Thank you all for joining us on today's conference call to discuss EyePoint Pharmaceuticals' third quarter 2020 financial results and recent corporate developments. With me today is Nancy Lurker, President and Chief Executive Officer, Dr. Jay Duker, Chief Strategic Scientific Officer, and Scott Jones, Chief Commercial Officer. Nancy will begin with a review of recent corporate updates. Dr. Duker will then discuss pipeline developments for EYP-1901, Scott will comment on recent progress made on our commercial activities. I will close with commentary on the third quarter 2020 financial results. We will then open up the call for your questions, where we will be joined by Dr. Dario Paggiarino, Senior Vice President and Chief Medical Officer. Earlier this morning, we issued a press release detailing our financial results as well as commercial and operational developments.
A copy of the release can be found in the Investor Relations tab on the corporate website, www.eyepointpharma.com. Before we begin our formal comments, I'll remind you that various remarks we will make today constitute forward-looking statements for the purposes of the safe harbor provisions under the Private Securities Litigation Reform Act of 1995. These include statements about our future expectations, clinical developments, and regulatory matters and timelines, the potential success of our products and product candidates, financial projections, and our plans and prospects. 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 most recent annual report on Form 10-K, which is on file with the SEC and in other filings that we may make with the SEC in the future.
Any forward-looking statements represent our views as of today only. While we may elect to update these forward-looking statements at some point in the future, we specifically disclaim any obligation to do so, even if our views change. Therefore, you should not rely on these forward-looking statements as representing our views as of any date subsequent to today. I'll now turn the call over to Nancy Lurker, President and Chief Executive Officer of EyePoint Pharmaceuticals.
Thank you, George. Good morning, everyone, and thank you for joining us. I'm encouraged by our third quarter revenue results, driven by a return of customer demand despite the COVID-19 pandemic and the country still not being fully open. We fully recognize that there is more work to do to get our commercial business back on an accelerating growth trajectory, and we're working hard to make that happen while operating within the safety constraints of a national pandemic. We have made significant progress since the pandemic caused the country to lock down in March, as evidenced by the following key events. Customer demand for DEXYCU is up over 120% in Q3 over Q2 for 2020. Customer demand for YUTIQ is up over 5% in Q3 over Q2 for 2020.
Of note, YUTIQ never saw the significant decline in Q2 customer demand that DEXYCU experienced due to COVID-19, the increase quarter-over-quarter is modest. We have added multiple new contracts with ambulatory surgery centers and integrated healthcare networks for DEXYCU, which should lead to increased orders over the coming quarters. We signed an important commercial alliance agreement with ImprimisRx in August, which has more than doubled the field force calling on physicians and ASCs for DEXYCU. We expect this to begin having a positive order volume impact over the coming quarters as field and ASC training efforts roll out. We expanded our YUTIQ field force from 10 to 16 over the course of 2020 and began calling on retinal physicians in addition to uveitis specialists who also treat posterior segment uveitis.
In August, we expanded our license agreements with Ocumension Therapeutics for YUTIQ and DEXYCU to also include South Korea and other jurisdictions across Southeast Asia. We have completed our GLP toxicology study for EYP-1901, our lead development candidate for wet age-related macular degeneration, or wet AMD, and we remain on track for filing our IND later this year with the goal of starting our phase I in early 2021. We amended our loan agreement with CRG to waive the 2020 net product revenue covenants and lower our 2021 net product revenue covenant with no additional incremental charges in connection with this amendment. We continue to manage our cash and burn, and as of October 31st, 2020, cash and cash equivalents totaled $30.5 million.
The increase in cash was driven in part by the purchase of approximately $5 million of common stock through our ATM facility by an established institutional biotech investor to increase an existing equity position. While we have more work to do, I am pleased with the commercial pipeline and operational progress we've made despite the challenges of the COVID-19 pandemic on our business. We are working diligently to ensure that we continue to drive revenues, manage our cash, move EYP-1901 forward, and ensure we have the capital to execute on these objectives. Turning specifically to our third quarter performance, driven by the very positive sequential quarterly increase in underlying customer demand, we reported total net revenues of $15.7 million, including net product revenue of $5.8 million, with $3.5 million for YUTIQ and $2.3 million for DEXYCU.
