Ladies and gentlemen, thank you for standing by, and welcome to the Bridge Biopharma Conference Call. Please be advised that today's conference is being recorded. I would now like to hand the conference over to your speaker today, Doctor. Neel Kumar, Founder and CEO. Please go ahead, sir.
Thank you so much and thanks everyone for taking the time, especially amidst a very busy morning for biotech and biology news. As is typical, we'll be making forward looking statements today and you can read through the details of those in the first two pages. I'll be referring to the announcement deck throughout call out page numbers so that you can follow along. This call is set up to address the transaction highlighted on Page 4 of that document. BridgeBio will be acquiring all outstanding shares of Itos Therapeutics for a 41% premium to the unaffected Itos closing price this past Friday.
The details of the deal are spelled out here on Page 4 and I'm sure we'll be speaking with many of you about them throughout the course of the day. What I wanted to spend my time with you on this morning, however, is not the structure of the deal, but rather why this deal is a good one, we believe for both iDose and Bridge and most importantly for the patients and the physicians that we serve. I'm going to move to Page 5 now. Very briefly, I believe and we believe that the time is right and the time is now for full investment in the promise of Eidos, its great team and its compound, Akaramidus, to ensure that no stone goes unturned in late stage development, commercial development and the commercial launch of this product. And we believe that this full excavation of value for patients and investors alike is most likely if iDose operates as a private entity under BridgeBio.
It once preserves ownership in the hands of the team that truly understands this molecule and its science and in many cases has been with it since its very beginnings, while placing it in a fully and without obstacle unencumbered ecosystem of innovation and development that will spare no effort or dollar to maximize the benefits of this compound. Let me on Slide 5 step back for a moment and revisit our better owner hypothesis. This is something we've talked about since the advent of Bridge, which was very close to the advent of our work with iDose. We passionately believe that operators that can connect early stage science, how to target a well described disease at its source to medicine and development plan and then again to the commercial landscape and the patient unmet need and physicians who might want to use the product should the data play out. That entity is best served in holding the drug all the way from early stage discovery to the marketplace.
And we believe that the team of Eidos within the BridgeBio ecosystem is just such a best owner with absolutely no barriers in doing the following. Number 1, pursuing the full development landscape of what's required to excavate the promise of acoramidis. Again, primary prevention studies, subpopulation analyses, diagnostic analyses and market build out. These types of things must be invested in today as we move this program forward. 2nd, marrying the current efforts that we have at iDose with additional precision cardiovascular and renal genetic opportunities across modalities to keep the community engaged, cardiologists and scientists alike and to build on learnings that we have both around TPR and related diseases as well as other precision cardiovascular diseases.
This will allow us not only to do more for patients in the future in this very specific disease state, but also to recruit the very best talent and to use the learnings that we have from one program to help increase the probability of technical success of others. 3rd, we need to start seriously on commercial development. This includes market growth activities around diagnostics, research and education as well as market access discussions in the BridgeBio ecosystem and Umbrella will allow the Eidos team to do this more capably. 4th, we'd like to pursue lifecycle management in a way that will allow for not only novel formulations, but also contemplation of potential combinations where it makes sense, meaning downstream clearance of amyloidotic plaque. And finally, we will be putting items within a bedrock of capital such that we can deploy consistently and not think about saving, but rather thinking about investing in the future of acoramatids.
All of this basically removes the barriers to full collaboration between iDAS and BridgeBio and will allow us to unlock the value of this very important hopefully drug for patients with TTR cardiomyopathy. I'll just flip briefly to Page 6 to address the question as to why now. As many of you know, we recently announced that we're fully enrolled in our Phase 3 clinical trial and we expect to have over 600 participants in that trial. One thing that we've seen over the course of the last 12 months and especially certainly since the COVID-nineteen crisis arose was just the level of excitement people have in and around this compound. It has truly been humbling to work with physicians and patients alike to try to keep this trial going and on time.
