Ladies and gentlemen, thank you for standing by. My name is Desiree, and I will be your conference operator today. At this time, I would like to welcome everyone to the Seres Therapeutics First Quarter 2025 Earnings Conference Call. [Operator Instructions] I would now like to turn the conference over to Dr. Carlo Tanzi of Investor Relations. You may begin.

Thank you and good morning. Our press release with the company’s first quarter 2025 financial results and business updates became available at 7 a.m. Eastern Time this morning and can be found on the Investors and News section of the company’s website. The company has also posted an updated corporate presentation to the website. I’d like to remind you that we’re making forward-looking statements, including statements about the timing and results of our clinical studies and data readouts, future product candidates, clinical development plans and commercial opportunities, communications with, feedback from, or submissions to the FDA, upcoming presentations, future payments related to the VOWST sale, operating plans and our future cash runway, our ability to secure partnerships and/or generate or obtain additional capital or financing, our planned strategic focus, anticipated timing of any of the foregoing or other statements which are not historical facts. Actual results may differ materially. Additionally, these statements are subject to certain risks and uncertainties which are discussed under the Risk Factors section of our recent SEC filings. Any forward-looking statements made on today’s call represent our views as of today only. We may update these statements in the future, but we disclaim any obligation to do so. On today’s call with prepared remarks, I am joined by Eric Shaff, Seres’ President and CEO and Marella Thorell, Chief Financial Officer. Additional members of the management team, including Dr. Matthew Henn, Chief Scientific Officer; Dr. Terri Young, Chief Commercial and Strategy Officer; and Dr. Dennis Walling, Senior Vice President of Clinical Development will be available during the Q&A portion of the call. And with that, I’ll pass the call to Eric.

Thank you, Carlo, and good morning, everyone. Today, I’ll share business highlights from the first quarter and provide an update on our progress advancing SER-155. During our recent full year 2024 results call, we provided an in-depth review of our programs and recent data. And therefore, we will keep our remarks more abbreviated today and focus on progress updates. Advancing SER-155 into the next stage of development in allo-HSCT remains our top corporate priority. And we are making significant progress towards initiating the next clinical study. As a reminder, our Phase 1b study showed that SER-155 administration resulted in a 77% relative risk reduction in bloodstream infections compared to placebo. This represents a highly meaningful outcome in this high-risk allo-HSCT patient population. We also observed a favorable safety profile in this study, consistent with the favorable safety profile we’ve seen historically across our live biotherapeutic product platform. The clinical results generated to date underscored the potentials of SER-155 to redefine the standard of care for allo-HSCT recipients and the many other vulnerable patient groups at risk of bloodstream infections. We believe that developing SER-155 and other live biotherapeutics to prevent infections in allo-HSCT in other adjacent patient groups, including autologous HSCT patients, cancer patients with neutropenia, CAR-T recipients, individuals with chronic liver disease and solid organ transplant recipients could represent significant improvement for patients and multiple substantial commercial opportunities for Seres. Last month, members of our team attended the recent European Society for Blood and Marrow Transplantation Conference. And we obtained encouraging commentary from the transplant community that provides support for our mission and echoes what we’ve heard from U.S.-based physicians. Healthcare providers emphasized that preventing bloodstream infections remains a major clinical challenge and new approaches are desperately needed. Many physicians also expressed enthusiasm for both the safety and efficacy…

Thank you, Eric, and good morning, everyone. I’ll start by noting that we have classified all historical operating results for the VOWST business within discontinued operations in the consolidated statement of operations for the comparative period presented, being the 3 months ended March 31, 2024. There is no ongoing activity in the current period related to disc ops. Seres reported net income from continuing operations of $32.7 million in Q1 2025 as compared to a net loss from continuing operations of $32.9 million in the first quarter of 2024. The net income in 2025 is primarily driven by the previously announced $50 million installment payment received from Nestle in January of this year, consistent with the company fulfilling its transition obligations. Research and development expenses for the quarter were $11.8 million, compared to $19.5 million in the first quarter of 2024, reflecting lower personnel expenses, a decrease in platform investments and lower costs related to the SER-155 Phase 1b study. General and administrative expenses were $11.9 million in the first quarter, a decrease from $14.9 million in Q1 2024, driven primarily by lower personnel and contractor expenses. As of March 31, 2025, we had cash and cash equivalents of $58.8 million. We are due a second installment payment of approximately $23.5 million net after deduction for employment-related obligations from Nestle in July of this year. We remain in compliance with the transition service agreement terms and therefore, anticipate receipt of this payment as expected. Based on our current cash balance, the expected installment payment from Nestle in July and our current operating plans, we expect to fund operations into the first quarter of 2026. On April 21 of this year, we affected a 1-for-20 reverse stock split of our common stock. Trading of our common stock on the NASDAQ Global Select Market commenced on a split-adjusted basis on April 22, 2025. Yesterday, we were notified by the NASDAQ listing qualification staff that we have now regained compliance with the bid price requirement. We remain highly disciplined in our financial management, ensuring that we are prioritizing activities that advance our clinical and strategic goals, and looking for means to preserve cash without compromising the achievement of these goals. As is prudent in today’s challenging financing climate, we continue to explore sources of capital in addition to partnerships to provide potential optionality for financing our Phase 2 study. I will now pass the call back to Eric.