These results are encouraging as underlying customer demand is approaching pre-COVID-19 pandemic levels. We are actively monitoring COVID-19 cases across the U.S. to ensure we are complying with health and safety guidelines while continuing to call on our valued customers virtually and in person when appropriate, and providing much needed access to our ocular products.
Turning to our pipeline, our team has continued to advance our R&D programs, including the recent completion of the IND-enabling preclinical GLP toxicology study for EYP-1901 on schedule. We plan to file our IND before year-end and dose our first patient in the first quarter of 2021, assuming the FDA allows our IND, with initial human data potentially available in the fourth quarter of next year. EYP-1901 is our potential six-month sustained delivery intravitreal anti-VEGF treatment being developed for wet AMD, with potential expansion into other retinal disease that represents a $13.1 billion global anti-VEGF market.
We're very excited about the potential for EYP-1901, as there is a significant need for extended treatments for patients to avoid frequent, often monthly eye injections for the rest of their lives. We remain focused on managing our balance sheet and our cash position. In August, we extended our exclusive license agreements with Ocumension Therapeutics for YUTIQ and DEXYCU to include additional markets in Asia. Under the extended agreements, we received a one-time $9.5 million payment from Ocumension for rights to commercialize both products under their own brand names in South Korea and other jurisdictions across Southeast Asia, and as a full and final payment of all milestones, but with royalties based on future sales still remaining payable to EyePoint. We're very happy to continue our work with Ocumension to bring our innovative products to the Asian markets.
Based in part on the promising customer demand trends seen this quarter, we were able to amend the existing debt facility with our partner CRG, resulting in a waiver of the net product revenue covenant for the 12-month period ending on December 31st, 2020, and a reduction of the fiscal year 2021 net product revenue covenant to $45 million from $80 million without additional charges to our company. We appreciate the continued support of our partners at CRG, who support our belief in the outlook for our products. As we approach the end of a challenging 2020, we remain focused on driving revenues of YUTIQ and DEXYCU and advancing EYP-1901 along its development plan while continuing to operate in a cost-efficient manner.
I'll now turn the call over to Dr. Jay Duker, our Chief Strategic Scientific Officer, to provide an update on our lead development candidate, EYP-1901, as well as other pipeline initiatives. Jay?
Thank you, Nancy, and good morning to all. Following the completion of the preclinical GLP toxicology study of EYP-1901, our team is actively working on completing and filing an IND application with the U.S. Food and Drug Administration in the coming weeks. EYP-1901 combines our bioerodible Durasert technology with vorolanib, an anti-VEGF tyrosine kinase inhibitor molecule, and is being advanced as a potential six-month sustained intravitreal treatment for wet AMD. Wet AMD is a progressive, debilitating ocular disease and despite several FDA-approved medications, remains a leading cause of blindness. There's a significant need for longer-lasting therapies to replace the relatively short duration of action of the currently approved anti-VEGF medications. This short duration of action, typically between one and two months, places an enormous burden on patients, families, providers, and the healthcare system.
Vorolanib has established efficacy signals observed in two prior human trials in wet AMD as an orally delivered therapy. Data from the prior phase II trial of oral vorolanib demonstrated a decreased intravitreal anti-VEGF injection burden and a longer time to first treatment as compared to placebo. A small portion of patients in each dose group did not require another anti-VEGF injection after screening and initiation of oral therapy. I will note, though, that this trial was prematurely stopped due to gastrointestinal and hepatobiliary toxicity signals. However, no significant ocular adverse events were observed during this trial or the previous phase I trial.
We believe that by placing vorolanib in our bioerodible Durasert technology to locally deliver the drug to the posterior segment via sustained zero-order kinetics will be comparable or could even improve the results observed for the oral delivery of vorolanib without the systemic toxicities associated with oral anti-VEGF treatments. Durasert has demonstrated its safety in thousands of patients in four FDA-approved sustained release ophthalmic products, including our own YUTIQ, and its bioerodible construct has no new excipients from the non-erodible construct. Preclinical studies of EYP-1901 administered into the eye have shown promising anti-VEGF activity with no serious safety issues observed.
