Clearside Biomedical Q2 2023 Earnings Call Transcript

Quartr
Provided by Quartr
August 14, 2023

There are 9 speakers on the call.

Operator

Greetings, and welcome to the Clearance Biomedical Second Quarter 2023 Financial Results and Corporate Update Call. At this time, all participants are in a listen only mode. A question and answer session will follow the formal presentation. Please note, this conference is being recorded. I will now turn the conference over to your host, Jenny Corbin of Investor Relations.

Operator

You may begin.

Speaker 1

Good afternoon, everyone, and thank you for joining us on the call today. Before we begin, I would like to remind you that during today's call, we will be making certain forward looking statements. Various remarks purposes of the Private Securities Litigation Reform Act of 1995. Actual results may differ materially from those indicated by these forward looking statements as a result of various important factors, including those discussed in the Risk Factors section of our annual report on Form 10 ks for the year ended December 31, 2022, our quarterly report on Form 10 Q for the quarter ended June 30, 2023, and our other SEC filings available on our website. In addition, any forward looking statements represent our views as of today and should not be relied upon as representing our views as of any subsequent date.

Speaker 1

While we may elect to update these forward looking statements in the future, We specifically disclaim any obligation to do so even if our views change. On today's call, we have George Lezefsky, our Chief Executive Officer And Charlie Deignan, our Chief Financial Officer. After our formal remarks, we will open the call for your questions. I would now like to turn the call over to George.

Speaker 2

Thanks, Jenny. The last 6 months have demonstrated that ClearSite is the clear leader in delivering agents We have a proprietary suprachoroidal space injection technology that utilizes our patented SCS microinjector. We're able to deliver small molecules and gene therapy behind the visual field targeting multiple retinal diseases. We have the 1st and only FDA approved SCS product with XIPERE and we have 4 external validating SCS delivery collaborations as well as an early stage internal research and development pipeline. Importantly, as we expand our development opportunities both internally and with our partners, Our versatile therapeutic platform continues to grow.

Speaker 2

Together with our licensing partners, there are now 6 ongoing SCS trials in 5 different indications utilizing 4 potential therapies. ClearSign's lead internal program is CLS AX, our proprietary suspension of axitinib delivered into the suprachoroidal space. CLS ax is targeting the multi $1,000,000,000 market for wet AMD. So let me take a moment to talk about the market opportunity And why we believe we can truly make a difference in the lives of the millions of patients suffering from this disorder. Wet AMD is a crowded arena The development of new products mainly due to the large and growing market as a result of the aging population, particularly in the U.

Speaker 2

S. With the higher demand, there's room for new treatments that provide significant improvement over current therapies, including reducing the treatment burden for patients and their caregivers. Based on the label for existing marketed products for wet AMD, Lucentis is recommended to be dosed 12 times a year, EYLEA 2 milligrams 6 times a year and recently approved BOVISMO up to 6 times per year. In contrast, we believe that CLS ax may be up to a twice a year treatment for wet AMD. This matters because it has been well documented that patient compliance It's a challenge and therefore a treatment option where patients maintain their vision with less frequent dosing may achieve improved patient outcomes.

Speaker 2

CLS ax could reduce the onerous treatment burden for patients who currently require frequent dosing and numerous office visits with existing approved drugs. CLS ax has the potential to be a better maintenance treatment option based on 3 main differentiating factors. 1st, CLS AX utilizes axitinib, which is the most highly potent tyrosine kinase inhibitor, delivering 10 times more potency than other TKIs in preclinical studies. 2nd, CLS AX is administered suprachoroidally using our proprietary SCS microinjector. This delivery mechanism does not require surgery And does not require an implant inserted into the eye.

