© 2024 Alpha Spread Limited. All Rights Reserved.
www.alphaspread.com is not operated by a broker, a dealer, or a registered investment adviser. Under no circumstances does any information posted on www.alphaspread.com represent a recommendation to buy or sell a security. The information on this site, and in its related newsletters, is not intended to be, nor does it constitute, investment advice or recommendations. The information on this site is in no way guaranteed for completeness, accuracy or in any other way. In no event shall Alpha Spread Limited be liable to any member, guest or third party for any damages of any kind arising out of the use of any content or other material published or available on www.alphaspread.com, or relating to the use of, or inability to use, www.alphaspread.com or any content, including, without limitation, any investment losses, lost profits, lost opportunity, special, incidental, indirect, consequential or punitive damages. Past performance is a poor indicator of future performance.
You don't have any saved screeners yet
Intrinsic Value is all-important and is the only logical way to evaluate the relative attractiveness of investments and businesses.
Good day, ladies and gentlemen, and welcome to Eyenovia's Third Quarter of 2023 Earnings Conference Call. [Operator Instructions] As a reminder, this conference is being recorded.
I will now turn the call over to [ Glenn Gorman ]. Please go ahead, sir.
Thank you, Judith. Good afternoon, and welcome, everybody, to Eyenovia's Third Quarter 2023 Earnings Conference Call and Audio Webcast. With me today are Eyenovia's Chief Executive Officer, Michael Rowe, Chief Financial Officer; John Gandolfo; and Chief Operating Officer, Bren Kern. This afternoon, we issued a press release announcing financial results for the 3 months ended September 30, 2023. We encourage everybody to read today's press release as well as Eyenovia's quarterly report on Form 10-Q for the quarter ended September 30, 2023, which will be filed with the SEC tomorrow, November 14, and our most recently filed Form 10-K.
The company's press release and annual report are also available on our website at www.eyenovia.com. In addition, this conference call is being webcast on the company's website and will be archived there for future reference. Please note that on today's call, we will be discussing product, product concepts and candidates, some of which have yet to receive FDA approval. Please also note that certain information discussed on the call today is covered under the safe harbor provision of the Private Securities Litigation Reform Act. We caution listeners that during the call, Eyenovia's management will be making forward-looking statements.
Actual results could differ materially from those stated or implied by these forward-looking statements due to risks and uncertainties associated with the company's business. These forward-looking statements are subject to a number of risks which are described in more detail in our annual report on Form 10-K. This conference call contains time-sensitive information that is accurate only as of the date of this live broadcast, November 13, 2023. Eyenovia undertakes no obligation to revise or update any forward-looking statements to reflect events or circumstances after the date of this conference call, except as may be required by applicable securities law.
And with that said, I'd like to turn the call over to Mike Rowe, Eyenovia's Chief Executive Officer. Michael?
Thank you. [ Glenn ], and welcome, everyone, to our third quarter 2023 financial results conference call. Eyenovia had a highly productive third quarter, both in terms of tangible results as well as setting the stage for our future success. I'm excited to share our progress and plans this afternoon as we prepare for our targeted launch of Mydcombi, the potential approval and launch of AP13007 and future partnerships in glaucoma and dry eye to leverage and monetize the Optejet technology beyond our own development programs. Let's start with our commercial preparations for the Mydcombi launch. For those of you who might not be familiar with Mydcombi, it's the first and only FDA-approved fixed combination of 2 popular pupil dilation drugs, and the first electromechanical spray platform using the Optejet.
Earlier this month, we were thrilled to announce that our contract manufacturer, Coastline International was approved by the FDA for Mydcombi commercial manufacturing. Production has already begun at coastline, and we expect to receive finished product into our warehouse in January 2024. In addition to manufacturing Mydcombi, we are also continuing to prepare the market and raise awareness about the product in the Optejet technology. Last week, we sponsored the course during the International Joint Commission on Allied Health Personnel and Ophthalmology's 51st annual continuing education program. The course was offered to ophthalmic technicians and provided hands-on experience with our Optejet dispensing technology and the use of Mydcombi.
