Good day, and welcome to the Quoin Pharmaceuticals third quarter financial results and business update conference call. All participants will be in a listen-only mode. Should you need assistance, please signal a conference specialist by pressing star, then zero. After today's presentation, there will be an opportunity to ask questions. To ask a question, you may press star, then one on a touch-tone phone. To withdraw your question, please press star, then two. Please note, this event is being recorded. I would now like to turn the conference over to Gordon Dunn, Chief Financial Officer. Please go ahead. Thank you, and good morning. We appreciate you joining us on today's conference call. With me on the call are Dr. Michael Myers, CEO, and Denise Carter, COO. We're pleased to provide an update on our progress for the third quarter of 2023, as well as discussing our Q3 2023 financial results. Please note that our operations and financial results press release is now available on Quoin's website. In keeping with our normal procedure, Michael will first provide an operations update, following which I will review our financial results. I'll then hand the call back to Michael for closing comments before we open the phone lines for questions. I'd like to remind everyone that statements made during this conference call will include forward-looking statements with a meaning of the Private Securities Litigation Reform Act of 1995, which involve risks and uncertainties that can cause actual results to differ materially from the information expressed or implied by these forward-looking statements. For more information regarding such risks and uncertainties, please see the risk factors outlined in the company's filings with the SEC. Any forward-looking statements are made only as of today, and we disclaim any obligation to update these forward-looking statements other than as required by law. Please see the forward-looking statement section in our financial results release issued this morning for more information. It is now my pleasure to turn the call over to our CEO, Michael Myers. Thank you, Gordon, and good morning, everyone. During this past quarter, we continued to make significant progress across multiple fronts, culminating in the release of additional positive clinical data for QRX003 from our ongoing open label clinical trial in Netherton Syndrome after the quarter ended on October 24. I will spend some time discussing this data, as well as our newly updated and optimized clinical plans for QRX003, which we are now pursuing as a result of this positive development. We believe that these planned protocol amendments will result in an even more robust clinical data set and potentially lead to a faster and possibly wider initial regulatory approval for the product. During the quarter, we entered into our ninth commercial partnership for QRX003, with the signing of an agreement with Pharma Mondo for Singapore. This new agreement increases the number of countries that we have entered into commercial partnerships for the product to 61. Furthermore, we are currently in late-stage discussions to enter into similar partnerships for additional countries in Southeast Asia and Latin America. This diligent and systematic approach to entering into commercial partnerships is entirely in keeping with our spoken mission to ensure that QRX003 will be made available to as many patients in as many countries as possible, once approved. As noted previously, these partnerships, along with our own planned commercial infrastructure for the U.S. and Europe, will facilitate what will effectively amount to a global launch of the product once approved, and also lay the foundation for similar global launches of our pipeline products once they also receive regulatory approval. We firmly believe that this global commercial network is unprecedented for a company our size and represents a highly differentiated and perhaps somewhat underappreciated advantage for Quoin. The potential incremental revenue-generating opportunity that this global commercial partnership network represents for our company, all of which will effectively fall to the bottom line, could ultimately be highly significant for the company and have a materially positive impact on our future profitability. During our last call, I also updated everyone on our M&A strategy. As discussed, given our strong balance sheet and potential access to additional capital, we have been acutely focused on expanding our product portfolio via acquisition, licensing, or other means. Following an extensive and broad-based process throughout this year, where we assessed well over 20 different opportunities, during the past quarter, we successfully narrowed that list down to three specific products for which we ultimately reached agreement on all key financial terms. As we have stated previously, while there can be no guarantees that a transaction will be consummated as there are external impacting factors, in particular, current market conditions, which, to say the least, are decidedly unfavorable, we are actively working towards closing out at least one transaction as expeditiously as possible.... While I'm not in a position to provide any specific details, I can tell you that all three assets are rare disease products that would strongly complement and enhance our current product portfolio. We hope to provide additional information on these opportunities in due course. I do wanna make one key point clear, however, we do not intend to close out any such transaction unless and until we have clear visibility on our ability to raise the necessary funds to fully support the clinical development of these assets. The last thing that we will do as a company is to acquire or license assets for which we cannot fund the clinical development of. As we have now stated on previous