Speaker 2

It's delivered by physicians in their office and has proven to be safe and reliable, both commercially and in multiple clinical trials. And thirdly, in our OASIS Phase IIIa clinical trial, we showed that a single administration of CLS ax demonstrated a favorable safety profile with no signs of inflammation. In terms of duration, in the extension study of OASIS In higher dose cohorts with a single dose of CLSAX, 2 thirds of the participants did not need supplemental treatment for 6 months or more. Also, these participants experienced a 77% to 85% reduction in treatment burden as measured by the number of anti VEGF treatments they received during the 6 months compared to the 6 month period prior to entering the OASIS trial. Importantly, we also observed signs of biological effect with stable mean best corrected visual acuity or BCBA and stable mean central subfield thickness or CST.

Speaker 2

Encouraged by the promising OASIS results and following the FDA draft guidance for drug development of treatments for wet AMD, last quarter we initiated ODiSI, Our randomized double masked multicenter Phase 2b clinical trial in participants with wet AMD. The overall objective for the trial is to evaluate the safety, And duration of CLSAX treatment and participants with wet AMD. The other arm in the trial is a current standard of care, EYLEA or oflibercept. Our goals for the ODiSI trial are to demonstrate similar visual acuity outcomes with a lower treatment burden for the CLSA exon And to obtain the necessary clinical data to determine a desired CLS ax fixed dosing regimen for a Phase 3 wet AMD clinical development program. We are pleased that the trial is off to a solid start and is progressing as planned.

Speaker 2

Multiple participants have been randomized to receive either CLSAX Clinical trial sites have been eager to be part of the trial and we have nearly all of our planned 30 sites currently open to enroll participants in the trial. As a reminder, Odysee is expected to enroll a total of 60 participants randomized to either CLS ax 1 milligram orflibercept 2 milligrams with a 2:one randomization schedule. This means that there is expected to be 40 participants in the CLSA exon And 20 participants in neoflibercevon. The treatment period is a total of 36 weeks. In the trial, CLS A X The primary outcome measures for the trial are the mean change in BCVA over the 36 week period as well as the assessment of Safety and tolerability of CLS A X.

Speaker 2

The secondary outcome measurements are treatment burden as measured by total injections including the need for supplemental therapy over the trial duration and other changes in visual function in ocular anatomy such as CST. An important component of ODiSI is the eligibility criteria. Our inclusion criteria is designed to ensure that Participants in our trial have active diseases screening. Eligible participants will be treatment experienced and will undergo diagnostic imaging after Screening visit followed by masked reading center confirmation of persistent active disease. This level of specificity is to ensure that participants are in need of treatment will likely respond to and benefit from treatment with anti VEGF therapy.

Speaker 2

We believe this will allow the proper assessment of the potential advantages of CLS AX in patients with wet AMD. We further believe CLSX will demonstrate the ability to maintain visual acuity with a longer duration of action in order to reduce the treatment burden for patients with wet AMD. We are confident in our overall trial design and the potential success in ODiSI and we look forward to reporting top line data in the Q3 of 2024. Moving on to XIPERE, we continue to receive positive feedback from clinicians regarding the use of XIPERE with patients. Our North American commercial partner for Zeikor, Bausch and Lomb, continues to conduct product education and training sessions for healthcare providers With more than 1200 retinal specialists trained to date, these sessions have been well attended and well received.

Speaker 2

Physicians report that the suprachoroidal injection procedure utilizing the SCS microinjector is easy to learn and that XIPERE is highly effective in treating their patients macular edema associated with uveitis. Looking forward, Bausch and Lomb is focused on increasing engagement with uveitis specialists across the country And working on reimbursement parameters that will make it simpler for physicians to use XIPERE for their patients. Our Asia Pacific partner Arctic Vision continues to move forward in 2 indications with their development of XIPERE, which they refer to as Arcadis. For the first indication of uveitis macular edema, Arctic Vision is currently enrolling a confirmatory Phase 3 trial in China. If positive, the data will allow Arctic to apply for marketing approval in China.

