NYSE:BHC Bausch Health Companies Q4 2023 Earnings Report $5.12 +0.63 (+13.89%) Closing price 04/17/2025 03:59 PM EasternExtended Trading$5.12 -0.01 (-0.20%) As of 04/17/2025 06:21 PM Eastern Extended trading is trading that happens on electronic markets outside of regular trading hours. This is a fair market value extended hours price provided by Polygon.io. Learn more. Earnings HistoryForecast Bausch Health Companies EPS ResultsActual EPS$1.15Consensus EPS $1.01Beat/MissBeat by +$0.14One Year Ago EPS$1.02Bausch Health Companies Revenue ResultsActual Revenue$2.41 billionExpected Revenue$2.29 billionBeat/MissBeat by +$114.49 millionYoY Revenue Growth+9.80%Bausch Health Companies Announcement DetailsQuarterQ4 2023Date2/22/2024TimeBefore Market OpensConference Call DateThursday, February 22, 2024Conference Call Time8:00AM ETUpcoming EarningsBausch Health Companies' Q1 2025 earnings is scheduled for Wednesday, April 30, 2025, with a conference call scheduled at 5:00 PM ET. Check back for transcripts, audio, and key financial metrics as they become available.Q1 2025 Earnings ReportConference Call ResourcesConference Call AudioConference Call TranscriptSlide DeckInterim ReportAnnual ReportEarnings HistoryCompany ProfileSlide DeckFull Screen Slide DeckPowered by Bausch Health Companies Q4 2023 Earnings Call TranscriptProvided by QuartrFebruary 22, 2024 ShareLink copied to clipboard.There are 11 speakers on the call. Operator00:00:00Greetings. Welcome to the Bausch Health Fourth Quarter and Full Year 2023 Earnings Call. At this time, all participants are in a listen only mode. A question and answer session will follow the formal presentation. Please note this conference is being recorded. Operator00:00:17I would now like to turn the conference over to your host, Maria Lycouris. You may begin. Speaker 100:00:23Good morning, and welcome to Bausch Health's 4th quarter 2023 earnings conference call. Participating in today's call are Thomas Ophio, Chief Executive Officer of Bausch Health and John Bareesi, Interim Chief Financial Officer. Before we begin, I'd like to remind you that our presentation today contains forward looking information. We ask you to take a moment to read the forward looking statements disclaimer at the beginning of the slides that accompany this presentation as it contains important information. Our actual results may vary materially from those expressed or implied in our forward looking statements, and you should not place undue reliance on any forward looking statements. Speaker 100:01:00Please refer to our SEC filings and filings with the Canadian Securities Administrators for a list of some of the risk factors that could cause our actual results to differ materially from our expectations. We use non GAAP financial measures to help investors understand our ongoing business performance. Non GAAP financial measures may not be comparable to similarly titled measures used by other companies and should not be considered along with, but not as an alternative to, measures calculated in accordance with GAAP. You will find reconciliations to our non GAAP measures in the appendix of the slides that accompany this presentation, which are available on Bausch Health's Investor Relations website. Finally, the financial guidance in this presentation is effective as of today only. Speaker 100:01:46We do not undertake any obligation to update guidance. Our discussion today will focus on Bausch Health, excluding Bausch and Lomb. However, we will briefly comment on Bausch and Lomb's results announced yesterday. We will refer to year over year comparisons with the same period last year unless otherwise noted. For the benefit of those who may be listening to the replay or archived webcast, this call was held on and recorded on February 22, 2024. Speaker 100:02:12With that, it is my pleasure to turn the call over to our CEO, Thomas Appiah. Tom? Speaker 200:02:18Thank you, and welcome to those of you joining the call this morning. I want to start today's call by highlighting the strategic priorities we set out to achieve this past year: growth, performance, focus and unlocking value. These priorities help support our ambition of being a globally integrated healthcare company trusted and valued by patients, healthcare providers, employees and investors as we relentlessly drive to deliver better health outcomes. We made significant progress on these priorities in 2023, reinforcing our strong global foundation, which consists of a large portfolio of products across a diverse set of therapeutic areas and geographies. Our significant presence in gastroenterology, hepatology, neurology, dermatology, medical aesthetic devices and international pharmaceuticals across the branded, generic and branded generic markets give us a solid platform for growth as we are excited about the opportunities in each of these areas. Speaker 200:03:27From a financial perspective, I am pleased to report we achieved or exceeded our February 