the future or to conform to these statements in relation to actual results unless required by law. You are cautioned not to place any undue reliance on these statements. Joining us on today's call from the executive team are Henry Gosebruch, Chief Executive Officer, and Aaron Cox, Chief Financial Officer. Eric Hedrick, Chief Clinical Advisor, Sooin Kwon, Chief Business Officer, and Dan Grossman, Chief Strategy Officer, will be joining us for the Q&A session. With all of that, let me now turn the call over to Henry Gosebruch, CEO. Henry? Henry GosebruchCEO at Galapagos00:02:20Thank you, Sherri, and thank you all for joining us today. It is truly an exciting time to be here. This call marks my one-year anniversary as CEO, and I couldn't be more proud of what we've accomplished together in the first year of our journey. We have transformed our management team and board, repositioned our portfolio, added an exciting set of new pipeline programs, and we are changing our name to Lakefront Biotherapeutics. This is not a story of small adjustments. It's a story of real transformation. A transformation like this requires the right people. At Galapagos, we've assembled a management team with world-class business development expertise and a shared mission of leveraging our unique position to develop new medicines for patients and to create significant value for our shareholders. Our executives bring world-class deal-making experience, and each has an enviable track record. Henry GosebruchCEO at Galapagos00:03:18This is a team built for this new phase of our company. We are focused on disciplined decision-making, careful capital allocation, reshaping our pipeline through business development, and focused execution that can create long-term sustainable value. As Galapagos transforms, it's also important that the board brings the right mix of capabilities and background. We are very pleased with the talented group that has joined us. The board's expertise and background brings the skills and experience that are needed to provide effective oversight of our strategy and the company. Our previous board chair, Jérôme Contamine, retired from the board following the 2026 AGM/EGM. I am extraordinarily grateful for Jérôme's service. He has been a great partner and provided valuable insights that have positioned us for this next phase of growth. I'm excited to work with Gino Santini as our new board chair going forward. Henry GosebruchCEO at Galapagos00:04:19Gino is a seasoned pharmaceutical professional with a 27-year career at Eli Lilly, where he served as Senior Vice President of Corporate Strategy and Business Development and led major acquisitions and partnerships. He has advised and directed numerous pharmaceutical, biotech, and venture-backed organizations and has relevant experience in M&A, commercial partnerships, and board governance. Gino's extensive operational, strategic, and business development expertise, shaped by decades of global leadership in our sector, will be invaluable as we execute on our strategy to deliver meaningful patient impact and sustainable shareholder returns. Just a few weeks ago, we announced that we have entered into a binding agreement with Gilead regarding the portfolio created by Ouro Medicines. This did not happen overnight. Henry GosebruchCEO at Galapagos00:05:10It was the result of a structured process, early relationship building, confidential reviews, negotiations, and ultimately successful agreement on a partnership with Gilead that has the potential to drive significant value for our shareholders. The transaction centers on Ouro's lead program, gamgertamig, a BCMA/CD3 T-cell engager for autoimmune diseases with multi-billion-dollar revenue potential. Currently in Phase 1b dose-ranging studies and expected to enter registrational studies as early as 2027. Gamgertamig, Ouro's lead molecule, is, in our view, a potential first and best-in-class T-cell engager that has demonstrated a compelling profile in clinical studies. The collaboration brings a meaningfully clinically differentiated high-potential asset into our portfolio. The proof of concept initial indications are orphan indications, where the clinical trials are manageable in size and scope, with significant potential for expansion into additional indications. Henry GosebruchCEO at Galapagos00:06:15We've seen compelling data from over 60 patients treated with gamgertamig across five distinct autoimmune indications. This clinical experience has highlighted the differentiated profile of gamgertamig, characterized by rapid induction of durable complete responses, minimal cytokine release syndrome with the current schedule of administration, and remarkable consistency in these findings across studies and disease indications. We look forward to sharing data with investors over the coming months in a series of publication and presentations at medical meetings. We believe that gamgertamig has a clear speed to market advantage. The initial focus on the treatment of rare autoimmune diseases has provided rapid proof of concept, enabling initiation of registrational trials as early as 2027. The program has also received Fast Track and Orphan Drug Designation in the U.S. for ITP and AHA, further supporting an accelerated development path. Henry GosebruchCEO at Galapagos00:07:16Finally, the spectrum of diseases that may be addressable by gamgertamig