And you can see it's reflected in these numbers and the pace of trial enrollment just how excited people are around this compound. We believe that that means that today is the day and certainly in these coming months, you'll see many actions from us in this vein to start to really invest more heavily in how we want to develop it even past the Phase 3. How do we think about teeing ourselves up for a primary prevention study? How do we think about potentially running a double blind head to head once we get our Phase 3 clinical data? How do we think about understanding how effective a more potent stabilizer might be in critical subpopulations, both of folks that have genetic or hereditary predisposition to the disease, as well as folks that might have more severe disease that were not helped by tafamidis.
Those are all the types of things that we think the BRIG bio ecosystem will allow for greater investment in and a greater contemplation of in terms of how we actually want to develop this drug using experts like Charles Holmesy and others who have been there and done that in the cardiovascular realm. Page 7 talks a little bit about what is this ecosystem that iDos will now be a part of. And you can see 1st and foremost that we've been building out at BridgeBio our commercial capabilities in and around our launch of MOCD Type A, a compound that we talked little bit about at our most recent R and D Day, as well as an upcoming launch in second line cholangiocarcinoma. All of these things have helped us to engage in a variety of different commercial capability building exercises that will be relevant for our drug at Inos, although it's in a different therapeutic area. And we've often said that the commercial ecosystem and synergies therein in the orphan drug landscape do not look like Call Point.
Rather they look like things such as market access, patient hub services, diagnostic services and partnerships, patient finding exercises, the funding of certain types of research, the support of certain types of KOLs, all of those things are going to be highly relevant and need to be done now in an increasingly competitive landscape that Acarameter finds itself in. And we believe BridgeBio can be helpful to iDose as we move forward in that vein. And on Page 8, you can see that and I think this is important, the now unencumbered access to a set of advisors that truly have been there and done that in the context of late stage development, commercial development in the cardiovascular realm, folks like Charles and Richard. A key aspect of BridgeBio is our Clinical Advisory Board or CTAB, which has many experts in the cardiovascular realm such as doctors Ethan Weiss, Michael Kit, Doctor. Harrington, obviously Bob Harrington and Mike Gibson and several others, Dan Gretler.
And this is married with a set of experts that I think actually are going to be quite important for iDose as it moves forward. As you move forward with a compound in any disease state, you start to learn a lot more about the basic science. So that basic science can point you in some interesting directions. For instance, one of the capabilities that I think will be very important to really tap into is the physical genetics capability that we've built out under Michael Pettigrew and Sun Gu. That capability will allow us to fully understand not only the impact of protective variants, but also potentially where else this compound might be of use within the broad landscape of cardiovascular disease.
There are many insights that can be gleaned from looking at the variety of different hereditary drivers in this disease and finding out more about number 1, what's driving disease and number 2, where our compound might be of health. This has been true in a great number of our other programs and I hope will be true here as well. Moving to Page 9, just a bit more about this ecosystem of innovation that the IDOS will find itself fully within now. This is a diverse set of compounds that we are developing. And you can see that iDUS is not the most advanced, so it can take advantage of some of the more advanced programs, but also take advantage of a lot of the innovation that's occurring in the cardiorenal division.
These are at least 2 of our announced programs in ADH 1 and PH1. And there are several other precision cardiovascular programs that we're working on. And I think that you'll hear about over the course of the next 6 months that complement greatly our interest in precision cardiology, which stem all the way back to what we were doing at 3rd Rock Ventures, obviously, So a lot of exciting activity here that I think could greatly benefit both from the iDose expertise as well as iDose benefiting from what's going on. And I think collectively, we've always said that scale matters, that learning from mistakes and from others within a broad portfolio of genetic medicines that target well described diseases that their source matters. We think it's important.
And now we've basically taken down the barrier so that we can all learn together and develop this very important drug. Page 10 talks a little bit more about our platform, which we've spoken about at the R and D day, discover, create, test and deliver. And I actually think there are ways that Ios could take advantage of all aspects of this platform, Deliver being the most obvious one alongside of test. We've spoken about what we need to do in late stage development and commercialization here. But there's many other things that we can think about or contemplate with respect to create.