Upon IND allowance by the FDA, typically 30 days, assuming no FDA questions, we plan to initiate an open-label dose-escalating phase I study of EYP-1901 in approximately 20 patients with wet AMD that were previously responsive to anti-VEGF therapy. The primary endpoint of the study will be safety, with important secondary measures of best-corrected visual acuity, central subfield thickness, and the need for rescue anti-VEGF injections using approved medications. Patients will be dosed at one of four dose levels of EYP-1901 one to two weeks after their last anti-VEGF injection, and then followed for 12 months, with the six-month time point being the key data readout. We look forward to rapidly initiating this study and dosing our first patient early in 2021. We believe EYP-1901 has the potential to be a disruptive and enormously beneficial option for patients and physicians for the long-term treatment of wet AMD.
EYP-1901 also has potential utility for the treatment of diabetic retinopathy and retinal vein occlusion, and we anticipate pursuing these in the future. For our other pipeline initiatives, we are looking at pathways to advance YUTIQ 50 into the clinic, and we are assessing additional pipeline expansion opportunities using our Durasert technology, along with potential product and technology in licensing. We look forward to keeping you updated on these initiatives as we progress them forward and into the clinic. I will now turn the call over to Scott Jones, Chief Commercial Officer, for the commercial update. Scott?
Thank you, Jay. Let me first echo the comments Nancy made at the beginning of the call on encouraging customer demand trends during the quarter for both YUTIQ and DEXYCU. These trends are the result of many factors, including our successful contracting efforts with larger ASC chains, more and more healthcare facilities resuming operations, thus allowing more patient treatments, as well as our ongoing product education initiatives. Let me begin with YUTIQ for chronic non-infectious uveitis affecting the posterior segment of the eye. Customer demand for YUTIQ was approximately 450 units in Q3 compared to approximately 430 units in Q2, driven by increased patient office visits in the period. Our YUTIQ commercial efforts continue to include in-person and virtual engagements focusing on the long-acting advantages of YUTIQ, especially during the COVID-19 pandemic, as we work to expand our reach into the retinal disease market.
In addition to providing steady and consistent anti-inflammatory control, YUTIQ can potentially reduce the frequency of patient office visits during the treatment, which continues to be a benefit during the COVID-19 pandemic. Our medical affairs team continues to seek opportunities to highlight YUTIQ in medical meetings, including the upcoming virtual AAO meeting. Let me now turn to DEXYCU for postoperative inflammation following cataract surgery. Customer demand for DEXYCU was up significantly over Q2, with approximately 4,700 units in Q3 compared to approximately 2,100 units in Q2. The advantages discussed with YUTIQ in the COVID-19 environment also apply to DEXYCU, as treating physicians have appreciated DEXYCU's extended duration therapeutic treatment from a single injection. We have continued to execute on our goal of securing additional contracts and volume-based agreements with ASCs and integrated healthcare networks to expand DEXYCU access for patients.
We recently secured agreements with Vantage Outsourcing and a large ASC chain to bring DEXYCU to more ASCs and their patients. Additional negotiations are ongoing virtually and in person, and we hope to drive these conversations and new agreements forward in the coming months. I will note that DEXYCU progress seen in the third quarter resulted nearly entirely from the existing EyePoint team, as our new co-promotion agreement with ImprimisRx was signed in August, and their sales specialists and inside sales team was engaged in product training through September. We believe ImprimisRx is an ideal partner to help expand the commercialization of DEXYCU as we're able to leverage their existing infrastructure and relationships with ophthalmologists, hospitals, and ASCs. ImprimisRx is now marketing DEXYCU as a top priority product and will initially focus on leveraging their established customers to develop DEXYCU trials.
EyePoint continues to retain responsibility for our internal sales and marketing teams, along with pricing, manufacturing, and contracting. Together, we hope to transition the cataract market to DEXYCU from the burdensome steroid eye drop regimen. We expect to see an impact on customer demand beginning in the fourth quarter from the ImprimisRx commercial alliance. While we are encouraged by the improving customer demand for both products during the third quarter, sustained growth will depend on the continued easing of restrictions surrounding the COVID-19 pandemic in various U.S. regions and the return of patients for these procedures. Given the unclear trajectory of the pandemic and governmental response, it's difficult to project customer demand and revenue for the coming periods, but we are optimistic on trends from the third quarter.