encompasses over 20 separate indications, giving us a pipeline and a product opportunity. In conclusion, we believe gamgertamig could represent a very important new type of treatment approach for immune reset therapy for patients across a large number of conditions. It has shown compelling clinical data so far, and it may have both a first-in-class advantage and best-in-class potential. Our partnership also includes three exciting preclinical programs, which we will look to progress with urgency. We look forward to sharing more about these programs in the future. Now, I'll turn the call over to Aaron to talk about financials. Aaron? Aaron CoxCFO at Galapagos00:08:01Thanks, Henry, and hello, everyone. As you heard from Henry, we are really excited about the Ouro transaction. Another major benefit is that it includes a partial waiver and modification of terms of our legacy Option, License and Collaboration Agreement, or OLCA, with Gilead, marking a meaningful step forward in our strategic and financial flexibility. This slide details the benefits of this transaction relative to our legacy relationship. In short, the participation of Gilead was far above the $150 million expected with the legacy agreement. I'm really proud of our team for negotiating far better terms and proving that we are able to work together with Gilead to achieve our common goals. Aaron CoxCFO at Galapagos00:08:44As noted in our transaction announcement, under the revised terms and subject to the closing of the transaction, $500 million is now unlocked for broader use beyond the Ouro Medicines investment, enabling Galapagos to pursue new opportunities and transactions independently of Gilead and expanding the universe of potential strategic targets. Up to $150 million of this $500 million may be used for return of capital to shareholders, subject to certain limitations, providing us with additional optionality to drive shareholder value. This partial waiver and modification to terms of the OLCA further strengthen our ability to deploy capital strategically and to pursue additional value-accretive opportunities. Last week, we also received approval from our shareholders to complete a share repurchase. We will provide an update regarding a potential share repurchase following the close of the Ouro Medicines transaction. Aaron CoxCFO at Galapagos00:09:40Turning now to our Q1 2026 financial results, as outlined in the press release issued last night, our total net revenues were EUR 6.5 million compared to EUR 75 million in Q1 2025. This decrease is mainly driven by the prior year comparison, which included EUR 57.6 million related to the OLCA revenue recognition. As noted with our full year 2025 results, the remaining deferred income balance related to the OLCA was fully released at year-end 2025. In Q1 2026, revenues were primarily driven by EUR 4.9 million in supply revenues from Jyseleca inventory sales to Alfasigma, and EUR 1.6 million in collaboration revenues, reflecting royalties from Gilead. On the cost side, we continue to see significant reduction in our operating expenses. R&D expenses decreased to EUR 31 million, contributing to an overall improvement in our cost base. Aaron CoxCFO at Galapagos00:10:40This reduction is driven by lower severance expenses as well as the absence of restructuring-related charges that impacted Q1 2025. As a result, operating loss improved to EUR 63.7 million compared to EUR 158.7 million last year, which included EUR 111 million in restructuring costs. Moving below operating income, we've reported net financial income of EUR 77.7 million, mainly driven by positive fair value adjustments and favorable unrealized currency exchange gains on our US dollar-denominated cash and investments of EUR 64.3 million. This led to a net profit of EUR 14.5 million for the quarter, compared to a net loss of EUR 153.4 million for the first three months of 2025. Aaron CoxCFO at Galapagos00:11:31Financial investments and cash and cash equivalents totaled EUR 2,982.2 million on March 31, 2026, as compared to EUR 3,297 million on March 31, 2025. The quarter-end cash balance meaningfully benefited from a decrease in the U.S. dollar to euro exchange rate, which moved from 1.175 at year-end 2025 to approximately 1.15 at the end of the quarter. Turning now to our guidance for 2026. With the closing of the Ouro transaction expected in the second quarter, we expect to spend EUR 60 million-EUR 75 million on Ouro-related cash expenditures, including operating costs and transaction expenses in 2026. Aaron CoxCFO at Galapagos00:12:17Along with the upfront payment of approximately EUR 713 million, this results in total Ouro-related cash expenditures of EUR 775 million-EUR 790 million for 2026. We continue to expect one-time cash costs of EUR 125 million-EUR 175 million related to the wind down of cell therapy activities. Inclusive of the Ouro-related expenditures and continued wind down of cell therapy, we now expect to end the year with EUR 1.975 billion-EUR 2.05 billion of cash and cash equivalents. Importantly, the company remains robustly funded. Following this transaction and including estimated R&D spend associated with gamgertamig until first approval, the company will continue to have a majority of its current cash remaining for additional strategic transactions and other capital allocation priorities. Aaron CoxCFO at