For instance, is there a way that we might even expand the aperture to something that could be interesting for ophthalmologic indications here? Are there other backup strategies or strategies in and around long term potential for a drug such as this or even adjacent indications that one might take it in, in the create and discover mode. Those are all questions that we'll be looking at as we move forward. Page 11 is a bit more about what this platform has delivered. And I think the Eidos family can hopefully take some confidence from this.
This has been a very productive platform across a variety of different indications. And so we expect and hope that we can all learn together as we progress this and other important medicines towards the finish line of Phase 3 over the course of the next couple of years. I'll end on Slide 12 with just a reminder of what this all means now for BridgeBio as a consolidated entity in terms of our key value drivers. We have 4 that we've been talking to many of you about over the course of the next 12 to 18 months now with iDose and its Phase 3 readout to happen late next year. We've been now fully enrolled our Phase 2 achondroplasia trial and expect data there towards the end of next year.
Our CAH trial, which we expect to initiate sometime early next year and our ADH-one trial, which is we announced last week now, we are Phase 2 ongoing. And we have enough cash on the balance sheet to get us through these catalysts. So we're hopeful that we can now put our heads down and really work on the important science and development that's required here and deliver against many of these promising opportunities for patients. So I'm going to stop there. It's a short deck, but I think it's a simple story, but a relatively profound one.
And I'm going to turn it over to our analysts for any questions.
Thank you. Our first question comes from Tyler Van Buren with Piper Sandler. Your line is open.
Hey, guys. Good morning and congratulations on bringing Eidos back home. You guys are paying a higher premium relative to the last approach last fall. But since then, we've also gotten the Phase II OLE data, which was positive. And additionally, this morning, as most people have seen, another precision genetic cardiology asset that you're very familiar with got bought by Bristol for 4 to 5 times the valuation you're paying for the remaining Eidos shares.
So can you just compare and contrast the 2 assets and opportunities and discuss your relative excitement for the opportunity ahead of Eidos?
Yes. Hey, Tyler. Thanks so much for the question. Yes, there was a lot in there. I mean, maybe I'll start with what's changed since our last offer.
It was not, as you mentioned, is OLE data, which obviously was exciting to us. But I think what was equally and potentially even more profound was the excitement we saw within the context of the clinical trial enrollment. Certainly, there were people that were taking their lives into their hands to come into the hospital so that they could get this drug. And I think that speaks not only to the high unmet need and the brilliant partnership of many of the physicians we spoke about, but also people's inherent belief that now with the separation of 20 80 mg and the fact that every time we do better in terms of stabilization, we'd be better in a safe mode for patients that this drug has the potential to do something special for a devastating disease. So all of that, I think it gave us more confidence to increase the offer.
I think as it pertains to myocardia, I can't comment on the specifics of their transaction. Obviously, I'm thrilled for our colleagues there. I think it's just a great thing for precision cardiology. I can remember the Series A deck that Charles and I presented at 3rd Rock when the company was coming together. And I think the most likely outcome or the best case outcome was acquisition was the acquisition of CV Therapeutics by Gilead or something like that was less than $1,000,000,000 So I think what you've seen is a real renaissance in the application of genetics to cardiovascular disease.
I think the more we look to be honest, you'll be hearing about some of this from us over the course of the next as I referenced in my comments over the next 6 months. The more you look, the more you'll see some really interesting genetic hooks in large subpopulations of what I would call cardiovascular syndromes. And myocardial is a brilliant representation of what's possible. And we think iDos could be the next and we think there are several other opportunities that could dovetail off of iDos. So yes.
Great. Thanks for taking the questions and congrats again.
Thanks.
Thank you. Our next question comes from Salim Syed with Mizuho. Your line is open.