We will continue to move our efforts forward virtually and in person when able to bring our products to patients in need. I would like to recognize and thank our commercial organization for their dedication and efforts through this changing and challenging market. I will now turn the call over to George to review the third quarter financials. George?
Thank you, Scott. As the financial results for the three months and nine months ended September 30th, 2020, were included in the press release that was issued this morning, I'll focus my comments today on a high-level overview for the quarter. For the three months ended September 30th, 2020, total net revenue was $15.7 million, compared to $2.5 million for the three months ended September 30th, 2019. Net product revenue for the three months ended September 30th, 2020, was $5.8 million, with $3.5 million for YUTIQ and $2.3 million for DEXYCU
Compared to net product revenue for the three months ended September 30th, 2019, of $1 million, generated primarily by DEXYCU. Please note that the net product revenue represents product purchased by EyePoint's distributors, whereas customer demand represents purchases of product by physician practices and ASCs from EyePoint distributors. Net product revenue from licenses, royalties, and collaborations for the three months ended September 30th, 2020 totaled $9.9 million, compared to $1.5 million in the corresponding quarter in 2019. This was driven by payments associated with the expansion of our license agreement with Ocumension for additional markets in Asia. Operating expenses for the three months ended September 30th, 2020 were $17.7 million versus $16.6 million in the prior year period.
This increase was driven by a $1.6 million increase in cost of sales, a $1.4 million increase in G&A expense, and a $0.6 million increase in R&D expense, being offset by a $2.5 million reduction in sales and marketing expense. Non-operating expense net for the three months ended September 30, 2020 totaled $1.8 million of net interest expense. Net loss for the three months ended September 30, 2020 was $3.8 million, or $0.03 per share, compared to a net loss of $15.6 million or $0.15 per share for the prior year quarter. Cash and cash equivalents at October 31, 2020 totaled $30.5 million, compared to $28.7 million at September 30, 2020, and $22.2 million at December 31, 2019.
We expect that our cash on hand and projected cash inflows from anticipated YUTIQ and DEXYCU product sales, licensing and research collaboration transactions, along with additional anticipated financing activities, can fund the company's operating plan into 2021. Given our current assumptions for the extent of the COVID-19-related closures in various regions across the U.S., our careful management of cash should enable us to achieve some important catalysts, including the filing of the IND with the FDA for EYP-1901 and the initiation of the phase I study. We continue to evaluate and pursue non-dilutive sources of capital, including ex-U.S. out-licensing opportunities for our commercial products and delivery technologies. I now turn the call over to the operator for questions.
As a reminder, ladies and gentlemen, if you have a question at this time, please press star then the number one on your touch-tone telephone. If your question has been answered and you wish to remove yourself from the queue, please press the pound key. Please standby while we compile the Q&A roster. Our first question comes-
Okay. I was wondering, regarding your commercial alliance with ImprimisRx, are you seeing an initial expansion of product reach considering this company is prominently marketing their telemedicine platform?
Yeah. Actually, you know the company well. Very good question. We are, we've more than doubled our field force. It does take time for the new sales representatives, both whether it's in person or tele-detail, to educate the Ambulatory Surgery Centers, get the surgical suite trained, and then have them submit for reimbursement. That we've always said you won't see the productivity really kick in for two to three quarters. I will say that we are starting to see orders now coming in from that ImprimisRx sales team, though.
All right. That's very encouraging. Thanks for taking my questions.
You're welcome.
Once again, ladies and gentlemen, if you have a question at this time, please press star and the number one. Our next question comes from the line of Andrew D'Silva with B. Riley. Your line is open.
Hey. Good morning. Thank you for taking my questions. Just a couple of quick bookkeeping ones to start. If you could just let me know what the CapEx and stock-based comp were for the quarter. While that's being pulled, if someone could just answer, I'm just curious on a couple of dynamics with DEXYCU. Are you now just ubiquitously including that agitation system to all centers that are expected to start selling the product? Do you believe that that's starting to bridge the proper utilization gap relative just to the handshaking? Just more on the regulatory standpoint, related to physician monetization front, from a pass-through standpoint, where are we on a potential extension? Where are you in initiatives to actually get a product-specific-injection reimbursement established?