We also have a significant exhibition booth at the American Academy of Ophthalmology and collected many leads and product requests from doctors who believe the technology addresses a significant unmet need in their practice. Last month, we presented data at the American Academy of Optometry Annual Meeting, demonstrating the Optejet's ability to maintain sterility even when exposed to a high microbial load. This presentation was particularly timely, given all the recent news about contaminated over-the-counter eye drops being pulled off the shelves of major drugstore chains and retailers due to the risk of serious eye infection and even blindness. In conditions that far exceed the microbial load that the Optejet would be exposed to in actual daily use, the device demonstrated its ability to maintain product sterility.
We are now in the process of validating the Optejet's ability to deliver topical medication without preservatives for an extended period of time. Our activities at these professional meetings have been a great avenue to continue socializing Mydcombi to ophthalmologists, optometrists and technicians and positions us well for a broader commercial launch of Mydcombi early next year. The current U.S. market for pupil dilation is valued at approximately $250 million, and we feel we are poised to take a good portion of that market share over the coming years, especially when we move to our next-generation device. More information, including ordering instructions and customer reaction to this unique product will appear shortly on mydcombi.com.
In 2024, we not only anticipate Mydcombi generating revenue for us, but we are looking forward to the potential FDA approval of APP13007 in early March 2024. We recently announced an agreement with Formosa Pharmaceuticals to acquire the exclusive U.S. rights to distribute and sell APP13007, or clobebazole pipionate ophthalmic solution. APP13007 is a potent steroid with a highly desirable safety and efficacy profile. It is currently under FDA review for postocular surgery inflammation and pain. Unlike almost all alternatives, this product is intended to be dosed twice daily without titration, which is significantly more convenient than the 4 times a day dosing regimens with titration for existing treatments.
There are approximately 7 million ocular surgeries annually and almost all of these procedures utilized topical steroids during the recovery process. This is potentially a significant market for us, and we expect to leverage our planned 10-person sales force for both Mydcombi and APP13007 and add significant value to optometry and ophthalmology offices in surgical centers. In addition to providing near-term revenue, APP13007 has the potential for additional indications in the Optejet, including dry eye, a multibillion-dollar market opportunity. Following the potential approval for the post-surgical indication on March 4 of next year, we look forward to working with Formosa and the FDA to determine the most efficient path forward for this new product.
We continue to explore additional partnering opportunities that we believe will benefit our company and our shareholders, specifically in glaucoma and dry eye, and we will provide you with updates on these developments when appropriate. I'll provide a brief regulatory update now. We have always believed that the Optejet due to its ergonomic design that eliminates the need for head healthy and handling small eyedropper bottles would be easier to use in many populations than currently available topical options. And in our own market research that we shared with you in the past, consumers and patients reported using eye drops was among the most difficult ways to use medication that they experience.
With that in mind, we recently held a successful meeting with the FDA to ask how we might demonstrate this benefit. We confirm with the agency that there is a path forward to include language in our labeling that covers patients who have difficulty or cannot reliably use eye drops as long as we provide evidence of a clinical benefit, either in efficacy or safety of the Optejet product compared to the eye drop product. We believe such labeling would not only help prescribers select our future products in classes such as glaucoma or dry eye, but this difference can lead to better formulary coverage for Optejet products as they would be the only products to provide an option for patients who have a challenging time with eye drops.
Now turning to Apersure, our proprietary topical on-demand pilocarpine-based therapeutic candidate that we are developing for the temporary improvement in near vision associated with presbyopia. Apersure is being designed with our more advanced Gen 2 Optejet device, which has been optimized for in-home use. These will be manufactured in our Redwood City facility, which is currently prioritizing manufacturing the Gen 2 device to supply our partners Bausch + Lomb and Arctic Vision with product for use in their pediatric myopia studies at the beginning of 2024. As a reminder, we are paid by our partners for reducing the supply, and that income helps cover a portion of our overhead for that facility.