Galapagos00:13:12Now, let me turn it back to Henry to wrap up. Henry GosebruchCEO at Galapagos00:13:14Thank you, Aaron. In closing, I'm just thrilled to introduce you to the new Lakefront Biotherapeutics. To us, Lakefront symbolizes the attractive opportunity in front of us and the new beginning we are creating. My most reflective moments often occur when I'm out exercising on Chicago's lakefront. Our new name captures what we aspire to achieve for patients, enhance quality of life, meaningful, positive impact, and more time for what matters most. It represents helping patients move toward a better future with greater hope and possibility. As of tomorrow, May 8th, we expect to be listed as LKFT on Euronext and Nasdaq, symbolizing another pivotal step in our transformation. With that, thank you all for your attention, and we will now open it up for your questions. Operator. Operator00:14:11Thank you. As a reminder, to ask a question, please press star one one on your telephone and wait for your name to be announced. To withdraw your question, please press star one and one again. We will now take the first question from the line of Brian Abrahams from RBC Capital Markets. Please go ahead. Brian AbrahamsAnalyst at RBC Capital Markets00:14:36Hey, good morning, guys. Thanks for taking my question and congrats on all the transformation over there. I was wondering if you could give us maybe your latest thoughts on what the dose ranging gamgertamig data will need to show specifically just in terms of B-cell depletion depth and durability, the CRS rate reductions to move forward in registrationals. How you're gonna be picking which registrational trials to begin first, and just any more thoughts on the potential size and complexity of these trials that could start next year? Thanks. Henry GosebruchCEO at Galapagos00:15:17Hey, Brian, it's Henry. Good morning. Thanks for the question. I'll start, and then I'll have Eric supplement. First of all, look, we, as we said on the prior discussion, we had a chance to really thoroughly diligence not only gamgertamig, but other programs out there with other T-cell engagers. We've seen really compelling data from over 60 patients that showed very rapid onset, very deep depletion and very good durability. Again, as we've talked about, that will come out here in the next couple of quarters in terms of individual releases at medical meetings and other publications. Henry GosebruchCEO at Galapagos00:16:10Just for context, I'll have Eric go through the specifics on the three points you raised. Eric. Analyst00:16:17Yeah. Thanks, Henry. Hi, Brian. Thanks for the question. You know, sort of expanding on what Henry just said, I think the team at Ouro has done really good work on, you know, exploring dose ranging here. I would say that the profile that, you know, would be an optimal profile for going into late-stage development would be one where you get profound B-cell depletion, but a dose duration schedule that minimizes CRS risk. I think at the current dose and schedule, you know, we've re-referred to this previously, it really does seem like alterations in the dose and the duration of therapy can really minimize the CRS risk. Analyst00:17:09I think the other aspect here that's important will be, you know, having a dose that results in a period of B-cell depletion that is deep but relatively short, right? That you can minimize the infectious risk, the need for supplemental intravenous immunoglobulin. Again, I think the team at Ouro is well on your way to identifying that dose. You know, we fully expect that, you know, by 2027, you know, we'll be comfortable with the doses that we take forward into phase III programs. Operator00:17:53Thank you. We will now take the next question from the line of Judah Frommer from Morgan Stanley. Please go ahead. Judah FrommerAnalyst at Morgan Stanley00:18:04Yeah. Hi, guys. Thanks for the update, and thanks for taking the question. You know, I think we saw another transaction recently for a BCMA/CD3. You know, there's several assets in this space. I'm just curious how you think this space might evolve and how you're thinking about development plans. Do you see room for multiple assets targeting the same mechanism within the same large indications? Do you think this is gonna be an area where various assets are going to kind of carve up sub-indications, maybe stick to smaller indications as opposed to necessarily all going after the same large ones? Thank you. Henry GosebruchCEO at Galapagos00:18:45Thanks, Judah. It's Henry. Again, just for context, we were able to diligence multiple opportunities in some depth. We're quite pleased that our top choice, i.e., gamgertamig, was the one that we were ultimately able to transact with. We continue to believe that gamgertamig is the best alternative out there and has the potential to be first in class. That being said, look, we're very encouraged by the fact that we're not the only ones excited about the space, that there's a lot of investment going into it. I think that's that is good to see and ultimately good for patients. Henry GosebruchCEO at Galapagos00:19:32The Ouro team has been really, really savvy in terms of picking very interesting indications that we believe are, you know, quite sizable, you know, multi-billion EUR potential easily. Where they have a clear timing advantage. I think in those places, we're in a