2023 guidance. For Bausch Health, excluding BNL, full year revenue was $4,610,000,000 and organic revenue growth was 6%, both slightly above our February 2023 guidance range and in line with our guidance update in November. For Bausch Health, excluding BNL, full year adjusted EBITDA was $2,360,000,000 in line with our guidance while funding incremental spend on R and D to support our Red Sea and amicillimod programs. Importantly, we ended the year on a strong note as the 4th quarter represented our 3rd consecutive quarter of year over year growth in adjusted EBITDA and we delivered adjusted operating cash flow of $708,000,000 above our guidance. For the Q4, revenues for Bausch Health excluding BNL were $1,240,000,000 up $38,000,000 or 3 percent on a reported basis and 2% on an organic basis. Speaker 200:04:45Adjusted EBITDA was $663,000,000 an increase of approximately 1% compared to the prior year. We made significant progress across our key R and D initiatives during the quarter. 1st, we received a positive top line data from our large global Phase 2 trial for amisolimod. 2nd, we completed enrollment for 1 of our 2 global Phase 3 trials for Red Sea with the second trial expected to complete enrollment in the first half of this year. And 3rd, in January, we received approval by the National Medical Products Administration or NMPA for Thermage FLX and the TR-four return pad in China. Speaker 200:05:34I will touch on these in more detail shortly. I am pleased with the continued momentum in our pipeline. Strengthening our balance sheet also remains a priority as we are focusing on managing our liquidity position. During 2023, we reduced debt net of cash for Bausch Health excluding BNL by 670,000,000 and in January 2024, we retired an additional $250,000,000 in principal value of debt through an open market repurchase program. We continue to defend our intellectual property rights for XIFAXAN. Speaker 200:06:13As discussed on our Q3 2023 earnings call, on October 6, 2023, the DC District Court held a hearing in Norwich's lawsuit against the FDA, where Norwich was seeking immediate approval of their ANDA. On November 1, the court denied Norwich's motion and granted summary judgment in favor of the FDA and Salix. In December, Norwich appealed the District Court's decision to the U. S. Court of Appeals for the DC Circuit. Speaker 200:06:47The DC Circuit has stayed the appeal until the Federal Circuit renders the decision in our XIFAXAN litigation. The consolidated appeals from the Delaware District Court are pending at the U. S. Court of Appeals for the Federal Circuit. On January 8, the Federal Circuit heard oral arguments. Speaker 200:07:07We expect a decision to follow late in Q1 or early in Q2. We are committed to vigorously defending our intellectual property and providing healthcare providers and patients with safe and effective treatments. You will recall that in January of 2023, we reached a tentative settlement with the IRS to resolve the Granite Trust matter. We continue to expect this settlement to be finalized in the coming months as we have previously said. The anticipated outcome of the settlement does not have a material impact on the company's results or cash flows. Speaker 200:07:46Turning now to the potential full separation of Bausch and Lomb. We continue to believe the separation of Bausch and Lomb makes strategic sense and we continue to evaluate strategies regarding the potential full separation with the objective of ensuring that this transaction results in 2 appropriately capitalized companies. Any decision regarding if and when a separation occurs or its structure will be based on and subject to an assessment of all relevant factors and circumstances. Any potential separation will also be subject to shareholder and other applicable approvals. And in the meantime, we are focused on managing our balance sheet. Speaker 200:08:31We ended the quarter with more than 1 $500,000,000 of liquidity. We repurchased a small amount of debt in the Q4 and in January 2024 repurchased approximately $250,000,000 in principal value of our debt. Finally, we are introducing our 20 24 guidance for Bausch Health excluding BNL, which reflects our confidence that we can deliver top and bottom line growth again in 2024. John will speak in more detail to this later in the call. Turning now to an overview of our segment performance for the quarter. Speaker 200:09:07In Salix, we continued to see strong demand in Q4 for our key products, including XIFAXAN. For XIFAXAN, we saw approximately 3% TRx growth in Q4 over the prior year with a strengthening trend in the back half of the quarter. This was led by strong growth for IBS D with a return to growth for HE driven by long term care channel. Putting this all together, we believe we are starting to see the benefits our investments in AI enabled sales force tools and DTC advertising to spread awareness of the underlying medical conditions and the options that