Great. Congrats on the deal Neil and team. I just had a few on acaramidis, if I can. The first is just some people think about TAVA and the 80 milligram versus the 20 milligram not really separating the 6 minute walk data at 12 months. I think folks will generally agree that karamidus is a better TTR stabilizer, but so is 80 versus 20.
And so I'm just wondering, Neil, how you're hearing out the risk as we go into the 12 month data there? I know the 80 also had a thicker patient population and maybe you can also comment on when do we get the baseline characteristics for Attribute Centimeters? The second question is just on the 600 patient number. Was that a number that you consciously chose to upsize the trial enrollment? And if so, why did you decide to upsize the trial enrollment by 20%?
And then lastly, does BRIDGE Bio or Eidos have any access to aggregated blinded data on the 6 minute walk thus far? Thank you.
Yes, great questions. Thanks, Helane. Appreciate it. So let me go from the backwards up to your first question and make sure I hit them all. Do we have access to aggregated blinded data?
No, I certainly don't. So we're not looking at that. None of my comments are informed by that. The 600 patient number was not something that was preordained. Actually, it's total product of the fact that we had many sites activating at the very end.
As you know, most of these trials tend to enroll like hockey sticks and you have this almost exponential like growth toward the end. So we just didn't want to have a site activate and then tell them that they simply can't put any patients into a trial. So it's just that relative excitement and just the scale of activation at the end that pushes over the edge there. And then in terms of your comments on 80 versus 20, yes, I mean, I think it's interesting, right. The evolution as you well noted of there being a lack of dose response when Attraction was first published, then we understood against 30 month mortality.
I think as you rightly point out, let's discriminate between that and 12 month 6 minute walk. But on 30 month mortality, what we saw was a 20% relative risk reduction on 80 versus 20 for just 10 percentage points more stabilization going from about 35% to 45% as they show on that scatterplot in the New England Journal and we're at 90 plus percent. So the presumption there is that hopefully we would have a meaningful relative risk reduction once again against mortality as compared to 80. The question that you're asking is why we didn't or whether we saw a separation at 12 months, 6 minute walk, 80 versus 20. Well, again, that's for the same reasons you wouldn't just because AD has a sicker patient population.
So if we're going to adjust for that, I'm sure you would see a signal there, but no one's done that type of analysis. So yes, that's kind of how we think about 80 versus 20. We continue to believe that increased stabilization will have an impact on all of the relevant endpoints, including 6 minute walk as well as and more importantly on mortality and rehospitalization. Neil,
on the baseline statistics for ATTRIBUT, do you think they'll look more like the 20 or the 80? Or when do we find out the baseline characteristics for your trial?
Yes,
I mean, I suppose when we publish the trial, the trial is basically set up to look as much like a track as possible. So we're sort of in the vein of that and I think we'll be pretty close actually.
Okay. Thanks. Thanks, Neil.
Yes. Thank you.
Thank you. Our next question comes from Mani Foroohar with SVB Leerink. Your line is open.
Hey, good morning. This is Rick on the call for Mani. Congrats on the transaction and thanks for taking our questions. Just 2 from us. So first, my question is around the timing of commercial investments.
It sounds like commercial development activities are going to begin pretty soon. Could you maybe describe the ramp of commercial build out we should expect, I guess specifically using the timings of the readouts for the Parts 1 and Part 2 of the ATTRIBUTE study as guideposts?
Yes, great. Well, thanks so much for the question and say I had a money for us. Yes, so we believe that the commercial build out their aspects of it that need to be long to launch and to certain other aspects obviously the hiring of a field force and things like that that need to be tight to launch. I think this is a unique space and in as much as you have behemoth like Pfizer that's out there with a compound that growing the marketplace, but it's really critical that several others of us get out there and educate people about what this disease is truly driven by and why potentially increasing stabilization should be better for patients. Obviously, we've seen that now across 3 clinical trials on the polyneuropathy side where we do better in terms of limiting toxic monomer amounts, we do better for patients.
