Good morning, ladies and gentlemen, welcome to the Fennec Pharmaceuticals Q2 2023 Earnings and Corporate Update conference call. At this time, all participants are in a listen-only mode. Later, we will conduct a question and answer session, instructions on how to participate will be given at that time. To ask a question during the session, you will need to press star one one on your telephone. You will hear an automated message advising your hand is raised. To withdraw your question, please press star one one again. As a reminder, today's conference call is being recorded. Now, I would like to turn the conference over to Fennec's Chief Financial Officer, Robert Andrade. Thank you, operator. Good morning, everyone. We are delighted that you could join us today for Fennec Pharmaceuticals Q2 2023 earnings conference call, during which we will review our financial results as well as provide a general business update. Joining me from Fennec this morning is Rosty Raykov, our Chief Executive Officer, and our newly appointed Chief Operating Officer, Adrian Haigh. Before we begin, I would like to remind you that during this call, the company will be making forward-looking statements that are subjects to risks and uncertainties that may cause actual results to differ from the results discussed in the forward-looking statements. References to these risks and uncertainties are made in today's press release and disclosed in detail in the company's periodic and current event filings with the U.S. Securities and Exchange Commission. In addition, any forward-looking statements made on this call represent our views only as of today and should not be relied upon as representing our views as of any subsequent date. We specifically disclaim any obligation to update or revise any forward-looking statements. This conference call is being recorded for audio rebroadcast on Fennec's website, www.fennecpharma.com, where it will be available for the next 30 days. With that, I will now turn this call over to Rosty Raykov. Thank you, Robert, and good morning, everyone. We'll be discussing our recent progress as we have achieved many significant milestones over the past several months. The focus of today's call is to review updates on the ongoing launch efforts underway for PEDMARK in the US and discuss our global opportunities, including the recent approval in Europe. Further, we'll detail our Q2 financial results, all of which were outlined in our earnings press release issued this morning prior to this call. As a reminder, PEDMARK is the first and only FDA-approved therapy to reduce the risk of cisplatin-induced hearing loss in pediatric patients one month of age and older with localized, non-metastatic solid tumors. The availability of PEDMARK has ushered in a critical breakthrough for the pediatric oncology community, which was enthusiastically awaiting a rigorously tested and FDA-approved option to safely increase the potential long-term quality of life of these young patients. In June, we announced PEDMARQSI was granted marketing authorization by the European Commission. PEDMARQSI is the first and only approved therapy in the EU for prevention of hearing loss induced by cisplatin chemotherapy in patients 1 month to 18 years of age with localized, non-metastatic solid tumors. Further, PEDMARQSI was granted Pediatric Use Marketing Authorization, PUMA, which includes 8 years plus 2 years of data and market protection. In terms of our commercial strategy, we're pleased to share the results of the Q2, as we believe they underscore the growth potential of PEDMARK. We remain focused on executing the following: establishing PEDMARK as the necessary complement agent when prescribing a cisplatin-based therapy for a child with localized, non-metastatic solid tumor, minimizing the barriers to access and ensuring rapid responses to product questions, and establishing Fennec as a premier partner of choice among the pediatric oncology community. To help address these goals, we have established a best-in-class patient services and support offering called Fennec HEARS, which is a comprehensive single-source program designed to connect PEDMARK patients to both patient, financial, and product access support. In addition, we have built out a strong commercial team to execute US marketing, distribution, access, and launch of PEDMARK with a sales team that is highly focused on targeting the approximately 200 pediatric hospital centers, including COG, NCI, and NCCN institutions across the US that drive 80% of cisplatin use. More specifically, we're pleased with the Q2's double-digit growth in new pediatric hospital centers prescribing PEDMARK and the consistent repeat orders from existing accounts. We have had recent success in larger academic centers, including formulary approvals early in the Q3 at major pediatric hospital centers. As a reminder, early adoption has come from both major academic centers and regional practices. More recently, we have had adoption coming from some of the most recognized pediatric centers of excellence. Geographically, all of our territories have seen HCPs prescribing PEDMARK, and we have seen