Thanks Marella. To summarize, we are making significant progress advancing SER-155, bolstered by encouraging clinical and mechanistic data, constructive regulatory feedback, and the clear unmet medical need identified by key opinion leaders and clinical experts. We are moving with speed and focus to submit our Phase 2 protocol to the FDA in the coming weeks and to prepare for the next clinical study. We are also making progress in our efforts to secure a partnership to capture the potential substantial therapeutic and commercial opportunities. I look forward to sharing additional updates as we advance our objectives in the months ahead and continue to attend medical and scientific conferences to increase awareness of and enthusiasm for SER-155. Operator, you can now open the call up for questions.

[Operator Instructions] And our first question comes from the line of Tess Romero with JPMorgan. Your line is open. Caroline Pötsch-Hennig: Good morning, team. This is Caroline Pötsch-Hennig for Tess Romero. Thanks for taking our questions, just two from us. First, are the partnership discussions being gated by progress the next steps for SER-155, in other words, are prospective partners looking for the protocol to be submitted or the trial itself to be initiated before finalizing the deal? And then I have a follow-up.

Yes. Caroline, thanks for the question and good morning. Without getting too deep into the play-by-play of our partnership discussions, let me offer a couple things. One is we are making progress, we are advancing those discussions. I will say that our interactions with the FDA have been constructive and let’s call it regular. We have been in contact with FDA, including as recently as last week, right. So, whereas the news reports are sometimes, I don’t know, dire, as it relates to what’s happening at FDA. I can tell you that we are getting feedback on our design of the next study. We are incorporating that feedback and we think we have a path. So, as it relates to our discussion with partners, we think that’s a significant positive. In terms of gating items to start the study, we have said before and I will reiterate today that the securing of a partnership for us is the key long lead time item for moving forward with the study. We are moving forward with all the key items that we have to do in terms of securing a CRO and manufacturing clinical material for the next study and thinking about site activation. So, we are doing the things that we need to do to be in a position to move, but the partnership itself for us will be a gating item for initiating the study itself. Caroline Pötsch-Hennig: Okay. Great. And then can you outline your proposed powering assumptions for the Phase 2 study of SER-155 and provide a little more clarity as to what you mean by an adaptive design in the context of the Phase 2 study? Thanks.

Sure. So, let me start and maybe I will tick it over to Dennis to comment. And I think we are not in a position to share the stats themselves. It is a standalone Phase 2 study, but we do think that the powering included in our design will allow us to use data from this study for both the efficacy and safety components of an overall package for submission to the FDA if we are successful. As it relates to the design of an interim look, let me offer a couple of comments. One is that, as we said in our prepared remarks, the timeline to get that read, we think is approximately 12 months. And that should give us a pretty good sense of where we are pointing in terms of efficacy. So, we are excited about that. But maybe I can ask Dennis to comment further on that question.

Yes, thank you. So, we think that the adaptive design with the interim analysis is an opportunity to get an early look at our efficacy and safety data in a way that we can begin to engage with the FDA earlier with discussions around what a potential pivotal Phase 3 program might look like. So, the plan would still require that we have that end of Phase 2 meeting conversations, but the interim analysis allows us a big head start to get to those conversations with the FDA early. Caroline Pötsch-Hennig: Great. Thank you so much.

Thanks for the question, Caroline.

Our next question comes from the line of Joseph Thome with TD Cowen. Your line is open.

Hi there. Good morning. Thank you for taking my questions. Kind of similar, but obviously they have a lot of FDA changes since you received your initial advice. And so is the department that you are working with, were there any large staffing changes there? And if anything, it almost seems like the new administration would be more supportive of microbiome therapeutics. So, just kind of curious if you have had any sort of changes in dialogue, either positive or it seems like not negative. And then is there any additional information that you can share regarding partnership discussions that give you confidence that you will be able to get this done kind of by the end of the year and your current cash runway guidance? And do you think the partner would want input on the Phase 2 protocol at all? Thank you.

