Innate Pharma S.A.

Hello, and thank you for standing by. My name is Lacey, and I will be your conference operator today. At this time, I would like to welcome everyone to the innate Pharma First Quarter 2025 Financial Results and Business Update Conference Call. All lines have been placed on mute to prevent any background noise. After speaker remarks, there will be a question and answer session. If you would like to ask a question during this time, simply press star followed by the number one on your telephone keypad. If you would like to withdraw your question, press star one again. Thank you. I would now like to turn the call over to Henry Wheeler, Vice President of Investor and Relations. You may go ahead.

Thank you. Good morning, good afternoon, and welcome everyone. This morning, innate issued a press release for our Q1 2025 Business Update and Financial Results. We look forward to highlighting the progress made during the year to date, as well as addressing future goals and milestones. The press release and today's presentation are both available on the IR section of our website. On slide two, before we start, I'd like to remind you that we'll be making forward looking statements regarding the financial outlook in addition to regulatory and product plan development. These statements are subject to risks and uncertainties that may cause actual results to differ from those forecasted. On slide three, to cover today's agenda, after an introduction from Jonathan, our CEO, Yanis Morel, Chief Operating Officer, will discuss the preclinical Anket platform and ADC updates. Sonia Quarantino, our Chief Medical Officer, will cover the clinical updates on the Q2MAB 6501 and 4502, who will then hand the call to Jonathan to wrap and close. We also have Frederick, our CFO, on the line for Q&A. Jonathan, over to you.

Thank you, Henry, and good morning to our US participants and good afternoon to everybody in Europe. I'm happy to have the opportunity today to update you on the latest developments at Innate Pharma. Starting with slide five, which illustrates our revised strategy, as you remember, we updated our strategic focus for 2025, which we shared during our presentation at the JP Morgan Healthcare Conference in January. As a reminder, this is illustrated on slide five. This strategy is focused on three key growth pillars that we believe will drive long-term value for Innate Pharma, our shareholders, and most importantly, for patients. The first pillar is our NKCELL Engagers, the Anket platform, which continues to be a critical component of our strategy. We are advancing three key programs from this platform. IPH65, our CD20 targeted Anket is currently in phase one. We're excited about IPH65's potential to address hematological malignancies and potentially autoimmune diseases. IPH61 rights will be returned to Innate as of July 1st, and it is progressing in phase two and with phase one data already presented. It was also awarded FastRat designation for the treatment of acute AML. We believe that this asset has potential to significantly impact patients' lives. IPH64, our BCMA targeted Anket is in phase one, in myeloma in partnership with Sanofi, and will be transitioned into autoimmune disease. These three assets continue to drive our leadership in NKCELL Engager therapies. The second strategic pillar is our antibody drug conjugates. We're particularly enthusiastic about IPH45, our Nectin-4 targeted ADC. The IND cleared last year, and the first patients were dosed in January 2025. This differentiated Topa-1 ADC targets high, moderate, and low Nectin-4 expressing tumors. With Nectin-4 being expressed at varying levels in a range of large tumors, IPH45's ability to bind low, moderate, and high expressing tumors pre-clinically significantly expands the potential product opportunity. We also have IPH43, our MIC-AB targeted ADC program, which is in research, further advancing our capabilities in ADCs. The third pillar is our current late stage assets. We're committed to advancing our late stage programs, particularly Lucutamab. Following positive phase two data, FDA feedback on next steps, and the US FDA breakthrough therapy designation, we're actively progressing partnership discussions. We are particularly pleased with the Lucutamab-BTD designation, which underscores its potential to treat cesarean syndrome patients with high unmet medical need. Additionally, Monaluzumab continues to progress well with AstraZeneca in the Pacific 9 phase three trial, and we remain optimistic about... Turning to slide six, which highlights our impressive pipeline. As you can see, we're advancing a robust pipeline with eight innovative assets currently in the clinic. The highlights include our proprietary asset, IPH65 for B cell lymphomas, and our soon to be proprietary asset, IPH60101 for AML. Our Sanofi partner's asset, IPH6401, which is now being developed in autoimmune disease, and our proprietary ADC, IPH45, targeting neckting for expressing solid tumors. In phase two, we have proprietary Coerthridl2 targeted antibody Lucutamab for CTCL and PTCL. And finally, we have our AZ partnered acid, Monaluzumab, which is being studied for neoadjuvant non-small cell lung cancer, and is in a phase three study for unresectable stage three non-small cell lung cancer. These assets showcase the productivity of our R&D organization and our commitment to delivering breakthrough treatments across a range of cancers and autoimmune diseases. Turning to slide seven, this summarizes the recent transaction with Sanofi. We're very pleased that Sanofi chose to make a 50 million euro strategic equity investment into a NAFARMA, which reflects their excitement and confidence in the Anket and our ADC platforms and the products which are in development. We're pleased to have Sanofi as a significant company shareholder with a 9% holding in our stock. As part of the agreement, Sanofi will return the rights to the CD123 targeting Anket IPH6101, which they were pursuing in AML. This will occur on July 1st. As part of their broader strategic reprioritization, this is why the asset was returned. We will evaluate the data for IPH6101 once received and determine the next steps for this program. As a reminder, Sanofi had progressed IPH6101 into phase two in treatment refractory AML patients and initiated a first line AML phase one study in combination with Venatoclaxone society. The other aspects of the agreement with Sanofi remain unchanged. They announced that they pivoted the BCMA targeted Anket IPH6101 from myeloma into autoimmune indications. They've also have IPH6101, the B7H3 targeted Anket and an undisclosed target as part of the agreement. The total potential milestones do on these assets is over 1 billion under our existing 2016 and 2022 agreements. Turning to slide eight, this highlights our upcoming ASCO presentations. We are very pleased that the long-term follow-up data for LACUTAMAP has been accepted for presentation at ASCO and we will have updates of both the CSERY syndrome data and the myococis fungoides data, which was used to support the FDA breakthrough designation. And we're excited that this data, which will be shared at ASCO continues to mature and improve with time. We also have a trial in progress presentation for our differentiated Nectin 4 targeted ADC, IPH4502. And AstraZeneca will present updates for Monalizumab from the Neuocost 2 trial ahead of the upcoming phase three readout for Pacific 9 next year. I'll now hand over to Yanis Morel, our COO, who will present the preclinical data for IPH4502 and IPH6501 and in particular new data, which was recently presented at AACR in Chicago and which further differentiates IPH4502. Yanis.