highly encouraging adoption within our target accounts that are increasing over time. In terms of patients, we have seen patient utilization across several tumor types, including hepatoblastoma, osteosarcoma, and germ cell tumors.... Given our broad and favorable payer coverage and streamlined reimbursement process, we have been successful in securing coverage for prescribed patients. We're pleased that the effort and execution of the team is starting to become evident in the 98% net revenue growth experienced in the Q2. We're continuing to execute against our strategic launch plans and are confident in our disciplined and targeted approach to building share within the US market. With regard to expanding in Europe, we announced in June the marketing authorization for PEDMARK, which will be marketed as PEDMARQSI. PEDMARQSI will be the first and only treatment approval in the European Union to address this area of significant unmet medical needs. We continue to evaluate the best commercial pathway for the company in Europe and the rest of the world, either go it alone or with a partner or both. Whatever pathway we select, we see Europe as another significant opportunity to create shareholder value. Finally, as announced today, I am very pleased to have Adrian Haigh join the executive management team of Fennec as Chief Operating Officer. Adrian has been a major contributor to Fennec's success since joining the board in 2014 and is part of the Fennec family. We are fortunate to have him available to help us at this pivotal stage in the commercial evolution of Fennec. Adrian comes to us from PTC Therapeutics, where his last role was Senior Vice President and Head of International. Prior to that, Adrian worked with our chairman, Dr. Khalid Islam, as Chief Operating Officer at Gentium, where he built and managed Gentium's commercial and medical affairs organization, and was also responsible for business development, playing a pivotal role in the sale of Gentium to Jazz Pharmaceuticals for $1 billion. Adrian, it's great to have you with us on this call. Can you give us a brief overview of the opportunity you see for Fennec, given your new role? Thanks, Rosty. I'm delighted to have been asked to join Fennec full-time as Chief Operating Officer. As many of you are aware, this has been quite a rollercoaster ride over the last 10 years. Through everything, we've remained laser-focused on our mission to ensure that all pediatric cancer patients at risk of hearing loss caused by cisplatin chemotherapy have access to PEDMARK. I left PTC at the end of last year after eight years building and leading the international commercial organization. Retirement was not for me, and I'm delighted that the board believes that my experience in leading global commercial teams, in generating significant pre- and post-approval sales, while at the same time evaluating all strategic options, is the skill set that Fennec needs right now. For example, at Gentium, the fact that we had a small commercial team in place across Europe with all the key HTA dossiers submitted are in preparation, combined with significant pre-launch revenue, that enabled us to generate considerable value for shareholders. Doing the same at Fennec will be a priority. Now that we have EU approval, work needs to be done and done quickly to ensure a speedy and successful launch, whatever strategic direction we ultimately take. Equally important is accelerating adoption of PEDMARK in the United States. As Rosty said, we've made considerable progress in the last quarter, we still need approval by a number of key pharmacy committees. Concluding these reviews and ensuring that PEDMARK is included as standard of care in all treatment protocols will be critical over the coming months. These will be my two priorities. Once again, it's a real pleasure to be a full-time executive team member, and I look forward to the next call, where we will provide further updates on our progress. With that, I'll now turn the call over to Robert to review our financial results for the quarter. Thank you, Adrian. Our press release contains details of our financial results for the Q2 of 2023, which can be viewed on the Investors and Media section of our website. Rather than read through all of those details, my comments today will focus on some key financial results. The company recorded net product sales of $3.3 million in the Q2 of 2023, versus $1.7 million in the Q1 of 2023, for a net revenue growth of 98%. As Rosty mentioned, we are pleased with the growing acceptance of Pedmark within healthcare providers during the Q2, and with the recent hospital formulary access approvals we have gained early in Q3. G&A for the Q2 of 2023 was $5.5 million, which compares to $4.4 million in the Q1 of 2023. The increase is largely attributable to non-cash employee remuneration. R&D expense is negligible, as the company reduced research and development costs when it received FDA approval of PEDMARK. The majority of traditional research and development expenses associated with PEDMARK are now recorded or capitalized into inventory and eventually recorded to cost of product