Because of this, we have moved the manufacture of registration batches for Apersure into the first quarter of 2024. We do not believe this change will materially impact the eventual timing of the Apersure launch as the market for topical presbyopia treatments continues to evolve and mature as evidenced by the performance to date of the only presbyopia eye drop currently on the market. Finally, for a corporate update, we are pleased to announce the appointment of [ Mr. Michael Geller ] to our Board of Directors as an Independent Director and Chair of our Audit Committee.
Mike comes to us with more than 35 years of senior financial leadership experience, including as former Chief Financial Officer of ADT Corporation, New York Stock Exchange year on next, Readers Digest Association and A.C. Nielsen. Mike previously served on the Boards of Cypress Creek Renewables and the Euronext Supervisory Board and is currently a Board member for Madison Square Boys & Girls Club and the University of Delaware. We are excited to have Mike on board and look forward to his guidance and insights. At this point, I'd like to turn the call over to our Chief Operating Officer, Bren Kern, for our manufacturing update. Bren?
Thank you, Michael. We have made significant progress in the third quarter as we continue to build up our manufacturing capabilities to support Mydcombi, our Optejet platform and the Gen 2 configuration in registration bases for Apersure. As Michael mentioned, we are delighted that the FDA approved the use of additional manufacturing site Coastline International to support the Mydcombi launch. Coastline has always already commenced manufacturing of commercial product in support of the vital commercial launch of Mydcombi in the first quarter of 2024.
As our Redwood City facility is currently under review with the FDA as an additional commercial manufacturing site for Mydcombi with a PDUFA date in February of 2024. Our Redwood City facility is also working towards qualifying our Gen 2 fill and finish line for both the clinical trials of our MicroPine and registration batches for Apersure. As Michael mentioned, we are targeting a delivery of batches for our partners and the initiation of aperture registration batches in the first quarter of 2024. Additionally, our [ renal ] facility continues to make significant progress in establishing base and injector manufacturing.
Recall, in our last earnings call, we indicated that we had installed the manufacturing equipment. Since then, the manufacturing team has been optimizing the operation of equipment including generating qualification protocols, and we are targeting the commencement of protocol execution before the end of the year. We continue to make significant progress in increasing our manufacturing capacity. I remain confident that we'll be well positioned to meet the anticipated demand for Mydcombi as well as for the other Optejet products in clinical developments. I would now like to turn the call over to our Chief Financial Officer, John Gandolfo, to provide a financial update. John?
Thank you, Bren. For the third quarter of 2023, net loss was approximately $7.3 million or $0.18 per share compared to a net loss of approximately $7.3 million or $0.21 per share for the third quarter of 2022. The third quarter of 2023 includes approximately $400,000 of nonrecurring expenses associated with the rework or replacement of certain clinical trial Gen-1 devices, which were found to be defective after shipment to a licensee.
The rework of replacement is not expected to have any impact on the enrollment or timing of Bausch + Lomb study. Research and development expenses totaled approximately $3.6 million for the third quarter of 2023 as compared to $3.9 million for the third quarter of 2022. For the third quarter of 2023, G&A expenses were approximately $2.9 million compared to $3.4 million for the third quarter of 2022. Total operating expenses for the third quarter of 2023 were approximately $6.5 million compared to $7.2 million for the third quarter of 2022. As of September 30, 2023, the company's cash and cash equivalents were approximately $20.7 million compared to $22.9 million as of December 31, 2022.