Thank you, Jonathan. I will now highlight the science behind our two strategic pillars that are the NKCEL Engager, Enquet, and the antibody drug conjugate. Enquet is our proprietary -in-class NKCEL Engager platform. It is a multi-specific plug and play technology aiming at engaging NKCELs to our tumor cells by triggering the most stable activating receptor expressed on NKCELs called NKP46. The interesting feature of this platform is that by swapping the tumor binding portion, it can produce multiple drug candidates addressing a variety of targets in oncology, but also in other disease like autoimmune and inflammatory disease. The recent transition into inflammation of SARS-514, also called IPH6401, our BCMA Enquet, developed by Sanofi, is illustrating that potential. On the next slide, slide nine, I like to highlight the structure of IPH6501, our lead proprietary Enquet, which is now in the clinic. It's a second-generation NKCEL Engager targeting CD20 that's specifically designed to eliminate B cells and to induce expansion of patients' own NKCELs. The unique design of IPH6501 involves several key components. First, there is an FAB targeting the tumor-associated antigen, here CD20, in a monovalent way. Second, like in a regular antibody, there is an empty portion that activates the NKCEL receptor CD16. Then the third and key component of the molecule is the NKP46 binder. It targets the NKP46 activating receptor, which is the most specific marker of human NKCELs, and which expression is stable on NKCELs in tissues, and especially in the tumor-infiltrating ones. Finally, the IL-2 variant portion provides the proliferation signal that is redirected towards NKCELs, helping them to increase their antitumor activity. On the next slide, slide 10, I like to highlight some of the key differentiating properties of IPH6501 over an approved CD20 T-cell engager. These data were published last year in Science Immunology. First, on the left, in in vitro assay, IPH6501 can deplete autologous CD20-positive B cells with greater efficacy than the T-cell engager. Also, on the right, you can see that IPH6501 induce significantly less pro-inflammatory cytokines than its T-cell engager counterpart in non-human primates, thus limiting the risk of cytokine release syndrome in patients. On slide 11, I will now highlight IPH4502, our lead proprietary ADC. We are very excited by this novel and differentiated NKT4-TOPO1 exatic NADC that is currently in phase one. This asset is built with a proprietary humanized anti-NKT4 antibody, which binds with high affinity to a unique epitope of NKT4. With an active FC, it's inducing as well ADCC and CDC, enhancing its immune response potential. The linker used is hydrophilic, stable and cleavable, ensuring high ADC exposure and low release of free exatican, which minimize potential side effects. The payload, exatican, is a potent topoisomer as one inhibitor. It has demonstrated bystander activity, as well as strong activity in model resistance to MMAE, which is a payload used in PADSEV, but also in several second generation NKT4 targeting agents. These properties allow IPH4502 to potentially target patients with low or heterogeneous NKT4 expression due to the bystander effect, as well as patients pre-exposed to MMAE, ADC, either because they do not tolerate MMAE or because they are refractory or became resistant to it. I will now highlight some of the recent data that we have presented at ACR in Chicago couple of weeks ago. Next slide. On slide 12, it is shown that IPH4502 can induce strong antitumoral efficacy in the bladder PDX model that became resistant to a fortumavidotin. Indeed, starting from a bladder PDX model, which is sensitive to EV on the left, repeated injection of EV induce resistance over time, and this resistance is related to the upregulation of the F-rex form MDR1 without loss of NKT4. Interestingly, as the expression of NKT4 is maintained, like it's observed in patients treated with PADSEV, and as Xatic-N is not sensitive to MDR1, a single injection of IPH4502 can overcome this resistance and induce complete tumor regression. On the next slide, slide 10, then we have shown that IPH4502 has strong antitumor activity in multiple non-bladder NKT4-expressing PDX tumor models, including here, head and neck, TNBC, and esophageal cancer. Interestingly, in these two last models, TNBC and esophageal, where NKT4 expression is low or heterogeneous, PADSEV didn't show efficacy, highlighting the potential of IPH4502 to address tumor types where PADSEV is not approved. Finally, on the next slide, in this last slide from our ACR poster, I like to highlight very interesting data benchmarking IPH4502 to PADSEV and to a homemade version of the NKT4 topo ADC from Eli Lilly, which is in phase one as well. As you can see in the upper row, when NKT4 expression is high, the three ADCs have similar efficacy. However, in the lung cancer model with low NKT4 expression, IPH4502 is the only one to show good efficacy. It's notable also that the biosimilar version of the Lilly candidate has no activity at all. And this is explained and actually shown in the poster by a poor internalization and a weaker bystander effect compared to IPH4502. I will now hand over to Sonja to highlight the clinical progress of our proprietary program.

