Good morning, and thank you to everyone for joining us today for our virtual R and D Day. I'm Beth Delgiaco, Vice President of Corporate Communications and Investor Relations at Argenx. We're looking forward to a time soon when we can meet again in person. We decided to use the virtual forum to our advantage and invited several of our Argenx scientists to speak today, likely team members that you haven't met before, but who are the beating heart of the company. They work closely with our molecules, our collaborators and our clinical teams and drive the ongoing translational studies to better understand the results we're seeing clinically.
On our agenda, you can see the depth of expertise of the speakers joining us today. Tim Van Hauer Miren, our Chief Executive Officer and Co Founder, will talk about where we are today as a company and how we are advancing towards ARGX-twenty twenty five. Hans Dehard, our Chief Scientific Officer and co founder, will talk about efgartigimod and the translational work we've done more recently on our Fc fragment. We'll then move to our new indications where we'll have both of the scientific leads speak, Vas van der Woening for myositis and Peter Verheesen for bullous pemphigoid. We had the pleasure of being joined by two top physicians to speak about the severity of these indications in a panel that is moderated by Albert Covera from our global marketing team.
Doctor. Rohit Agarwal joins the panel from the University of Pittsburgh to talk about myositis, and Doctor. Russell Hall from Duke University to talk about bullous pemphigoid. Finally, we'll share data on our next immunology asset, ARGX-one hundred seventeen. The lead physician on the team, Olivier Van Dessen, and the lead scientist, Inge Vandewala, will cover the potential of C2 as a target, data from our Phase I study in healthy volunteers, and our path forward into multifocal motor neuropathy patients.
We'll end the event with a Q and A session with our speakers and broader management team, including Whit Perrese, Chief Medical Officer Keith Woods, Chief Operating Officer and Karl Gubitz, Chief Financial Officer. Our Q and A session will be audio only to allow you the opportunity to dial in and ask questions. We expect the event to wrap up shortly after eleven a. M. Eastern.
Also, to maximize the virtual format, we're hosting a microsite with several presentations from physicians and patients to support today's event. On this site, you can view disease overviews from both Drs. Agarwal and Hall on myositis and bullous pemphigoid, respectively. We additionally asked two of our patient partners to talk about living with myositis and bullous pemphigoid. It's the patient perspective that motivates our team every day, and we encourage you to hear directly about the disease and treatment burden they face and how their lives changed after receiving their diagnoses.
To provide more information on our global launch, we worked with Doctor. Changbo Zhao to talk about the MG opportunity in China, which we believe to be substantial. And finally, on the Microcyte, we included a second panel discussion with two vascular experts, Doctor. John Casseline and Doctor. Daniel Rader.
We continue to learn more about FcRn and its dual role in recycling IHGs and albumin. In this panel, we'll talk about the role of albumin as it pertains to our autoimmune patients. We also encourage you to visit the MicroCite to read relevant publications around the topics discussed today. All presentations will be available on the microsite for up to one year should you want to rewatch at a later date. And with that, let's start the event.
Tim?
Thank you, Beth, and thank you, everyone, for joining us today. We have very exciting content to share with you that we hope will outline important future programs at Argenx. When we founded Argenx, Hans Thorsten and myself, we chose the name Argenx because it refers to the ancient myth of the Argonauts, a team on a mission to do the unthinkable. I still stand behind this choice because it underscores our purpose. We are a team, a quickly growing team that wants to bring a revolution to our patient communities in how we understand and perceive autoimmunity.
You can see within this infinity symbol that we believe our opportunity is limitless when it comes to immunology innovation. We see nothing but an abundance of opportunity ahead. In order to embrace this opportunity, we lean equally on both the science and the patient. It is the critical unmet needs of the patient that drives us, but it is the breakthrough science that allows us to do something about it. There's no one without the other.
Our efgartigimod journey started in 2013. We had new modality, thanks to our collaborator, Sally Ward, the opportunity to be first in class targeting FcRn and an innovative way to do so with our Fc fragment. We showed the first clinical proof of concept with an FcRn antagonist demonstrating a clear correlation between the PD effect, I. E, total IgG reduction, and efficacy in MG with improvements both on the MG ADL and QMG disease scores. Once we validated the deep science, we turned to the patient.
We relied on our patient partners in designing the innovative ADAPT trial, evaluating the potential of individualized dosing for the snowflake disease. The patients each experience their own individual course. We have now committed our time to engaging with the MG community through our advocacy efforts, our patient marketing efforts, and our real world evidence study, MyRealWorldMG, involving over 2,000 MG patients. We believe that we are standing on the precipice of a change in autoimmunity that reminds us of a monumental shift that has occurred in oncology. For decades, oncologists had only systemic, blunt tools to treat tumors, classifying tumor types by the organ of origin, for example, lung or breast.
There has been a shift in therapy to one that is tumor type agnostic, where we don't have therapies specific to lung or breast cancer, but to a mutation that is present in many tumor types. We have also seen therapies like the PD-one inhibitors, approved in multiple tumor types with unifying biology. We believe that autoimmunity is set to undergo this revolution from traditional blunt tools like corticosteroids or chemotherapy to therapies like efgartigimod, precision tools that reduce pathogenic IgGs regardless of the target antigen. The immune system holds the unifying biology that ties together diseases of the muscle, blood and skin. The power of a tool that is target antigen agnostic is twofold: one, it means the breadth of opportunity in terms of patients we can reach as fast.
We're not limited to diseases of the muscle. We can look systematically at where the IGGs play. Two, we have a discovery tool in our hands. Best way to determine if a disease is IgG mediated is to use a targeted approach like efgartigimod. As we reach new patients, we will reach new frontiers of biology.
With myositis, we have exactly this opportunity to use efgartigimod as a precision tool to better understand the role of IgGs in the disease biology of each of the myositis subsets we will evaluate. You will recall that with MG, we had before us a very well characterized autoimmune disease. We knew that ninety five percent of patients had a form of disease that is driven by either acetylcholine receptor, MuSK or LRP4 targeting autoantibodies. CIDP, the disease is already more heterogeneous. We knew from the literature that about forty percent of patients had characterized IgGs against the peripheral nerve.
What we learned from our interim analysis is that more CIDP patients have an IgG mediated form of CIDP where the autoantibodies are just not characterized. Our gono go showed this. Now, with myositis, we have an opportunity. We see a diverse group of autoantibodies, which are either known to drive disease or are associated with disease. This is about seventy percent of patients across subtypes, which means that about thirty percent are yet to be characterized.
With efgartigimod, it's okay that we don't know the identity. If it's an IgG, we will clear it. It is this principle that we rely on as we continue to interrogate biology with new indications. With bullous pemphigoid, we have a different story to tell. This is the second indication within autoimmune skin blistering diseases and has some key similarities to pemphigus.
In both, the role of the specific autoantibodies is well characterized. In the case of pemphigus, they target DSG1 and DSG3 and in bullous plenfigoid, they target BP180 and BP230. We have equally as convincing data from therapies that are good proxies to efgartigimod, like IVIg, plasma exchange and preferably immunosorption. And we hear from patients it's similar high unmet medical need for fast acting, safe therapies that allow them to taper corticosteroids. In the more fragile BP population, this need to taper is even more critical.
We will use similar principles from the pemphigus Phase T trial design to go straight into a registrational trial with BP. Our skin blisting franchise is quickly shaping up with these two serious autoimmune diseases. Efgartigimod emerged from the heart of our science, which is our immunology innovation program. As I said earlier, the unique way in which efgartigimod interacts with FcRn as an Fc fragment mimicking the natural interaction of a wild type IgG with FcRn. This is all due to collaboration.
ARGX-one 17, our second immunology asset, which we also talk about today, emerged from a productive collaboration with Utrecht University and Professor Eric Hacht. As we look at data from the Phase I healthy volunteer trial, we'd be hard pressed to find a better way to interrogate C2. If this is your target of choice, we believe ARGX-one hundred seventeen to be the best way to address it in terms of complement knockdown and durability of PD effects. Both efgartigimod and ARGX-one hundred seventeen are children of the IIP mold. We know that to identify first in class targets, we need collaboration.
We know that to build the best molecules, we need collaboration. We are also realizing that to interpret why we see the clinical results that we see, we need to go back to collaborative science and to run the translational studies. This seamless knowledge transfer is the power of the IIP program. Going forward, we plan to shift our priorities to those assets that fit our growing franchises of neuroinflammation, hematology, skin and kidney. The most proliferative of our therapeutic franchises is within neuroinflammation.
We will talk about both efgartigimod and ARGX-one hundred seventeen in detail today, our two lead candidates. But we also want to talk briefly about our investment into the candidates that will follow. There is a wealth of opportunity within neuroinflammation alone. In its way, the franchise is shaping up to be a company within a company. Unmet need across MG, CIDP, myositis, MMN is serious.
We see this need extends to diseases like SMA, ALS, congenital MG, various muscular dystrophies and rare neuropathies. ARGX-one hundred nineteen will be a very exciting part of the story, but there is a lot of more work to do. As we look forward to the cadence of launches ahead within the neuro franchise, the importance of building infrastructure now becomes abundantly clear. We can leverage what we've built for MG into CIDP, MMN and myositis as well as ARGX-one hundred nineteen over the next five years. Focusing our energy and resources into a franchise not only creates economies of scale, but also allows us to attract top talents and deep in house expertise.
I would like to end my presentation with a peek into the future. Today, we are in the middle of 2021 and by the end of this year, we expect an approval of efgartigimod by the FDA for our first indication, myasthenia gravis. We have been grateful for all of you who have joined us on the journey of bringing efgartigimod to this point. We are always thinking to the future and want to share some of the expectations we have for an argenx twenty twenty five. While much will change as we reach more patients living with autoimmune disease, we are committed to keeping true to the roots of argenx.
We were built out of an antibody engineering discovery platform, an entrepreneurial spirit and a belief that collaboration drives innovation. We see these traits, innovation, entrepreneurship, collaboration as core to our culture and core to our growing pipeline. These are priorities as we grow and as we bring forward a new asset each year. We have capitalized on our innovation in various ways, including through partnerships and company creation opportunities. This is the forest you see on the slide.
We plan to prioritize programs that fall within our therapeutic franchises going forward, but we also know good signs when we see it. Value can come in many forms. Now in moving up the tree, the IIP feeds our immunology pipeline. Today, we are in six abcartigimod indications, and we have committed to get to 10 indications as quickly as possible. And the work doesn't stop there.
Thanks to our Zai collaboration and our commitment to externally sponsored research, we expect to be well beyond 10 indications by 2025. ARGX-one hundred '17 is on the heels of efgartigimod. We are starting with NMN that have laid out exciting opportunities within our current and future therapeutic franchises to capture the breadth of potential of C2 as a target. 2025, we expect to see multiple late stage ARGX-one hundred seventeen trials. We also spoke about ARGX-one hundred nineteen today, which, while early, could be an important part of our story by 2025.
Finally, shifting to the patients, the leaves of our tree. Our patients and their communities will remain a core priority for us. The autoimmune market is growing. And as I said earlier, we hope to be standing at the precipice of a revolution within it. In a market we expect to surpass USD 150,000,000,000 by 2025, we want to make efgartigimod as broadly available as possible.
We want to be available in many markets across six of the seven continents, whether through our own commercial capabilities or through partnership. We will be active in indications across five therapeutic franchises. This comes with significant team growth. We plan for our team to double in 2021 from 400 to 800 and for that growth to continue to accommodate the global commercial and robust R and D business. Let me end by expressing my gratitude to all my colleague Argonauts.
It is thanks to their relentless enthusiasm and unconditional commitment that we are where we stand today. The journey has been an intense one and the hope of our patients is a deep source of inspiration to all of us. I would now like to hand over to my colleague and co founder, Hans DeHaert, who is our Chief Scientific Officer. Hans?
Thank you, Tim. I'm very excited to be here today to talk about the Fc fragment of efgartigimod, the unique design properties that emerged from our collaboration with our partner, Professor Sally Ward, and why we believe these properties are directly connected to the differentiated clinical outcomes we have seen. You will recall that Sally Ward's work on FcRn contributed to an immunology breakthrough. She found that FcRn is not only responsible for the transfer of IgGs from the mother to the baby, but also responsible for IgG homeostasis. In other words, for the long serum half life of IgG.
This picture shows the function of FcRn and explains how this receptor gives IgG a long serum alpha life. Small volumes of blood including the serum proteins are taken up into endothelial cells. Due to the pH dependent binding of IgG to SGRN, these immunoglobulins bind to the receptor at the low pH of the endosome. Other serum proteins and excess IgGs that are not bound to FcRn will disappear into the lysosome and be degraded. The FcRn IgG complexes will recycle back and at the neutral pH of the blood IgG will be released and will go back into circulation.
It is important to realize that albumin is the only other protein next to IgG which binds in a pH dependent way to FcRn and is also recycled, resulting in a long serum half life of this molecule. As is shown in the yellow square, albumin binds to a different site of FcRn as opposed to IgG and therefore both molecules can interact simultaneously with a single FcRn molecule. We are learning that not all FcRn antagonist molecules act the same and that there are different ways to antagonize this receptor. We choose the design of the Fc fragment as it is a natural ligand of FcRn and induces a highly potent and specific antagonism. The picture shown here illustrates the differences between the various anti FcRn molecules.