And we've seen that now with the dose separation on the Centimeters side. So all of the Com Dev that we're doing now is fairly consistent with what you would typically see in a larger cardiovascular arena, the things we're doing around medical affairs, the things we're doing around sponsored research. I think where we really want to or seek to invest going forward is additional development. For instance, I think subpopulation analyses, the diagnostic partnerships, I think will be a key element to our go forward strategy as well, ensuring that really we're finding as many patients as possible and fully understanding the heterogeneity associated with this disease. So those are the things that I think are the first wave of any commercial piece.
In addition to just commercial build out and planning, we'd like to launch this product not only in the U. S. But also in Europe and that takes some building and time. So you can expect to see some build out of infrastructure in geographies that are not the United States analogous to what we put together here in terms of our MSL force as well as our PSP and several of our other operating forces on the commercial side in the U. S.
And as it pertains to Part A versus Part B, look, I think the obviously the Part B data, which will come probably 6 months after launch as you sort of put it all together. So it won't be a huge delay between when we launch off of Part A and when Part B data comes. We think that there will be a set of physicians that will look at this depending on the data obviously from Part A and say, okay, we sort of understand how this disease works. We understand that this is a markedly better stabilizer than is tafamidis as all data shows. And we understand that every time we do better in terms of stabilization, we're doing better for patients.
And if we do better on the 6 minute walk, they can connect the off from that to our OLE data to serum TTR levels to stabilization levels and potentially start to use the drug then. So I do think it will be very important for us to begin our education and have a strong launch of 6 Minute Walk. But I don't disagree that the launch will be fully enabled by mortality and rehospitalization data coming after Part B.
All right. Got it. My second question was, so the press release described investments in novel formulations and additional studies for acoramidis. Can you maybe describe any ongoing work that is happening here with novel formulations and maybe a little more detail about what we could expect in the future as far as the formulations and additional studies?
Yes. I mean, I think our first focus is obviously look, I mean, at its baseline in the orphan market, efficacy is what wins and efficacy and safety for a disease this devastating. But we do think all other things being equal, it's better to go once a day versus twice a day. And so we've been working on an extended formulation, if you will, that would allow us to go once a day. That's been the primary focus thus far.
I think thinking about delivery to a few different tissue or organ sets like the eye or the brain could be of interest in the context of some other diseases that we've been thinking about. So that's another area of ongoing research, although it's too speculative and early for us to really comment on that.
All right, great. And actually just one more if I can. Could you just remind us of the status of the Phase 2 open label extension study and if can expect any additional readouts from this in the future?
Yes, good question. No, we it's ongoing as many OLEs would be and we have no expectation of sharing data at this point. We're focused on our Phase 3 and what the readout looks like.
Great. Well, thanks for taking our questions and congrats again.
Thank you.
Our next
question comes from Paul Choi with Goldman Sachs. Your line is open.
Hi, thanks. Good morning, Neil, and congratulations on the consolidation and thanks for taking our questions. Just one question from our team, please. With regard to as you think about the valuation here and the offer, I think investors are probably pretty comfortable with the Phase 3 at this point. But could you maybe elaborate a little further on where you see value creation beyond lifecycle management, the areas that you talked about?
And just how do you think about the continual investment rate for iDose going forward here? And what particular opportunities would you focus on going forward? Thank you very much.
Yes, great question and thanks for it. It's nice to hear from Paul. I think with respect to the ongoing investment, let me start there and the value that could be unlocked through the full consolidation. It goes beyond lifecycle management. I think pretty profoundly it starts with the full development landscape.
The types of things that we've been talking about, this disease is really a mass action disease as you and I discussed. So probably earlier on in your life, you've got this tetramer that's destabilized. You've got deposition of amyloidotic plaque. It's happening over time. The earlier you can pick up these patients and intervene, especially if you have a safe small molecule, the better it's going to be.