Thank you very much, Yanis. And in slide 16, I will now cover the proprietary clinical programs, IPH6501, our CD20 targeting and CASEL engagement, IPH4502, the NKT4 ADC, and then lacutamab, the anti-Kirk 3DL2 antibody developed in CTCL. In slide 16, you will find a high level overview of timelines for IPH6501. This first in-human trial is recruiting well and throughout this year, we plan to complete the dose escalation and we'll look for initial safety data, PK and pharmacodynamic readouts, as well as any preliminary efficacy signals. As a next step, we will open the dose optimization part of the study to select the optimal dose for subsequent studies and then open expansion cohort in non-homogeneous lymphoma subtypes. The emerging safety profile and the therapeutic window from the dose escalation will also indicate if this asset may be positioned in B-cell mediated autoimmune diseases where rituximab is often used as a standard of care. In the next slide, we can move to the next program, IPH4502, our lead targeting NKT4. And following the IND clearance at the end of September, 2024, the first patient was dose earlier in January this year and the first dose cohort was dose within a week. We have recently received health authority authorization in France and the French sites are also now operational alongside the US sites. The study is recruiting very well. We are actively working to progress the dose escalation as quickly as possible and we can foresee to be in the pharmacologically active range in the second half of the year. We are therefore looking to generate preliminary phase one safety data by the end of 2025 and then to establish activity in NKT4 expressing tumor types that express different level of NKT4 from low to moderate and high. As a reminder, the rationale and design of this study will be presented as a trial in progress at the ASCO annual meeting in a couple of weeks. Now in the next slide, I'm excited to share the progress with Lacutamab, our first in class anti-KirT3DL2 antibody. This is an antibody that depletes the tumor cells that express KirT3DL2. And this currently under development for the treatment of cutaneous tissue lymphoma and peripheral tissue lymphoma, both of which are cancers with high unmet needs. Our phase two data in Caesare syndrome and mycosis fungoides were presented at ASH 2023 and ASCO 2024 and they were highly encouraging, showing that Lacutamab have the potential to make a significant impact on these patients. We are thrilled to have received FDA breakthrough therapy designation. In addition to the previous FDA FASTRAC and EMA prime designation for SS patients, we've failed at least two prior systemic therapies. This designation paved the way for a faster path to approval and are also a testament to the strength of the data. Additionally, Lacutamab has also been granted orphan drug designation for CTCL in the US, further emphasizing the critical role it could play in treating rare and challenging cancers. We are very excited about the ongoing development of Lacutamab and its potential to provide a significant benefit to patient with this difficult to treat cancers. And we are actively preparing the regulatory package to the FDA and for the EMA to receive authorization to proceed with the phase three trial. We continue to remain engaged with the FDA to finalize the phase three protocol and discussion are progressing according to internal plans. In the next slide, we also look forward to the ASCO presentation on the long-term follow-up for Lacutamab in mycosis fungoides and Caesare syndrome, and the compelling data that supported the breakthrough therapy designation. Now, with the strong MF and SS data that we previously presented at ASH 2023 and ASCO 2024, the breakthrough therapy designation and the supporting long-term follow-up data that we are going to present at ASCO this year, there is an increased confidence in the potential of Lacutamab. Our aim is to ensure that Lacutamab gets to patients who need it as quickly as possible and to maximize the value via an accelerated approval. We look forward to looking, we look forward to update you with the PTCL trial that is performed by the Lysac group, and the trial is currently progressing well. I will now hand over back to Jonathan to close this meeting.