For a brief update on our licensing revenues, in addition to the cash balance noted above, we have receivables from our license partners of approximately $400,000 as of September 30, 2023, and in addition, we expect the product development milestone payment of approximately $1.8 million from [ our division ] that we anticipate in the first quarter of 2024. I'll now provide an update on our existing licensing program with Bausch Health for MicroPine in the U.S. and Canada and Arctic Vision for all 3 of our products in China and South Korea. Bausch + Lomb is continuing to enroll in the ongoing Phase III CHAPERONE trial of MicroPine, a proprietary atropine formulation for the reduction of pediatric myopia progression.
It has been shown in clinical studies to slow myopia progression by 60% or more. There are currently no FDA-approved drug therapies for this indication, and if left untreated, this can result in retinal detachment, myopic retinopathy and vision loss. Our agreement with Arctic Vision covers Greater China and South Korea, and covers MicroPine, MicroLine and Mydcombi and provides a sales royalties in addition to development milestones. MicroPine in particular, is a significant opportunity in China for pediatric myopia. If approved, MicroPine could be a significant source of nondelivery funding for our company over the long term.
To date, our license agreements have generated approximately $16 million in license fees, and with the potential to earn an additional $60 million in net license and development milestones and reimbursable expenses over the next 4 years. If our products are approved upon commercialization, Eyenovia is also well to both on significant sales royalties. We are continuing to assess potential pipeline expansion opportunities similar to our promos agreement, we will continue to leverage the Optejet technology to address unmet needs in additional large ophthalmic indications. In conclusion, we are very pleased with our performance in the third quarter of 2023. And to summarize our key highlights today, we acquired exclusive U.S. commercial rights to APP13007 as a potential treatment for postsurgical ocular pain inflammation from most of pharmaceuticals.
We achieved our first commercial sale of Mydcombi in August 2023 and continue to carry out our targeted launch. Gen 2 Optejet production continues to advance and we're continuing to build out our manufacturing capabilities to support Mydcombi production with coastline manufacturing now on production in a Redwood City facility anticipated to come online early 2024. And our licensing agreements with Arctic Virgin and Bausch + Lomb are progressing well and remain a promising avenue for a significant development and regulatory milestones as well as the potential for additional sales royalties. This concludes our prepared remarks. We would now like to open the call to questions. Operator?
Thank you, sir. Ladies and gentlemen, we will now be conducting a question-and-answer session. [Operator Instructions]
Our first question comes from Tim Lugo of William Blair.
This is John on for Tim. So I was wondering if you could give us any color on what any gating factors you have remaining to getting 13007 into the clinic for dry eye disease? Or are you just waiting for the PDUFA perform moving forward? And as a follow-up, just wondering if you could provide any early thoughts on the trial design study indication.
We are waiting for the PDUFA because once that is done, then we can reference that file for all of the preclinical and safety information saves us a lot of time. So the idea would be -- with the product, we could go directly into Phase III. We've spoken with the FDA. It would be 2 relatively short-term Phase III studies because the initial indication would be in acute dry eye. So this would be used as an adjunct for flare-ups, for example, which is common because the current dry eye products don't do a particularly good job at solving the issue.
So we've had the discussions. We know what the design would be, and we're waiting at this point for the approval because to go forward, we would want to reference the approved drug.
Our next question comes from Matt Kaplan of Ladenburg Thalmann.
This is Raymond in for Matt. Congrats on all the progress. Just wanted to ask about perhaps the drivers and moving parts for Mydcombi revenue as the launch in near term. I was wondering, is it state licenses, sales force rollout? Any additional color would be helpful. And I just have one more follow-up question.
Sure. Thanks for calling. The state licenses are falling into place. So at this point, it's manufacturing, which is underway. So we need to get the product into the warehouse in January. The 2 sales force leaders have been hired. They're now going to hire the remainder of the sales force, and that's time for when the product actually is available. So at this point, everything is moving the way we would expect it, and I would anticipate first sales at the end of January.
I see that. Yes. And I guess you mentioned in the prepared remarks, the Gen 2 device, the FDA mentioned clinical efficacy, is that more superiority or noninferiority over eye drops?