On the left hand side you can see how one IgG molecule in a very specific way via its Fc tail interacts with two FcRn molecules. In the middle you can see efgartigimod, which is the Fc fragment derived from human IgG1 and that has been engineered to have a higher affinity binding for its receptor while maintaining the pH dependency. It is clear that efgartigimod binds exactly in the same way to SUM as IgG is doing. Anti SUM monoclonal antibodies have been selected to recognize an epitope close to or overlapping with the site to which IgG binds. However, it is approximate binding and not an exact fit.
Our hypothesis and what we address with our translational studies is that these different ways of binding to FcRn will lead to different subcellular trafficking pathways so that efgartigimod can mimic the pattern of endogenous IgG, while a monoclonal antibody that targets FcRn with its two Fab arms will not. To learn more about the differentiation of efgartigimod, we launched a series of translational experiments with efgartigimod and a monoclonal antibody targeting FcRn. Remember that we already published our microscopy experiments in the JCI paper from 2018, where efgartigimod and an anti FcRn monoclonal antibody were fluorescently labeled. These experiments revealed that efgartigimod was recycling whereas the positive control on the FcRn monoclonal antibody rapidly disappeared into the lysosome. The experiments which I will discuss here are making use of fluorescently labeled FcRn and unlabeled efgartigimod and an anti FcRn monoclonal antibodies.
In these movies you can see that efgartigimod does not affect the fate of FcRn since over time it gives a similar picture as the untreated cells. However, in the movie of the control anti FcRn monoclonal antibody, FcRn seems to rapidly disappear and by co staining of lysosomal markers we found out that FcRn ends up in the lysosome. I am going to play the movie again so you can carefully watch this effect of efgartigimod and monoclonal antibody and see how this compares with the untreated cells. When plotting the HUN volume as done on the graph on the right, you can clearly see that untreated cells and efgartigimod treated cells give similar amounts of HUN but do not change over time. Whereas for the positive control on the HUN monoclonal antibody, the FcRn signal rapidly goes down.
Since FcRn disappears for the positive control on the FcRn monoclonal antibody, a decrease in IgG can be expected upon treatment. Since albumin is recycled by FUN as well, this serum protein is expected to be reduced in circulation also. In contrast, efgartigimod does not reduce FcRn levels so the lower IgG levels observed in treated patients in healthy volunteers can be explained by the fact that efgartigimod is occupying the IgG binding site of FcRn. Therefore, the drug should not reduce albumin levels. We are continuing to educate ourselves on albumin because this is an important player of the FcRn story.
In the literature it is clear that in the severe autoimmune population we are aiming to treat, maintenance of albumin levels is of crucial importance. Albumin has different functions as depicted on this slide but I would like to highlight the role it has in lipid mechromeostasis. I encourage you to visit the event website where you can hear more from a panel of experts on the importance of albumin in lipid metabolism. These are data from our Phase three ADAPT trial in one hundred and sixty seven mg patients. The patients were treated in cycles where in each cycle efgartigimod was given by weekly administrations followed by an observation period.
Depending on clinical deterioration a new cycle was given so patients were treated in a personalized way. On the left, the PD effect is shown for all patients during the first cycle. A deep reduction in IgG was observed which resulted in an unprecedented clinical benefit as has been described in the Lancet Neurology publication which came out earlier this month. On the right hand side in the top panel, you can see the albumin levels of efgartigimod treated patients shown with blue symbols and for the placebo patients shown in red. Clearly no reduction in albumin levels was found in efgartigimod treated patients as illustrated for the first and second treatment cycle.
In the lower panel, the LDL levels have been plotted and again no difference was observed for efgartigimod treated patients as compared to placebo. We already published before that no albumin reductions were observed in our Phase I healthy volunteer study and the Phase II studies in MG and ITP patients. Also in the Phase II pemphigus trial where patients have been treated with one hundred twenty five mgkg efgartigimod for a period of thirty four weeks, we did not observe albumin reduction or an increase in LDL levels. These clinical results make sense based on the translational work that I shared with you today. This is a perfect example of the interplay between clinical and science epigenetics.
We use breakthrough science to build a differentiated molecule. We have achieved very strong clinical results. And now we go back to the science to learn about our molecules' behavior in the most complete way possible. In conclusion, we are rapidly expanding our safety database with the trials we have run to date and the ongoing global registrational trials. We have gathered PD data, efficacy data and albumin data from each indication and have seen consistent results on safety and tolerability.
And we have also now dosed over one hundred and twenty five patients with efgartigimod for over twelve months. To date we have not incurred any toxicity limitations in healthy volunteers or patients which therefore enables us to dose and to achieve our maximal clinical response and a maximum PD effect. These outcomes are very important as we look ahead to bring efgartigimod to as many patients as possible who are living with severe autoimmune disease. I now like to introduce my colleague, Bas van der Vornen. Bas is a research fellow at Argenyx and also the scientific lead for our myositis program.
Bas, the floor is yours.
Thank you, Hans. Hello, my name is Bas van Arvani and I am the lead scientist on this myositis program. During this presentation, I will explain our rationale to target idiopathic inflammatory myopathy with efgartigimod. I would also like to encourage you to learn more about myositis from the presentation by Doctor. Achalal which you can find on this website.
Idiopathic inflammatory myopathy or myositis is a very severe and disabling immune disorder that has a devastating impact on the quality of life. There are no FDA approved therapies for myositis. We believe that some of the subtypes of myositis are autoantibody mediated and can therefore be treated with efgartigimod. These subtypes are immune mediated necrotizing myopathy, intrasynthetase syndrome and dermatomyositis. The classification of subtypes within myositis can be done on the basis of myositis specific autoantibodies.
Those of you who have already seen the presentation by Doctor. Achawal will recognize this chart. It shows that in dermatomyositis there are five different targets of autoantibodies. Then there is polymyositis. This can be subdivided into antisynthetase syndrome and immune mediated necrotizing myopathy.
In antisynthetase syndrome, there are autoantibodies against many different tRNA synthetases. To file most of these autoantibodies in antisynthetase syndrome are directed against YO-one. In necrotizing myopathy, patients have either antibodies against necrotizing myopathy or against hMGCR. Subclassification can also be done on the basis of clinical symptoms using the classification criteria from ECR URA. Either way, subclasses can be formed where autoantibodies associate with clinical symptoms.
The involvement of autoantibodies in the pathology of myositis is best understood in immune mediated necrotizing myopathy. Here we can distinguish complement dependent and complement independent processes. In necrotizing myopathy, anti SRP and anti H and GCR can bind muscle fibers thereby activating the complement system and the formation of the membrane attack complex. This leads to a process that we call myolysis. The membrane attack complex pulls actually holes into the cells of these muscle fibers and this leads to an increase of muscle enzyme levels that can be measured in the blood samples of these patients.
The affected tissue becomes necrotic and the recruitment of macrophages leads to microphagocytosis and the release of pro inflammatory cytokines such as IL-one, IL-six and TNF alpha and they have to complement independent process. Normal muscle regeneration occurs by the activation of resident satellite cells, namely myoblasts, that they fight and engage in a fusion process forming myotubes to generate mature muscle fibers. Muscle regeneration is directly impaired by autoantibodies to ectopically expressed autoantigens on the regenerating fibers. What is not on this figure is that autoantibodies also can directly upregulate markers of atrophy. As compared to necrotizing myopathy, the role of autoantibodies in the pathogenesis of dermatomyositis and antisynthesis syndrome is less well understood.
But there are two mechanisms that are clearly involved in dermatomyositis and antisynthetase syndrome that are likely triggered by autoantibodies. These are complement activation and type I interferon production. First, the activated complement targets muscle tissue directly leading to myolysis and necrosis. Second, the complement system targets the microfasculture of the muscle tissue leading to the destruction of capillaries and the hypoperfusion of the muscle tissue. Independent of the complement system, immune complexes can also induce the production of type I interferon by specialized dendritic cells.
Interferon impairs myocardial formation and muscle angiogenesis leading to the hypoperfusion of muscle tissue. Factor one interference also stimulates the adaptive immune system to produce even more autoantibodies resulting in a positive feedback loop. In case these pathogenic processes are not controlled well, this will eventually lead to atrophy. In summary, autoantibodies are involved in the pathophysiology of myositis by activation of the complement system that targets the muscle tissue directly or by the activation of the complement system that targets the microvasculature in these muscle tissues. Immune complexes trigger specialized dendritic cells to produce type one interferon and then there's the direct inhibition of myo tube formation either by direct binding to ectopathy expressed autoantigens or via Type I interference.
Now I have explained the role of autoantibodies in the pathophysiology, let's take a look at the identity of these autoantibodies. There are many different myositis specific antibodies. These antibodies are specific for myositis and can even be used for the sub classification of the different subtypes of myositis. There are also patients that have myositis associated antibodies. These autoantibodies can also occur in other autoimmune diseases.
And lastly, there are patients that have autoantibodies against yet unidentified targets. Regardless of the target antigen, efgartigimod will clear all these altered antibodies as these are predominantly IgGs. Preclinical experiments have demonstrated that the passive transfer of IgGs from patients generate all disease features of the recipient mice. Although there are no approved targets for the treatment of myositis, common immune therapies like rituximab and IVIG have demonstrated that autoantibodies are foundational drivers of the disease. In patients there is also a correlation between autoantibodies and muscle damage across all of these subtypes of myositis.
There is also a direct link between autoantibody levels and the disease activity. So let's take a deeper look at the clinical data showing the correlation between autoantibody titers and disease characteristics. CK is a muscle enzyme and a marker for active meiosis in blood samples. This figure shows a perfect correlation between autoantibody titers and CK levels. In the sera of these eight patients the CK levels exactly follow the trend of the anti SRP levels.
Similarly, anti hMGCR, YOH1 and MI2 titers have been demonstrated to correlate with CK levels and muscle strength. Furthermore, anti MDA5, YARG1 and anti MIA2 titers have been reported to correlate with extra muscular disease activity like interstitial lung disease and skin disease. Many years ago, the efficacy of rituximab was tested in a large myositis trial in four hundred and two hundred patients. That trial failed for several reasons, but what we learned from this trial is that autoantibodies are predictive biomarkers for the efficacy of rituximab. Retrospective analysis demonstrated that those patients positive to MI2 or YO-one met the definition of improvement earlier than all other patient groups tested in the trial.
Recently, OctoChem reported a positive outcome of their IVIG trial in dermatomyositis. This is the PROGRAM study. Based on these results, OctoChem IVIG has now been approved in Germany for the treatment of dermatomyositis that sets precedence for the total improvement score as an outcome measure. How exactly IVIG works is not fully understood. Clearance of altered IgGs is for sure one of the mechanisms of action.
Let's take a look at the preclinical experiment. In these preclinical experiments, the passive transfer of IgGs purified from the plasma of anti SRP positive or anti hMGCR positive necrotizing myopathy patients results in the loss of grip strength and muscle strength in these mice. As you can see in the figure on the left, injection of mice with purified IgGs from anti SRP positive necrotizing myopathy patients results in the loss of CLIP strength as compared to mice injected with IgGs from healthy controls. When mice were injected with IgG depleted plasma, no loss of crib strains was observed indicating that this is purely driven by IgGs. Similarly, mice injected with IgG from an anti hMGCR patient resulted in the loss of muscle strength.
Two histopathological features of necrotizing myopathy are necrosis and complement their position on the muscle fibers. And exactly that is what has been observed in recipient mice that were injected with these autoantibodies. These data show that auto RTGs are responsible for induction of the disease. While necrotizing myopathy anchors the market opportunity with the best characterized pathophysiology around autoantibodies, we take a basket trial approach to develop efgartigimod also in antisynthesis syndrome and dermatomyositis. Thereby we will be reaching out to even more patients with high unmet needs based on a plausible autoantibody based biology rationale.
Having a precision medicine like efgartigimod targeting solely the IgGs may allow us to redefine all three subsets as being truly IgG mediated diseases. Let's take a look at our trial design. Given one, the high unmet medical needs across these three subtypes two, the unifying IgG based disease priority and three, the existence of an overarching primary endpoint being the total improvement score, we designed the following trial. Approximately one hundred and eighty patients stratified for the three different subtypes and for the severity of their muscle weakness will be enrolled. Patients will be treated weekly either with one thousand mg efgartigimod subcu on top of standard of care or with placebo on top of standard of care.
The challenge is that we don't know whether all three subtypes will respond equally well, but here is where we can make the difference. This is an adaptive enrichment trial design. This means that we have the opportunity to perform an interim analysis after the proof of concept Part two part of this trial. Guided by an independent DSMB advice, we will have the ability to continue with one, two or all three of these myositis subsets and adjust the trial size accordingly. The primary endpoint will be based on the total improvement score and the key secondary endpoints will include the durability of benefits, the quality of life and the individual components of the total improvement score.