are available to treat them. For 2024, we anticipate maintaining our current level of investment in these areas to drive further growth in this important franchise. Speaker 200:09:57Finally, TRULANCE and RELISTOR continued to deliver double digit TRx growth in the quarter. Turning to international, we saw strong year over year revenue growth on both a reported and organic basis. In all regions during the Q4, continued growth in our promoted brand portfolios in key markets including Poland, Mexico and Canada More than offset the impact of the MRADE recall earlier in 2023 and increased generic competition for certain products particularly in Canada. Our focus in 2024 will be continuing to invest in our promoted product portfolio, while looking for business development opportunities to drive long term growth. In Sultum Medical, revenues increased by 4% on a reported and 5% on an organic basis, reflecting solid growth in China as well as growth in the broader Asia Pacific region. Speaker 200:10:59Revenues in the U. S. Declined slightly in the quarter. Highly focused on maintaining our momentum in Asia, including driving Thermage FLX performance in China. And in 2024, we'll also be focused on growing our U. Speaker 200:11:14S. And EMEA markets, where we believe there is meaningful opportunity to expand our presence. To support these efforts, we have added talented key leadership to the Solta business to advance our leading portfolio of products and have invested in the expansion of the U. S. Field force. Speaker 200:11:31We are also focusing our R and D organization on our pipeline of new market authorizations and next generation products as we continue to build upon this world class durable aesthetics business. In Diversified, we saw another quarter of healthy performance, particularly in neurology as we continue to capitalize on opportunities in the market created by competitor supply constraints. We remain focused on managing this mature portfolio of products for profitability and cash generation in a challenging competitive and pricing environment and continue to look for opportunities to make targeted investments where appropriate. Dentistry revenues were in line with a strong Q4 in the prior year and in the coming year we are looking to accelerate growth with a focus on the sales force and new marketing tools. In dermatology, CabTrio is now launched and available for patients in the U. Speaker 200:12:30S. At the end of January 2024 and we are excited to be able to provide this new once a day triple combination topical acne treatment for patients. We continue to expect that Cabtrillo will be launched in Canada in the second half of twenty twenty four. Turning to the latest developments in our R and D pipeline, starting with our GI pipeline. In December, we announced positive top line results from our Phase 2 study evaluating amicilimod, an S1P antagonist in the treatment of ulcerative colitis or UC. Speaker 200:13:09We are very pleased that the study met the primary and key secondary endpoints including clinical remission and endoscopic improvement during the double blind period of the study with no unexpected adverse events. We are preparing for our next steps to progress this program, including presenting the detailed results at upcoming scientific conferences and planning to meet with the FDA for an end of Phase 2 meeting. We are planning to advance into Phase 3 in moderate to severe UC patient and could possibly target all UC patients based on our results. We anticipate a step up in R and D spend to support these Phase 3 efforts as well as exploring opportunities to expand into other therapeutic areas, primarily Crohn's disease with a Phase 2 program. We expect to initiate our global Phase 3 program for UC in late 2024. Speaker 200:14:09Our Red Sea program for rifaximin for reduction of early decompensation in cirrhosis continues to advance. The global program is focused on delivering a novel formulation and assessing the efficacy of rifaximin SSD formulation versus placebo to delay the occurrence of HE related hospitalizations. We completed enrollment for 1 of 2 large global Phase 3 trials as of the end of the year with enrollment for the second trial expected to be completed during the first half of twenty twenty four. Together, these studies are expected to include approximately 1,000 patients across the major markets of North America, Europe and Asia Pacific. Turning now to our aesthetics pipeline. Speaker 200:14:57We are very pleased to have received approval for Thermage FLX and TR-four return pad from the NMPA in China in January. We are excited about the opportunities in this market and we see a runway for growth. We expect to start realizing the benefits of this starting in the Q2 of this year. We plan an FDA submission for our next generation Fraxel, a fractionated laser device for skin resurfacing in the Q2 of 2024, we expect approval could be received in the second half of this