sales. The company began recording selling and marketing expenses when it expanded its payroll to include an internal sales force. Selling and marketing expenses include distribution costs, logistics, shipping and insurance, advertising, wages, commissions, and out-of-pocket expenses.... The company recorded $2.3 million in selling and marketing expenses in the Q2 of 2023, compared to $2.5 million in the Q1 of 2023. Our GAAP net loss for the Q2 of 2023 was $5.4 million, or $0.21 per share, compared to a GAAP net loss of $5.0 million, or $0.19 per share. Finally, our cash position. We ended the Q2 with approximately $15 million in cash, cash equivalents, and investment securities. This includes $25 million of capital drawn in the Q2 under our existing Petrichor convertible debt facility. Our cash burn for the Q2 was approximately $3.4 million, compared to $5.5 million in the Q1 of 2023. As a reminder, we anticipate approximately $2 million in monthly cash operating expenses during 2023. We believe our available capital, when coupled with PEDMARK revenue assumptions, will take us out for at least the next 12 months. Operator, with that, we are ready for questions. Thank you. We will now conduct the question and answer session. As a reminder, to ask a question, please press star one one on your telephone and wait for your name to be announced. To withdraw your question, please press star one one again. Please stand by while we compile the Q&A roster. Our first question comes from the line of Chase Knickerbocker of Craig-Hallum. Your line is now open. Good morning, everyone. Thanks for the questions, guys. Maybe just concerning the ramp of accounts you have cleared P&T at, we're now on the tail of that six to nine-month period it takes to get through those P&T committees at the larger accounts. You know, good to hear about the account growth. Maybe putting a finer point on it. You know, of those 200 focus accounts we talk about, you know, what do you think your number of accounts is today or just general penetration there? You know, however you want to define it, I think just a finer point there would be helpful for investors. Hi, Chase. This is Rosty. Thank you for the question. We're shying away from giving details in terms of number of accounts. What I would say is that what we have at the moment is actually quite significant compared to where we were at this time last quarter. As I mentioned in my prepared remarks, the growth in accounts was double-digit. What's... This is prescribing accounts. In addition to that, we have had some major P&T wins in some of the most recognized and larger institutions in pediatric oncology. Hopefully, some of these accounts will be coming through this quarter. Again, that would, that would really help further with the double-digit growth. We still have significant opportunity ahead of us, as there are more P&T committees coming up. Got it. You know, maybe speak to the ongoing cisplatin shortages we're seeing in the US. You know, what are you hearing from customers? Do you think, you know, that's having any impact on your ramp at this point? No, that has not been. We have heard about the cisplatin shortages. They have been ongoing for the last at least 4 months. That has not been an issue in pediatric oncology. As you know, in pediatrics, there are not that many patients to begin with, and cisplatin is goes to those hospitals first. We actually, we're hearing a lot about melphalan shortages at the moment, but not cisplatin. Got it. Yeah, how should we be thinking about, you know, bringing Adrian Haigh on here in the COO role? You know, is this, you know, is the implication that, you know, Adrian Haigh has been playing a large role in partnership discussions in Europe, and thus, you know, it's kind of just cementing the role there? Or should we be thinking, you know, there's an increased appetite from you guys to maybe go it alone in Europe now, and, you know, Adrian Haigh, through his PTC experience, launching their international businesses, is obviously would be a good fit there, building those capabilities out? In our prepared remarks, well, you know, personally, I've known Adrian for over 10 years now, and we at Fennec, we're a small company. We work very, very closely with our board members. I'm very, very thankful that he was able to join us at this pivotal moment. As you could see from his resume, he has the necessary experience to help us with all of the above. This goes from from helping set the ground up for launch in Europe to overseeing the US sales organization and medical affairs, and access to partnering opportunities, both in Europe, globally or all of the above. Maybe, Adrian, you, you may, you may want to say a couple of things as well here. Yeah, yeah. Not, not a lot really to add. I think my, my experience is that, you know, I've. You know, this will be the 3rd time if we do build a commercial organization, that I've done it. I know how to do this. I know how to do it quickly, and I know how to do it at, you know, minimal cost. As, as Rosty said earlier on in the prepared remarks, you know, at, at Gentium, I was heavily involved in