Good afternoon. My name is Krista, and I will be your conference operator today. I would like to welcome everyone to the Jazz Pharmaceuticals Third Quarter 2023 Earnings Call. I will now turn the conference over to Andrea Flynn, Vice President, Head of Investor Relations. You may begin.

Thank you, operator, and good afternoon, everyone. Today, Jazz Pharmaceuticals reported its third quarter 2023 financial results. The slide presentation accompanying this webcast is available on the Investors section of our website. Investors may also refer to the press release we issued earlier today, which is also posted to our website. On the call today are Bruce Cozadd, Chairman and Chief Executive Officer; Renee Gala, President and Chief Operating Officer; and Rob Iannone, Executive Vice President, Global Head of R&D; Kim Sablich, Executive Vice President and General Manager, United States, will join the team for Q&A. On Slide 2, I'd like to remind you that today's webcast includes forward-looking statements, such as those related to our future financial and operating results, growth potential and anticipated development and commercialization milestones and goals, which involve risks and uncertainties that could cause actual events, performance and results to differ materially from those contained in these forward-looking statements. We encourage you to review the statements contained in today's press release, in our slide deck and in our latest SEC disclosure documents, which identify certain factors that may cause the company's actual events, performance and results to differ materially from those contained in the forward-looking statements made on today's webcast. We undertake no duty or obligation to update our forward-looking statements. Turning to Slide 3. On this webcast, we'll discuss non-GAAP financial measures. Descriptions of these non-GAAP financial measures and reconciliations of GAAP to non-GAAP financial measures are included in today's press release and the slide presentation available on the Investors section of our website. I'll now turn the call over to Bruce.

Thanks, Andrea. Good afternoon, everyone, and thank you for joining us today. I'll start on Slide 5. In the third quarter of 2023, we delivered strong commercial results, advanced multiple late-stage programs within our pipeline and maintained our focus on driving operational excellence. Our results for the quarter exemplified the successful execution that has led to an exciting transformation and diversification of our business across our commercial portfolio and R&D pipeline, and we remain well positioned to achieve Vision 2025. As we highlighted in today's press release, we've updated our 2023 guidance, raising our full year total revenue and oncology revenue guidance at the midpoint. And as our pipeline continues to advance, we are increasing our R&D guidance, primarily driven by investments in Zanidatamab development across multiple HER2-expressing cancers that we believe will allow us to deliver an important new therapeutic option with the potential to raise the standard of care for patients and create long-term value for Jazz. It's important to note that our disciplined approach to capital allocation has allowed us to invest in R&D as well as key commercial franchises, while remaining on track to deliver on our full year GAAP net income and non-GAAP adjusted net income guidance. With regard to our commercial business, we are seeing strong momentum across all three key growth drivers: Xywav, Epidiolex and Rylaze. Combined revenue from these products grew 24% in the third quarter compared to the same period last year. We remain confident in the durability of our oxybate franchise and the growth of Xywav in both narcolepsy and idiopathic hypersomnia, or IH, even as high sodium branded and authorized generic competition has entered the narcolepsy market. Xywav is annualizing at $1.3 billion in revenue, remains the oxybate of choice and is the only approved treatment for IH. Underlying demand continues to drive Epidiolex growth. We remain confident in its potential to reach blockbuster status and contribute more than $1 billion in revenue to our Vision 2025 revenue target. Outside the U.S., we expect additional launches and indication expansions through 2024. In oncology, Rylaze has continued to grow in the U.S., supported by strong demand from pediatric patients and our increasing emphasis on the adolescent and young adult market. In addition, we recently received marketing authorization for the product in Europe under the trade name Rylaze. The performance of these products, together with Zepzelca revenues is fueling the ongoing diversification of our commercial business. More than half of net product revenue this quarter came from Epidiolex and our oncology products combined, and Xywav represented more than two-thirds of our oxybate revenue. This marks a significant shift from just a few years ago when Xyrem represented three-quarters of total revenue. This diversified revenue stream is a direct result of our outstanding commercial execution along with successful corporate development and internal R&D efforts. Moving to our pipeline. We now expect up to five late-stage readouts through the end of 2024. Rob will cover our R&D progress in more detail later in the call, but I want to highlight that we view Zanidatamab as the most derisked and highest priority program in our pipeline. We plan to initiate a rolling biologics license application or BLA submission this year for accelerated approval of Zanidatamab for second-line treatment of biliary tract cancers or BTC. This is an important step in delivering Zanidatamab to patients with BTC and other HER2-expressing cancers with limited treatment options. Given the strength of clinical data to date and its promise in multiple indications, we believe Zani has the potential to deliver more than $2 billion in peak revenues. On the operational front, our commercial execution, along with attention to operational excellence has put us in strong financial position. We continue to generate significant cash flow from operations, which combined with our strong balance sheet gives us the capacity to invest in the products, pipeline programs and corporate development opportunities with the highest potential to deliver sustainable growth and enhance value. Turning to Slide 6. We are very pleased with our progress in the third quarter and believe it has advanced us towards achieving all three components of Vision 2025 as we continue our transformation into a high-growth global biopharma leader. I'll now turn the call over to Renee to review our commercial performance, after which Rob will share an update on our R&D progress. I'll provide a financial overview, and then we'll open the call to Q&A.