calls, another company has filed an IND with the FDA and received a Study May Proceed Letter to initiate the clinical development of their product as a potential treatment for Netherton Syndrome. As of this morning, following a review of the ClinicalTrials.gov website, it appears that this study still has not been initiated, and Quoin remains the only company to be actively conducting clinical studies in Netherton Syndrome under an open investigational new drug application, or IND. Furthermore, while other companies have also spoken for some time, either about filing INDs or initiating Netherton Syndrome clinical studies under open INDs, we continue to see a consistent pattern of those timelines being pushed further and further out, or indeed, being abandoned completely. As we continue to make significant progress on the clinical front ourselves, we and our now nine global marketing partners, are more excited than ever by the potential commercial opportunity that of what could be the first regulatory approved product for this horrendous disease. As we have consistently stated, Quoin, unlike many of our biotech peers, focuses not only on the clinical aspects of product development, but also on the CMC side of development as well. I'm pleased to announce today that our contract manufacturer, or CMO, for the active ingredient in QRX003, has successfully developed and scaled up a new and fully GMP manufacturing process for the drug substance. You may recall that the active ingredient in QRX003, although a very well-characterized molecule, has never been approved as a drug for any indication, and that there has been no source of GMP quality material previously available. As a result of this successful collaboration with our CMO, that is no longer the case, and the availability of fully GMP material from a scaled-up manufacturing process for the active ingredient, represents yet another positive step forward in the development of our product. Bear in mind, that this source of GMP material is exclusively contractually available to Quoin only. We are also actively exploring whether new intellectual property may be developed from this exciting development. Turning now to our ongoing clinical studies in Netherton Syndrome patients. On October 24th, we announced the release of positive clinical data from our single-arm open label study. This data was from the first six evaluable subjects in the study. As outlined in our press release, on that date, the data was positive across several measured endpoints. Recall, that in this open label study, subjects are currently receiving off-label systemic treatment and will continue to do so in conjunction with QRX003 for the duration of the study. It is worth noting that all subjects in this study have been treated with this off-label systemic therapy for at least one year, and in a number of cases, for multiple years. Notwithstanding this ongoing and long-term systemic therapy treatment, all patients recruited into the study exhibited clear signs of Netherton Syndrome at the point of entry into the study, including compromised skin and significant pruritus or itch. As a result of this long-term systemic therapy, subjects recruited into the study provided a natural baseline for us to assess if treatment with QRX003 over a duration of 12 weeks would lead to any therapeutic improvement across a number of clinical endpoints. As reported, for five of the six subjects, their pruritus or itch was either absent or negligible according to the standardized scoring system after treatment with QRX003. Absent or negligible pruritus is defined as a 0 or very low single-digit score in a 0 to 10 scoring range... for the sixth subject, their pruritus was effectively unchanged from baseline on completion of the study, possibly reflecting a not uncommon refractory nature of the pruritus associated with this disease in their particular case. We are extremely pleased with these results, as pruritus can be extremely distressing and debilitating for Netherton patients. What is particularly noteworthy is that despite receiving long-term off-label systemic therapy, all 6 subjects were experiencing significant pruritus at baseline, and for 5 of those 6, that pruritus had largely disappeared following treatment with QRX003. In addition, all 6 subjects evaluated demonstrated an improvement in skin appearance according to the investigator's scoring system. For three of the six patients, there was a well-defined improvement in skin appearance according to this endpoint on completion of dosing with QRX003, while for the other three subjects, there were signs of improvement in skin appearance at various points throughout the study, though not necessarily on completion of testing. This is potentially further important evidence of the possible efficacy of QRX003 as a treatment for NS. Importantly, also, all six subjects expressed satisfaction with QRX003 across a number of assessed metrics, leading to a positive overall experience with the product. As you know, QRX003 is an easily applied and user-friendly topical lotion, which makes it attractive to use for patients and caregivers. Finally, and also importantly, there were no significant adverse events reported throughout the study, and the overall safety profile of QRX003 to date is extremely favorable and highly suggestive of a potentially safe treatment for this disease. Taken together, the body of clinical evidence generated to date from both an efficacy and a safety perspective, has led to a number of exciting developments for our two ongoing clinical studies. Enabling us to move into an optimization phase, which we believe may ultimately result in an even more robust and diverse data set and potentially to a faster approval for the product. These new developments have been submitted to our open IND for QRX003, and I will now provide