business development and ultimately in the sale of, of Gentium to Jazz. You know, dare I say, I think I tick all the boxes. As I said earlier, you know, the board believes- I'm the right person at the right time, and quite honestly, I was getting very bored in retirement and had been quite actively engaged with Fennec over the last couple of months, helping as a board member, and we all agreed, kinda makes sense for me to take on a full-time role. Yep, yep, that makes a lot of sense. Just last for me, I'll hop back in the queue, guys. Any kind of update on how we should be thinking about launch in Europe? You know, you know, whether or not it's, you know, on your own or, you know, with a partner. You know, how should investors be thinking about a potential launch timing there? Well, I think we're evaluating all options. I think a launch will be towards the end of the Q1 next year, but to enable that to happen, we have to do a lot of work. For example, you have to apply for a special license in Germany called the NUB license. That has to be submitted by the end of November. If that isn't in place, then there's no way that anybody can sell in Germany, in hospitals in 2024, and that requires quite a lot of preparation. We've also started the work preparing all the HTA dossiers for the key countries, and as you know, that doesn't happen overnight. It takes several months. We're, we're doing whatever it takes to ensure that when PEDMARK is launched, whether it's through, through Fennec or whether it's through some kind of a partnership, it's the most successful, speedy launch possible. Yep, got it. Congrats on the progress, guys, and great to have you on board, Adrian Haigh. Thanks. One moment for our next question. Our next question comes from the line of David Nierengarten of Wedbush Securities. Your line is now open. Hey, thanks for taking the question. I just had a couple, kind of on the penetration of the markets. First, have there been centers... I know, you know, thankfully, childhood cancer is a rare occurrence, but have there been any centers that have repeated, you know, or have, you know, repeat patient dosing of patients? Then on your coverage of the academic centers, do you have an estimate on how many patients utilize those centers, you know, as a percentage? You know, like, is it 40, 50, you know, 80%? Thanks. Hi, David. Yeah, maybe I can answer the second one first. Yeah, if you look at the centers overall, it varies. You have centers where the, the, the repeat customer orders, where they're utilizing, most physicians are utilizing it. There's some centers where half the physicians are utilizing it, so it varies. It's, it's sort of center by center, comfort by comfort, from physician to physician, disease by disease, of course, because our label plays into several tumor types. Their experience and the growth that we're seeing comes from, from really, writing scripts, putting patients on drug, and seeing the outstanding results, both from an efficacy perspective, but importantly, safety perspective, with this product. I mean, here we are, you know, almost 9 months into launch, and they, there hasn't been an A reported, which speaks to how good this drug is. Rarely would you see anything in pediatric oncology that, or any oncology product for that matter, that has that. That's what makes us very, very excited, because we, we have a really, really good treatment for these kids. Sorry, what was the first question again? I think the first question was actually on the repeat customers. The next one was the, you know, kind of the number of academic centers or, you know, the number of academic centers signed up and the, you know, percentage of patients, you know, typically that they treat in a year out of the total population. Yeah. -majority is 70% or something. Yeah, thanks. Yeah, it's like I said, it's pretty well distributed. Maybe, Robert, you have some great granularity on these numbers, but it's pretty well distributed between the academic centers and some of the smaller hospitals, which typically in the early launch tend to be some of the early adopters. Yeah, I'll, I'll, I'll add, David, similar to what Rosty said, every center is unique in the sense of the amount of patients, the type of patients it sees, and their philosophy on how, on how they, they, they roll out, whether before formulary approval or after formulary approval. You know, similar to what we said already, we have gained some major academic centers recently, and so we're, we're, we're quite excited about that, and anticipating some orders there. You know, hopefully as the months go out, we actually learn more from all our centers in terms of patient numbers, PEDMARK applicability. Thanks. Thank you. This concludes our question and answer session. I would now like to turn the conference back to Rosty Raykov. I would like to thank you all for joining us today. We look forward to updating you on our continued launch progress and corporate milestones in the future quarterly calls. Thank you and have a great morning. This concludes today's conference call. Thank you for participating. You may now disconnect.