Thanks, Bruce. It's been an exciting few weeks as I assumed my new role. And while I'm working across a different part of the organization, my focus remains the same: driving the continued growth and transformation of our business. Starting on Slide 8. Our confidence in the durability of our oxybate franchise has only increased as we gained more visibility into how market dynamics are evolving with the availability of branded and authorized generic high sodium oxybate. Total oxybate revenue, which includes Xywav and Xyrem revenues, together with royalties from Xyrem authorized generics, is annualizing at $1.9 billion, and we are well positioned to achieve our stated goal of $2 billion in oxybate revenues as part of Vision 2025. Xywav revenue was approximately $332 million for the third quarter of 2023, representing growth of 30% compared to the same period in 2022, driven by continued adoption in both narcolepsy and IH. Exiting the third quarter, there were approximately 9,500 narcolepsy patients taking Xywav. Our focus on educating patients and prescribers about the benefits of reducing sodium intake continues to drive growth. And we recently launched a new campaign to support these initiatives. Importantly, we are seeing adoption from both high sodium oxybate and oxybate naive patients. In IH, we see continued growth of new prescribers, and exiting the third quarter, there were approximately 2,550 active IH patients on Xywav. Xywav is uniquely positioned to address the multiple symptoms of IH, including sleep inertia, excessive daytime sleepiness and cognitive impairment, all of which have a significant impact on patients' quality of life and daily function. Based on the opportunity to improve the lives of people living with IH and our confidence that the IH indication represents a durable growth driver for Xywav, we are increasing our investment to further build the market. This will include educational initiatives and expanding our field team to include members specifically focused on IH to increase the breadth of prescribers. Slide 9 highlights our latest educational campaign for narcolepsy treaters 'Less Is More', which reinforces the compelling low sodium health benefits of Xywav. Narcolepsy is a debilitating chronic condition, and we have focused our educational efforts around the lifelong burden of high sodium intake for narcolepsy patients who live with a two to three times higher risk than the general population of cardiovascular comorbidities such as stroke and heart failure. Xywav is the only approved low sodium oxybate containing 92% less sodium than high sodium oxybate and importantly, is the only oxybate without a labeled warning about high sodium intake. You've heard us use a number of comparisons for the sodium load of high sodium oxybate versus Xywav, including eating four large orders of fast food french fries or five large bags of potato chips every night before bed, or that it would take 12 years of treatment with Xywav to equal the sodium intake of one year of high sodium oxybate treatment. Regardless of the parallels we draw, the bottom line is clear. The sodium reduction offered by Xywav has significant potential health benefits, including lower blood pressure and improved cardiovascular health. We recently presented data at the World Sleep Meeting that built on our body of research demonstrating the clear relationship between sleep disorders and increased cardiovascular risk, as well as the meaningful improvements possible with treatment plans that consider a patient's holistic health, such as reducing sodium intake. And earlier this year, we shared data at the American Academy of Neurology meeting that showed narcolepsy patients treated with high sodium oxybate had a higher risk of new-onset hypertension diagnosis or anti-hypertensive medication initiation within 180 days of starting therapy when compared to a matched control group of narcolepsy patients not being treated with high sodium oxybate. The risk of those taking high sodium oxybate was approximately twice that of the control group. We believe that the majority of patients and health care providers will continue to prioritize long-term health when evaluating oxybate therapy, and we are finding the direct competitive messaging in the 'Less Is More' campaign to be effective. Additionally, since we know this disease and its treatment are complex, the campaign also highlights the advantages of individualized dosing regimens for Xywav patients and the support services that Jazz makes available for HCPs and their office staff to have Xywav prescriptions approved, reimbursed and delivered to patients. We also offer a range of patient services that include co-pay assistance and disease education. Turning to Slide 10, on Epidiolex. We achieved another quarter of growth with net product sales increasing 9% year-over-year to approximately $214 million driven by underlying demand in both our U.S. and European markets. Key drivers of this demand growth include Epidiolex' strong product profile including data around benefits beyond seizure control, increased penetration in the long-term care setting and strong uptake in key European markets, all of which provide us with continued confidence in a blockbuster potential of the product. Turning to Slide 11. We are focused on multiple opportunities to drive Epidiolex to blockbuster status including continued data generation and we expect to present several data sets at the upcoming American Epilepsy Society meeting in December. Our educational efforts around caregiver reported outcomes beyond seizure control from the BECOME survey have been especially impactful, further differentiating Epidiolex from other antiseizure medicines. To accompany this caregiver reported data on improvements in cognition, behavior and other non-seizure benefits in LGS and DS, we have initiated the post-marketing EpiCom trial in TSC. EpiCom was designed in collaboration with HCPs and patient advisory groups to evaluate the impact of Epidiolex on behavioral and cognitive functioning and outcomes using a range of validated scales. Our commercial team also has an enhanced focus on dosing optimization, further penetration in the adult setting and continued growth outside the U.S. Turning to Slide 12 and our oncology franchise. Net product sales for Rylaze were approximately $105 million for the third quarter, a 43% increase year-over-year. Demand for Rylaze remains strong, and we see a number of factors that are driving what we believe is sustainable growth. First, health care providers have indicated that they are returning to best clinical practice and switching therapy at the first signs of hypersensitivity, which was often not possible under the supply limitations with Erwinaze. Second, while Rylaze has been almost universally adopted in pediatric oncology protocols, we are now also seeing increased pediatric usage in several other areas. These areas include physicians switching patients from E. coli-based asparaginase due to other treatment-related issues that arise as well as some use of Rylaze in first-line treatment based on its advantages of a short-acting profile relative to current first-line asparaginase therapies. Third, we continue to see increased adoption of the Monday, Wednesday, Friday, 25-25-50 milligrams per meter squared dosing, which is more in line with preferred clinical practice and allows for a dosing schedule that ensures sustained asparaginase levels through the course of treatment, which is essential to improved outcomes for patients. Fourth, we are seeing increased use of Rylaze in the treatment of adolescents and young adults, or the AYA market, and we expect continued growth in this segment. Our field teams have been expanding their educational efforts to AYA treaters this year with a focus on physicians who have previously used asparaginase therapy. Outside the U.S., we recently received European Commission approval under the trade name Rylaze and are planning to begin a rolling launch later this year. With respect to the market opportunity, the commercial landscape in Europe has a number of differences compared to the U.S., including competition and market access dynamics. Turning to Slide 13. Zepzelca remains the treatment of choice in second-line small cell lung cancer and has generated more than $800 million of revenue since launch, proving to be a highly accretive and well-executed corporate development transaction for Jazz. Net product sales for the third quarter increased 11% year-over-year to $78 million driven by an increase in underlying demand. A portion of this demand relates to the continued shortage of platinum chemotherapy, which has led to oncologists choosing Zepzelca for some patients they may have historically rechallenged with platinum therapy. Although this dynamic may be temporary in nature, it is currently resulting in greater use of Zepzelca, particularly in the community setting, where its clinical profile and ease of administration have been well received. While we have achieved significant penetration in the second-line setting, there remains an important unmet need for patients diagnosed with small cell lung cancer. We expect top line PFS data from our pivotal Phase III trial of Zepzelca in combination with Tecentriq in first-line small cell lung cancer at the end of 2024 or early 2025. A positive outcome in this trial would provide a further opportunity to both improve patient lives and outcomes as well as drive future growth in our oncology franchise. With that, I'll turn it over to Rob for an update on our pipeline and upcoming milestones.