year. Finally, our program for clear and brilliant touch, a fractionated laser device for skin rejuvenation continues to advance with regulatory submission still on track for 2024 in Europe, Canada and Asia Pacific markets. Speaker 200:15:50As a leadership team, we remain committed to driving growth by leveraging our existing assets, making targeted investments and executing with commercial excellence, while continuing to progress our pipeline all with a patient centered mentality. With that, I will turn the call over to John Barresi who will provide further details on our Q4 performance and financial outlook for 2024. John? Thanks, Tom. Hello, everyone, and thanks for joining us. Speaker 300:16:23We closed the 4th quarter with consolidated revenues for Bausch Health of $2,410,000,000 up 10% on a reported basis and 4% on an organic basis over the same quarter last year. On a consolidated basis, revenue increased 8% for the full year on a reported basis and 7% on an organic basis. 4th quarter revenues for Bausch Health excluding BNL were $1,240,000,000 up 3% on a reported basis and up 2% on an organic basis over the same quarter last year with growth in our international, diversified and Solta segments, while Salix was in line with last year. Bausch Health excluding B plus L ended the year with revenues of $4,610,000,000 up $255,000,000 or 6% on both a reported and organic basis compared to 2022. Let's dive into the revenue performance for each segment in more detail starting on Slide 13 with Salix. Speaker 300:17:204th quarter Salix revenues increased $2,000,000 on both an organic and reported basis to $583,000,000 driven by TRx growth in our key products, including XIFAXAN, RELISTOR and TRULANCE. Comparisons to the prior year's quarter were impacted by changes in the timing of wholesaler buying patterns. As you will recall, sales reported 13% growth in the Q3 of 2023 compared to the Q3 of 2022. As we noted then, we saw an increase in wholesale channel inventory in Q3 earlier than we had anticipated. And this quarter, we saw inventory in the wholesale channel decline compared to a build in Q4 of 2022. Speaker 300:18:02For the full year, Salix reported revenues of $2,250,000,000 an increase of approximately 8% over 2022 on a reported basis. We realized an approximately 3% increase in net price along with an approximately 5% increase in volume with the volume increase split roughly equally between underlying demand and the impact of higher overall wholesale inventory levels year over year. While inventory in the channel declined relative to Q3, we did end the year higher than we ended 2022. XIFAXAN continued to represent approximately 80% of Salix segment revenues this year and saw strong growth in underlying demand. Retail prescriptions grew 3.1% in Q4 versus the prior quarter. Speaker 300:18:47We saw growth in TRx for IBS D and importantly, we also saw solid growth of approximately 6% year over year in Q4 in TRx for the long term care channel as well as strong growth in non retail units attributable to outpatient clinics. For the quarter, XIFAXAN revenues were in line with the prior year as this TRx growth was offset by the timing of wholesaler buying patterns discussed earlier. For the quarter, RELISTOR delivered 44% growth over the prior year due to both higher demand and improved net pricing, while TRULANCE revenues were flat as TRx growth was offset by lower net pricing and shifts in wholesale inventory. International revenues were $290,000,000 during the quarter, an increase of 11% on a reported basis and 6% on an organic basis compared to the prior year period, with strong performances across the EMEA, Canada and Latin America regions. For the full year, international revenues were $1,070,000,000 for 2023 compared to $988,000,000 for 2022, an increase of $83,000,000 or 8% on a reported basis and 6% on an organic basis. Speaker 300:20:01This year's international segment performance was driven mainly by an increase in net realized pricing as growth in our portfolio of promoted products was offset by the impact of increased generic competition and the effects of the MRADE recall in the 2nd quarter. Ulta Medical revenues were $103,000,000 for the 4th quarter, an increase of 4% on a reported basis and 5% on an organic basis over the prior year period. Growth in the quarter was led by China and to a lesser degree the remainder of Asia Pacific, while sales in the U. S. Slightly declined compared to the prior year. Speaker 300:20:38Ulta Medical ended the year with revenues of $347,000,000 an increase of 16% on a reported basis and 18% on an organic basis compared to 2022. Revenue growth was driven by strong demand in China, including the effect of comparison to 2022 when China and to a lesser degree the rest of the Pacific region were affected by COVID related lockdowns. With approximately 80% of the revenue for this business coming from consumables, the recent Thermage FLX approval in China and possible