The IND filing is planned for the end of twenty twenty one, pending on the interactions with the Division of Clinical Outcome Assessments and the Complex Innovative Trial Design Division of the FDA. In conclusion, over thirty thousand patients in The U. S. With necrotizing myopathy, intrasynthesis syndrome or dermatomyositis suffered from proximal muscle weakness. The diverse panel of IgGs, autoantibodies, emerged as a key driver of muscle inflammation.
There is clinical evidence that links IgG levels to the disease activities. The catalyst of the antigen, efgartigimod, will clear all of these autoantibodies as these are predominantly IgGs. Thereby efgartigimod will contribute to the elucidation of the myositis biology. Our adaptive enrichment trial enables us to enroll a broader patient population with a high unmet medical need. This basket trial design for myositis may support for future multi indication trials based on a unifying biology.
For more information on Myositis, I'd like to remind you to take a look at the presentation by Doctor. Acheron. That presentation can be found on the website. Thank you for your attention. I'd now like to introduce my colleague, Peter Verhaesen.
He is a principal scientist at iGenx who is also the scientific lead for our skin blistering programs: Pemphigus and Burlicus Pemphigus.
Thank you, Vas. This part of the presentation I will give a quick overview of another new indication for efgartigimod, which is bullous pampered poise, provide an overview of the disease and the pathophysiology, show how different therapeutic approaches impact the autoantibody levels and disease activity in budesonide and present the design of the registration study for efgartigimod. I also encourage you to learn more about brunus pemphigoid from the presentation by Doctor. Hall which you can find on this website. Brunus pemphigoid is the most common autoimmune blistering disease and is driven by autoantibodies affecting the skin.
Disease typically affects elderly people and early key symptoms are itch and rash and patients develop fluid filled blisters during disease progression. Let's have a quick look to the prevalence, burden, current treatments and unmet needs. The prevalence of blundespagliflozin is twelve per one hundred thousand adults and the incidence increases with age. Bunus pemphigoid has a high burden on affected patients and the disease has a strong impact on the quality of life and has a high mortality. The mortality of blundespantagoid in The U.
S. Is two point four fold higher than the mortality in the general population of the same age. There are currently no approved therapies available for blundespantagoid. First line treatment consists of topical or systemic corticosteroids which result in substantial mobility and increased mortality, conventional immunosuppressants as corticosteroid sparing agents, rituximab and IVIG. The unmet needs for patients are the time to remission, a high relapse rate and side effects from corticosteroids.
Brilus pemphigoid represents a significant market opportunity for efgartigimod. Brilus pemphigoid is a well understood autoimmune disease in which the binding of autoantibodies initiates a cascade of inflammatory events resulting in blister formation. Cellular targets of the autoantibodies are two hemidesmosomal proteins BP180 and BP230. These molecules are involved in the stable attachment of kiogenocytes to the underlying matrix. The autoantibody actions include mechanical disruption of keratinocyte adhesion and cytokine release.
Immune complex formation initiates complement activation leading to the recruitment of mast cells, neutrophils, eosinophils and other immune cells and to the release of proteases and inflammatory mediators. All these effects, which start with the binding of the autoantibodies, induce the blistering observed in buddhist antibodies. There is preclinical evidence of the pathogenicity of the anti BP180 antibodies. In neonatal mice, pathogenic BP180 antibodies induce typical BP skin lesions clinically and histologically. When these mice are pretreated with high dose IgG and injected with an identical dose of pathogenic IgG, we see that the competing high dose IgG leads to lower anti BP180 antibody levels and reduced disease scores.
The disease phenotype is completely abolished at higher high dose Ig doses. Interestingly, with the same experimental settings FcRn deficient mice are resistant to the pathogenic BP180 antibodies due to the reduction in circulating level of these antibodies and this shows the importance of FcRn in this. The clinical benefit with therapies targeting IgG in budesonide was demonstrated in studies with IVIG, plasmapheresis and immunohadsorption. In a Phase III study with IVIG in 56 BP patients who were unresponsive to corticosteroids, clear therapeutic benefit was observed with a stronger response in severe disease and the observed improvement in the disease activity was fast. In a K series with plasmapheresis, all patients achieved complete remission and concomitant prednisone doses were reduced by seventy percent.
With protein A immunohistorption, which selectively removes IgG antibodies in patients with severe or refractory bullous plentidoid or with particular high disease activity as first line treatment, it was shown that there was a strong initial drop in the O2 antibody levels and the effect was also continued after treatment. The improvements were observed in previously treated and treated naive patients and all showed a significant reduction in O2 antibody levels throughout the observation period. The majority of the patients achieved complete remission and the proportion of them would taper off corticosteroids completely. Most patients needed only one cycle of immunoabsorption. In this slide, we see some data from the same studies.
From the Phase III study with only a single cycle of IVIG, here shown on the X axis, we can observe the improvement on the disease activity and the first onset of effect. From the plasma exchange case series, we can see that all budespantricoide patients achieved remission and we can observe the seventy percent prednisone dose reduction. From the immunohistorption data, again selectively removing IgG antibodies, we can see that together with the reduction of O2 antibody levels, patients improved from active disease, here shown in black, to clinical remission or partial remission, shown in green and red after one month, and all to clinical remission shown in green thereafter. Together, these data show that rapid depletion of serum O2 antibodies may be an effective treatment option in patients with Willis pemphigoid. We have learned a lot about efreticimod in pemphigus, which is also relevant for bilispenticoids.
In pemphigus, we have seen a clear correlation between IgG level reduction, including autoantibodies and improvement in disease scores. We have observed a fast onset of activity which was confirmed by a high rate of disease control at an early time point and a high rate of patients achieving complete remission with corticosteroid doses which were much lower than normal. We have observed that with sustained maintenance treatment and keeping IgG levels low the patients continued to improve on their disease activity. Antaparticimod demonstrated a very favorable safety and tolerability profile. Both pemphigus and dulis pemphigoid are well characterized autoimmune diseases in which the autoantibody levels are part of the diagnosis and are used to measure treatment progress.
For both diseases, international groups of experts have defined scoring systems and consensus endpoints which we can use for our clinical studies. Specifically for British pampicoid, which affects more fragile, elderly people, it is the favorable tolerability of aperiticamotid pemphigus and other indications that convinced key opinion leaders to support a trial in bruits pempevoid. With the proof of concept established in pemphigus, the clear biology rationale and the availability of international consensus guidelines, we believe that we can go right into a registrational trial for belastanfavourite. Study population will be newly diagnosed and relapsing patients within one year of diagnosis. We aim to develop efgartigimod as first line treatment.
Patients will be randomized one to one between the efgartigimod and placebo treatment arms and will be treated for thirty six weeks. Standard of care concomitant medication will consist of prednisone at the starting dose of zero point five mgkgday and the dose will be adjusted with the disease activity and tapered off as quickly as possible. Primary endpoint is the proportion of participants in complete or partial remission of oral corticosteroids. Secondary endpoints relate to corticosteroid sparing, onset of activity, prevention of relapse and quality of life. And the study will be followed by an open label extension study.
To summarize this presentation, brittle spampagoid is a well defined disease that is the most common autoimmune blistering disease and represents a significant market opportunity. Biluspamphigoid is characterized by autoantibodies against the key antigens BP180 and BP230. Autoantibodies are crucial players in the pathogenesis of biluspamphigoid. We have learned a lot about efgartigimod from our study in pemphigus and the efficacy and safety data from Pemphigus serve as proof of concept for bullous pemphigoid. Clinical study of efgartigimod in bullis pemphigoid is designed to be registrational.
I hope this presentation has given you a greater insight into bullis pemphigoid as a new indication for efgartigimod. I would now like to introduce my colleague, Albert Covera, Senior Director of Global Marketing at Argenx and Marketing Lead for all new neurology indications. Albert?
Good morning. My name is Albert Covera, and I am a member of the global marketing team at ARGX with a specific focus on indications and development. Today, I am very pleased to have two leading physicians with us to discuss our new efgartigimod indications, myositis and bullous pemphigoid. We have Doctor. Rohit Agarwal, Professor of Medicine, Medical Director of the Arthritis and Autoimmunity Center and Co Director of the Myositis Center at the University of Pittsburgh Medical Center and Doctor.
Russell Hall, the J. Lamar Calloway Professor of Dermatology at Duke University Medical Center. Welcome, Doctor. Agarwal and Doctor. Hall.
Thank you so much for being with us today to share your insights and expertise. So I'd like to begin with you, Doctor. Agarwal, if I could. And if you could provide us with a brief overview of your clinical practice and the number of myositis patients you treat as well as
Sure. First of all, thanks for having me on this panel discussion with Doctor. Hall. So we have a Myositis Center at University of Pittsburgh. We call it as UPMC Myositis Center.
And currently, we have about two hundred to two twenty five active myositis patients that we follow. Overall, in our registry, we have more than one thousand myositis patients over the last couple of decades. And in terms of research interest, I specifically focus in myositis in clinical trials for novel therapeutics as well as outcome measure, meaningful outcome measure development.
Thank you very much. And Doctor. Hall, if you could answer the same questions as well, please.
Sure. Thank you very much. And it's a pleasure to be here and to talk about bullous pimphiboid. I am the J. L.
Mark Calloway Professor of Dermatology. And as such, we have a very active autoimmune blistering skin disease section. And we also follow many patients with luspinifiboid, following at any one time 40 to 50 patients with approximately 10 to 20 patients new each year that we see. Our effort is a collaborative effort, and these patients are oftentimes enrolled in various clinical trials for the treatment as well as for the pathogenesis of the disease. My research interests have focused on both discovering new treatments through clinical trials as well as using those clinical trials to do mechanistic studies that can help us understand how these drugs work, whether they work on the B cells or the antibody or the inflammation or what exactly is the pathogenic mechanism for which these drugs work.
Thank you very much both. And Doctor. Hall, I'd like to continue with bullous pemphigoid for a moment as we move to the next topic, which is the role of the autoantibody in each disease. Could you please highlight the role or roles of autoantibodies in bullous pemphigoid? And how well understood do you feel that these roles and or functions are within the dermatology community?
Well, the story of antibodies in autoimmune blistering skin disease is a very interesting one in the sense that started in the late '60s and early '70s when we first developed antibodies against human immunoglobulins. And a medical student at the University of Buffalo decided to look and see if there were any antibodies in the skin of patients with pemphigoid. And they looked and found that there was indeed a very specific deposition of IgG that's seen in the skin of patients with closed pemphigoid that was localized exactly where the blister formed after they found that this IgG was also found in their blood and did not react and reacted with normal human skin, suggesting that it was an autoantibody. That is, it was an abnormal antibody directed against a normal antigen. This was followed very closely thereafter by the definition of the antigens for bullous pemphigoid, which are predominantly the bullous pemphigoid antigen 180, or BP180, and a bullous pemphigoid antigen of two thirty kV, BP230.
With the establishment of these antigens, we were able to develop an antibody test that could look at the levels of the antibody, and we found that the antibodies did correlate, especially in large populations, with the development of the disease activity. So the evidence became very strong that these antibodies did play a critical role in the development of this disease. And it is well accepted that these antibodies are part of the specific manifestations of bullous pimplegoid.
So Doctor. Agarwal, I would argue that perhaps the function of the autoantibody in myositis might be, let's say, somewhat less understood, as Doctor. Hall was highlighting in the case of bullous pemphigoid. Maybe even this difference occurs between subsets such as immune mediated necrotizing myopathy, antisynthetase syndrome, dermatomyositis, etcetera. So could you also perhaps elaborate a bit on the pathological manifestations of these differences between the subsets?
Sure, sure. Well, first of all, I agree with you that, the role of autoantibody is not as established and as historical as Doctor. Hall was saying in BP. However, in last two decades, we have recognized the role of myositis specific antibodies in myositis more and more. Whether you start from animal models of pathogenesis, whether the autoantibody leads to, you know, immune complex formation and then ultimately leading to complement activation, leading to the injury of the muscle, or you talk about interferon pathway activation through antibody.
Regardless, these their models put together with this suggests there may be a direct pathogenic link of these myositis specific antibody. Moreover, these myositis specific antibodies are highly specific. That means if you have these antibodies, then you have the disease. It doesn't matter. You may vary with about your clinical presentation, but you have that particular category of the disease.
Thirdly, we have done studies in which we have showed that the serum level of myositis antibodies correlate with the disease activity over time. And also, we know that there's a significant role of these myositis antibodies in terms of
And there's multiple it sounds as if there are multiple myositis specific antibodies across the various subsets. Would there be an instance where one myositis specific antibody may be used for diagnosis for two, three, or four different subsets? Or how does that differentiate?
Yes. I think that's a very good point. So we since then, since 1975, Born and Peter criteria, we have updated a new classification criteria, which is which has been validated and adapted by American College of Rheumatology and European League Against Rheumatism, and it's called ACI Europe classification criteria. And in that criteria, you see that there's an entry of at least the most common myositis specific antibody called JO1 antibody. Most experts believe that criteria should be changed to any myositis specific antibody.
And I tried to explain them when the criteria was developed, we just didn't have enough data on all other antibodies because this is you talked about ten, twelve years ago. But now we have a lot more data that suggests that any myositis specific antibody should be included in the classification criteria just because of its high specificity itself.