Thank you, Renee. Slide 15 provides an overview of our robust diversified pipeline that includes neuroscience and oncology programs across all phases of development. Consistent with our mission and strategy, these programs are focused on advancing the treatment of serious diseases for which there are limited or no options. Moving to Slide 16. This is an exciting time for our organization as we approach multiple catalysts across the pipeline. We now expect up to five late-stage data readouts through 2024, with all five addressing areas of significant unmet need. Starting with neuroscience, recruitment in our Phase III trial of Epidiolex in Japan is progressing well, and we now expect top line data in the second half of 2024. We are pleased to announce that we have completed enrollment in our ongoing Phase II trial of JZP-150 in PTSD. Based on timing of the last patient last visit, we are updating the anticipated timing of our top line data readout to January 2024. We also have ongoing trials for suvecaltamide, or JZP-385, in both essential tremor and Parkinson's disease tremor, with top line data from the ET trial expected in the first half of 2024. If results are positive, we believe this trial could serve as part of a pivotal package. In addition, we anticipate initial proof-of-concept in healthy volunteers later this year for JZP-441, our Orexin 2 receptor agonist. Moving to oncology and Zanidatamab. We expect to report top line data from the ongoing Phase III frontline gastroesophageal adenocarcinoma trial next year. Later in the call, I'll provide an overview of our regulatory strategy for Zanidatamab, including an update on BTC. As Renee just mentioned, top line progression-free survival data in Zepzelca in combination with Tecentriq as first-line maintenance therapy for extensive stage small cell lung cancer is expected at the end of 2024 or early 2025. I'll now discuss some of our key programs in detail. Starting on Slide 17, with Zanidatamab, our highest priority pipeline asset. Given its potential across multiple HER2-positive tumor types, we are expanding and accelerating our development plans for this exciting molecule. Zanidatamab is a novel bispecific antibody that can simultaneously bind two nonoverlapping epitopes of HER2, known as biparatopic binding. This unique design results in multiple mechanisms of action, including dual HER2 signal blockade, receptor clustering on the cancer cell surface, leading to internalization by a biparatopic binding and potent immune activation, including antibody-dependent cellular cytotoxicity, antibody-dependent cellular phagocytosis and complement-dependent cytotoxicity, leading to encouraging antitumor activity in patients. Additionally, Zanidatamab can prevent HER2 from combining with other HER2 proteins and with ERBB receptor family members like HER3, which can further block growth signaling. Zanidatamab has shown compelling activity across a broad range of HER2-expressing tumors. And we presented promising efficacy and early survival data at ASCO in BTC and ASCO GI and GEA earlier this year. Most recently, BeiGene, which has development rights in some Asia Pacific markets outside of Japan, reported results at this year's ESMO meeting from a Phase II trial of Zanidatamab in combination with chemotherapy, atezolizumab, BeiGene's anti-PD-1 antibody in first-line gastric and gastroesophageal junction cancers. Data included an overall response rate of 76%, with a median duration of response of 22.8 months and a median progression-free survival of 16.7 months at the time of the cutoff. These data, along with our own GEA program, are building a body of evidence supporting the potential of Zanidatamab in treating first-line GEA. Based on compelling Phase II data, we plan to initiate a rolling BLA submission this year for accelerated approval of Zanidatamab for second-line treatment of biliary tract cancer. We expect to complete the submission in the first half of 2024 and anticipate that our confirmatory trial in first-line BTC will be open and enrolling patients prior to the completion of the rolling BLA submission. Turning to Slide 18. BTC and GEA are the first of multiple indications we plan to pursue for Zanidatamab. We believe Zanidatamab has the potential to raise the standard of care for some of the most difficult-to-treat HER2-expressing cancers, including breast cancer, where we see a significant potential to help patients in both early and late-stage disease. We are executing a comprehensive development plan and are excited about delivering this innovative therapy to patients. If approved, we expect to initially enter the market in second-line BTC where physicians would gain important experience with Zanidatamab. Following BTC, we expect to have a path to approval in first-line GEA with a supplemental BLA submission, which provides a more streamlined approval process compared to a full BLA. We strongly believe that a substantial opportunity remains to address the unmet patient need in first-line GEA, including in the HER2-positive PD-L1 negative patient population where the care remains trastuzumab plus chemotherapy. For patients who are PD-L1 positive, we believe that Zanidatamab has the potential to be the HER2-targeted treatment of choice, while also combining with a PD-1 inhibitor in order to treat those patients with GEA whose tumors expressed PD-L1. There also makes an opportunity to move into earlier stages of GEA where we see the potential to help those patients in the neoadjuvant and adjuvant settings. GEA represents a significantly larger patient opportunity compared to BTC. And a prior approval in BTC may accelerate adoption into GEA treatment time lines and protocols. We look forward to data from the ongoing pivotal Phase III GEA trial expected in 2024, which may support U.S. and global regulatory submissions. Breast cancer also represents a considerable opportunity, supported by promising early data for Zanidatamab as monotherapy in multiple combinations and across stages of disease and lines of therapy. Based on the efficacy and safety seen in studies to date, we believe Zanidatamab is well suited for early-stage disease including potential use as neoadjuvant and adjuvant therapy. Zanidatamab has also shown promise in HER2-positive and hormone receptor positive breast cancer as part of a novel combination. Based on these encouraging signs of activity, we have ongoing trials in neoadjuvant breast cancer, including an arm in the I-SPY platform trial, which is studying Zanidatamab for the neoadjuvant treatment for locally-advanced breast cancer. We are also evaluating the opportunity to expand into both combination regimens and later lines of therapy in HER2-positive and HER2 HR-positive breast cancer. Finally, we are also evaluating Zanidatamab in multiple early phase trials in other tumor types, where a few HER2-targeted treatment options are available. We are impressed with the strength of data and clinical activity Zanidatamab has shown across a diverse set of HER2-expressing indications such as colorectal cancer, non-small cell lung cancer and multiple other cancers where there continues to be a need for safe and effective targeted treatment options for patients. In summary, we are committed to rapidly advancing and expanding our development program for a molecule that has the potential to transform the current standard of care in multiple HER2-expressing cancers. Turning to Slide 19, JZP-150 is our novel, highly selective fatty acid amide hydrolase, or FAAH inhibitor. We are developing JZP-150 as a once-daily oral medication with the potential to impact the pathophysiology and symptoms of PTSD. By addressing the underlying cause of PTSD, impairment of fear extinction and its consolidation, JZP-150 has the potential to improve patients' associated symptoms such as anxiety, insomnia and nightmares. Preclinical and early clinical data showed activity on fear extinction and stress response. JZP-150 has a novel and promising mechanism of action, providing irreversible inhibition of FAAH, which we believe may have advantages over reversible FAAH inhibitors in development, and we anticipate top line data readout in January 2024. On Slide 20, I'll highlight JZP-441, a potent highly selective orexin-2 receptor agonist designed to activate and restore impaired orexin signal. Through this mechanism of action, JZP-441 has the potential to exert pronounced weight-promoting effects in people with sleep disorders. Orexins are excitatory neuropeptides that play an important role in the regulation of sleep and wakefulness. Patients with type 1 narcolepsy have a loss of orexin-producing neurons with impaired orexin signaling. And clinically, these patients often present with chronic disabling symptoms that significantly impact patients' ability to function normally during the day. Slide 21 illustrates the design of our Phase I program, evaluating safety, tolerability, pharmacokinetics and pharmacodynamics of JZP-441 in healthy volunteers. Our single ascending dose study is being conducted in sleep-deprived healthy volunteers and includes an evaluation of the weight-promoting effects of JZP-441 using the maintenance of wakefulness test, or MWT. This is a recognized disease model that historically has translated to patient efficacy. We also have an ongoing study evaluating multiple ascending daytime doses in healthy volunteers intended to provide safety of chronic dosing in support of a multiple dose study in patients. Importantly, we have structured the program to maximize our learnings at this stage, including identifying appropriate dose ranges, which we believe will accelerate later development in patients. We're excited about the potential of JZP-441 and look forward to updating you on our progress later this year. Turning to Slide 22. Our team is advancing multiple preclinical compounds to a clinical stage development. JZP-815, a molecule that has emerged from our collaboration with RedX, is one of our most recently initiated Phase I trials. JZP-815 is a highly selective potent pan-RAF inhibitor with a differentiated mechanism of action. It targets specific components of the mitogen-activated protein-kinase pathway that are known oncogenic drivers, active against multiple ARAF, BRAF and CRAF mutants and a spectrum of BRAF fusions. Activity against ARAF mutants may be an important point of differentiation as recent data suggests the importance of ARAF in the context of mutant RAS activation. JZP-815 also potently inhibits both monomer and dimer-driven RAF signaling and prevents paradoxical pathway activation induced by BRAF selective inhibition. Slide 23 illustrates the design of the ongoing JZP-815 Phase I trial, evaluating the safety, dosing, pharmacokinetics, pharmacodynamics and initial antitumor activity of JZP-815 in participants with advanced or metastatic solid tumors harboring mutations in the MAP kinase pathway. It consists of two parts. Part A will characterize the safety and tolerability of JZP-815, determining a maximum tolerated dose and PK profile and determining a recommended Phase II dose to be further investigated in the expansion phase or Part B. Part B will investigate the antitumor activity at the recommended Phase II dose in various tumor types based on mutation status. Overall, our R&D team has been advancing multiple programs from our neuroscience and oncology pipeline, and we have multiple upcoming catalysts and near-term data readouts. Now I will turn the call over to Bruce for a financial update.