Speaker 2

In addition, Arctic recently announced that the Therapeutic Goods Administration of Australia Has formally accepted its new drug application for suprachoroidal use of Arcadis for the treatment of uveitic macular edema. The acceptance of the NDA in Australia is an additional validation of the of the suprachoroidal administration being an innovative recognized form of ophthalmic drug delivery and another step towards the global commercialization of XIPERE. The second indication of ARCTIC is diabetic macular edema. ARCTIC has completed a Phase 1 clinical trial and we expect them to report the data from the trial later this year. This data could provide helpful insight into potential for broadening the use of XIPERE in other indications.

Speaker 2

We're excited about the progress Arctic Vision has made to expand the use of XIPERE and we look forward to further updates from them. We also continue to work closely with our partners developing breakthrough technologies to deliver gene therapy and ocular oncology treatment utilizing suprachoroidal delivery with our Earlier this month, REGENXBIO announced updates on its ABBB RGX-three fourteen program for the treatment of wet AMD and diabetic retinopathy being developed in collaboration with AbbVie. In July, REGENXBIO presented interim data from the Phase to AV8 and ALTITUDE trials demonstrating suprachoroidal delivery of 314 administered to patients with prophylactic steroid eye drops resulted in 0 cases of intraocular inflammation. Additional data from REGENXBIO on both trials is expected over the next 6 months. Interim efficacy data from the ALTITUDE trial in diabetic retinopathy is planned for American Academy of Ophthalmology meeting in November of 2023 and the interim efficacy data from the ABA trial in wet AMD is expected to be presented at the Hawaiian Eye and Retina Meeting in January 2024.

Speaker 2

Our oncology partner, Ora Biosciences, announced their progress last week with their drug candidate, Belsar, for the treatment of choroidal melanoma. Their global Phase 3 clinical trial is expected to dose the first patient in the second half of twenty twenty three and is designed as a superiority trial comparing Belsar versus sham with the primary endpoint as time to tumor progression. Oura has qualified trial sites globally with multiple sites ready to enroll patients in the U. S. In addition, Ora expects to present updated efficacy data in the second half of twenty twenty three.

Speaker 2

The Phase 2 data will include 12 months medium follow-up of patients treated with the therapeutic regimen intended to be used in the global Phase 3 trial. With that summary of our programs, I'll now turn the call over to our CFO, Charlie Deignan for a financial update.

Speaker 3

Thank you, George, and good afternoon, everyone. Our financial results for the Q2 were published earlier in our press release and are available on our website. Therefore, I would just provide a summary of our financial status. As of June 30, 2023, our cash and cash equivalents Totals approximately $35,000,000 We continue to prudently manage our cash as we move forward with our programs and we have worked To fine tune our budget over the next year, based on our current outlook, we now expect to have sufficient resources to fund our planned operations into the Q3 of 2024. Over the next few months, we look forward to participating in several investor conferences, including the H.

Speaker 3

C. Wainwright Ophthalmology Conference this Wednesday, the Cantor Global Healthcare Conference in September and the Jones Trading Healthcare Summit in October. We look forward to keeping you updated on our progress. I will now turn the call back over to George for his closing remarks.

Speaker 2

Thanks, Charlie. In closing, Our state of the art suprachoroidal injection technology continues to advance globally. CLS ax is targeting a large market opportunity in wet AMD With a new mechanism of action utilizing pan VEGF inhibition and a unique suprachoroidal delivery using our SCS micro injector. We are confident in our Phase 2b ODiSI trial design and the potential for CLSAX to offer patients a therapy that will maintain their vision while reducing Our current partners are making meaningful progress as well and reporting encouraging clinical data across their respective programs. We continue to receive positive feedback on our SCS microinjector and the potential advantages of drug delivery to the suprachoroidal space.

Speaker 2

We remain very active within the medical community at scientific meetings and in ongoing discussions with key opinion leaders in the treatment of back of the eye diseases. Clearside has pioneered drug delivery behind the visual field to treat retinal disorders. We will continue to explore opportunities to And the use of our suprachoroidal injection technology platform. Now I'd like the operator to open the call for questions.