In the next five to seven years, what do you think generally that we will be able to understand more effectively?
What it will prove is that DM itself is just an umbrella term. And each autoantibody is a unique disease itself. So we're going to move from clinical classification of dermatomyositis and immune mediated necrotizing myopathy or antisynthesis syndrome to more serological classification. We're to call them MDA-five positive disease or HMGCR positive disease or SRP positive disease because we will recognize that each one of them, these myositis specific antibody, play a very unique role in not only pathogenesis, but also can help in management prognostication. As I told you, the levels of these antibody also fluctuate.
If somebody flares, the level go up. Somebody goes in remission, the level goes down.
All right. I'd like to have a few questions for you, almost coming from the view of the patients and their perspective. And, you know, with the other indications that argenx is investigating, you know, we've seen that there are some common patient related themes across the various autoimmune diseases. And one of these common patient themes really is the, let's say, terrifically arduous journey for the patient to ultimately or finally obtain an actual diagnosis for their condition. Now, Doctor.
Hall, in your opinion, can you talk a bit about what you consider to be the typical patient journey to a diagnosis, and perhaps how that quality of life for the individuals is impacted along that journey before he or she comes to you in your office?
Sure. I think that one of the most interesting things about, the most Hempaglottin in terms of its journey to a diagnosis not to see a dermatologist, but rather to see the general your private practitioner, whether it's a general internist or a family physician or your primary care provider. And in that instance, this rash generally comes on very quickly, and it has the characteristics of a rash that's red and itchy, and it's giving the patient a lot of problems. So their journey may start at their primary care provider who looks at the rash, says this looks like an inflammatory, itchy rash, and it needs some steroids. Just like you would treat somebody with poison ivy or allergic contact dermatitis, you give them a short two week course of steroids, it gets better and it goes away, and it never comes back.
And so the patient gets treated with steroids, and it goes away. And in the course of five to seven days, it markedly improves, and the doctor says, That's great, we'll take you off the steroids, send you on your way, you shouldn't have any problem with this again. But then three to five days after going off the steroids, or even as the steroids are being reduced, it flares up again and shows even worsening characteristics. And it's at that point that these patients oftentimes go to the dermatologist, and it's at that point they get the diagnosis. Luckily, because our organ is so accessible, and we can do biopsies very easily on these patients with very little morbidity to the patient and very little cause, these patients are biopsied generally at that visit, and the diagnosis of bullous pemphigoid is made because the tests are very commonly available now, no matter where you live or no matter how the expertise of the dermatologist, reading slides, the biopsies can be obtained and the diagnosis can be made.
This is complicated in pimavoid because these patients are oftentimes over the age of 60 and 70, in fact with a median age, oftentimes in the 80s for the onset. So these patients oftentimes have other problems that make the use of steroids quite difficult. They'll have difficulty controlling their diabetes or their hypertension. They may have a lot of peripheral edema. They'll see changes in their mood and their behavior sometimes with the high dose steroids.
So at that point in time, it's an issue of both the diagnosis has been made, it's how are we going to manage it and treat it with the effective therapy that can minimize the adverse events, yet control the very significant symptoms of generalized blistering and incredible itching. And that's when they come in to the academic dermatologist, and that's where other therapies such as steroid sparing therapies, immunosuppressive therapies, or even new therapies in clinical trials often come. And that is why the patients are very eager to get these new medications because their symptoms just cannot be controlled without the severe adverse events associated with systemic steroid use. So now Doctor. Agarwal, being mindful, and we
talked about the different subtypes, Is there or can you take a moment to describe the I don't know if typical is the right word, but the path to diagnosis for what patients may go through in your scenario?
Yes. So I think the journey, to some extent, depends on what subtype are we talking about. But I will try to, you know, generalize everything. What happens in myositis world, they have various different clinical features that don't always present all in one go. So there is a lack of understanding initially amongst the patient themselves.
Sometimes when they present with muscle weakness, they kind of shrug it off as maybe I'm just not have done enough exercise or maybe I'm getting older, maybe my ligament is full or something else is wrong with me. There's nothing serious wrong with me, and then they kind of brush it off until it gets more and more severe. And sometimes we have patients who come to us at a stage where they're not even able to get up from their chair, where they need two people to pull them out of the car because they just can't get up or they can't even lift a grocery bag or any or a gallon of milk or anything significant, they can't just hold it or having difficulty in shower. To do shower, you have to raise your hands over your head, and they just can't do that anymore. So there's oftentimes a significant delay from patient themselves.
Sometimes they develop joint pain and rashes that they don't understand. Eventually, they get to a primary care doctor who obviously have very little experience about this disease. This is a rare disease. They have never probably seen in their whole practice, may have had one or two cases in their whole life span of ten, twenty years of their practice. So they don't know.
So oftentimes, they say, okay, let's give a little bit of steroid. Let's just do some lab work. And lab work could also be pretty much normal if they're not looking for muscle enzyme, for example. After a couple of visits of the primary care doctor, the primary care doctor recognized this could be rheumatological because not only a muscle weakness, rash, you're having joint pain, you have multiple different symptoms. Once they get to a rheumatologist, generally, there's about three to six month wait to get to a rheumatologist.
Eventually, they reach a rheumatologist. Now, rheumatologists or dermatologists or neurologists often able to recognize this could be inflammatory myopathies. However, there are many mimickers of inflammatory myopathies, so they want to be sure. For that, they often refer to centers like us who see myositis patients day in, day out. Again, now there's another two, three months or six months wait, depends on where you go, to a specialist neurologist, dermatologist or rheumatologist.
And once the patient comes to us, clinically, recognize based on the history and exam that, yes, we are dealing with myositis. However, we need to be sure as well. So we have
to run
a series of battery of tests, whether it's an EMG, muscle MRI, muscle biopsy, skin biopsy and so on to confirm what we think is correct. And then the treatment journey starts. The diagnostic journey is very convoluted and problematic. On an average, it could be anywhere between six to twelve months before they can get treatment initiated. So the diagnostic journey itself is a problematic journey itself.
Now you asked about treatment, I think, as well. So even the treatment journey isn't that easy. We have to use high doses of steroids for long term to improve strength of these patients or improve rash and other clinical manifestation. Now the treatment itself becomes a big headache for us because these high doses of steroids for long term period leads to significant comorbidities, whether it's osteoporosis to muscle atrophy, to obesity, cardiovascular disease, avascular necrosis, you name it. I can go on and on about the side effects of long term steroids.
But we have to use them. Otherwise, these patients are not going to be functional. And these patients have functional disability in their day to day life. So we exchange one problem for another problem, essentially, you know. And then we often have to use nonsteroid immune suppressive drug.
Again, we are trying to lower the dose and the length of steroid use by using these nonsteroid immune suppressive drugs. Now these non steroid immunosuppressive drugs are not specific for myositis. These are general immunosuppressive drugs. So obviously, they're not going to work excellent for all our patients. It do in some cases.
But we feel that onethree of our patients, at least the ones that get to us, are refracted to these treatments. And even another one third who initially improve and we taper their immune suppression, they flare up, they relapse. So we have a significant problem in terms of management of these patients. Now many of these patients then eventually go to clinical trials and other areas. But even though, at least in our center, with our experience, we are able to improve a lot of our patients, even then, if you truly interview our patients, whom I would say we have done fantastic job in improving their condition, they will tell you that is not true.
They will tell you, I suffered every day. I have fatigue issue. I have muscle endurance issue. I'm not able to do what I used to do. I can't keep up with the hours of job that I'm doing.
Remember, the myositis patients are in the age group of 30 to 60. These people have to work in every day, forty to fifty hours a week to able to keep up their income, which is not easy when you've been hit by disease like myositis. So that's it's so there is a significant unmet need in terms of effective treatment, which does not lead to the significant side effect profile that we currently have.
So Doctor. Hall, if you could spend a moment and highlight what is your typical current treatment algorithm for a bolus pemphigoid patients today? And the second part of the question is if you could highlight any key needs for a new medication to manage
bolas Today I think the most critical factor for a patient with bolas pemphiboid when they present to you acutely is you've got to do something to stop incessant and really debilitating itching and the development of blisters and acute inflammatory reactions in the skin. And that needs to be stopped as quickly as possible. That's very disruptive to every aspect of the patient's life, their social life, their physical life. And so at this point in time, that is done by systemic corticosteroids.
And generally we can achieve control on a fairly good dose of steroids, on a modest dose of steroids, within twenty one to thirty days. We can do that. It's just that we cannot maintain high dose steroids for long periods of time without significant morbidity in a population that has a median age of 80. So the results of that are we have to search for a steroid sparing agent. And we have a whole host of drugs that we choose from, ranging from drugs that work against the inflammation, such as doxycycline or dapsone or other kind of anti inflammatory drugs, to drugs that are more traditional immunosuppressive drugs, very similar to what is used for myositis with azathioprine or mycophenolate or methotrexate or other sorts of anti inflammatory immunosuppressive drugs.
And those are usually used, and we try to manage those to control the disease while we're getting people off systemic corticosteroids. And these patients oftentimes take a year to two years to get totally off of systemic steroids, and it can be a very arduous task. And that's our real challenge. And I always tell patients the first time I see them is that we have a sign up, they can't see it. I have it painted in ink that only our long term patients can see that I will never go on prednisone again.
And so that's what we want as our goal of our patients. Now we don't always meet that goal. But that's what we strive for, and that's what our patients want. And we need to find new drugs that will allow us to do that, because frankly our current drugs are as very hit and miss. And some work for some patients and some don't work for other patients.
So Doctor.
Agarwal, from what you discussed previously and listening to Doctor. Hall now, it seems as though perhaps the philosophy treatment algorithm paradigm might be similar for myositis patients. Can you talk to us about that for a couple of minutes?
Sure. What Doctor. Hall talked about could really be said for myositis as well. There are only a few differences that I wanted to point out, but first, some similarities. The manomyositis inclusion, immune mediated necrotizing myopathies, antisynthesis syndrome, we don't have any FDA approved treatment.
So we face same significant trouble in getting nonsteroid immune suppressive drugs to our patients to help them manage their disease. The second point, think one Doctor. Hall was mentioning that we are able to give steroid and in a month or so, patients improve. Here, I would say there is slight differences in dermatomyositis inclusion immunometric necrotizing myopathies and antisynthesis syndrome. So when we treat our patients with steroid, it takes months, not few days to weeks to see improvement.
We typically bring them back in three months to even notice if there is any improvement that is happening or not. You know, each treatment, we have to try for at least three to six months to say, okay, this is not working. We need to move on to another treatment. So that means even if we have to find the right drug and if the right drug is available, it may take six to twelve months to eighteen months to get to that drug just by the fact that, you know, you're going to try different combination of steroid and nonsteroid immunosuppressive drugs. And all this time, you're going to have to use steroid to keep the patient under some control.
And I will add a third aspect, that even if we are able to maintain for in some patients, are able to maintain their treatment, their disease under significant control, when you ask the patient, patient is still symptomatic. They still have fatigue, endurance, muscle pain problems. We just have improved the disease to a certain extent that the doctor is satisfied. Okay, the rash is minimal, muscle weakness is minimal, lungs are doing okay, you don't need oxygen. We are satisfied, but the patient is not because they have disability in their day to day life.
I'd like to ask this to the both of you. And as this is important for argenx, as we continue our clinical development in the indications that we've been discussing today, What would you say, to summarize, are the key attributes of future therapies for either bullous pemphigoid or myositis? And I'll begin with you, Doctor. Hall.
Well, think that the discussion has led us hopefully has led us to this point in the sense that it's clear that our most important aspect is that we achieve a very rapid and effective control of the initial symptoms of itching and blistering on the skin. And we have to get that under control in as short a time as possible. So quick acting control of itching and blistering in the skin disease is the number one criteria. Second or sort of Part B of that first two things is do that with as little dose of systemic corticosteroids as possible, or hopefully at some point in time no systemic corticosteroids to develop that initial early control of itching and control of blistering. The second criteria it has to be is that whatever this therapy is, is able to induce a complete remission and able to sustain that complete remission without the use or with minimal use of corticosteroid.
So those two factors, quick and sustained remission with minimal to no systemic corticosteroids, are two of the most important criteria. The third criteria that has to be included is minimal adverse events, the increased mortality that we see in our patients over the time of their disease. Even though patients are elderly, the death rate for those pemphigoid is two to three times that for their age matched peers. So we would like to try to improve that so we can improve their lifespan. Thank you.
And Doctor. Agarwal, are some
of those attributes or characteristics similar?
I think Doctor. Hall spoke very well about all the points that I would make. The only difference, in terms of the sequence, And Doctor. Hall spoke about treatment that can cause complete remission. I would put my goal a little bit lower.
I would be happy if I find a treatment that even improves the disease by moderate improvement, by moderate response. But it has to be sustained long term. And we cannot continue to use the steroid the way we're using the steroid. I would be more lenient, maybe not a few weeks. I will be happy with few months of steroids even.
But we cannot continue to give years and years of high doses of steroids for these patients.