untapped potential in the U. S. And EMEA, we believe Solta Medical is positioned for continued near and long term growth globally. Speaker 300:21:18Diversified revenues were $259,000,000 during the 4th quarter, an increase of 1% on a reported basis and 2% on an organic basis compared to the prior year period. Neurology delivered year over year growth as we continued to capitalize on opportunities in the market created by supply constraints among competing products in the Q4. In dermatology, revenue declined by 12% for the quarter relative to the prior year as volume increases for JUVIA and ERASLO were offset by continued net pricing pressures and continued pressure on our non promoted products. And as Tom mentioned, Captrio is launched and available for patients as of late January 2024. And in addition to the important benefits this product is expected to bring patients, we view this as an opportunity to return the dermatology business to growth. Speaker 300:22:09The generics business continues to be a profitable, cash generative business. However, it also faces a highly competitive environment from both pricing and volume standpoint. While it plays a role with our LOE products, with the timeline of many of those LOEs and the competitive environment we expect to face for the long term, we have revised our expectations for this business and recorded an impairment of goodwill of $91,000,000 in the quarter. Dentistry revenue of $29,000,000 was in line with a strong Q4 in 2022. We continue to invest in the dentistry business for the long term and are looking to accelerate growth in 2024. Speaker 300:22:48For the year, Diversified segment revenues declined 4% on a reported basis and 3% on an organic basis relative to the prior year with varying degrees of declines in neurology, dermatology and generics reflecting the pressures we've discussed throughout the year. As shown on Slide 18, Bausch and loan revenues were $1,170,000,000 during the 4th quarter, up 18% on a reported basis and 7% on an organic basis compared to the prior year with growth across all Bausch and loan segments. Similarly, Bausch and Loan revenues for the year increased by $378,000,000 on a reported basis or 10% and 8% on an organic basis compared 2. Turning to the 4th quarter P and L on slides 2020 gross margin was 71.6%, 130 basis points higher compared with the prior year. Full year consolidated adjusted gross margin was 71%, 10 basis points higher than last year. Speaker 300:23:53For Bausch Health, excluding BNL, adjusted gross margin for the Q4 was 80.2%, approximately 30 basis points lower than last year's Q4. For the full year, adjusted gross margin was 80.1%, a decline of 50 basis points, which included the impact of the Emerald A recall earlier in the year. At B and L, adjusted gross margin was 62.5 percent for Q4 of 2023 compared to 57.9% for Q4 of 2022, driven primarily by product mix including Xiidra. Consolidated adjusted operating expenses for the Q4 were $891,000,000 an increase of $121,000,000 For Bausch Health excluding V and L, adjusted operating expenses increased by approximately $16,000,000 during the quarter as higher A and P was driven by investments in the Salix segment. D expenses also increased primarily related to our Salix initiatives. Speaker 300:24:51Adjusted G and A for Bausch Health excluding B and L was slightly favorable to the prior year as we annualized stabilization of the post IPO structure and focused on cost containment. B and L reported an increase of $105,000,000 in adjusted operating expenses due primarily to increased selling in A and P driven by product launches. Consolidated adjusted R and D expense for the quarter was $151,000,000 an increase of 6% compared to the prior year and represented 6.3% of product sales compared with 6.5% for the prior year period. For Bausch Health excluding BNL, R and D expenses of $72,000,000 increased by approximately $8,000,000 for the Q4 as compared to the same quarter last year. As Tom mentioned, we expect another meaningful step up in R and D expense throughout 2024 to support the next phase of development for amicilimod. Speaker 300:25:47We also will continue to progress our 2 global Red Sea Phase 3 clinical trials. 4th quarter consolidated adjusted EBITDA was $897,000,000 an increase of $56,000,000 or 7% on a reported basis. Adjusted EBITDA for Bausch Health excluding BNL was $663,000,000 for the quarter, a slight increase from $659,000,000 in the 4th quarter of 2022. For the full year, consolidated adjusted EBITDA was $3,110,000,000 and for Bausch Health excluding B plus L was $2,360,000,000 both slight increases from 2022. Turning to cash flow. Speaker 300:26:29On a consolidated basis, Bausch Health generated $390,000,000 of operating cash flow and $305,000,000 of adjusted operating cash flow in 4th quarter. Full year cash flow from operations on a consolidated basis was $1,030,000,000 adjusted cash flow from operations on a consolidated basis was $763,000,000 