Yes. Joe, thanks for the questions. On the first one, maybe I answered part of it in my last comments. But it’s hard for us to speak about FDA in general or the environment in general. What we can talk about is our own interactions and our own interactions have been highly constructive and regular and certainly we were concerned about it. We continue to monitor it, but we have been in regular contact with FDA and we have gotten robust specific feedback from them, which has been useful in us determining how we think about moving forward. Now, remember, we have breakthrough designation. So, we think that, and this is just my speculation, I think that’s probably helpful. I mean the FDA on the heels of our Phase 1b results determine that based on the unmet need and the early clinical signals that, SER-155 was worthy of that designation. And so perhaps that is helpful in thinking about prioritization of work. But again, we don’t speak for the FDA. All I can say is that, we have been pleased with the interactions that we have had to-date and it allows us to move forward the way that we had hoped that we would. On the partnership dynamics and maybe timing, look, it’s hard to predict. I would say based on our experience, there is not always a linear line between starting a process and ending a process. So, it’s a little bit difficult for me or challenging for me to opine, Joe. All I can tell you is that we are making progress. We are having discussions in terms of our design and our feedback from FDA with our partners or potential partners. And we are also mindful of our catch resources and time. And so, we are moving forward with absolute urgency and you can expect us to continue to do that.

Great. Thank you. And then maybe just on the Phase 2 itself, just that I understand the interim analysis, I guess when that occurs, do you have the optionality to increase the size of the study if you want more information? And obviously, given that you do have the breakthrough therapy designation, do you think there is a path for the FDA could say, let’s just expand this Phase 2 and make the Phase 3 confirmatory or do we kind of know that a Phase 3 would need to be the base case here? Thank you.

Yes. Joe, thanks for the question and maybe I will start and I will invite Dennis to comment too. It’s a little tricky. We are careful not to speak for the FDA. There will be optionality as it relates to information that we could learn from the interim and how we might use it either for 155 or as we have said beforehand, thinking about adjacencies from allo into say, auto. So, we are incredibly excited about the design of this interim look. We think it will give directionally a sense of where we are pointing. It will give us information. It will give FDA information. Our expectation is that the data that we get from this Phase 2 study will help inform a Phase 3 study or a pivotal study and that overall package will be used for licensure. But we don’t speak for the FDA. We are very careful not to get ahead of them. And so as usual, we will follow the data in consultation with them as we have in the past and we will in the future. But Dennis, any other comments on that one?

Yes. I think it’s important to understand that this Phase 2 study design is appropriately powered for a very robust and large data set that we will be able to analyze. And so the optionality at the interim is important to understand is that we do have the opportunity to make decisions if necessary at that time point. But the other important thing to understand is that we expect that this data from the Phase 2 will be supportive of the total package that the FDA would evaluate for a potential approval. And as Eric said, it’s premature to speak for the FDA is what they might want to do or not. But we are expecting to have robust engagement and conversations with them at the interim level and at the end of the Phase 2 to complete a pivotal Phase 3 design that would get us to an approval.

Excellent. Thank you so much.

Thanks for the questions, Joe.

And our last question comes from the line of John Newman with Canaccord. Your line is open.

Hi guys. Good morning. Thank you for taking my question. I just had two actually, in terms of the Phase 2 study and the primary endpoint, could you talk about how much follow-up the FDA might be looking for? And just curious if this particular study would be designed for you to be able to follow-up for overall survival or if that would be something that you would maybe add as a secondary endpoint in the Phase 3 or simply follow-up as observation? Thanks.

Yes. Thanks for the question. Maybe I will start and Dennis can kick in. So, just at a high level, as we have said before, we have engaged with the FDA. They provided feedback to us that we have incorporated into our design. We think that we have what we need to move forward. We were submitting the protocol, as we said, in the next couple of weeks. If there are questions or proposed adjustments, we expect to hear back. But again, the partnership for us really is the gating item in moving forward. But maybe Dennis can comment specifically on the follow-up question.

So, I mean as we have said before, the FDA has given us a breakthrough therapy designation on the endpoint of bloodstream infection reductions. And that is our intended primary endpoint in this Phase 2 study. The protocol is still being finalized. Obviously, we are going to be looking at a number of different things that could be potential efficacy signals as well as safety. So, at this point in time, we will have to see what the data show at the Phase 2 and then have those discussions with the FDA about what are the appropriate types of efficacy measures we would evaluate for Phase 3.

Great. Thank you.

This is Matt here as well. I will give you one other piece of information regarding that. I mean, as you know, we always design rigorous studies that are data rich. And there are large cohort studies that have shown associations of the gastrointestinal microbiome with survivability in this patient population. And so we will obviously be collecting the kind of data to look for signals there. But as Dennis said, the protocol is still in development with respect to those types of endpoints.

Okay. Great. Thank you very much.

Thanks for the question.

That concludes the question-and-answer session. I would like to turn the call back over to the management for closing remarks.

So, thank you, operator, for your help this morning and thanks to everyone for joining today’s call. And we look forward to our continued engagement. Thanks. Have a great morning. Have a great rest of the week.

Ladies and gentlemen, this concludes today’s conference call. Thank you all for joining and you may now disconnect.