Thanks, Rob. I'll start with our top and bottom line results on Slide 25. As a reminder, our full financial results are available in our press release and 10-Q. In the third quarter of 2023, we achieved $972 million in total revenues, driven by continued growth of our key products in both neuroscience and oncology. We're pleased with the continued trajectory of Xywav during a period when high sodium oxybate competition has been introduced into the market. Coupled with Epidiolex momentum, the strong growth of Rylaze and solid performance of Zepzelca, total revenue increased 3% compared to the third quarter of 2022. Our adjusted net income for the quarter was $340 million, and we reported adjusted EPS of $4.84. The decreases in ANI and EPS this quarter compared to the same period last year were driven primarily by an increase in R&D investment, partially offset by higher revenues and a lower effective tax rate. The majority of our R&D increase this quarter is related to Zanidatamab. Our adjusted EPS also reflects a lower number of diluted shares outstanding compared to the same period last year. We continue to generate significant cash from our business. We recorded $307 million of cash from operations in the quarter and $925 million through the first three quarters of the year. Our strong overall financial position means we have significant flexibility to invest in priority commercial and R&D programs as well as corporate development opportunities. Turning to Slide 26. We have raised the midpoint of our full year 2023 revenue guidance to a range of $3.75 billion to $3.875 billion. As a reminder, we raised revenue guidance last quarter and have continued our strong commercial execution on key growth drives: Xywav, Epidiolex and Rylaze. Our guidance represents year-over-year total revenue growth even as we faced the headwind of oxybate competition. Our 2023 neuroscience guidance remains unchanged and reflects expectations of continued growth of Xywav and Epidiolex, offset by the expected decline in Xyrem with a revenue range of $2.715 billion to $2.825 billion. With regard to high sodium authorized generics, royalties from high sodium oxybate AGs were $29 million in the third quarter of '23, which reflect a significant increase over the first half as we move to a six-month fixed rate royalty per the AG agreement with Hikma. The royalty rate will increase again after this six-month period, at which point, it will remain fixed for the duration of this agreement. AG Royalties are included in our neuroscience guidance. We have raised the midpoint of our 2023 Oncology revenue guidance to a range of $975 million to $1.05 billion, which reflects 16% growth at the midpoint. I would like to draw your attention to several items on Slide 27. Our strong cash generation, combined with our disciplined capital allocation provides us with flexibility to make strategic investments in our business. This includes an increase to our R&D guidance and an increase to the midpoint of our SG&A guidance while remaining on track to deliver ANI growth in 2023 compared to 2022. Our updated guidance midpoint equates to an adjusted operating margin of approximately 44%. While margins will vary over time, we believe we are well positioned to achieve our Vision 2025 goal of driving a 5% improvement from 2021 to 2025. One note regarding ANI as we look to the future. In the third quarter, we benefited from a lower effective tax rate partly driven by tax benefits derived from our increased R&D expenditure, expiration of statutes of limitation and changes in product mix. We expect that our ETR will increase next year as global tax rates are harmonized. Consistent with our capital allocation strategy, our enhanced investment in R&D is a direct result of our success in diversifying and advancing our pipeline. We have increased our R&D guidance for 2023 to a range of $780 million to $820 million, reflecting our confidence in our pipeline programs. In particular, we are making substantial investments in Zanidatamab to more aggressively pursue development opportunities that we believe will benefit patients and create long-term value for Jazz. Looking at SG&A, we are updating our guidance to the range of $1.065 billion to $1.105 billion as we invest in a disciplined manner to drive further growth in key brands. We believe there is tremendous unrecognized value potential in our stock. We, therefore, continued share repurchases under our existing repurchase program. In the third quarter, we completed approximately $75 million of share repurchases. At the end of the third quarter, approximately $261 million remained available for share repurchases under our current plan. Importantly, given our strong overall financial position, we are able to include share repurchases in our capital allocation strategy without compromising our ability to execute business development opportunities and invest in our innovative R&D program. Additionally, we are reiterating our adjusted EPS guidance of $18.15 to $19. I'll conclude our prepared remarks on Slide 29. Our top line performance this quarter was driven by focused execution and strong commercial results, evidenced by the durability of our oxybate franchise, continued growth of Epidiolex and strength of our oncology business. We continue to advance our pipeline, invest in long-term growth, and we expect up to five late-stage data readouts through 2024 that have the potential to further diversify and transform our business. We remain focused on strategic capital allocation. With our strategic investments, expanding product portfolio, R&D progress and focus on operational excellence, we believe we are well positioned to achieve Vision 2025 and deliver further diversification, sustainable growth and enhanced value to patients and shareholders. That concludes our prepared remarks. I'd now like to turn the call over to the operator to open the line for Q&A.