Operator

Thank you. At this time, we will be conducting a question and answer session. Thank you. Our first question is coming from John Wallobin with JMP Securities. Your line is live.

Speaker 4

Hey, thanks for taking the questions and the updates. A couple for me, George.

Speaker 2

You mentioned almost

Speaker 4

30 sites are open now. Wondering if you still feel good about that number, if you think you'll add more, you have enough? And then also, I think you commented that patients are being dosed. Can you tell us how many have been dosed so far in the study?

Speaker 2

Okay, John. Our goal was 30 and we're very close to 30. We feel comfortable with 30. We have a lot of interests. We may enroll a few extra over 30, that's possible.

Speaker 2

But right now, our goal is 30 and we're just about there. So we're feeling very good with that. In terms of updates, we have reported that we've begun the randomization process. So So we've had multiple patients be randomized between the CLSAX arm and the oflivercept arm. But at this point in time, we're not giving updates on the actual number

Speaker 4

Okay. And then interesting nuance in the design for Odyssey is the ability to redose CLSAX depending on when someone hits rescue criteria. Wondering about your modeling about How many patients do you think will be re dosed with CLSAX or rescued with EYLEA based on the OASIS data? I think this could give us a lot of Interesting information we're not going to get from other TKI studies.

Speaker 2

Yes. Listen, we've designed this trial in a way that we think We're going to be have a lot of success in getting this to be a 4 to 6 month treatment. And I'm very hopeful and I Expect a high degree of success of getting the vast majority of the patients towards 6 months. I don't believe, Unless there's deviations from protocol, I would be very surprised if we have any rescues that are less than 12 In the CLSA Exxon. That would our expectation is there's be very few, if any, Early stage rescues in less than 12 weeks after the first CLS A X dose, which if you remember, we've got the 3 loading doses and We're dosing CLS ax at the second loading dose of aflibercept.

Speaker 2

So we're doing aflibercept on label for both groups in terms of loading and then we're going Switching to in the aflibercept arm, they're being dosed every 2 months on label. In the CLS ax arm, we're going to dose At least every 6 months with CLS A X unless supplemental therapy is required earlier. But I really don't anticipate Any significant number of patients being rescued before 12 weeks after the initial dose.

Speaker 4

Okay.

Speaker 2

I think OASIS really the OASIS data really gives us that kind of encouragement. Again, we have to run the trial, we To do carry out the trial according to the protocol, but if we run it according to the protocol and based on what we saw in Oasis, I think there'll be very few.

Speaker 4

Can you talk about the opportunity for treatment extend with CLSAX versus potentially looking at A treatment naive population of subsequent study and I'll hop back in the queue. Thanks again.

Speaker 2

Okay. John, just real quick, could you repeat that again? I just missed the last part of it.

Speaker 4

How you think about the treatment extend opportunity like you're studying now or potentially looking at a treatment naive population in a subsequent study?

Speaker 2

Well, like I said, we're going to make sure that everybody in the CLS ex arm gets a dose At 6 months, if they didn't require one earlier. I think our real hope is that there'll be people that are being treated at 6 months That by virtue of looking at BCBA changes and CST changes really don't require it. So we're looking at a multiple dose But we're also going to be looking at the biological indicators, the anatomical indicators and Being able to report out whether it was they really met a need. And so what we're trying to do here is we're really trying to determine what Proper fixed dose is to go into Phase 3 because I believe that we need to go into Phase 3 with a fixed dosing regimen. You know, FLBRESA has a fixed dosing regimen, but physicians quite often use the treatment extend.

Speaker 2

I think patients are going to be coming into the office. They're not going to come into the office twice a year or once a year. They're going to be coming back every couple of months, every other month. And if they come in at 6 months after getting their CLSAX dose, in practice, if it was approved and their BCBA is stable and the CST is stable. I think it will be just like any other therapy that people feel comfortable doing treatment extend.