some details of these planned protocol amendments. One such amendment is the elimination of the lower 2% dose from our double-blinded study. This decision was based on the very clean safety profile observed to date for the higher 4% dose across both studies. Going forward, the double-blinded study will now comprise of the higher 4% dose and a placebo, and as such, will become a 2-arm study instead of the current 3-arm study that it is. In addition, with a view to maximizing the potential clinical performance of QRX003, we are modifying the dosing frequency of the product from once daily to twice daily across both studies. Again, based on the body of clinical evidence generated to date, in conjunction with the very clean safety profile observed so far, we believe that twice-daily dosing of the product has the potential to deliver a more robust clinical evidence of efficacy across all measured endpoints. Finally, the number of subjects in the open-label study will be increased from the current 10 to 20, with all new subjects being tested with QRX003 dosed twice daily going forward. For the blinded study, the number of subjects to be enrolled will be increased from the original 18 to 30, and going forward, this will be a two-leg study with QRX003 at a 4% dose tested against a placebo, with both test materials now being applied twice daily. This now means that both studies will each have a cohort of subjects dosed once daily and a second cohort dosed twice daily, enabling us to evaluate if increasing the frequency of dosing does indeed lead to an incremental therapeutic benefit for subjects in the studies. We are very excited about these new developments in our clinical programs, and as discussed, we believe these protocol amendments may ultimately result in a faster approval for QRX003 in Netherton Syndrome and with a more compelling data set. With that update on our operational progress, I will now ask Gordon to discuss our third quarter financial results. Gordon? Thank you, Michael. As of September 30th, our cash and marketable securities was approximately $14 million compared to $15.4 million as of June 30, which we expect will be sufficient to fund our operations through the end of 2024. Our operating loss for the third quarter was $2.1 million, compared to $2.3 million for the third quarter of 2022. The decrease was primarily due to lower professional fees and other general and administrative costs in the quarter. I'll now turn the call back to Michael to make some closing remarks and begin our Q&A. Thank you, Gordon. We are entering a very exciting period for Quoin. Based on the positive clinical data reported recently, we are making a number of protocol adjustments to our ongoing clinical studies, which we believe may lead to a more rapid approval with a broader and more robust data set. In addition, following a thorough process throughout the year, we have identified and agreed financial terms for the acquisition or licensing of a number of exciting new assets in the rare and orphan disease space that we believe could be highly complementary to our current development portfolio. While we are diligently working on finalizing at least one transaction as soon as possible, there can be no assurances that this will actually occur, as we will only close out any deal if we can raise the incremental funds required to complete the clinical development for that asset. We intend to use our current funds primarily to advance the development of QRX003 and our other pipeline products only, and the development of any additional products will need to be funded by new capital. We believe that in these highly challenging market conditions, such prudent use of our cash resources must remain a key priority for the company as we head into 2024. With that, operator, we are now ready for questions. Thank you. We will now begin the question-and-answer session. To ask a question, you may press star then one on your touchtone phone. If you're using a speakerphone, please pick up your handset before pressing the keys. If at any time your question has been addressed and you would like to withdraw your question, please press star then two. At this time, we will pause momentarily to assemble our roster. Our first question comes from James Molloy with Alliance Global Partners. Please go ahead. Hey, guys. Good morning. Thank you for taking my questions. I had a question on the changes to the phase 2/3 trial from 10 to 20 and from 2 arms to 1 arm and changing the doses. I think expectations are for mid-2024 data. Does this change the expectation for being able to file potentially should the data, you know, bear up based on this trial in say late 2024? Hi, James. So thanks for the question, and thanks for participating. We don't believe there's gonna be any material change to the timelines. It doesn't affect the pace at which data will be released, but overall, we believe we remain on track, and possibly able to speed up the approval of the product. So these developments are positive overall. Oh, great. Thank you. And then, on the timing of. I know, bringing in this, the one transaction that you see you're very close on, can you walk through again, presuming, and you mentioned you'd only bring it in if you could raise the funds to do so. Can you walk through, in an ideal world, when you would like to bring that in, and how much you think it would take, you need to raise to run, to get that through clinical trials? Yeah. So I'm not going to get into any details, James, about how much it would take to complete the clinical development of the product on this call. In an ideal world, I would like to get this closed prior to the end of the year. We are, as you well know, we're not living in an ideal world at the moment, so we're. I can't really give a timeline. I can just say, look, we have agreed financial