Your first question comes from the line of Jessica Fye from JPMorgan.

This might be a little tricky to respond to, but recently there were some headlines stating that Jazz might be exploring various strategic options, including breaking up the company or a sale of a business unit. I generally think of Jazz as more likely to buy a business than sell a business. But is there anything you want to clarify for folks regarding how you're thinking about business development and the strategy.

Jess, welcome back. Good to hear your voice. So I'll point out that Jazz made no such announcement. There was a story in one place with unnamed sources. I'll also remind you, as an Irish takeover panel company, that we can be forced to clarify publicly if there's something actually going on in pretty short order and that did not happen. We remain very focused on corporate development as a way to grow our business. Well, that's been part of our strategy historically. It specifically called out as part of Vision 2025. And we think the strong financial position of the company, ending the quarter with $1.6 billion in cash and a strong cash flow of $925 million over the first three quarters, and the substantial continued deleveraging of the company put us in a really good position to continue to put cash to work to grow our business.

Your next question comes from the line of Jason Gerberry from Bank of America.

I am interested in the changing competitive landscape in the oxybate market with LUMRYZ, especially after their update about enrolling 1,000 patients. I'm wondering if your guidance indicates that your assumptions about competition haven't changed since the beginning of the year. Are you noticing anything in the market that stands out? Or do you believe that the competitor might be attracting more of their business from either uninformed patients or those who have historically stopped using Xywav? That information would be helpful.

Yes, Jason, thanks for the question. And before I turn it over to Kim for a little more color, I'll just say in your comments, you're exactly right that we foresaw competition in the oxybate space this year, both from authorized generics of Xyrem and the branded fixed dose high-sodium product, and built that into our guidance. We've actually raised our neuroscience guidance last quarter and continue to perform in line with our guidance. But Kim, maybe you could give a little more color on the oxybate landscape.

Yes, sure. So yes, Xywav is still growing in narcolepsy. We're pleased to see despite the additional competition from the high-sodium oxybate introduced this year. Yes, our growth in narcolepsy has slowed in line with our expectations and our own forecast as there remain fewer available patients to transition from Xyrem given our early success with Xywav and some patients have decided to go ahead and give FT218 a try. But generally, in terms of what we're hearing from health care providers right now, they are still telling us that they place a high value on both the low sodium value proposition of Xywav as well as on the fact that they've gotten used to being able to individualize or customize the dosing regimen for individual patients depending on their needs. Many HCPs have expressed an interest in gaining eventually some experience with the new fixed dose, high-sodium oxybate product and where they're typically doing that, they're telling us is among those patients that have come in and have insisted on giving it a try. So overall, we remain very confident in the strength and durability of our oxybate franchise. We do see Xywav continuing to be the active choice now and in the future, and it is still the only one approved for the treatment of idiopathic hypersomnia. And lastly, when we continue to look at our data in terms of the portion of patients who are naive to oxybate treatment, they're being started on their first oxybate treatment. The vast majority of these patients continue to be being initiated on Xywav. So we think that's very strong evidence that overall overwhelmingly physicians still feel it's most important to focus on the patient's long-term health.

Your next question comes from the line of Ami Fadia from Needham & Company.

Can you discuss why you believe JZP-150's mechanism is potentially different from a reversible FAAH inhibition? Regarding your ongoing trial focused on the CAPS-5 endpoint, what would you define as a clinically meaningful change that you hope to observe? Additionally, can you elaborate on the trial's power and whether we should anticipate a statistically significant result? Lastly, could you explain why there are two doses in the trial instead of just using the higher dose?

Rob?