All right. Well, on behalf of the Argenx organization, I'd like to thank you both again. This has been incredibly helpful for our audience, for myself, to hear about these serious debilitating autoimmune diseases and how you manage your patients that are living, with these conditions. We absolutely appreciate your time and commitment this morning. And I hope to have the pleasure of speaking with you both again in the future.
So thank you both very much.
Thank you very much.
Thank you for having us. Thank you.
Thank you, Albert, Doctor. Agarwal and Doctor. Hall. We're now going to move on to ARGX-one hundred seventeen. I'd like to introduce my colleagues, Inge and Olivier.
Thank you, Beth. Today, we will talk about ARGX-one 17, a monoclonal antibody that blocks complement factor C2. I want to start by giving a bit background on the complement pathways. Complement cascade consists of three pathways: the classical pathway, lectin pathway and alternative pathway, and is essential in the defense against all kinds of pathogens. All three pathways lead to the activation of the central molecule C3 that in turn activates a final common pathway leading to the formation of the membrane attack complex, resulting in membrane damage and inflammation.
So why do we target C2? First, it targets upstream of C5. And as you can see here, the inflammatory potential starts at the C3 level. Secondly, we leave the alternative pathway intact. And by doing this, you still have an antibacterial defense reducing the risk for infection.
Third, we wanted to target both the classical and the lectin pathway. So two options are possible, C2 or C4. Of those two, C2 was attractive because it has less abundant presence in circulation and has the mildest phenotype of all classical pathway deficiencies. C4 deficiency has a higher risk for developing lupus compared to C2 deficiency. ARGX-one hundred seventeen is a first in class antibody optimally engineered for C2 blockade.
If we look at its features, it binds in the pH and calcium dependent manner to C2. And it has an IgG backbone, which is equipped with the LALA mutation to knock down effector functions and an enhanced mutation to enable half life extension. All those features result in a unique mode of action of ARGX-one hundred seventeen. Weeping antibody as depicted in the figure on the right. First, ARGX-one hundred seventeen binds to C2.
It is taken up by finelysidosis entering in the endosome where C2 is dropped off and degradated, whilst ARGX-one hundred seventeen is recycled back to pick up new C2 molecules. So Olivier will explain the Phase I trial.
Thank you, Inger. Thank you for introducing ARGX-one hundred seventeen. Today, I will share and present to you some of the key elements and study results that we have generated of our ongoing Phase I clinical study with ARGX-one hundred seventeen. In this Phase I first in human clinical study, we are testing ARGX-one hundred seventeen to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of a broad dose range administered to healthy subjects. And in this particular study, we typically have included a typical single ascending dose part and a multiple ascending dose part of the study.
ARGX-one hundred seventeen has been administered both intravenously as well as subcutaneously in these two study parts. And in our single ascending dose part of the study, we tested up to eighty mgkg administered intravenously and we tested up to sixty mgkg administered subcutaneously. In our multiple ascending dose part of the study, we tested quite a broad different dose regimen. Dose regimen that were defined and selected to assess on safety and tolerability of repeated administrations, but also dose regimen in particular to generate the dataset to optimally inform a PKPD model. And this PKPD model will inform us on future dose regimen that will be tested in subsequent patient studies.
Overall, we are pretty pleased with the progress we have made in this clinical study and as a substantial number of study participants have been included to date. In particular, 70 subjects have been included in the single ascending dose part of the study and 32 subjects have been included in the multiple ascending dose part of the study. And overall, this has allowed us to generate a very comprehensive and robust clinical data set. So let's now have a closer look at some of the data that we have generated. In the first step, we'll zoom in on the key safety results.
But I would like to caution that our study is still ongoing. And as a sponsor, we are still blinded to these safety results. Being blinded implies that we can only share high level results on a core level. As a reminder, this first in human clinical study is currently ongoing. We tested a broad dose range of different doses the single ascending dose part and multiple ascending dose part of the study.
And specifically for each cohort that has been tested, I would like to emphasize that we randomized subjects in a three:one ratio. This means that for every cohort, six participants received ARGX-one hundred seventeen and two participants received placebo. From a safety perspective, we attempted to summarize the key safety results through this table. In this table, you will see the number of study participants and the percentage of study participants who developed treatment emerging adverse events on a cohort level. The left We did see indeed treatment emerging adverse events across all cohorts and that is typical for a first immune Phase I study.
But the majority of these treatment emergent adverse events were categorized to be grade one or mild in nature. Very few grade two or moderate treatment emergent adverse events have been observed, and furthermore, no clear dose relationship with respect to treatment events were observed across the different cohorts that had been tested. As you can see, in the two point five mgkg dose cohort, one subject developed a series adverse event. This serious adverse event was characterized by an abscess that required a drainage and that was categorized as such to be serious adverse event and this drainage basically resolved the AE. According to the principal investigator, the serious adverse event was considered to be not related to study drug and that provided additional reassurance for us.
Overall, based upon the totality of treatment emerging adverse events and specifically zooming in on the infections, we have indeed concluded that no increased risk of infections was observed across the different cohorts that have been studied. But taking all the safety results into account, and specifically safety results that we presented here, we basically can conclude that single and multiple administrations of ARGNIC-one hundred seventeen or placebo yield a favorable safety and tolerability profile supporting the investigation of study drug and patient studies. So let's now have a closer look at the PK and PD results from our first immune study. And now I will give the baton to Ingred.
Thanks, Olivier. In this slide, the pharmacokinetics and the pharmacodynamics of ARGX-one hundred seventeen of our single ascending dose cohorts are shown. If we look at the PK curves on the left, we see a classical PK pattern with a dose proportional increase of Cmax. You can immediately notice that ARGX-one hundred seventeen stays long in circulation due to the enhanced mutation and has an estimated elimination half life of around sixty five to seventy days, which was even longer than expected and as a result from single ascending dose cohort three on, subjects were followed up for a longer period. At the graph on the right, free C2 levels are depicted, which is one of our PD readouts.
We observe a dose dependent reduction of free C2 levels, and this reduction is sustained as free C2 levels are reduced by 95% or more than one hundred days after one dose of thirty milligrams per kg or more. On the next slide, we see the pharmacodynamics and pharmacokinetics of the multiple ascending dose cohorts. First looking at the PK profiles on the left. Accumulation of ARGX-one hundred seventeen is observed after multiple dosing as expected because we haven't reached steady state yet. These dosing regimens were chosen to optimally build a robust PKPD model.
When looking at the Vc2 levels on the right, again, sustained reduction in Vc2 is observed after multiple dosing. When targeting complement, you need to consider the high levels of circulating complement factor that are present in circulation. That is the reason why the concept of a high loading dose followed by a maintenance dose concept was tested. As you can see in the yellow curve, sixty mgkg loading dose leaded to an immediate and fast drop of C2, which could be sustained over time with lower doses of ten milligrams per kg. All those PK and PD data were used to build a robust PKPD model, enabling us to optimize dose selection in further development of ARGX-one hundred seventeen.
On this slide, three dose regimens are modeled, suggesting potential for infrequent dosing. To reach full complement blockage, which corresponds to more than 99% reduction in Vc2 levels, several dosing regimens can be applied. Here we show the concept of loading dose of sixty mgkg, followed by a maintenance dose of ten mgkg, shown in green, compared to every four weeks forty mgkg dose or every eight weeks, sixty milligram per kg dose. All those regimens are reaching the targeted PD effect. So to conclude, the model suggests a broad range of dosing possibilities.
To briefly recap the Phase I data of ARGX-one hundred seventeen, we have shown that ARGX-one hundred seventeen has a favorable safety and tolerability profile, that the sweeping antibody design enables infrequent dosing. We also have shown a consistent PKPD profile across IV and subcu dosing. Overall, these data support a Phase II proof of concept trial in multifocal motor neuropathy. MMN or multifocal motor neuropathy is a serious neuromuscular debilitating autoimmune disorder. It is characterized by slowly progressive muscle weakness due to motor neuron degeneration.
It mainly affects hands and forearms making patients become dependent. In The US, there are about thirty thousand patients with MMN and this number is still increasing. Mainly men are affected and the median age is around 40 years. Diagnosis takes around one point five years as it is initially often misdiagnosed as ALS. The first line treatment is high doses of frequent IVIG and MMN patients account for more than half a billion of the IVIG sales.
So why did we select MMN? First, in IgM, IgM autoantibodies will bind to GM1, which is located on the nerve cells, more specifically on motor neurons at the Rhodochrombier and it is also expressed on Schwann cells. Upon binding, these autoantibodies will activate the classical pathway of the complement as IgM are potent activators of the classical complement pathway. As shown in the graph, the GM1 antibody titer is correlated to classical pathway complement deposition. Complement activation leads then to muscle damage and loss of grip strength.
The current standard of care is IVIG and IVIG reduces C3 deposition in vitro, resulting in less complement deposition. Through our collaboration with Erik Hag and Ludo van der Pol from UMC Vitrev, we have generated in vitro results showing that ARGX-one hundred seventeen efficiently can block complement deposition on nerve cells. This is shown on the slide. Let me start by explaining the model. Motor neurons or Schwann cells are plated and cultured on glass slits.
Next, serum from MMN patients containing IgM autoantibodies against GM1 were added to the cells. These will bind to their target GM1. Next, serum which is a source of complement is added, resulting in complement activation. This can then be measured using a microscope and staining for C3. You can see strong C3 deposition when adding an isotype control on both Schwann cells and motor neurons, meaning that R2 antibodies from MMN patients activate classical pathway of complement.
When IVIG is added, reduction in C3 deposition is observed, but not a full blockage. If you use C2 depleted serum, no complement is deposited and when supplemented again with C2, C3 deposition is restored. Very nice to see is that when you add ARGX-one hundred seventeen, it is capable of fully blocking C3 deposition on both motor neurons and swarm cells and this happens in a concentration dependent manner, which is shown on the next slide. Here you observe the dose dependent reduction in C3 deposition, often higher concentrations of ARGX-one hundred seventeen. And moreover, it is dependent on C2, as C2 depleted serum did not activate C3 deposition And reconstitution of the depleted serum with C2 up to physiological levels dose dependently restores C3 fixation.
So to conclude, ARGX-one hundred seventeen blocks C3 deposition in a dose dependent manner. Next to that, we also collaborated with Hugh Quillison from the University of Glasgow to evaluate ARGX-one hundred 17 in an ex vivo model of acute maternal neuropathy. These transgenics mice were used, which exclusively expressed gangliosides on their neuronal cells. From these mice, muscles were isolated and incubated with anti GM1 antibodies, human serum as source for complement and ARGX-one 17 for a nisotite control. Here you can see that this ex vivo system, GM1, are able to activate the complement system as seen by C3 deposition at the nerve terminal.
This complement activation leads to neuronal damage as observed by the loss of the neurofilament staining. In contrast, when you use ARGX-one hundred seventeen instead of an isotype control, ARGX-one hundred seventeen blocks complement activation as no C3 deposition was observed and hence the nerve terminal stays intact, as seen with the positive staining for neurofilaments. So to conclude, XENX-one hundred seventeen protects the integrity of the exome by blocking complement. All this data has led to the initiation of a Phase II trial in MMN patients, which will be explained by Olivier.
Thank you, Inge, for nicely summarizing our in vitro and in vivo work. So based upon a very strong preclinical foundation and the clinical safety PK and PD results we have generated and that I presented earlier on, we are indeed well positioned to assess ARGX-one hundred seventeen in our first inpatient study in MMF. And I will now present and explain some of the study design elements of this Phase II dose range finding study. But please bear in mind, our protocol is still in development and we could potentially implement some changes in the very near future. As you can expect, the study design has been developed with the input from an esteemed panel of international experts and we have taken into account many of the lessons learned from other clinical studies that have been conducted in this patient population.
The proposed Phase II study will include approximately 45 patients with definite or probable And here we will use an adjudication committee by an independent panel of experts, an education committee that is actually very similar to what the HFrEHim or CIDP study is implementing. The patient populations that will be included in our study will furthermore be characterized by the fact that they will be on stable IVIG regimen at screening and they will have to fulfill the criteria for IVIG dependence. Following completion of the screening period, patients will enter an IVIG monitoring period. And during this IVIG monitoring period, we will basically assess clinical outcomes while patients receive their standard regimen. Reason for having this IVIG monitoring period is obviously to assess the clinical safety and efficacy of IVIg treatment.
But in addition, we would like to demonstrate that IVIg has indeed some weaknesses where we believe that ARGX-one hundred seventeen can potentially make a difference for patients when they get study drug. Following completions of the IVIG monitoring period, patients will be randomized to one of three treatment arms. We have defined two ARGX-one hundred 17 arm and one placebo arm. Following the randomization and first IMP administration, patients will go through a 16V double blind treatment period. During this treatment period, we will assess safety and tolerability, our primary study objective.
But in addition, obviously, we will be looking at a series of efficacy outcome measures. We will be looking at time to IVIG retreatment. We will be measuring grip strength. We will be looking at MRC SUMS score. We will be testing nine hole PEG test and MMN ROS.