really favorable position. That being said, we don't view gamgertamig behind in any other indication as well, and those are being very actively explored. To your question, whether ultimately, you know, the best drug takes all of it or the market gets split up in some way, I think, you know, we'll defer that when we go a little bit further. Again, we're based on our diligence of multiple programs. Henry GosebruchCEO at Galapagos00:20:17We think we got the first and best in class alternative here with us. Operator00:20:28We will now take the next question from the line of Phil Nadeau from TD Cowen. Please go ahead. Phil NadeauAnalyst at TD Cowen00:20:38Good morning. Thanks for taking our questions, congrats on the progress. Two from us. First on gamgertamig, you've mentioned that it's perhaps best in class. Can you go into a little bit more detail about how it is differentiated structurally or otherwise from the other BCMA CD3s? That's first. Then a follow-on to Brian's question. In terms of moving into pivotal development, can you talk about the framework with which you're evaluating the different indications and opportunities, and how you prioritize the first one or several to move forward into pivotal development? Thank you. Henry GosebruchCEO at Galapagos00:21:15Eric, why don't you, take the first one, and then perhaps, Dan can, take the second one. Analyst00:21:22Yeah, sure, Phil, thanks for your question. I think in terms of, you know, differentiation amongst these BCMA-directed T-cell engagers, one of the things that was attractive about the Ouro molecule, I guess there was two aspects. One is the detuning of the CD3 binding arm, which, you know, we think goes a long way in addition to dosing and, you know, significantly reducing the CRS risk. That was important. The BCMA binding arm is very potent, right? We're comfortable that, you know, from the data we've seen so far is, you know, is sort of resulting in very deep B-cell depletion and, you know, the sort of response in disease that you would associate with profound B-cell depletion. Analyst00:22:19I think those were the main aspects of the molecule that were attractive to us. Again, you know, the Ouro Medicines team has really advanced this very well in the clinic, and I think you're seeing the clinical representations of those molecular features. Maybe Dan, if you wanna comment as well. Dan GrossmanChief Strategy Officer at Galapagos00:22:38Yeah. Sure. I'm happy to talk about indication selection. You know, first I'll echo what Henry said in terms of appreciation for the Ouro team's strategic judgment in choosing initial indications in which you could get a very rapid and very clear signal of the actual clinical potency of the molecule, and particularly in those in the, you know, the benign hematologic indications. You know, beyond that, I mean, we kind of see gamgertamig as the vanguard of, you know, TCE T-cell engager therapy for autoimmune disease broadly, which could really be revolutionary over the next 10 years. Dan GrossmanChief Strategy Officer at Galapagos00:23:09We anticipate that There's a high likelihood that in 10 years, it'll be hard to imagine there was a time when this was not, you know, this kind of technology was not part of standard of care across, you know, across these B-cell mediated autoimmune disease. You know, we are really looking for quite a bit of breadth and to get the product out, you know, into the clinic and then into the hands of physicians to see what it can do across not just different diseases, but different therapeutic areas. Of course, the first filter is always going to be a mechanistic hypothesis that deep B-cell depletion will result in meaningful clinical benefit to patients. You know, that's sort of effectively a proxy for PTRS. Dan GrossmanChief Strategy Officer at Galapagos00:23:50You know, within that, we see, you know, a range of disease states in which the standard of care today and anticipated over the next couple of years is woefully inadequate. There's the room to, you know, do the most good for patients, where there are material size patient populations, and where, you know, the feasibility of running clinical trials and bringing the product to the commercial market is most feasible. We're gonna be balancing those factors, but really looking to show the broad potential of this kind of technology. Henry GosebruchCEO at Galapagos00:24:24Yeah. Phil, it's Henry. Just to add to Dan's answer. You know, one thing that again, really attracted us in our, in our diligence is that given how profound the impact is on patients that we've been able to see, you really need just pretty small numbers of patients in these diseases to really figure out. Dan GrossmanChief Strategy Officer at Galapagos00:24:43Yeah Henry GosebruchCEO at Galapagos00:24:44You get the right dosing scheme to take it forward into larger studies. We quite like the fact that this is very capital efficient. Again, in due time, we'll provide a little bit more on sort of our R&D spend, et cetera. Aaron gave it for this year, of course. But that's another very important feature that there's really relatively modestly sized studies needed. You can go into pivotals, which are also quite modest, given again, this profound impact on patients we've seen. Dan GrossmanChief Strategy Officer at Galapagos00:25:17We can do a lot with a little at this effect