Yes. Thanks, Bruce. Thank you for the question, Ami. So starting with the first part of that around why the mechanism is differentiated. I would first say that we're interested in JZP-150 because of FAAH as an underlying part of the pathophysiology potentially. So we know that PTSD patients have low levels of anandamide, and by inhibiting FAAH, you can raise those levels. So we think this is one of the mechanisms that potentially directly addresses the underlying pathophysiology. We think we're differentiated in being irreversible, as you mentioned, because you can create a more sustained FAAH inhibition. In other words, you ultimately have to resynthesize FAAH in order to get back to baseline levels. So it just allows for consistent inhibition of FAAH which we think is more important. In terms of clinically meaningful effect sizes, we haven't said what we're necessarily striving for in this, but you could certainly look across different mechanisms and see what has been achieved in terms of the CAPS-5. In our trial, we think we're certainly well powered for a clinically meaningful effect given the 270 patients that we've enrolled across those three arms. And to your point about a low dose and a high dose, in this trial, we included two dose levels because we wanted to evaluate what we felt was based on prior receptor occupancy data, full constant inhibition of FAAH versus a lower dose that would be just under that full inhibition. And that sort of brackets the range of exposures that you might want to see and allows us to collect safety data in that range and then would put us in a better position to select doses for a pivotal trial, if and when we move forward with that.

Your next question comes from the line of Marc Goodman from Leerink Partners.

Yes, I was hoping you could give us a little flavor on what's going on with Zepzelca. It seems to finally have grown after many quarters, it's just seeming flat. So if you can just give us a little color there. And then could you just give us the total oxybate patient number for us, please?

Yes, I'll take the second part of the question first. And then, Kim, maybe you could jump in on Zepzelca growth, which I agree looks really nice this quarter. On total oxybate patients, we've stopped giving that number. As you noted in the royalty revenue off the AG of $29 million during the quarter, that has jumped up significantly, and that revenue, of course, is derived from patients that would not be included across Xywav and Xyrem. So essentially, total patients don't track to our revenues anymore because that Xyrem plus Xyrem royalty is a little bit distinct. We've continued to give patient numbers in narcolepsy and idiopathic hypersomnia as we exit a quarter to give you a sense of growth of the Xywav asset, but I'll just point out total revenues and total patients don't track the way they have historically for Jazz until this quarter. In the first half of the year at the much lower royalty rate on the AG and earlier at the AG launch, the difference wasn't significant. It is significant now and will only continue to be. On Zepzelca, I'll just point out we're really happy with this deal when I talked about why we do corporate development and add assets to the company. I think Zepzelca, having generated over $800 million in revenue since launch, has shown that to be a deal that was highly accretive and continues to reward our investors. So Kim, do you want to talk about dynamics there?

We are pleased with the 11% year-over-year growth we achieved in the third quarter. The increase in demand this quarter is partly due to the temporary shortage of platinum chemotherapy in the U.S., which led to the use of Zepzelca in some patients. Traditionally, oncologists may have considered another round of platinum therapy after the first-line treatment, and we've been emphasizing that Zepzelca shows impressive results in this area. However, it has been challenging to convince some customers to switch to it. Recently, we've provided new data that we hadn't shared before, specifically for the platinum-sensitive patient population, to help alleviate any concerns about using Zepzelca. We presented results on overall survival and progression-free survival, which, along with the chemotherapy shortage, encouraged many customers to try the drug. We believe they are seeing positive outcomes and, even as the supply of platinum chemotherapy improves, some healthcare providers may return to their previous practices while others may start using Zepzelca more frequently. Additionally, we have observed many healthcare professionals gaining experience with this product in community and outpatient settings, and we are impressed with its ease of administration and clinical profile as it does not require inpatient monitoring. We think this business may remain strong even after the shortage. Overall, Zepzelca has become the preferred treatment for second-line small cell lung cancer, and we see significant future growth potential for this brand in the first-line setting, where we currently have a Phase III trial underway.

Your next question comes from the line of Balaji Prasad from Barclays Capital.

Looking at the well-defined patient populations in narcolepsy or IH or oncology, this is one where the market sizing still seems incomplete. So can you discuss the opportunity in the adult setting, as you spoke about this afternoon, the additional ex-U.S. launches? And what would this translate to in terms of an expansion of market size? Maybe an extended - a related question, as you continuously call out that it's well on its way to $1 billion. What can we expect beyond this in terms of longer-term growth trajectory? Is it going to be mid-single digits or high single digits? How can we think about it?

Thank you for your question, Balaji. I'll address that. While we don't provide specific guidance on products, I can share insights on the broader opportunity and then let Kim discuss some specific dynamics we're observing in the U.S. For the current quarter, we experienced a 9% year-over-year growth, and notably, we saw a 14% increase when looking at the first nine months compared to the previous year. We are confident that we are on track for significant success in line with our Vision 2025 goals. Regarding Epidiolex, there are three key growth drivers to consider. First, it is a global product, which offers vast opportunities for expansion. We are currently approved and reimbursed in 24 countries, and we expect results from a pivotal study in Japan by the end of next year. Additionally, there is strong underlying demand in the U.S., which Kim will discuss shortly. Second, we believe Epidiolex is a long-term asset with a solid portfolio of patents, most of which extend to 2035 and some to 2039, positioning it as a significant revenue generator for the future. Third, it is a highly differentiated treatment. Epidiolex is well-characterized and well-tolerated, making it suitable for polypharmacy, which is common in this field. We have accumulated substantial data supporting its use, which healthcare providers find beneficial. These three factors collectively reinforce our confidence in its long-term potential. Regarding international dynamics, we launched in several countries and indications throughout 2023, and we anticipate this trend to continue into 2024. Now, I'll hand it over to Kim to discuss the adult long-term care segment and other demand drivers.