Speaker 2

I'm not sure if that's completely responsive to your question, but I really look forward to seeing a fixed Dosing regimen where we can clearly, as I mentioned in the opening remarks, I mean, if you look at on label now and even with vevismo, Which was just recently approved. That dose is every 4 months at a maximum. And there's a number of people that have to be dosed after 4 loading doses in every 2 months For 3 months. I think if we're in the 4 to 5 month 5 to 6 month category, that's a major improvement for patients. And I think even at that point, doctors will still look to treat and extend past that.

Speaker 2

So we may be going past 5, 6, 7 months in number of patients.

Speaker 4

That is helpful, Drew.

Speaker 2

We see the data and we have we really have to go into Phase III, I believe, with fixed dosing regimen Rather than the way it was done in the past where there's a kind of a treat and extend and we'll see how far we go. Our goal is to really set up that The fixed dosing regimen.

Speaker 4

Got it. All right. Thanks again.

Speaker 2

Sure.

Operator

Thank you. Our next question is coming from Andreas Arguerides with Wedbush Securities. Your line is live.

Speaker 2

Hi, Andres.

Speaker 5

Good afternoon. This is Caroline actually on for Andres. Hi, Caroline. Hi. Sorry,

Speaker 2

I can't see anything.

Speaker 5

It's okay. No worries. Thank you for taking our questions. Just 2 from us. Can you discuss your targeted Timeline for enrollment in ODiSI and how enrollment is progressing?

Speaker 5

Are you seeing any impact from the availability of the bismo? And then second, can you just discuss the powering assumptions for Odysee?

Speaker 2

Okay, sure. The powering assumption, We're not conducting a non inferiority trial. We're not conducting a superiority trial. So there really isn't a powering assumption in here. What we're looking at is flibercept on label and see what over the 36 weeks yes, 36 weeks, How those patients in the flibercept arm do in terms of keeping a stable BCBA and CST?

Speaker 2

And then we're going to look at the CLS ax arm and what we're trying to do is to see whether the BCVAs and the CSTs are Similar between the two groups and what our ideal dosing regimen would be on a fixed basis going into Phase 3. Should it be every 4 months? Should it be every 5 months? Should it be every 6 months? Maybe can we go longer than that?

Speaker 2

Okay. So there's not this is not set up As a trial that has sufficient patients to have a powered outcome as you would think of in a non inferiority trial in particular. So we think that the Phase 2 design here in terms of total patients that are in the treatment arm It's very consistent with way a number of the recent Phase II trials have been run. We're not looking to convert this into a Phase III. We're looking to run a standard Phase 2b trial here, trying to compare in an estimation on an estimation basis, How well we're doing and where we should go into Phase 3 on a fixed dosing.

Speaker 2

In terms of the enrollment, As I mentioned in the press release and in the opening remarks, we're nearly at the 30 targeted sites that we want. We have All of our previous sites from Oasis are included in Odyssey. So we have very people that are very experienced with CLSAX already in. We'll be closing that out soon. And then on enrollment, we're not going to give enrollment updates Per se, but what we are not changing is our disclosure regarding when we think top line data is Going to be available.

Speaker 2

We're still looking at Q3 of next year and the way we've been able to enroll sites And as we see enrollment of participants going on, we're still very comfortable with Q3 of 2024 in terms of top line data.

Speaker 5

Okay, great. Thank you so much and congrats on the progress.

Speaker 2

Thank you.

Operator

Thank you. Our next question is coming from Sean Kim with Jones Trading. Your line is live. Yes, hi. Thank you for taking my questions.

Operator

I guess first question for me. Hi, Sean. Hi. My first question is that In light of recent safety issues reported with an FDA approved therapy in geographic atrophy, Would you please remind us if there has been any retinal vasculitis reported with any of suprachoroidal injections given thus far? And a related question is in comparison to intravitreal injections, whether this prochloroidal drug delivery approach might be intrinsically More likely or less prone to causing retinal vasculitis and related adverse events?