For Bausch Health excluding BNL, adjusted operating cash flow was $278,000,000 for the 4th quarter $708,000,000 for the full year compared to adjusted operating cash flow of $340,000,000 for the Q4 of 2022 $637,000,000 for the full year 2022, with the changes primarily reflecting the timing of working capital movements and for Q4 the timing of interest payments. The full year 2023 also exceeded our guidance of $625,000,000 driven by our focus on expense management as well as by the timing of cash collections based on the wholesaler buying patterns I discussed earlier. As we've discussed in prior quarters, as a result of the accounting treatment for the senior notes issued as part of our 2022 debt exchange, a portion of our cash interest payments are classified as financing cash flows. Adjusted cash flow includes payments of the full contractual interest as well as adjustments for the payment of separation costs, business transformation costs and litigation and other matters net of insurance proceeds. Speaker 300:28:00Now let's turn to our balance sheet on Slide 22. We continue to prioritize liquidity management and the delevering of our balance sheet. In the Q4 of 2023, we reduced our debt net of cash for Bausch Health excluding BNL by approximately $250,000,000 We continue to evaluate alternatives to reduce our overall leverage while also focusing on our maturity profile. Despite only retiring a small amount of debt in Q4, in January 2024, we retired $250,000,000 in principal value of 2025 and 2026 maturities through open market repurchases, capturing approximately $12,000,000 of discount in the process. At the end of the Q4, Bausch Health excluding BNL had $350,000,000 outstanding under our accounts receivable facility and had no outstanding borrowings and approximately $950,000,000 of availability under our revolving credit facility. Speaker 300:28:59As shown on Slides 2324, total debt for Bausch Health excluding Bausch and Lomb at the end of the quarter was $16,400,000,000 which consisted of approximately $15,000,000,000 of restricted debt issued by Bausch Health excluding BNL and approximately $1,400,000,000 of unrestricted debt, which includes the $1,000,000,000 of senior secured notes issued by the unrestricted subsidiary created in the Q3 of 2022 and the $350,000,000 drawn under our accounts receivable facility. Excluding B plus L debt, approximately 85% of our debt is fixed and approximately 70% of the company's debt on a consolidated basis is fixed. Debt net of cash for Bausch Health excluding BNL is down approximately $670,000,000 since the beginning of 2023. We ended the year with over $1,500,000,000 of liquidity, including approximately $616,000,000 of cash and $950,000,000 of availability under our revolving credit facility. We will continue to evaluate the best uses of that liquidity, including focus on our maturity profile and our overall leverage. Speaker 300:30:12Overall, we are pleased that revenues, adjusted EBITDA and adjusted operating cash flow for 2023 for Bausch Health excluding BNL met or exceeded expectations. With that as the backdrop, I'll now discuss our guidance for 2024, which you can find on Slide 26. In 2024, we expect revenues of $4,700,000,000 to $4,850,000,000 with growth of 2% to 5% on an organic basis. For 2024, we expect foreign exchange impact to be a slight tailwind. Full year adjusted EBITDA for Bausch Health excluding BNL is expected to be $2,360,000,000 to $2,460,000,000 For Salix, we expect to see mid single digit revenue growth. Speaker 300:31:00Based on the investments we've made, we expect volume growth from a TRx and extended units perspective to expand relative to what we saw in 2023, although changes in wholesale or purchasing dynamics may temper how that growth translates into revenue growth. We also intend to maintain our investments in selling and A and P consistent with 2023 levels. Lastly, as we've noted in the past, we typically see a seasonal step up in sales in the second half, particularly in XIFAXAN, primarily due to wholesaler inventory dynamics as well as patient level patterns related to insurance deductible activity. For international, we expect mid single digit organic revenue growth led by the EMEA and Latin America regions. We are excited by the potential for new product launches in these regions. Speaker 300:31:48In Canada, we plan to further grow the recently launched products Realtris and UCERIS and continue to focus on obtaining approval of Kebtrio. We're also making targeted investments in sales teams and promotion across the different regions. For Solta, we anticipate strong double digit organic revenue growth across all major geographies. We have new leaders in key positions in this business and have invested in expansion of the U. S. Speaker 300:32:13Sales team. Therefore, we anticipate growth led by China and Asia Pacific as well as double digit growth in the U. S. And EMEA regions. For Diversified, we expect an overall