Sure. Thanks, Renee. So yes, I think we've talked about for the last year or so, we've really been putting increased focus on the adult segment there, particularly as it pertains into the U.S. and the long-term care setting where many of the adults with these conditions revive. And we're seeing really nice growth there in that population disproportionate to what we're seeing in the brand overall. So that is a nice growth driver. But across both the pediatric and adult market, there are, I'd say, three other things that are really driving the growth, and I think speak well for the future. Renee mentioned the data. We've talked quite a bit with you about the data. We are sharing the data regarding combination with clobazam and the beyond seizure benefits of Epidiolex particularly as it relates to behavioral improvements and cognition improvements specifically because we're trying to expand the definition of efficacy and really differentiate the brand from existing products today. And I'd say both of these pieces of data really are eye-opening and do a great job of that in the marketplace, particularly that beyond seizure data in the LGS and Dravet space. The third one is that we have done a really nice job, I think, over the last couple of years of expanding, I would say, or improving the quality of access to Epidiolex. Pretty much since launch, we had a very high percentage of commercial lives that have coverage as well as Medicaid lives that have coverage for Epidiolex. But what we've really seen in the last couple of years and this year in particular, is that the quality of that coverage is improving in terms of the utilization management criteria becoming less burdensome. The utilization management criteria being broader in terms of providing easier access to Epidiolex for a broad range of patients with refractory conditions. And ultimately, we are hearing from our customers' feedback that they are finding it easier to get their patients Epidiolex, which of course, only reinforces their confidence in prescribing it. And then lastly, persistency has been really a hallmark of this brand since it was launched similar to activate once patients get through the early titration period, they tend to stay on Epidiolex for a long time. But despite this, we still have seen room for opportunity to invest in improving that persistency, both at the beginning of the treatment and when patients have been on it for some time, and we're seeing nice improvements there, particularly if we can get HCPs to support patients and get them up through that titration period. Overall, we see them stay on the drug for a pretty long time. So lots of things there to point to as current and future growth drivers in the U.S.

Your next question comes from the line of Akash Tewari from Jefferies.

This is Amy on for Akash. So we have one quick question on orexin. So you are guiding to data for JZP-441 in healthy volunteers by year-end. I guess, what level of MWT do you need to see to move this program forward? Also, what makes you feel comfortable about the liver toxicity profile?

Sure. Should I take that one, Bruce?

Yes, please.

Yes, we have some benchmarks from other orexin agonists currently in clinical trials. For the healthy volunteer MWT study, we are looking for comparable efficacy, which seems to be applicable to patients as well. We are also able to compare various doses we are testing against other compounds, not just within the orexin class but also with other wake-promoting agents. This should give us a strong understanding of when we have achieved a satisfactory level of efficacy. And what was the second part of your question?

The liver toxicity profile is something that makes you feel confident, yes.

Yes. We believe that liver toxicity is not a broader class effect and likely pertains specifically to that structural class mentioned by Takeda. Even when we in-licensed from Sumitomo, we were working with a different chemical series, so we don't see that risk applying to us. Our preclinical toxicology studies also showed no concerns regarding liver toxicity.

Your next question comes from the line of David Amsellem from Piper Sandler.

So I also had a question on the orexin agonist, JZP-441. So we've seen some early tolerability data at World Sleep for the other compounds, urinary urgency being one that comes to mind, also visual disturbance. I wanted to pick your brain on how you're thinking about those as being on-target effects or is something else going on? And just your general level of, I guess, vigilance is the right word on those kinds of AEs?

Yes. So I mean, listen, the early days across these compounds, we have a lot to learn. But I would say the therapeutic index is going to be very important, whether that be to what we perceive as on-target effects like the urinary frequency that you mentioned or potential off-target like hepatotoxicity. The therapeutic index is going to be important. Part of that may relate to the half-life of the compound. I mean, if you have something that is too long a half-life, you may see residual effects into the evenings causing them insomnia, which is obviously counterproductive from the therapeutic intent. And so having a favorable half-life from being able to dose in a way that creates a therapeutic index for either on-target or any potential off-target toxicity will be important. And that's part of what we're doing in our healthy volunteer studies, both of the single dose as well as the multiple dose is really exploring the therapeutic range and various dosing that will allow us to select an optimal regimen to be evaluated in patients.

Your next question comes from the line of Joon Lee from Truist Securities.

This is Jeremy on for Joon. How are you looking at the oxybate market evolving both in terms of Xywav and Xyrem? And has the AG impact been as expected?

Yes. I'll start on that one and just say, again, the way things have played out this year has been very much in line with our expectations. Xyrem has been declining for years now, largely because we've been successful with Xywav giving patients a healthier lifelong treatment option. That decline has continued this year. Obviously, complemented by having new entrants in the marketplace. But that revenue stream for us is now very small relative to our total business at about 16% of our revenues this quarter if you add up Xyrem and our royalties on the AG. And we're focused on growing Xywav. We think the product has great durability as an asset. We are very excited about the opportunity to continue growing the idiopathic hypersomnia market. We know there are more patients to reach. We know diagnosis can improve. And as physicians gain more experience using this product and seeing the benefit in their patients, the mirrors what we saw in clinical trials, we think that's very favorable for their intended increased use of the product. And we still think there's growth left in the narcolepsy market. We haven't seen much of a change in the overall growth dynamics since the Avadel launch, but it's usually true that having multiple companies out talking about a disease that is sometimes underdiagnosed can be helpful. So we're excited to continue to grow Xywav.

Your next question comes from the line of Gary Nachman from Raymond James.

First, can you talk about Rylaze expanding in Europe and specifically your expectations on how much that product will contribute ex-U.S. over time? What's a reasonable target there? And then just on your point, Bruce, on Xywav in idiopathic hypersomnia, how concentrated is the current prescribing base? And what are some of your initiatives to try and expand that further? And at what pace do you think you'll be able to do that to tap into more of those patients?

So two different questions. Maybe I'll hit Xywav first and say the prescriber base for IH is very overlapping with the narcolepsy prescriber base, about 90%. As you heard in our comments on the call, we are increasing our effort behind IH to have some folks focus on that specifically to get out to some physicians who may be a little less familiar with using oxybate to support them, but the prescriber base is very similar. Renee, do you want to talk about Rylaze a little bit?

Yes, I'm happy to. So we're really pleased to be able to make this product available in Europe. And as we stated, we expect to begin that rolling launch later this year. I will stress that the market dynamics are very different in Europe versus the U.S. So in Europe, we have Enrylaze on the market as a competitor. We have quite a different pricing scheme and a number of steps to take from a market access perspective to ensure that Rylaze is secured on protocols, which will take some time. So taking all of these things into consideration, I would say that being on the market in Europe will provide growth, but characterize that as relatively small and something that would be achieved over time relative to the overall opportunity in the U.S. And then on the topic of the U.S., maybe I'll turn to Kim to provide a few comments on what we're seeing there.