Well, I'll give you an example, and I'll use safety as an example. We know that the Optejet delivers 1/4 or 1/5 the dose, for example, of conventional eye drops. So if you use beta blockers as an example, if you take a beta blocker as an eye drop, and this is in the literature, it actually slows your heart rate by 1 or 2 beats per minute as a systemic side effect because the majority of that beta blocker you're going to end up drinking because you're overdosing the eye.
If you use the Optejet, you will have significantly less available systemically and it is likely that we would be able to show that you don't have that impact, that safety impact because you are getting a lower dose. That's the kind of thing that could end up in the label to differentiate the product.
Our next question comes from Len Yaffe of Stoc*Doc Partners.
I wanted to ask you a question about APP13 bond. And I was wondering, I was very excited to talk about the dry eye application because that's seeming a very large market. Could you discuss to the extent you have data in the U.S., the size of that market? How much of it is [ XDR ] and [ RESTASIS ] versus over-the-counter drops? And you mentioned initially, you'll be competing in the acute dry eye segment, how big of the total dry eye market is that? And it seems like this would be a perfect drug to be put in the Gen 2 Optejet device, how much more do you think that could potentially expand the use of the drug given that you'd have it available in Optejet?
And I think I'm going to steal that AP13 bond from now on, it's easier to say. We think it's a tremendous opportunity. And let me start with why ending Optejet, and I'll go back to when we talk to the FDA about differentiating the Optejet from an eye drop. One of the issues with steroids as a class is that historically, when you use them for an extended period of time that can cause something called an IOP spike, which is a transient intraocular pressure increase, which you don't want to see in patients who are sensitive like patients who have glaucoma. So the FDA is very concerned about that.
Now [ clogetazole ], the formulation we have in clinical trials, we only saw that in 1 patient out of 180, which is basically the same as you would see in the general population without drug. So we think this is a particularly good drug for dry eye because you don't see the IOP spike to begin with. But the benefit of using the Optejet is because you're delivering 1/4 to 1/5 a dose, is that if these IOP spikes are related to dosing, you should see it even less, which would be the additional benefit while still getting the dry eye pain and inflammation relief. So that's why we want to put it into the Optejet to get that additional benefit.
As for the market opportunity for people who are on cyclosporine or RESTASIS or on lifitegrast, many of you know that, that's not enough. And you're still using artificial tears and you're still having problems. So this would be a product, if approved, that you would use for those times where it's getting just a little bit too much and you need something for 14 weeks to calm down the ocular surface. In terms of market size, it doesn't really compete with the other drugs. It's used in addition to them from time to time. There are millions and millions of patients out there. So this could easily be a multibillion-dollar opportunity for the right drug, and we think we have something that is really special with AP13 bond. Thank you.
Okay. And secondly, could you comment on when the MicroPine studies would be complete either by Bausch or Arctic so the drug could be ready for filing given that, that market, especially post pandemic and younger folks spending so much time on their cell phones either texting or playing video games for the incidence of progressive myopia is increasing. It seems like it's a very large market.
Yes. I can't speak for either of those companies as they're operating their own studies. I can tell you that in previous conversations, I know that they would like to finish their enrollment in 2024. So assuming that's the case, it's 3 years to an efficacy endpoint after that, which would take you to the end of 2027. So I think any kind of filing would probably be in 2028. .
Great. And when you refer to it as bond, I'll take a little like CRP with my name after it. So [ fair enough ]. Thank you.
Thank you. Ladies and gentlemen, we have reached the end of the question-and-answer session. I will now hand over to Michael Rowe for his closing remarks.
Thank you, operator, and thank all of you for joining us today, and that concludes today's call. We are very pleased with the year we have had so far, and we are excited to close out 2023 with strong momentum.
So thank you again for joining us. We look forward to our full fiscal year update in March or April of next year.
Thank you. Ladies and gentlemen, that concludes today's event. Thank you for joining us, and you may now disconnect your lines.