Speaker 2

Well, I think the first part of the question first, as far as I know. Certainly, with CLS ax, we've had no events, no indication of any kind of inflammation, including retinal vasculitis. So that is covering both the product itself, CLS AX, the Tyrosine Kinase inhibitor, As well as the injection technique and the injection procedure. We've not seen any of that. And as far as I'm aware, we don't have any Significant reports or any reports at all of retinal vasculitis.

Speaker 2

I'd have to double check that to be sure, but there's nothing that comes to mind In our partners trials or in our previous trials getting XIPERE approved that that was a significant problem. Certainly, if you look at the injection procedure itself using our SES Micra injector, it's been very reliable, safe, Very repeatable. The physicians that are trained on it find it once they're trained on it and the training doesn't take All that long, it's not that complicated, but it is important. Once they're trained, they find it an easy procedure, a very acceptable procedure And very comparable in a sense to from a patient experience and a physician experience to intravitreal injections. So retinal vasculitis has just not come up as a problem that I can recall in any of our clinical trials or our partner's Now to be fair, REGENXBIO had did have some inflammation in some of their earlier trials, But they've recently reported that with the topical steroids in their Phase II trial, I believe it was in wet AMD, They've seen no signs of inflammation and I've certainly not heard of any reports of retinal vasculitis.

Operator

Okay, that's helpful. Thank you. And related to the ODYSSEY trial, if I understand correctly that One of the goals for the ARTASIS trial is to define the fixed dosing schedule for potential Phase 3. So my question is, What endpoint would it dictate that dosing interval for Phase 3? Would it be BCBA there change?

Operator

Or would it be more of totality of data across different efficacy points?

Speaker 2

I think the most important and certainly from the FDA's point perspective, the most important Endpoint would be the BCBA. They certainly want to Doctor. Chambers with the FDA It's very focused 1st and foremost on vision preservation or vision improvement. And so I think the real most important factor would be the BCBA stability for the duration. How long can we keep that BCBA stable without requiring any kind of supplemental intervention?

Speaker 2

So I think that's the most important thing. Other things like CST are important, but I think BCBA is the most important factor there.

Operator

Okay. Got you. And just a quick follow-up on that is, just curious what your Expectations might be for the efilibercept control arm in terms of that BCDA change for 6 months, specifically in the target population for the Allis trial?

Speaker 2

I'm not sure what to expect Regarding BCPA, I would hope that I would expect not so much I would hope, but I would expect if the patients are The typical patients that go into that and they get dosed appropriately on label with aflibercept, they'll have a similar Outcome, there'll be a similar overall outcome to what you've seen with aflibercept dosed on labeled Before in the hands of other people. I don't know why it would be any different in our hands than other people. We looked at how VAVISMO did versus opliberceb using opliberceb as their control in Phase 3, and we saw how Vabaisma did against that. And we think that we can do as well against aflibercept as bevizumab did against aflibercept, but we believe that our Dosing interval is going to be longer than the vivisimos turned out to be in their Phase 3. So I don't expect any difference In the way oflifloversat patients respond to aflibercept other than what you've seen in other trials in wet AMD That enrolled a similar population.

Speaker 2

Okay. And it really does come down to the enrollment, what kind of patients are you putting in? Are you If you're putting in patients that really don't have strong signs of active disease, those patients are going to do really, really well Because they may not have required any real intervention to begin with. There's lots of literature that will talk about patients that are relatively dry with the disease, but no active signs of no signs of active disease might go for a long period of time between injections. But We're trying to make sure that the two groups have people that are responsive to anti VEGFs and have active disease when they're enrolled.

Speaker 2

And then I think the outcome in the Flubr subgroup will be pretty consistent with history.

Operator

Okay, great. Thank you.

Speaker 2

Sure.

Operator

Thank you. Our next question is coming from Rohit Bassin with Needham and Company, your line is live.