In addition, we will collect a lot of data on patient reported outcome measures as well as pharmacokinetic and pharmacodynamic results and we will be looking at disease relevant biomarkers. Following completion of the double blind treatment period, patients will indeed have the option to enter a long term extension study and be exposed to prolonged treatment with ARGX-one hundred seventeen. Again, as I've said in the beginning of my talk, we are in a pre final stage of preparation of our Phase II patient study, but we are on track to start a study by the end of twenty twenty one.
Next to MMN, ARGX-one hundred seventeen is a pipeline and a project opportunity. As you can see here, there are a lot of classical and lectin pathway mediated diseases across our therapeutic franchises. Currently, we are preparing to select a second indication for ARGX-one hundred seventeen. I've come to the end of the ARGX-one hundred seventeen presentation, so thank you all.
Thank you to all presenters. We're now going to open up the call to Q and A, which as a reminder, will be audio only. Operator, can you please provide instructions on how to ask a question?
If you are streaming the presentation via the webcast, you may submit an Our first question comes from James Gordon with JPMorgan. Please go ahead.
Hello, James Gordon, JPMorgan. Thanks for taking the questions. My questions were just about timeline. So for BP and myositis, when would you most likely have clinical data? For BP, I can see it straight to pivotal.
But for myositis, can you do something a bit like you have done in in CIDP with the phase two sort of feeds straight into a phase three if it works well? Or you definitely need to do a separate Phase two and pivotal trial? And actually, just on that, could you talk about these timelines for other trials as well? So for 01/2017, ranges timelines might the Phase two be on? And how are you finding recruitment and trials going for ITP and PV?
And time lines there as well, please.
Thank you for being with us today, James.
I highly appreciate it.
This is Tim speaking. I'm going to invite my colleague, Vin Parez, who's our Chief Medical Officer, to comment on your question regarding timelines and the ability to do something similar with the myelitis trial as what we have been doing with CIDP. Wim, can you take this question, please?
Yes, sure. I hope you can understand me well.
Yes, we can, Win. Sorry?
Okay. I trust you can hear me well?
Yeah, we can, Ben.
Okay, thank you. So the situation with myositis is, of course, a different one compared to CIDP, where we talk here about combining three different expressions of the disease. And therefore, that requires a different approach. What we could be looking at is an enhancement of the subtypes that could show and in that sense, it's a derisking scenario. And you might say it's similar compared to CIDP because we also had an early derisking.
Here we do the derisking for the specific subtype. So we will be able to enrich any subtypes where we see a response. We could still change the sample size accordingly, referring back to predefined criteria. So in that sense, there is de risk within de risking within the design, but it is different from the CIDP situation. And as I just mentioned, because it's a different approach with three different subtypes included.
Thank you. And with regards to starting of the trials in budesonide, myositis and MMT, can you comment on big picture timelines to starting these trials?
Yes. We are focusing on end of the year or early next year. So it will be a very busy time period, but that's the timeline we are aiming for. Some of the timelines depend on interactions that are ongoing, as mentioned, in the presentations, especially for myositis. We are paving the path here, so to stay so to speak.
We are trailblazing in the sense that in terms of endpoints, we have interactions with the FDA also with respect to the innovative trial design. And depending those interactions, the timeline could be early, so still this year or early next year for a start.
Thank you, Wim. And then James, on finishing studies, of course, we continue to stay away from any guidance here. We're still in full COVID pandemic in big parts of the world. So what we will do in the future going forward is what we said we would do that is if the men's studies are fully recruited, we will talk about it in our quarterly earnings calls. And of course, you can monitor the start or the initiation of these trials through clinicaltrials.gov.
Thanks for the question. Thank you.
Our next question comes from Tazeen Ahmad with Bank of America. Please go ahead.
I think I was muted. Sorry.
Can you
hear me?
We can hear you. Thank you. Okay.
Excellent. Thank you so much. Good morning and good afternoon. I'm just wondering, given that the myositis indication might be quite large, and you talked about, you know, potential subgroups, can
you talk to us a
little bit about how you're thinking about, whether certain of those subgroups might be more amenable to, treatment and whether or not, you know, your plan initially could be to study specific subgroups? And then as a follow on question, I think, one of the comments made during the presentation is that for myositis treating with steroids often takes a long time to start to see efficacy. Based on what you know about the profile here, how long do you think it would take to start to see efficacy in patients? Thanks.
Hey, Tazeen, thank you for being with us today, and good morning to you. It is true that myasitis, of course, is a set of indications. Here, I think, in the R and D slides, which were presented by Bas, we basically showed you how we went about identifying these subsets where we think there is most compelling evidence for IgGs mediating the disease, you know, starting with IMNM, then ACEs and dermatomyositis. And maybe, Bust, you can briefly repeat why we zoomed in on these three subsets. But we think within the universe of myositis, myositis is a three plausible subset to interfere in a meaningful way with efgartigimod.
Baz?
Indeed, in necrotizing myopathy, the rationale is very clear that both antibodies are driving the disease. There have been preclinical animal models that clearly showed that if you take and purify IgGs from the blood of patients and inject it into mice, Then these mice, they develop exactly the same disease features as have been observed in these patients. So that's a fairly direct evidence that the other IgGs are involved. Now for antisynthetic syndrome and dermatomyositis, these direct evidences are not available yet. But what has been done for antisynthetic syndrome, and remember what Professor Achalal mentioned that the anti Yo antibody is the most prevalent antibody in myositis, and it's an antisynthetase antibody.
So what there has been done is it is not a direct transfer of IgGs into mice, but what has been done is that mice have been immunized as the target of the antibody. This is is just to do T RNA transferase. And what these mice what happens in these mice is that these mice, they develop a very high title of these antibodies against their target, so kind of the mouse anti Yo antibodies. And these mice, they also developed the same disease features, so these mice, they developed muscle inflammation and lung inflammation similar that is observed in patients with antisynthetic syndrome, interstitial lung disease and muscle weakness. Looking more at the clinical evidence, looking at rituximab in myositis trial ten years ago, there you see that patients that have antibodies against YOH1, so the antisynthesis or against MI2, that's an antibody in dermatomyositis.
These patients, they met the definition of improvement earlier than in other patients tested in that trial. And what is also demonstrated that the titers of these antibodies, and that's very important, that these titers of these anti Yo antibodies and also for the MR2 antibodies, they correlate with all these core set measures
of the total improvement score. Yes.
Thank you, Bas. And we have the benefit of having Doctor. Agarwal on the phone. So maybe Doctor. Agarwal, you want to build on what Bas has been saying?
And maybe also comment on the fact that steroids seem to take some time to act and maybe draw a proxy from IVIG or another proxy you think is relevant for trying to estimate what time of response could be on an IgG lowering agent? Doctor. Agarwal?
Yes. So first of all, Bass really nicely summarized the first question that the speaker asked about the evidence of autoantibody or evidence that lowering globulins may work. And I will add to just one more point that there are also evidence in dermatomyositis in certain subsets. For example, anti MDA-five positive antibodies, they have been thought to be sort of prognostic and the levels of anti MDA-five antibody sort of predicts how active or severe the disease is going to be. Similarly, an antibody called anti TIF1 gamma antibody, which is associated with cancer
What has been seen is once dermatomyositis is active, these antibodies goes up. When it gets into remission, antibodies drop the level. And if the patient has a flare up in future, you see, again, risk sufferance increase in demanding increase in these auto antibodies. So I was just completing the few additional points that Bass has already summarized nicely. And then the question, how long does it take for patient to see a response?
It's typically first of all, depends on the onset of action of the drug. So let's say the drug works in four weeks or eight weeks. I've always maintained it takes about three months for patients to see clinical response, a significant clinical response. Now based on IVIG Octagam data, we know the clinical response starts as early as eight weeks. But to reach a threshold, a significant clinical response, I believe it still would take about twelve to sixteen weeks.
And that's why when we do myositis clinical trial nowadays, I recommend to have at least sixteen week primary endpoint or up to twenty four week primary endpoint, longer is better because then you have a more assurity that you will see the response in the given time. I hope that answers the question.
Yes. Thanks for all of that color. So would you have a guess on how much faster efgartigimod can work?
David, in the area of speculation, of course, Dazeen. So we do not know that. And of course, that's something which we will study in this clinical trial. We have designed a clinical trial in close concert with the experts, including Doctor. Agarwal.
So we believe the duration of the trial is sufficiently long to pick up a convincing signal in any of the T subsets in case efgartigimod would work. How fast it's going to work, we don't know yet. So I think we will need to wait for the data.
Okay.
Thank you, Tazeen.
Our next question comes from Greg Suvanovich with Goldman Sachs. Please go ahead.
Thanks. Can you hear me okay?
Yes, we can. Hello, can you
hear me okay?
Greg, we can hear you. Yes, we
can hear you, Greg. Thanks for joining
thank you. Thanks for the R and D Day and all the details. I guess I've got two questions that are kind of related to each other. One, you know, thanks for announcing five and six and I'm sure there are a lot of questions around five and six but I wanted to pick out on your comments around perhaps seeing efgartigimod approved in as many as 10 indications or getting to 10 indications. And so how are you thinking from a rationale or strategy in terms of indications seven through 10?
And, you know, how do you prioritize whether it's based on the biology or the commercial opportunity? And kind of following up on that, I know in past presentations going back a couple of years you've highlighted indications such as lupus and EB and ANCA vasculitis or RA. So I'm wondering if you can comment on whether you think those indications that are still up for consideration. And then my last question for Doctor. Agarwal.
It goes back to perhaps something Tazeen might have asked about but I'll ask it a different way which is as you think about the three subtypes that the company is going after in terms of myositis, how would you rank kind of based on the strength of the biology or the science, you know, of the three where you think efgartigimod is most likely to find efficacy if you have any initial impression? Thanks.
Thank you, Greg. I will take question one and then indeed hand over to Doctor. Agarwal to talk about probabilities of success in the key subtypes of myositis which we have jointly selected. With regards to indication selection, Greg, we're not going to change strategy. We always start from a convincing, a solid biology rationale.
The type of rationale which we presented to you today in the slide slides, ideally the CPLEX immunosorption data like we have shown you from luspenthygoid, but we also believe that's the type of evidence we collected from myositis, including some of the transfer models Vas described, is pretty compelling. So I think there's a very plausible biology rationale for both. Of course, the feasibility of running clinical trials is the second filter we consistently apply.
And I
hope that we could show you today an intelligent logical trial design for both indications. And then third, the commercial rationale, of course, I think we showed you data today on prevalence, data on what we think an addressable market or patient population could be for both indications. These are sizable, meaningful market opportunities. And as you can see today, we have been prioritizing indications which help us to build out the commercial franchises being neuromuscular and being skin today. So we will continue to apply similar logic to selecting the next indications seven to 10 or beyond 10.
The list is very long. I would also like to call out the strategic collaboration we have with Zai Lab, our partner. Zai Lab is not only the company which will be our commercial partner in China to take efgartigimod to patients there, but we publicly disclosed that Zai Lab will also be our partner to start adding proof of concept studies in additional indications. So you will see us ramp up to 10 hopefully fast. On your question regarding lupus or rheumatoid arthritis, I think it's very interesting today that with myositis, we start to sit at the interface between muscle and probably rheumatology because some of these patients are being seen by rheumatologists.
So we're putting a toe in the water here in the rheumatology space without disclosing anything more. And we continue to believe that the kidney could become a next franchise based on the biology of some of the indications, which would be amenable for efgart or for ARGX-one hundred seventeen. So I would say stay tuned. We're just in a logical, consistent fashion, expanding our reach into high conviction indications. And with that being said, I would like to turn again the call to Doctor.
Agarwal to comment on his view on probabilities of success across the three subtypes which we have selected. Doctor. Agarwal? Yes.
Thank you. So I think it was an excellent question, what's the probability. It's still difficult to say. But I if you go by the evidence, you have the direct evidence, most direct evidence in IMM and M, okay? So from that standpoint, I would say I will pick IMM and M as the top like the most likely the one that's going to show efficacy.
The second one, I would pick it antisynthesis syndrome because I think in terms of the total amount of evidence from mouse model and clinical studies done, we have the best evidence in second best evidence in antisynthesis syndrome. And dermatomyositis, we do have evidence, but it's sort of more smaller studies and more circumstantial rather than a direct solid evidence. So that's why I would put it at number three.
Thank you, Doctor. Agarwal. Thank you very much.
Our next question comes from Joon Lee with Truist Securities. Please go ahead.
Hi. Thanks for taking our questions and for all the presentations. The PKPD of January, sweeping mechanism of action is really promising. Would you I mean, it's sort of an out there kind of question, but would it make sense for you to collaborate with AbbVie, say, to make a sweeping version of Humira as well? I mean is there a limit to the target that you can sweep?
And is this sweeping technology something that is protected by your IP? Or is this more, you know, in house know how? Or can others do that as well if they so desire? And the second question is on the recent data from Alta Morris on gMG. You know, looked pretty impressive with evident efficacy at week one already and durable, you know, response out to week 52 with the two eight week dosing.
Does this in any way change your commercial strategy for efgartigimod? And what would you say is the biggest differentiator of efgart against Ultomoris and gMG? Thank you.