On Rylaze specifically, I'm very pleased with the product's performance. We haven't had the chance to identify the peak market potential due to supply constraints, so we don’t provide product-specific guidance. However, we are seeing strong demand which indicates significant patient need. Some growth drivers were anticipated, while others were unexpected in this supply-constrained market. We expected healthcare providers to switch patients more quickly due to hypersensitivity responses, but we are also noticing a substantial amount of switching related to other treatment issues, particularly from E. coli-based asparaginase. Additionally, although we do not market it for first-line use, there has been considerable first-line application due to its broad acting profile compared to existing first-line therapies and concerns among providers, particularly regarding treatment issues in adult patients. We have also observed notable growth in our efforts this year within the adolescent and young adult market, with increased usage in these groups, which is somewhat different from our original expectations. Overall, the market has embraced Rylaze, particularly in pediatric protocols, but we are also seeing a rise in the use of erwinia-based asparaginases among adolescents and young adults.

Your next question comes from the line of Gregory Renza from RBC Capital Markets.

Bruce and team, congratulations on the update. Bruce, could you provide more specific insights on the competitive landscape of oxybate that you mentioned earlier? I'm curious about the value or potential loss associated with the LUMRYZ FT218 patient. How significant is the experience of trying LUMRYZ and the corresponding prescriber for that patient in the market strategy Renee outlined? Do you see any potential to attract or re-attract such patients as this option becomes more established in the market?

Yes. I love the way you ended your question, which is right where I was going to go with my answer, which is we absolutely expect a new product to get some use. But we think all high-sodium patients, be they on Xyrem, AG Xyrem or the LUMRYZ product or potential future Xywav products, as we saw from the data we shared earlier this year at the neurology meeting, we can see even in as little as 180 days, an increase in hypertension diagnosis or initiation of anti-hypertensive therapy when starting on high-sodium oxybate products. So as physicians and patients have already discovered this matters, and we believe that will continue to be important, making Xywav the oxybate of choice.

Your next question comes from the line of Charles Duncan from Cantor Fitzgerald.

This is Elaine Kim on for Charles. Congrats on the quarter. Regarding PTSD, what are your perspectives on the unmet need and the potential for psychedelic medicine such as MAP's MDMA and possibly organizations like Compass's therapy? And where do you see JZP-150 fitting in the emerging treatment landscape?

Rob, do you want to jump in on that?

Sure. So when I think about a treatment like MDMA and what is associated with that in terms of the support that one needs ultimately, I think that that's going to be appropriate for a subset of the population. PTSD is overall very, very common. And so we think JZP-150 could potentially be much more broadly applicable.

Your next question comes from the line of Jeff Hung from Morgan Stanley.

For suvecaltamide, what's the bar for success in the essential tremor study? And can you talk about what gives you confidence that the Phase IIb will read out positively?

Yes, I believe we have a good understanding of what constitutes a meaningful change on the TETRAS endpoints, with a particular focus on the ADL and a portion of the performance scale. From our Phase II studies and discussions with KOLs and the FDA, we have clarity on what will represent a significant change. Additionally, several other studies that have been published could serve as relevant benchmarks. What distinguishes JZP-385? Several factors contribute to this differentiation. Firstly, it is a state-dependent inhibitor, acting selectively on active ion channels, which is expected to enhance the therapeutic index. We also offer a once-daily formulation. Based on our previous studies, we chose a threefold dose range for the Phase IIb trials—10, 20, and 30 milligrams—which we believe has enabled us to optimize dosing and exposure for maximum efficacy. We are optimistic that this will lead to strong efficacy across that dosage range.

Your next question comes from the line of Mohit Bansal from Wells Fargo.

I have a question about the oxybate franchise. Can you provide insights on the pricing of Xywav in relation to LUMRYZ and the generics available in the market? I'm asking this because we've noticed a sequential decline in this franchise since AG's launch. I would like to understand your perspective on achieving the $2 billion target you mentioned for 2025.

So the quick answer on pricing is there has not been a significant change in terms of sort of our revenue per patient in the past few quarters. In terms of the revenue decline, that's driven by a loss of Xyrem revenues, which, as I've said, have been going down for a long time and are now representing a smaller and smaller portion of our overall revenues while Xywav continues to grow. So those two things at present, as was built into our guidance for the year, essentially are offsetting each other to some degree, but our focus is on growing that Xywav business in narcolepsy and importantly, in idiopathic hypersomnia even as we see royalty income off the AG continue to increase.

Your next question comes from the line of Troy Langford from TD Cowen.

Congrats on the progress in the quarter. Just with respect to the opportunity with Zanidatamab, I guess what else do you guys think you need to check off that list before you can complete the regulatory submission for the product in H1 '24 or H1 next year. And related to that, do you all think that you would need to significantly amplify your current oncology sales force to effectively commercialize the product?

Yes, I'll jump in on that one and just make some comments about our level of excitement about Zani and then ask Rob to comment on the path forward from a regulatory perspective. So as we mentioned on the call, we are extremely excited about this opportunity. This is a highly derisked asset, a global asset for us, and then also one with significant revenue potential. We talked a bit about the data that's been generated to date since doing this transaction. We continue to be impressed with what we in terms of just robust antitumor activity in HER2. And that's in both monotherapy and in combination with other agents, and that gives us a ton of confidence to put both significant investment behind the molecule, but then also to outline the opportunity as having peak revenue potential of over $2 billion. In terms of the near-term need from a commercialization perspective, we don't believe that this is going to require significant augmenting of our current field force. We believe that, that will be quite efficient. And of course, we are focused on going to market first with BTC, as Rob outlined, and then we'll build from there. So Rob, you want to comment on development?

Yes. I think the specific question was what else is needed to complete the BLA submission for BTC. And it's just the usual components. As you might expect, some of those components are going to be available sooner than others. And with breakthrough designation, we've been given the opportunity to do a rolling submission. That allows us to submit components as soon as they're ready to give the FDA sort of a head start on reviewing those components. And then as we said, within the first half of the year, expect to be able to provide everything that's needed to complete that submission.

And we have no further questions in our queue at this time. I will now turn the call over to Bruce for closing remarks.

Thank you so much. I'd like to close today's call by recognizing our Jazz colleagues for their efforts in delivering new therapeutic options to patients and also thank our partners and shareholders for their continued confidence and support. Thank you all for joining us today.

This concludes today's conference call. Thank you for your participation, and you may now disconnect your lines.