So investing immediately and trying to understand what those populations are and which populations within that population, if you will, of people that have depositing amyloidotic plaque, but they have enough events such that you could run a trial or study within. That's going to be very critical for us to set up a primary prevention study, which ultimately is I think how we move from acute treatment of someone who's already very sick and may have 10% to 20% of their heart by weight as amyloidotic plaque to people who are just on the early stages of this disease. So we can pick them up and hopefully prevent them even getting quite sick. That coupled, I'd say with subpopulation analyses, I mean, one of the things that we've been intrigued by was the relative lack of efficacy that tafamidis had in late stage patients. But that's interesting.
We also know that tafamidis has a differential finding to several of the important mutations, whereas we don't as we published in now I think 3 years ago. So those types of subpopulation studies, although they may be difficult to do in a formal Phase 3 setting, I think would be very interesting to do in the context of almost like a Phase 3, Phase 4 investigational study. So we'll be investing in that. We'll be investing in some of the commercial development stuff I just talked about during the last question. And I think importantly, we're going to be investing in at least one important new precision cardiovascular program that I think kind of brings this together in the context of you started with I think hypertrophic cardiomyopathy was the first real kind of new thing in precision cardiology.
And then I mean, if you book the CSK-nine aside for a moment, which is sort of a different thesis, although still following genetics. But if you go from HCM to TTR, there are several other diseases that look like that, that are high unmet need. And I think putting this program in the context of those will help us to do several things. Number 1, obviously learn from the variety of different programs that are ongoing. But 2, also to recruit better talent, to think about greater development advisory boards, to get physicians more excited.
I think all of that stuff matters. I think BioCardia did a great job of that. And hopefully, we can do the same here. So that's sort of how I think about it. I think that the incremental investment that would be required isn't massive for stuff like that.
It just requires focus and a team and a set of folks that have been there done that. Does that answer
your question? Thanks for the color, Neal. If I could just ask a follow-up, just in terms of those additional precision cardiology opportunities, when do you think you would be in a position to either announce a candidate and or an indication potentially?
Yes, I think we typically talk about the new I mean, sort of been thinking about talking about our new programs that around the JPM timing. We did that last year. We sort of introduced a couple of new programs. So I think you could expect that again this year.
Okay, great. Thank you very much.
Yes. Thank you.
Our next question comes from Geoff Meacham with Bank of America.
This is Greg Harrison on Congratulations on the deal. How do you think this deal changes your ability to develop agramidus beyond the current structure. Maybe to put it another way, were there any specific obstacles you encountered or anticipated working with iDose as a separate company?
Yes. Greg, thanks for the question. Yes, I think when you have 2 different owners, obviously you have 2 different boards, you got to get everything approved as you move from one company to the other. We've built out a lot of infrastructure at BridgeBio, but question always comes in and around how much do you need to charge for this service and should the one board approve it for the other. And obviously, I was not the middle of those types of discussions, but they take a long time.
And I'm a big believer, it's my wife works for Apple and they focus on total removal of barriers to just like open your computer and have a ridiculously good experience. I think the same is true for drug discovery and development and actually a lot of things in life. Just small things nudge you away from doing everything that's optimal. And I think in this case, taking away that onerous 6 to 8 week process of getting this approved and that approved and saying, hey, immediately I can call up our CTAB or I could avail of our expertise in CMC here. Those types of things I think will make a meaningful difference.
And I really do believe that every minute is going to count here because we've got a limited period of time in a pretty competitive marketplace to maximize the value of this asset for patients and investors. So yes, I think those hiccups will be gone. I think everyone just being focused on maximizing the value of the asset just like every other affiliate does at BridgeBio, I think will be really powerful and more fun for the team too. And I think it'll be more fun to be in an environment where you're doing a lot of really interesting things in cardiovascular disease and renal disease more broadly and to be attached to that. That just tends to be an ecosystem where people thrive.
So we're excited.
Okay, great. That's super helpful. And then do you expect any meaningful synergies in the transaction? And is that something you could quantify at this point?