mid single digit decline in organic revenue. Speaker 300:32:28We expect growth in dermatology led by the introduction of CabTrio and in dentistry driven by continued investment in the sales force and related tools with continued pressures in our neurology and generics businesses. From a gross margin perspective, we expect to continue to mitigate the impact of inflation on our cost of goods sold and we expect our gross margin to remain comparable to last year at approximately 80%. On the expense side, we anticipate that selling and A and P will grow in line with sales growth as we maintain the base we established in 2023 and make targeted investments to drive growth in businesses including Solta and dentistry. Additionally, as we've discussed previously, there will be a meaningful increase in R and D spend throughout the year as we invest for the future in our GI and aesthetics pipeline programs. We think it is critical to continue to allocate capital to this area for the long term as it will benefit patients and healthcare providers while positioning our business to deliver stakeholder value. Speaker 300:33:29Lastly, we expect adjusted operating cash flow for Bausch Health excluding BNL in a range of approximately $775,000,000 to $825,000,000 for 2024. And as I said earlier, adjusted cash flow includes adjustments for the payment of separation costs, the payment of the full contractual interest on our existing debt and also includes lower tax payments in 2024 relative to 2023 inclusive of the impact of the tentative Granite Trust settlement. I'll now hand the call back to Tom. Speaker 200:34:02Thank you, John. In summary, as you heard today, we made significant progress against our 2023 strategic priorities and we enter 2024 with strong momentum and a clear set of objectives. We are excited about the potential of our Salix business led by XIFAXAN and we will continue to advance our pipeline with Red Sea and amicilimod. We believe Solta is poised for long term growth with Thermage FLX in China and untapped potential in the U. S. Speaker 200:34:36And EMEA. The broad portfolio of products and geographies in our international business will continue to provide balanced growth. And in our diversified business, we believe dermatology with the launch of Cabrio and dentistry will deliver growth with the remainder of the portfolio remaining profitable and cash generative in a challenging competitive and regulatory environment. With the year ahead, we are focused on building on the foundation we have set across our diverse global business by driving a results oriented culture of accountability delivering on our revenue, adjusted EBITDA and adjusted operating cash flow commitments executing with operational excellence and cost focused mindset across the enterprise, intensifying our focus and operating rigor behind R and D and business development and continuing to evaluate strategic alternatives. We will execute against these objectives with a focus on operational excellence with a patient centered mentality. Speaker 200:35:54I am thankful for and proud of our Bausch Health team for their achievements this year. They have worked tirelessly and are all in to position our business for the long term. Life won't wait, neither can wait. Every patient deserves better health and the chance to make the most of life. This drives us on with urgency and efficiency to deliver the products patients need most to enrich their lives. Speaker 200:36:25On behalf of our entire Bausch Health team, I thank you for your interest in and support of our company. With that, we will now take questions. Operator, please open the line for Q and A. Operator00:36:38Thank you very much. At this time, we will be conducting our question and answer Thank you. Your first question is coming from Glenn Santangelo of Jefferies. Glenn, your line is Speaker 400:37:17live. Yes. Thanks for taking my question. Hey, Tom, I just had two quick ones. I appreciate all the details on the 2 pipeline programs. Speaker 400:37:25But as we think about doing some long term modeling, I was wondering if you could maybe help us think about broad timelines for both these programs as we think about the path to approval? And then maybe secondly, in recent quarters, I mean, the company has talked about a number of different recapitalization opportunities. And in your prepared remarks, you talked about how you retired $250,000,000 of debt in January. And I'm just sort of wondering, given where the debt trading, where BLCO is trading, given that Salt is doing much better, without getting specific, do you see any meaningful opportunities for further recapitalization efforts in 2024? And I'll stop there. Speaker 400:38:07Thanks. Speaker 500:38:10Hi, Glenn. Thanks. Appreciate the question. So overall when we take a look at these two programs, clearly if we take a look at Red Sea, we think this is a great opportunity. Clearly, the patient pool here is large, much bigger than