size. Phil NadeauAnalyst at TD Cowen00:25:20That's very helpful. Thank you. Operator00:25:22Thank you. We will now take the next question from the line of Sean McCutcheon from Raymond James. Please go ahead. Yang HongAnalyst at Raymond James00:25:32Hi. Good morning, team. This is Yang on for Sean. I have two questions. Maybe the first one is, could you speak to the optionality on continued BD activities and the prioritization, for instance, targets or indications driven that may have a clear strategy to have a synergism with gamgertamig in autoimmune disease? I have a follow-up. Henry GosebruchCEO at Galapagos00:26:02Yeah, thanks for the question. It's Henry. A couple things. Again, we've said that the majority of our capital is available for other strategic initiatives and future BD. Aaron walked through the EUR 500 million bucket we now have that we can do deals independent from Gilead, and we can take a portion of that for return of capital as well. We're very excited about that flexibility and the substantial capital we have left to look for other BD. That being said, we're very excited about Ouro and the potential that we just in the prior question outlined, and the three preclinical assets we have that could also be a meaningful opportunity. Henry GosebruchCEO at Galapagos00:26:44I would say, the hurdle for the next BD deal is very, very high. Just, you know, the hurdle for the first one was also high, but the next one is very, very high because we've got a really, really nice portfolio. We do have increased capability now, and we of course have a set of, you know, diseases that it could make sense to build on, as you say, to introduce some, you know, development or even commercial synergy down the road. I think the message right now is, look, we're excited about what we have. We're gonna be very, very busy executing these programs, and we're in no rush to do a second BD deal here, given how much we have in our plate. Yang HongAnalyst at Raymond James00:27:29Great. Thanks. Could you also please comment on the infection risk hematology event associated with gamgertamig and all the BCMA TCE class in general, and the company's view on the differences it may be associated with CD19 TCE for autoimmune disease? Thanks. Henry GosebruchCEO at Galapagos00:27:55Eric, why don't you take that one? Analyst00:27:58Yeah, thanks for the question. You know, I would say that, you know, the, you know, sort of in relation to the comment I made previously, you know, the infectious risk here really has to do with the duration of B-cell depletion and plasma cell depletion, right. You know, when we're giving, you know, when team at Ouro is giving this drug, you know, in the current dose and schedule, we're comfortable that we're getting to the point where the period of B-cell depletion will be such that the infectious risk should be manageable. That will be a key point in sort of determining the dose to go forward. Analyst00:28:44Again, I think, you know, the key point is that you can dose this drug in such a way that you can have an impact on the period of B-cell depletion, and then the infectious risk should really go along with the durability of B-cell depletion. Again, the team at Ouro has done a really nice job at dose ranging and trying to like, you know, optimize that period. Yang HongAnalyst at Raymond James00:29:14Got it. Thanks. Operator00:29:17Thank you. We will now take the next question from the line of [Matthias] from KBCS. Please go ahead. Analyst at KBCS00:29:28Hi. Yeah, Matthias coming in for Jacob. I had a question on the Galapagos 36,667 program. What are the strategic options you are currently considering? Could one of the potential outcomes be that you choose to develop the program in collaboration with Gilead, or how do you look at that program at the moment? Thanks. Henry GosebruchCEO at Galapagos00:29:56Yeah, thanks for the question. It's Henry. As we said previously, we're analyzing various alternatives relating to 3667. That process continues, although it's quite well advanced at this point. We're coming close to the end of that process and making a decision which way to go, and we're assessing kind of a broad range of options. More to come on that in the not too distant future, but it's inappropriate at this point to comment further on it. Analyst at KBCS00:30:27Great. Thanks. Operator00:30:29Thank you. I would now like to turn the conference back to Henry Gosebruch for closing remarks. Henry GosebruchCEO at Galapagos00:30:37Very good. Well, thank you for your time today. We look forward to closing the Ouro transaction here in the second quarter and welcoming the team from Ouro to join us here. More broadly reflecting on the last year, it's just really been a fantastic year, and I'm super proud of what we've accomplished together. I'm also super excited about the year ahead for Lakefront Biotherapeutics. Thank you, and we hope you have a great day. Operator00:31:07This concludes today's conference call. Thank you for participating. You may now disconnect.Read moreParticipantsAnalystsAaron CoxCFO at GalapagosBrian AbrahamsAnalyst at RBC Capital MarketsDan GrossmanChief Strategy Officer at GalapagosHenry GosebruchCEO at GalapagosJudah FrommerAnalyst at Morgan StanleyPhil NadeauAnalyst at TD CowenSherri SpearHead of Investor Relations at GalapagosYang HongAnalyst at Raymond JamesAnalystAnalyst at KBCSPowered by