Thank you, Sonja, for the update. As you've heard, we have several upcoming R&D catalysts that can be meaningful to our long-term growth. We have several programs coming out of our Anket platform like our proprietary Tetra-specific Anket IPH 6501, which is progressing well in phase one. We also look forward to the first data from IPH 4502, which is also progressing well in phase one. Near term, we're looking forward to the next steps for Lacutamab, including finalizing the phase three confirmatory study with FDA following the BTD designation, while advancing partnering discussions, which are well underway. Turning to slide 22, I'd like to conclude our prepared comments with a few thoughts outlined on the slide. We have a differentiated pipeline with several first in class opportunities. We now have eight products in clinical development with four that are currently proprietary and four that are partnered. Our cash position of 72.5 million euros as of the end of March, excluding the 15 million received from Sanofi's equity investment, will enable INNATE to fund our operations through to mid-2026. I would now like to open the call for Q&A.

At this time, I would like to remind everyone to ask a question, press star, then the number one on your telephone keypad. We will pause for just a moment to compile the Q&A roster. Your first question comes from the line of Dana Graibosch with LearInc Partners. You may go ahead.

Thanks.

This is a question, guys. Sorry about my voice. I wonder if you could talk about as you look at the IPH6101 CD123 NCAT, as you look through the data coming from your former partner, and then the data that you have from the IPH6101 partner and for Ellen Boeing, what's your bar there that it would be worth further investments internally from INNATE, specifically on efficacy and safety? Thank you.

Thank you. Yannis, do you want to take that one? Yeah.

I think, hi, Dana. Yannis is speaking. Yeah, thank you for your question. I think it's a bit too early. We actually just signed the restructuring of this agreement. We didn't get the entire package of the data. We will start transitioning the asset back to INNATE with an effective transition completed with a due date for the completion of the transition by July 1st. So it's currently a process that is ongoing.

I understand the process, and I understand you haven't seen the data yet, but do you not have any strategic guiding principles before you see the data about what your bar would be before looking at it?

Maybe I can come in here, Dana. I think it depends on the setting we look to take it into, and I think that depends on seeing the data. We need to see whether this is a product for the refractory setting, or is this a product that should be used for maintenance, and to be able to make those decisions, we need to see the data and understand where that can take us. I think there would obviously be different bars for each of those different settings, and it would lead to a potentially different decision. So it's a little early to answer your question, but yeah, watch this space. I think hopefully in the next few weeks we will get at least the first cut of data back from Sanofi, so we'll be able to understand a little better what's been happening in those studies. And then I think that can guide us, and then hopefully by the time of the full transition at the end of July, we'll be in a position to make some firmer statements about what we plan to do with the product.

Your next question comes from the line of Swayampakula Ramakant. With HCW, you may go ahead.

Thank you. Thanks for the call. Jonathan, just at the high level, with the 87 and change in million in the bank, you have three assets that you're kind of working on with the Sanofi product coming back, and also the 6501 and 4502. So what's the high level strategy here in terms of making sure that you can take these products forward? It looks like the industry is having a tough time with financing right now. So how are you thinking through in terms of utilizing your resources in the right way?