June, thank you for being with us today, a good morning. With regards to the sweeping technology, let me first comment on your question on to what extent it is proprietary. And then I will give the floor to my colleague, Hans Behat, to conceptually address the question on what type of targets are most amenable to a sweeping approach. And then I will give the floor to Keith Woods, of course, my colleague on the commercial front, to talk about differentiation from ULTOMIRIS and how we look at our own data in light of this data release. So from an intellectual property point of view, in order to make a sweeping antibody, you need actually to have a couple of mechanisms built in into your molecule, right?
So your antibody molecules should have a pH or a calcium dependent binding to its targets, And that's something which we discovered to be a natural property of our C2 targeting antibody, so coming straight out of discovery. We did not have to engineer for that. On the other hand, you need, of course, an increased binding to FcRn in order to favor the recycling path over the degradation path and give your molecule a long half life. And here, of course, we have a unique patent position when it comes to the patents which we in licensed from Sally Wards University, UT Southwestern. These are patents which we are prosecuting.
We already have secured granted patents the main territories, and we continue to prosecute them. So not everybody can make a sweeping antibody. I think it's a small select group of people who can make them and be one of them. Hans, maybe you want to add conceptually what type of targets we would consider for a sweeping approach, please?
Yes, hello. I hope that you can hear me. The type of targets which we consider are the targets which are abundantly circulating. So I think complement factors are an excellent example as Inge also explained. But I think you were also referring to ULTOMIRIS, where C5 is the target and that is also abundantly circulating.
So for TNF, for HUMIRA, I don't think it really makes sense because there are not such abundant amounts of TNF circulating the bloodstream. So these are the most interesting targets. Another targets which can be considered are receptors, which take away the antibodies. So for instance, Shugai targeted the IL-six receptor antibody and with an antibody, which had a very short half life. And more recently they published about a version of Actemra, which was made sweeping, meaning that it can be internalized by binding to the IL-six receptor, but in the endosome due to the pH dependent binding can be released.
And when you combine this with mutations in the Fc like ENHANZE, you really can enhance promote the recycling back to the surface of the cell. And then again, the antibody is released and can bind to other IL-six with separate targets. So these are the typical targets which we consider for the sweeping concept.
Thank you, Hans. And let me remind the audience here that we do have a collaboration with Shugai, where actually we have been accessing some intellectual property, which we think is of interest going forward into the future, trying to build real differentiated molecules under our IIP umbrella. Pete, I would like to hand over to you to briefly comment on the question on the recent data released for ULTOMIRIS in GNG.
Sure, Tim. Happy to do so. So I guess the first thing to say is, I don't think the data was that big of a surprise. It's a C5, it's similar to SOLIRIS. We figured that it would have similar results.
It did. It was about a fifty seven percent clinical response rate on MG ADL. That's very comparable to the REGAIN study that was at about sixty percent. It doesn't change the fact that it's a C5 and that's only going to affect your acetylcholine receptor positive patients. And it is also only dealing with the element of complement at the neuromuscular junction.
And as we all know, the actual autoantibody plays complement is just one of three roles that the autoantibody plays at the neuromuscular junction. With efgartigimod, we believe we play upstream of C5s because our mechanism of action is removing that autoantibody from the neuromuscular junction. Therefore, if it's not there, you're not recruiting complement. I'm not comparing trials, but I will say I think we've set the bar quite high. If you look at a clinically meaningful response rate of about seventy eight point five percent of patients that are exposed to efgartigimod for one to two cycles have a clinically meaningful response.
You know it's a very rapid onset of action, about eighty four percent of those patients respond after one or two doses. And what's really meaningful is in a responder rate, almost two thirds of patients reach minimal symptom expression. So I still believe we're going to play upstream. And you know that we also had the seronegatives in our secondary endpoints as well, So potentially broader.
Thank you, Keith. Thank you,
next question comes from Yatin Suneja with Guggenheim Partners. Please go ahead.
Hey guys, can you hear me well?
Yes. Welcome, Yatin. Good morning.
Good morning and good afternoon, everybody.
Thank you for that great presentation. Two questions for me. These are quick ones. So on the adaptive design for the myositis study, what are the criterias for you to abandon one of these subtypes? If you can walk us through that.
And the other question I have is, you know, with regard to the IgG reduction required for different type of skin diseases? Actually the question is there a different requirement for IgG reduction for skin diseases versus something with more of a systemic presentation? And then can you get enough skin tissue distribution or penetration with your subcu administration?
Yes. Two great questions. Thank you, Jatin. So on myositis, I'm going to give the floor to Wim, our Chief Medical Officer, with us today. We are not disclosing the fine details of the study designs, but indeed there's an ability with an interim look at the data by the ASMD to actually advise us to continue in one, two or three subsets and also have the ability to potentially enrich in all the subsets.
Wim, do you want to talk conceptually about what it would take to continue in a subset, please?
Yes. Sure, can do that. But I don't know whether I can disclose much more than what you already said, Tim. I think it is important that there will be an adjudication committee, as was mentioned, to make sure that we have the in the three subtypes of population that fulfill the criteria for the disease. The futility analysis will enable us and we will remain blinded, but
the DSMB will look at
Pardon me. It appears we've lost connection to our speaker.
But it is okay. So Jatin, there's not too much we can see about the statistical rule we're going to use to declare an indication, a continuation indication, yes or no. But I think when captured the essence of it, That is a futility analysis where you would apply your typical statistical rule in order to continue, discontinue. And I think it's about it involves a significant number of patients in order to come to that point. On your question on IgG reduction, of course, is a question we cannot answer completely.
You know with efgartigimod, we have a PD effect of maximally reducing total IgG 70% to 75%. But maybe I can give the floor first to Peter to talk about his view on the ability of efgartigimod subcu to meaningfully reduce IgGs in the skin based on what we have seen for epamphigus. Right, Peter? Yes, thank
you very much, Tim. So indeed, so we have completed our Phase II study in pemphigus and what we have learned there from the IV formulation is that together with the IgE level reduction, the autoantibody levels were quickly reduced and this translates into improvements in the disease activity scores. But we have also learned that when we kept dosing for longer time periods that patients continued to improve and that also the autoantibody levels were improving further. So that's very interesting. Now what we do in skin indications in pempicus and in bruleus pempivode with the registration of trials is we have indeed changed to the subcutaneous formulation.
And what we note from the subcutaneous formulation, gives a very similar pharmacodynamic profile as the IV formulation that we have used. So we have very beautiful mimic there. So for brusempegoid specifically, what do we know there about autoantibody level reductions and improvements on disease activity scores? You can, for instance, look to that Phase III randomized controlled trial of these 56 patients on response to corticosteroids and they have of IVIG. Nevertheless, we have observed these improvements, these fast improvements with an autoantibody level of about 50%.
Five-zero, 50%. Fifty %, yes. And what we also know is, for instance, with corticosteroids, also the autoantibody levels are reduced to about the same degree for patients in remission. But of course, it takes us much longer time to get to that point, and it takes months to get this 50% reduction. So yes, Tim, we
think that that 50% is well within reach for a molecule like efgartigimod. Vas, do you want to comment on anything we know about myositis in this regard?
Yes. I think that Professor Achela already gave the answer. There is a correlation between the autoantibody titers and also the disease severity, also regarding to certain symptoms. Regarding to your questions, whether it could have an effect in the skin as well, I think there we have the example of the PRODUMP trial with Optacam IVIG where they met the endpoint on the total improvement score, but also had a very positive effect on the CDASI score, and that's the cutaneous dermatomyositis disease area and severity index.
Thank you, Bas. And just for sake of clarity, I think we should be able to match or beat the IgG level reduction observed with IVIg rise, given this very specific mode of action of efgartigimod. Thank you for the questions.
Thank you, Tim.
Thank you.
Our next question comes from Jason Butler with JMP Securities. Please go ahead.
Hi, thanks for taking the questions and for all the presentations today. I had two. First on myositis, how are you thinking about
the
individualized dosing plan like you have in MG? And then for falsamphagoid, just again, how do you think about developing the drug or evaluating the drug as a monotherapy versus tapering steroids, I. E. Adding the drug on top of a tapered or lowered steroid dose? Thanks.
Thank you, Jason, and a very good morning. Thank you for being with us today. On your second question, before I hand over to Wim to talk about dosing and thinking about dosing frequency and myositis, bluspensiboid, let me just clarify, we are dosing on top of standard of care, which is steroids. And yes, the protocol will cater for the possibility to taper steroids as of when a patient is achieving sufficient response. So we will do that and that is very similar by the way to the global Phase three registration trial, which is ongoing for pemphigus.
When do you want to comment on our views on dosing frequency and the ability to go into individualized dosing in an indication like myositis?
Yes, sure. And I hope that I'm not kicked out this time while responding to the question. So of course, this trial will give us a lot of insights on how efgartigimod reacts and the patients react to efgartigimod in the different subtypes. One could imagine that given the pathology that a more sustained therapy could be needed. But of course, as I mentioned, this trial will give us a lot of these insights to see how we continue in the registrational part of the study.
Think
yes, thank you, Ben. And I can imagine that similar to CIDP, once we have a convincing signal in the blinded study in an open label extension, you would actually allow for the ability to, to a certain extent, phase out the dosing when patients go into remission wise. So that's a topic for the OLE. Jason, did we answer your questions?
Yes, that's great. Thanks a lot, Sam. Appreciate it.
Thanks for being with us. Thank you.
Our next question comes from Joel Beatty with Baird. Please go ahead.
Hi, this question is for the company or the docs. As you add more indications for efgartigimod, do you anticipate there may be a role to use diagnostics to pick out patients more likely to respond to treatment, either in clinical trials or the real world?
I'll give the floor to Doctor. Agarwal to comment on, you know, how, in general, the diagnosis and subtyping of myositis is evolving more and more based on serology. But she's the expert we have in here today, so I would like to make maximum benefit of that. So Doctor. Agarwal?
Yes. So I think it's a good question. But what I would say is in ten years, last ten years, we have seen significant advances in standardization and improvement in the diagnostics of these myositis specific antibodies to an extent that ten years ago, when a commercial lab would report an autoantibody, I wouldn't really believe it. I would check it in my research lab. Whereas now in last couple of years, we have abandoned doing repeat autoantibody testing in our research lab because the commercial assays are giving us very good results.
So there will be there has to be an accompanying autoantibody testing. But what I would say is you don't need to develop a different accompanying diagnostic. Those diagnostics that companies is already available in the commercial market, and those itself are getting better and better in terms of the sensitivity and specificity.
So that's all. And Doctor. Hall, I think for BP that is a very simple answer, right?
Yes, I think for BP, the role of the antibody is central. And I think that there's definition of responsiveness will probably be focused on just antibody levels and how high they are in disease severity. But I think that the relationship is so strong that there won't be a big differentiation in terms of biomarkers about who will be responsive because of the key role the antibody plays in the pathogenesis.
Thank you, Doctor. Hall.
Our next question comes from Danielle Brill with Raymond James. Please go ahead.
Hi, guys. Good morning. Thank you for the question. Doctor. Agarwal, I believe you mentioned that dermatomyositis is actually an umbrella term.
And I'm just wondering if you could elaborate a bit on how disease pathogenesis or if the treatment response varies based on the autoantibody involved. And then as a follow-up, Tim, in your planned trial, will placebo controls be matched at the antibody level? Thank you.
So, good question. So dermatomyositis is a specific diagnosis of it's a clinical diagnosis. When you come to a serological diagnosis or serological classification, then you see the dermatomyositis is actually made up of five different subsets serologically. And each different subset is represented by the myositis specific antibodies. And these each myositis specific antibodies have some unique clinical features on the top of the common clinical feature of dermatomyositis.
For example, anti TIF1 gamma antibody obviously have classic dermatomyositis, but also have higher association with cancer. Anti MDA-five antibody has different pathogenesis and has an association with interstitial lung disease. And TMI two is your garden variety, very good prognosis, you know, dermatomyositis. So you see there's a commonality of clinical diagnosis or classification of dermatomyositis, but then there is uniquely different features. And these each unique different features stem from unique different pathogenesis that what we believe that each of these antibodies not just represent unique clinical features as a biomarker, but they also represent an underlying pathogenesis, all of which lead to a common clinical phenotype of dermatomyositis at the end of the pathway basically.
Thank you, Doctor. Agarwal. And on the second question, I think that's simple. We will be balancing the two arms, so active versus placebo, based on disease severity and not necessarily based on antibody type. And now we are monitoring antibody titers to do some retrospective analysis, but we don't use it to basically balance the two arms.
Okay?
Got it. Thank you.
Thank you for the questions.
Our next question comes from Yaron Leber with Cowen. Please go ahead.
Yes. Hi. Good morning. Good afternoon. Thanks for including me.
So, Tim, I I got a couple of questions. The first one for BP. Just how big is the study? And are you dosing weekly until response? And at that point, once they taper steroids, they can vary the dosing scheme?
Or does that happen really after the thirty six weeks? And then I have a question on myositis afterwards.