Andy, that's a lot of questions, but thank you. Okay, I've got them all down. While George is coming up with the CapEx and options. You had one question which is pertaining to what we call our vortex. For those listeners on the call, you have to shake the suspension of DEXYCU before you administer it, because it does separate in the pre-supplied vial. It's important that it's well-shaken. We've now put into all our offices, the answer is yes, it's an automatic ultrasound spinner, which in 30 seconds, as opposed to actually, no, it takes five seconds as opposed to having to shake it for a bit. You now get consistent suspension just by hitting that ultrasound shaker for about five seconds. The answer is yes, that is helping a lot. We're pleased with that.
The second thing is we've also, not only do we have that, but we've also implemented a few other things to make it easier for the offices and the ASCs so that they call it a pearl at the bottom of their eye. We now have that addressed and making sure that we try to get an injection code. I'm going to turn those questions over to Scott, our Chief Commercial Officer. He's leading those efforts.
Good morning. Thanks for the question. On the pass-through, we're still actively working on this. We do have, I think you've probably heard this before, but there is existing legislation which would give CMS authority to extend pass-through based on the public health emergency. Those bills are waiting. We hope that they could be included in an upcoming stimulus package if one does happen either this year or next. Related to the injection code, the professional fee for the injection code, we are in the process of putting our application together. That would be for an early 2021 deadline and meeting in 2021 with the expectation of a code in 2022. Again, that's the process that we're going through right now, and we will be filing that shortly.
Thank you. George, did you happen to find that CapEx and stock-based comp number for the third quarter?
Yeah. Andy, we'll file the Q, I think tomorrow. I think that in rough terms, our capital investment is under $200,000 year to date. We've been very tight with our spending, and that is largely driven on our expanded GMP facility here in Watertown, to manufacture both YUTIQ and EYP-1901. Stock-based comp is around $4 million year to date. That's a non-cash item.
Okay. That's perfect. Thank you. Just a couple more quick ones for me. Can you give us just a little bit more color around, or at least talk around what the commission or rev share is with ImprimisRx? I think last time you mentioned it was between 20% and 40%. If you could help narrow that down a little bit, it'd be quite useful in modeling.
Yeah, Andy, we can't disclose that. That's confidential. We're not at liberty to disclose that, certainly without ImprimisRx agreement. We're not gonna disclose that. Let me just continue to stress, it's at the market rate that you would see for a deal. We're not overpaying, but we wanna also make sure that we incentivize them to sell the product. They are ramping that up.
Okay. This last question is related to YUTIQ. You may have mentioned this, but it was a little bit choppy from a connection standpoint. Is stocking mirroring customer demand at this point? If you'd give any other just color around what you're seeing with just inventory levels and how you kind of see the year playing out with those dynamics that would be great. Thank you very much.
Yep, good question. We have definitely reached an equilibrium, and we're not seeing any more of the gyrations that we saw last year. We're very confident that what you're seeing, again, there's a delay between when the orders come in and how that flows through the distribution channel. We're seeing a consistent alignment between demand and what ultimately gets ordered by the distribution channel. That's what gets recorded as revenues. Right now, I would not expect that we would see any choppiness between those two, which is also why we're now disclosing customer demand. Again, I wanna caution everyone, you can't take the customer demand orders and just multiply that by our WAC and say, "That's what the quarter's going to look like," because you have a lag which goes on through the distribution channel.
As I said, the gap between what's in the distribution channel and what's coming in has narrowed substantially, and we don't see that changing.
Okay, wonderful. Thank you very much for taking my questions and best of luck at closing out the year.
Thank you.
Thank you. I'm not showing any further questions, so I now turn the call back over to Nancy Lurker, CEO, for closing remarks.
Yes, thank you everyone for taking the time to listen. I want to continue to stress that we are working very hard to ensure that we manage our cash, and that we minimize the need to continue to draw additional cash in. We're highly conscious of the fact that we want to make sure that we're driving revenues while we're advancing our pipeline and very, very tight cash management. We remain confident in our ability to hit our milestones going into 2021. Thank you very much, and look forward to continued discussions.
Ladies and gentlemen, this does conclude the program. Thank you for participating.