Speaker 6

Hi, this is Rohit on for Serge. Thanks for taking our questions. Hi, Rohit. Hi, Rohit. Hi, how's it going?

Speaker 6

Are you still evaluating new potential new collaborations for the SCS micro injector platform? And then is the current Cash balance sufficient to get us to a top line readout of Odyssey? Thanks.

Speaker 2

All right. I'll take the first part of that question and I'll let Charlie take the second. Yes. We are in discussions with other companies about potentially partnering In various disease states or with various therapeutic agents that we think might be useful delivered supercorporally. We conduct those kind of business development activities on a regular ongoing basis.

Speaker 2

We don't Jump into them lightly. We want to make sure they're very strategic and very positive for us and would be a positive for the company. And so we need to make sure that we have the right terms, the right partner and it fits our strategy for partnering. We typically try to partner in areas where the collaborator has technologies that we cannot access, That we don't have any expertise in, for example, gene therapy. That is not a core competency of us, of ClearSign.

Speaker 2

So that's why we partner in the look to partner in the area of gene therapies in particular. But there could be other small molecules That are proprietary to other companies that want to be put into our suprachoroidal delivery system, and we're certainly open to that. And we have A constant set of conversations with people trying to put together the right deal that makes sense for us as well as for them. And Charlie, I'll let you take the cash runway call.

Speaker 3

Thanks. Hey, Rohit. Yes, so as we said, our data is coming, planned to come Q3 next year and our cash can get us into Q3 of next year. That's obviously, we want a cushion And we can't until we finish enrollment know exactly within the quarter, the data will come. But We will continue to look to extend our runway much past When the data comes in and that's what we're doing now is looking at all dilutive and non dilutive ways to extend our runway.

Speaker 7

Great. Thank you.

Operator

Thank you. Our next question is coming from Jack Padovanov with Stifel. Your line is live.

Speaker 8

Hi. This is Jack calling in for Annabel.

Speaker 2

Hi, Jack.

Speaker 8

Hi. Just Quick question for me. Could you briefly go over again some of the economics with your partners and if there's any chance that you might be able to see some additional near term Expected catalysts or milestones from them?

Speaker 2

Charlie, is that something you would want to address?

Speaker 3

Yes. Sure. So as a reminder, We haven't announced or we're not allowed to announce particular milestones, but as some of these Our collaborators are getting into Phase 3. Typically, there's Phase 3 development milestones that go with them. But that's That would affect our EPS and revenues, but just don't forget that when we monetized our royalties with HCR Healthcare Royalty, those milestones will get wrapped up and go towards the cap we have to pay.

Speaker 3

If you remember, We took $32,500,000 from them and we'll have to pay 2.5 times that back, so approximately $81,000,000 So those any milestones that come in will go directly to HCR on our partnered programs.

Speaker 4

Thanks.

Speaker 5

Did I

Speaker 3

answer your question? Yes.

Operator

Thank you. Our next question is coming from Yi Chen with H. C. Wainwright. Your line is live.

Speaker 7

Thank you for taking my questions. Your partner, REGENXBILE recently reported some progress with their candidate for what AMD. I don't know if you can comment on whether their candidate in the future could potentially become a competitor to CIS AX?

Speaker 2

I'll take that question, Yi. I suppose it could. It depends. I think As I understand their therapy, their therapy is a gene therapy that generates a lucentes type molecule. And again, what CLS ax does is a different mechanism of action than what REGENX The REGENXAbbVie product would have, right.

Speaker 2

So that's It's pretty much standard anti VEGF therapy, just like EYLEA, VAVAZOVEL, etcetera, and Nucyntis. There I think their potential claim to fame is they're going to last a long time And binding, the circulating VEGF. From our perspective, we're taking a different mechanism mechanistic approach And that is we're blocking the VEGF receptors 1, 2 and 3. So any circulating VEGF including if it's not Completely bound. They're still circulating VEGF and they're binding again VEGF A.