No, Jeroen, this is a great question and a great opportunity for my colleague, Peter, to comment on trial size in BP and also how we envision the possibility of tapering the background corticosteroids. Peter? Thank you very much
for the question indeed. So what we see for registration of trials in BP is that the trial size is between 8,120 patients typically. So we also go with the proposal of about 120 BP patients randomized one to one. Of course, we have the ambition to taper off corticosteroids as quickly as possible and to allow for that so that will be initiated two weeks after achievement of disease control, so consolidated disease control two weeks later the taper will start.
Thank you, Peter. And then, Yaron, to the second question, please.
Okay. So the second question on myositis. What's the background? This is it sounds like this is a monotherapy study, right, with no background. Are patients naive or they relapse in myositis?
And at what point do you expand into sort of the Phase III potential pivotal part of the study?
Yes, so first of all, the treatment is efgartigimod or placebo will be on top of standard of care, that's first of all. And then we will, of course, do the randomization one on one of the three different subtypes of myositis and at interim we can do the futility analysis where we can either continue Phase one, two or three of the subtypes and do the sample size estimation accordingly.
And background medication would typically be bus in myositis, really like this? Yes.
This is a low dose of steroids plus maximally one nonsteroid immunosuppressant.
Yeah, thank you. Yaron, is that answering your question?
Yeah, and then is it a chance that you can go into each individual subtype can go into a full pivotal head to head against control with the size of the estimation, right? It's going to be seamlessly integrated in that sense.
That is correct. So if it works, we can gain a significant amount of time as compared to a classical scenario where you would do your Phase II without your Phase two, at the end of Phase two meeting, then you know, get your Phase three on the rails, but it is taking a significant amount of time. So the aim of the design is to minimize time loss between the futility analysis and the readout of the Phase III registrational portion of the study. Thanks for the questions. Thank you for being with us, and we invite the next question, please.
Thank you. Our next question comes from Douglas Tasso with H. C. Wainwright. Please go ahead.
Hi, good morning. So just for the myositis trial, I'm just curious again, I guess this is on top of standard of care. So are there any treatments that are excluded, or is it basically just up to the clinician in terms of what they are allowed to have, what therapies are allowed?
Thanks for the question, Doug. So looking here at my colleagues, Peter and
Buss, probably a typical therapy which would
be excluded would be IVIG, right? Is that correct? Peter, you go first.
Yes, I think standard of care therapies that we exclude are typically, of course, actually containing therapies for monoclonal antibodies. So IVIG, we know is, of course, having a natural Fc fragment, so it could be allowed as rescue medication in certain trials.
Rescue medications. And Vasu, about myositis?
Yes, I think that the patient should be off therapy on IVIG or rituximab. For a minimum period of time. For a minimum period of time. Okay. So very similar.
I hope
that it's answering your first question, Doug. Do you have
the second Yes, it
does. Then just also, just in terms of the individualized dosing, I'm just curious from Doctor. Agarwal's perspective, how applicable or relevant do you think that is versus what they're able to treat in aspenia gravis?
From my friend's mind?
Yeah. I mean I may not have understood the question, but I think it obviously you have to not allow IVIG and rituximab as concomitant drug. So what we really allow in most clinical trials is concomitant drug, which is basically, you know, little bit of steroids, limited plus one other immunosuppressive drug. But for this particular trial, obviously you can't allow rituximab and IVIG as a concomitant drug trial. But we even allow that for other trials as such.
I'm not sure I got the right question then otherwise.
No, Doctor. Ederwald,
was just asking the dosing Yeah, so what we did in Mycena gravis, which is what we call a snowflake disease, that means that each individual patient is experiencing his or her disease in a unique individual way. We basically allowed in the trial, the Phase III trial, a tailored dosing, so individualizing the dosing cadence to the individual needs of the patients. As we've already explained in an earlier Q and A, we think that for myositis, we would probably walk down the path like CIDP, where we will be looking for more chronic dosing bites. Thanks for the question. Thanks, Doug.
I appreciate it.
Our next question comes from Yanan Zhu with Wells Fargo. Please go ahead.
Hi, thanks for taking my questions. So one question for the doctors and two questions for the company. The question for the doctor, Doctor. Arguell and Doctor. Hall is that in patients who achieved remission with efgartigimod in either the myositis trial or the BP trial, do you foresee maintenance treatment with efgartigimod?
I mean, not in a trial, but in a real world setting, would you foresee applicability of maintenance usage of efgartigimod, or do you foresee patients come off therapy for an extended time before they get retreated?
I'll answer for my side is I think what I would expect would happen is what something that has happened in IVIG, where basically you give IVIG to put patients in remission, okay? So which could be a six month treatment, maybe a year of treatment, and then you taper it off, assuming that the patient would not relapse or hoping the patient would not relapse and you taper the treatment off. And in most cases, the patients actually do very well on a very minimum amount of maintenance doses of a standard immunosuppressive drug like methotrexate or mycophenolate. And that's what we do in IVIG. But in some cases, we see when we taper the IVIG, at the time when we tapering or at the end of the taper, we'll see the disease starts to flare up, not that much, but disease starts to come back.
And then we know, okay, this patient, we're going to have to do maintenance treatment with IVIG for longer time point. So we continue a lower frequency and dosing of the maintenance treatment for another six months or a year, and then we try to taper again. And then we again, in many patients, we are successful, in some patients, we are not. So but that's for minority of the patient. For most of the patient, I would expect that once the patient is in remission, patient is able to maintain the remission on the basic immunosuppressive drugs.
Maybe it will take six months or a year, it depends.
Doctor. Hall?
Yes, I think that the first answer to the question is there will be some patients that require long term therapy based on the persistent production of autoantibodies by their body. And the how we'll identify those patients and whether we'll go into a tapering program, as Doctor. Agarwal suggested, will depend on the clinical response, do they develop small levels of disease, but also by monitoring the antibody levels, both in the skin and in the blood, so that we will be able to watch patients. And I think the nice thing about the skin is we can see minimal disease activity, so we can taper adjust the taper to the degree activity. So that my anticipation is that there will be a long period of therapy, perhaps up to a year, and then a gradual tapering dictated by clinical response and autoantibody levels both in the blood and in the skin.
And that over the course of the next two years, most patients will be able to taper completely off the therapy.
Thank you, Doctor. Hall. And then you had a second question, right?
Right. Two questions for the company. One is that thank you for providing some additional color on albumin. It looks very encouraging. I just I think I saw a little bit of increase in albumin in the efgartigimod treated patients compared with placebo patients.
Just wanted to hear your thoughts on whether there's anything there. And lastly, could you touch upon the ongoing your dialogue with the FDA on the BLA of efgartigimod in myasthenia gravis? Have you had mid cycle meeting with them? And what's how would you characterize your interaction with them so far? Thank you.
I appreciate taking the questions. Thank you.
And thank you for these questions, Shannon. Let me start by answering the second question. I would invite my colleague, Hans, to comment on the albumin level, which we presented and the thinking behind it. With the FDA interactions, I can confirm to you that we did have the mid cycle meeting. And the way we would be able to summarize the interactions is that so far so good.
So this is, as you know, an ongoing Q and A. You get written questions, you supply written answers and that goes on and on. Meantime or meanwhile, inspections are taking place for the clinical sites. We do know the plan for the inspection of the manufacturing sites. So, so far so good.
Hans, maybe you want to take the question on the albumin level, please?
Yes. Thank you very much for this question. So indeed, in some trials, we did see a small, stable, transient increase in albumin within range of clinically normal, so not more than 10% increase. This confirms the fundamentally different subcellular fate with efgartigimod as compared to the full length FcRn targeting antibodies achieved with the CST ultimate evidence of the difference between those two classes of FcRn antagonists. We are not aware of any literature associated with adverse events with this level of albumin increase.
And we checked with our KOLs and they confirmed the same and said it could be even beneficial at these levels. So across clinical trials, even with longer chronic exposure, we remain within this band of normal. I hope that this answers your question.
Does. Thank you. Thank you.
This concludes our audio questions. I would like to turn the conference over for any questions submitted via the webcast.
Thank you. We have one. It's in the two new esgartigimod indications. Do you expect that patients will need to fail steroids first?
And then
a second part of that is in BP, given the age of the patients, how long do you think the duration of treatment will be?
Thank you, Beth, for providing us with this question from the chat box. Again, I'm going to make use of the benefit here of having Peter and Buzz in the room. But what about inclusionexclusion criteria to the extent we can be public about them? Do we expect people to fail steroids before they can come on trial? Peter, you go first?
Well, we aim to develop efgartigimod as first line treatment in BP. So we will enroll newly diagnosed patients, and they start at zero point five milligram per kilogram per day of corticosteroids. So that's
the answer for BP. Thank you. And what's for myositis?
Yes, it's actually the same for myositis. So, basically, newly diagnosed and also basically can be on steroids during the trial if that's a low dose.
But they need to meet a
minimum standards with regards to disease severity, right? Yes, absolutely. Okay.
I think that answers the first question, right?
Yes. And another one on the review of the BLA. Do you think it's possible given the regain primary endpoint that they would want to see data at twenty six weeks? And how would you handle this, if so?
Well, the only thing I can say there, Beth, as an answer is, of course, we have been crafting the design of the ADAPT trial in close collaboration with all the stakeholders, you know, not just the patients who express their desire for individualized dosing and the physicians subscribing to that, but of course, also with the regulators. So we had buy in in the ADAPT trial design from both the FDA and the PMDA. So we do know what they think about the individualized dosing, the primary endpoints and the stringency of the primary endpoint because remember, in order to be a responder in the ADEPT trial, you needed to have a clinically meaningful benefit in four consecutive visits, not just in one. So I don't have any specific concern in my mind concerning the acceptance of the primary endpoints.
Okay. And I'm just going to put two more out there at once, and then we'll be done with the chat questions. The first is, could you give an update on our partnered programs and include cusatuzumab in that? And then the second is, could you talk about, the opportunity of efgartigimod in BP you know, to some of the potential competition like Dupixent?
Okay. I'll give the second question to Peter here to briefly comment on competitive landscape and actually lack of approved therapies. On the first question, I'm happy somebody is indeed still thinking about all the other opportunities which are progressing in the hands of our partners. And I actually can be very brief about it. I think our partnerships with Leopharma, with AbbVie, they continue to progress.
So these molecules continue to make progress in the clinic. As you may remember, we're only allowed to talk about these programs if and when they transition between the different phases of clinical development. But I can be affirmative, the leopharma and the AbbVie collaboration are live and progressing well. Same, I think, for the Agamap opportunity and the statin opportunity, which continue to do well, either in the preclinical or the clinical phase. For what concerns gusatuzumab, we are doing what we said we would be doing.
We're doing a very thorough analysis of the data. We will plot the path forward with CUSA in a database fashion. I think what we said in the press release is that we believe there is value in the molecule, there is strength in the data, and we're exploring through a business development angle how we can actually take cusatuzumab forward. We will not bring cusatuzumab back in house. We will not distract our ongoing efforts for our autoimmune programs.
I've got taken off ARGX-one hundred seventeen and ARGX-one hundred nineteen, but we think we owe it to the AML patients to seek a path forward through some sort of partnership. Thanks for the question, Beth.
This concludes our question and answer session. I would like to turn the conference back over to Tim Van Hauermeeran for any closing remarks.
Yes. I would just like to make a few concluding remarks for the audience. I really hope you enjoyed the R and D Day presentations, both at our in house people and with our partners on the clinician sites. And as we explained, collaboration is in the DNA of this company. We believe the future belongs to those who collaborate best.
So I would like to thank Doctor. Agarwal and Doctor. Hall for their active contribution, but also all the other people and patients who contributed to disease evaluation, clinical trial design, etcetera. So I hope you like the compelling vision for ARGX twenty twenty five. We think the global autoimmune market is exciting.
It is growing. We believe we're at the forefront of what could be a revolution in the way we think about autoimmunity, the way we treat autoimmune diseases, now that precision tools like efgartigimod and ARGX-one hundred seventeen are becoming available, actually to the extent that we have an opportunity to reclassify or redefine certain autoimmune diseases as being truly IgG mediated or complement mediated. This is the fifth and the sixth indication we're discussing today. We will be back to you talking about the other indications seven to 10 and hopefully beyond 10. And we will continue to build vibrant franchises in the neuromuscular space, the heme space, the skin and potentially the kidney space.
ARGX-one hundred seventeen, we think, is an exciting molecule. The way it's coming out of Phase I is with very solid Phase I safety data, warranting investigation in patients. We believe this is again a pipeline in a product opportunity with MMN being the first of hopefully many indications, which will fit the growing franchises. And rest assured, we continue to invest in our IIP program. We're building a company for the long haul.
We have an abundance of opportunity in front of us through the immunology innovation program. And ARGX-one hundred nineteen, I would say, stay tuned on that. That is the first one coming out of the autoimmune discovery efforts next to ARGX-one hundred seventeen. And I would like to end by thanking all my colleagues working hard in the lab, in the clinical trials, on the commercial and pre commercial front. It's only thanks to their dedication and commitment that we stand where we are today.
So a big thank you, very grateful for working with such a great team. Thank you, Beth, and thank you, colleagues.
The conference has now concluded. Thank you for attending today's presentation. You may now disconnect.