Well, if you mean cost synergies, no.
Okay. Thanks.
Thank you. Our next question comes from Tom Schroeder with BTIG. Your line is open.
Good morning and congratulations, although you've been pretty transparent about this intent. So you're doing a lot of talking about subpopulations more than I've heard in the past. Is there a sense already in the community that tafamidis doesn't do well in certain mutations? And are you doing any screening in Phase 3 to try to make sure you have enough of several important candidate mutations? Or do you think that comes later?
Yes, good question. So first of all, thanks for taking the time to dial in. The subpopulations, I take it in 2 ways. Number 1 is obviously the later the disease, why isn't it that the why is it the hazard ratio was less attractive and could it better stabilize or potentially either halt or do something interesting for those patients that were Class 3. So that's number 1, which I think is interesting.
Number 2 is people still progress and certainly the mutants continue to progress in the context of TAF and there has been some relative understanding of a binding mode that it's less useful in some of the context. Certainly as KD2 is totally different in some of the mutations versus what AG10 looks like. And so that's what we would like to explore is whether or not that biochemistry could translate to something that is clinically meaningful. And I think all the while we're going to learn quite a bit more about when you stabilize like in the context of time and also how potently you stabilize in the context of how thermodynamically destabilize that tetramer is. All of those subpopulation analyses will help us to fill in these critical gaps as to how this disease is working and what an optimal therapeutic might look like.
So that's why I think some of these subpopulation analyses are interesting. I also think they're interesting from a commercial standpoint because you got to remember that these clinical trials are not powered to look I mean everyone slices and dices them, but as we've often talked about, I think you and I have talked about the trials are like less than 50% power to really make these subpopulation like cuts. And so the more study we can do to connect those dots in more obvious way, I think the better it's going to be for physicians that are trying to make a decision.
So just enriching for particularly destabilized mutations would probably come later?
Can you say that again? Sorry.
A trial enriching for the worst subpopulations in terms of stability, that would be a later trial, do you think?
Yes. But we think yes, exactly. But you sort of have to start planning for it now. So I think getting all of those trials kicked off just as soon as we start to get a hint as to whether or not this drug is going to be useful for patients after Part A. I think that's going to that's when we would kick off a lot of those studies.
Thank you.
Thank you. Our next question comes from George Farmer with BMO Capital Markets. Your line is open.
Hi, good morning. Thanks for taking my question. Neil, could you comment on if there's anything in the OLE that you saw that kind of compelled you to make this move try to make this move again? And is there any sort of mechanics involved in the actual transaction whereby minority shareholders need to be better informed as to what's going on with the actual trial, specifically data going on in the OLE? And then also could you comment on, again, thinking about synergies by absorbing iDose into the whole bridge framework, you have a lot of other kind of cardiovascularleno like drugs, which maybe could be potentially rolled up to the iDose framework.
Is that something that you might consider?
Yes, great question. So I'll start with the last and work my way backwards. Just in terms of rolling up iDos into the broader framework of Cardio Renal, yes, I mean that's one aspect that we think is very exciting. There's actually a lot of iDos employees that are already working in some aspects on, for instance, ADH1, which we think is one of our more compelling cardiorenal programs just kicked off of Phase 2. And some of the other programs that we talked about, some of which we've disclosed, some of which we haven't.
So, yes, I think that's a really compelling part of this thesis. I think it's going to be really fun for the team as well as they spread their wings and take their key learnings from what's gone right at Eidos and hopefully spread it to other programs. So yes, that's a big part of this. In terms of OLE data, no, there was nothing in OLE data that prompted us to do this now or anything like that. And minority investors and the special committee are fully aware of everything that we're aware of.
Okay, great. Thanks very much.
Yes. Thank you.
Thank you. And there are no other questions in the queue.
Thanks everyone for your time. Appreciate it.
Ladies and gentlemen, this concludes today's conference call. Thank you for participating. You may now disconnect. Everyone, have a great day.