Yeah, I mean, first of all, we were very happy to receive the strategic investment from Sanofi, which I think, as you just pointed out, brings our cash to almost 90 million. That gives us some options in terms of what we do next. Built into our plans, we basically have the ability to take 6501 and 4502 through to the next decision points, which are clearly high in our strategic thinking. There are key priorities in terms of making sure that we get through to those points, which will hopefully generate data, which will allow us to potentially secure further funding via partnerships or via an investment raise. So that basically is the strategy is around getting through to those next inflection points, particularly for 4502 and 6501. And that's where we're putting our focus and our effort. And then, of course, making sure that we establish, hopefully, a partnership for Likutumab, which will fund the future development of Likutumab and the confirmatory study that will be required to take advantage of the accelerated approval opportunity in the US for the Caesare syndrome. So they're really, from our perspective, where we're putting our time and attention and making sure that we're adequately funding those programs to make sure that we can go as fast as possible. And I think we've demonstrated that we're going fast. I think 4502 is a good example of that, where we went from IND to first patients recruited at the end of January this year in a very quick period of time. I think it's probably as good as it gets in our industry. We're seeing that program continue to move very quickly in terms of recruitment, which will hopefully put us in a place to be able to share data later in the year. So that's really the strategic focus from the company at this perspective. Now we have to take IPH 6101 on top of that and really identify what we want to do with this asset. Do we want to partner it out again? That's also a potential opportunity. Do we want to find a way to be able to take this forward ourselves? And again, as I mentioned in the previous question, we need to understand the data a little better to understand which setting is the right one to take the product into to understand what it would take to do that in terms of funding. So that's where we're at today. But I think the key messages are focused around 4502 and 6501.

Thanks for all that color. On the LACUTA map, the long-term follow-ups data that you're going to put out in a couple of weeks here, how much of that data is being sought after in your conversations with potential suitors?

That's data that is in the data room that we provide to the companies that are basically under CDA. And that is an important part of the consideration of partner companies because, as I alluded to earlier, and as Sonja alluded to, the data with time continues to get better and significantly better. And that makes the argument or the case around LACUTA map even stronger, which is why FDA gave a BTD designation for the product a couple of months ago. So yes, it's important data.

Thank you. Thank you, Jonathan, and good luck with everything.

Your next question comes from the line of Raj and Sharma with Goldman Sachs. You may go ahead.

Hello. Thanks for taking my question. So I had one on the B7H3 Ankit. I think it's IPH62, which is partnered with Sanofi. It seems like the B7H3 development landscape is becoming quite crowded, so it would be helpful just to get your perspectives on the rationale for the target. And also, if you could just discuss why this may be a better target for the Ankit platform rather than an ADC, which seems to be the modality that most companies are using to target it. Thank you.

Thank you, Raj. And I think Yannis can take this one.

Yeah. Hi, Rajen. So this program is actually the basis of our collaboration expansion with Sanofi in 22. It's a target on which we were working for quite some time at the research level and for which we had a very good and impressive efficacy data in preclinical models. So that's why Sanofi decided to take a license on this one. And then I would say for the mid to long term development strategy, it's more a question for Sanofi. I agree with you that the target is getting more and more attention, especially through the ADC. But having this alternative orthogonal mechanism, which is an immune mechanism with Ankit cells, could be also a very interesting way to target the B7H3.

Thank you, Rajen. Operator, could you go on for further questions? And then I have another question offline.

If you would like to ask a question, please press star 1 on your telephone keypad.

OK. Thank you. So a question I received offline from Osama Dengir at Odo. On financial visibility, does the current financial visibility include the Phase 3 for Lucutumab? Are you considering financing options? And if yes, what options would be favored in that case? So

maybe I can take this one. So in our current cash runway, it does not include the Phase 3 confirmatory study for Lucutumab. In terms of how we're looking to move forward, our preferred option, I think, as we mentioned, is to establish a partnership where the partner would basically pick up the cost of the confirmatory Phase 3 study. Having said that, what I think we've said many times is we won't do a bad deal for Lucutumab and we won't give this product away because we believe that this has a significant potential in excess of $500 million. It's hitting a very high on medical needs for patients. It has a very good reputation as a product amongst clinical investigators. So we're clearly not going to give this away. So we are exploring alternative options, and you can imagine all of the various alternatives that will be possible. We're looking at those options, and our objective is to have basically a range of options to choose from at the point when we need to initiate the Phase 3 study, either with a partner or finding a way to fund this ourselves if we need to. And that's basically where we're at today. Okay, I think that was it. I think that was the one. There are no more questions. So I'd like to thank you for your attention, and we'll close the call. I wish you all a great day.

Ladies and gentlemen, that concludes today's call. Thank you all for joining. You may now disconnect.