Speaker 2

And in many cases, there's an overexpression of patients Once you start to bind the VEGFA, especially on a longer term treatment after a couple of years getting VEGFA anti VEGFA therapy, That there's an overexpression of C and E in particular, which can cause potential neovascularization. So I think while it's potentially competitive in that they're going after wet AMD as are we with CLS ax, I think they could be complementary if you want to put a positive spin on it. I think they'd be complementary because the mechanisms are different. And theirs would unlikely based mechanistically unlikely to address any of those Patients that become resistant to VEGF anti VEGF A therapy, and because in many cases overexpression of CNE, while Our mechanism through using a tyrosine kinase inhibitor would block all 3 VEGF receptors. So even if there was overexpression of C and E, We would be blocking the interaction of VEGF C and E at the receptor sites.

Speaker 2

So I think there's room for multiple products. I often refer to this area as starting to develop the characteristics of cancer therapy, where there's multiple approaches, multiple products to use for the treat particular cancer. And I think it could be that the 2 products end up being able to be used together rather than just Competing straight up for all wet AMD patients. So I think there's room for both and we'll see. The proof will be in the clinical data for both products.

Speaker 7

Thanks. My next question is, I don't know if you can comment on the prescription volume of XIPERE and whether your quarterly license revenue is correlated to the Prescription model.

Speaker 2

Okay. I'll let Charlie handle that. That's his

Speaker 3

Yes. So we don't have prescription information. I think those of you that track Retina drugs, difficult to get. So we can't give any guidance or trends on sales. We're contractually obligated to Bausch not to discuss unless they do so.

Speaker 3

Until they start reporting out publicly the sales, I can't help you with that.

Speaker 7

Got it. And lastly, could you comment on The potential timeline to for your partner to obtain the approval of XIPERE in Australia?

Speaker 2

Well, our understanding of the filing in Australia is that it's typically it's very similar to the United States and that Your expectation should be about a 12 month review to approval cycle and they filed a month or so ago. And so I would think it'd be they'll have news by this time next year. But that's kind of an educated guess on my part, but We do understand the Australian process for approval runs about in a similar timeline to the United States, which is about 12 months.

Speaker 7

Got it. Thank you.

Speaker 2

Okay. Sure.

Operator

Thank you. We have reached the end of our question and answer session. So I will now turn the call back over to Doctor. Lizewski for any closing comments you may have.

Speaker 2

Thank you. Thank you all for joining us on the call this afternoon. We really appreciate your continued interest in Clearside. We look forward to updating you on our progress throughout the year. And at that, operator, you can now disconnect the call.

Speaker 2

Thank you again all.

Operator

Thank you, sir. This concludes today's conference. You may disconnect your lines at this time, sorry. And we thank you for your

Powered by Quartr

Key Takeaways

  • ClearSite’s proprietary suprachoroidal injection platform now includes the first FDA-approved SCS product, XIPERE, plus four external collaborations and a growing internal pipeline.
  • The lead internal asset, CLS-AX (axitinib suspension), showed in the OASIS trial that a single dose led two-thirds of participants to avoid supplemental treatment for 6 months, with a 77–85% reduction in anti-VEGF injections and stable BCVA/CST.
  • The ongoing Phase 2b ODiSI trial for wet AMD is designed to compare CLS-AX’s safety and efficacy against on-label aflibercept, targeting similar visual outcomes with potentially twice-annual dosing.
  • Commercial progress includes Bausch + Lomb training over 1,200 retinal specialists on XIPERE in North America, while Arctic Vision advances Arcadis in Phase 3 China trials and an accepted Australian NDA.
  • Financially, ClearSite reported approximately $35 million in cash as of June 30, 2023, with sufficient runway to fund operations into Q3 2024.
AI Generated. May Contain Errors.
Earnings Conference Call
Clearside Biomedical Q2 2023
00:00 / 00:00