terms that we believe are favorable to Quoin, so we're excited about that. And we think this asset has potential to be a very significant commercial product once approved. But there are other factors at play here that are somewhat outside of our control. So we will remain diligent, but we will remain focused on ensuring that we don't put ourselves in a position where we bring in a new asset, and it has to sit on our shelf because we can't fund the development of it. So I would ask you to be patient, and hang in there as we work through the process. Absolutely. Maybe last question to you. Any updates? I know you're focused, obviously focused and correctly so on QRX003. Any updates on QRX004, QRX007, QRX008, for the other various early stage programs, or are those sort of on hold for the now, for the nonce? So QRX004, which you know, is our program for EB, remains on hold as we continue to evaluate the commercial opportunity for our product. There has been developments in this space in the past year. There's been approval here in the U.S. There was a product that was approved in Europe, though rejected in the U.S., and there are some other pivotal data that should come out in the next several months as well. So we remain vigilant, we remain watchful, but not putting any resources into that at this point. QRX007 and QRX008 continue to make progress with our partnership with Queensland University of Technology in Australia. As we've said for quite some time now, these are early-stage programs, and on a different trajectory than zero three, but we believe ultimately they, they could be important contributors as well. So, moving forward, but as I said, at a different pace than zero three. Great. Thank you for taking the questions. Thanks, Jim. Again, as a reminder, if you have a question, please press Star, then one to be joined into the queue. The next question comes from Michael Marin with Ladenburg Thalmann. Please go ahead. Thank you. So the clinical data, you've done a very strong job in securing distribution. As you said, you have nine agreements in place. The clinical data that you've reported, do you expect that this will accelerate conversations with other potential distribution partners? Great question. So thank you for asking, Erin. Potentially, yes. Look, we receive a lot of inbound interest regarding this product. You know, we've consistently said, look, we will commercialize ourselves in the U.S. and Europe, but still there's a lot of interest from companies who have an established infrastructure, and like where the product is going. So I think you're right. It will increase interest. We're hoping that interest will be in countries where we haven't partnered. Though, to be honest, there aren't that many of them left at this point. So I think the short answer is yes. Okay. Thank you. Our next question comes from Dennis Palumbo with Ladenburg Thalmann. Please go ahead. Hi, good morning, gentlemen. Thank you for taking my question. My first question, I'm sure you guys have got, you know, done some back-of-the-envelope math and, you know, figured out some price points. Could you, could you tell us a little bit about your total addressable market, the TAM, for the, for the NS product? Yeah. Hi, Dennis. Thanks for the call. Hi. Nice to talk to you again. So we believe, combined in U.S. and Europe, there's probably somewhere between 7,000-8,000 patients. And in the countries that we've partnerships, there's probably an additional 10,000-15,000. The numbers are difficult to come by, as I'm sure you know, 'cause this is a very rare disease, and diagnosing it, it can be challenging, but these are numbers that we feel pretty confident with. In terms of price point, we haven't drilled down to a point where I'm comfortable saying, you know, giving you an exact number, but the opportunity here, we believe, is substantially in excess of $500 million in total and could be significantly higher. Wow! That's a pretty strong number. And my last question is, you know, you were talking about acquiring another, some more assets for another company. You know, right now, with your company trading for $0.30 on the dollar for your cash, how are some companies not knocking your door down, trying to get you guys to buy you guys up? I mean, rare disease drugs aren't easy to come by, especially you're so far down the pipeline compared to your competitors. Another great question, and one I can't really provide any details on, but I think you, you've hit the nail on the head. People are looking at this company, see what we're doing. But look, we are just focused on what's in front of us. We believe we have a great asset. We're looking to add to that asset with additional products, and we will continue to deliver. Whatever conversations come our way, we have a board of directors to address that. So, okay. Yeah, that much makes sense. I mean, so if offers are coming in, you guys are looking at them. Not going to comment, but, you know. I think you can see where we're going. Yeah. Yeah. No, I appreciate it, and you guys are just so undervalued, it's ridiculous. I mean, you're getting the pipeline for free, and like I said, getting all your cash for 30 cents on the dollar makes very little sense. Anyway, thank you, and have a great day, and look forward to some updates. Thanks, Dennis. Take care. With no more questions, this concludes our question and answer session. I would like to turn the conference back over to Michael Myers for any closing remarks. Yeah. So just to say thanks to everybody for participating here today. As always, we are readily available by phone, email. If there are any follow-up questions or concerns, we'd be happy to address them. Other than that, have a great day, and thanks again. The conference has now concluded. Thank you for attending today's presentation. You may all now disconnect.