today's patient pool that we're looking at because this is a prevention trial. Speaker 500:38:33So as we one of the things that we did this year was really energized and put more money behind those studies to make sure we got the recruitment. As I said in my prepared remarks, we had the first the one study completely recruited and then the second study we're expecting that in the first half. So trying to really accelerate that program, So we have a launch probably in sometime in 2027. This is going to be again a large pool. It is prevention. Speaker 500:39:10So clearly there is a good really good opportunity for us. On the amicilimod side, of course we are really pleased with the data on the Phase 2 program. This was a very large Phase 2 program. We're working right now to see what the timing will be of the Phase 3 program. We're expecting at the end of the decade to be able to launch the product in UC. Speaker 500:39:38As I said in my prepared remarks, there is an opportunity here to continue to expand as if we looked at Crohn's and running a Phase 2 program and then if the data is good, clearly running a Phase 3 program, which would push approval something into the first half of the next decade. So I really think these two programs give us a really good momentum on our R and D programs as we Speaker 300:40:10look forward. I'll turn off turn the call over to the question over to John to talk about the debt. Yes. Thanks, Glenn. Yes, as we've said, we're always looking at the options that we have to manage our balance sheet, manage our debt. Speaker 300:40:26We're not going to comment on any specific strategies or actions that we may undertake at any point in the future. But what I will say is if you think about where we sit today, we have over $1,500,000,000 of liquidity between our cash and the revolver flexibility. We're guiding to $775,000,000 to $825,000,000 of adjusted operating cash flow and we typically use a fair amount of that manage our debt. As you noted, we do have the flexibility on the roughly 8% of BLCO that we still own that we have the option to monetize at some point. And we are focused on reducing debt. Speaker 300:41:03So we're always looking at all the tools and all the options, but we're not going to comment on anything specifically at this point. Speaker 400:41:09Appreciate all the detail. Speaker 200:41:10Thanks. Thanks. Operator, next question. Operator00:41:14Thank you very much. Your next question is coming from David Amsellem of Piper Sandler. David, your line is live. Speaker 600:41:23Hi. This is Skyler on for David. So first, what are your thoughts on how amicelimod could fit into the UC space in the context of existing approved S-1Ps and a pretty competitive pipeline? And then separately, could you also talk about the extent to which you will further invest in XIFAXAN as it moves through the later part of its commercial life? Thanks. Speaker 500:41:45Yes. What I would say is on amiselimod, clearly among S1Ps, the positive top line data suggests it could be a promising therapy in terms of efficacy and safety in the space. There are a few others in the space. When we look at the data, we think we have a real competitive product here. So as we continue to really look at the data and build our Phase 3 program, we'll see where that fits. Speaker 500:42:17But we think again on the positive top line data, it looks really good. What I would say is on XIFAXAN, we have multiple formulations on XIFAXAN. We're always looking from an R and D perspective of where we could use these new formulations as the Red Sea program. Clearly, we're using one of our new formulations, but we're always looking for and looking at the link between the gut and the brain. And then clearly that is a focus for the team. Speaker 500:42:53If you want to talk about investing in XIFAXAN on the commercial life side of it, I still think even though XIFAXAN is late in its life cycle, as you saw the results for 2023, They are strong. We believe we can continue to grow our franchise, the investments we have put behind AI for the field force and that has been rolled out to the entire the field force on both the primary care and specialty care side. If you look at the data that we saw in the Q4 as we exited the year, the data was strong. And so that those tools are really going to help us move forward with XIFAXAN. The other thing also is, is when I take a look at XIFAXAN, clearly there's a lot of unmet needs still there and I think we can tap that with the programs and the investments that we're making between AI and DTC as I said in my prepared remarks. Speaker 500:44:01So I really the team has really done a really great job this year with XIFAXAN and getting the growth on it and then the unmet need that is still there in both the IBS D side of the business and the HE side of the business, there's still an unmet need that we can treat more patients. Operator, next question. Operator00:44:25Thank you very much. Your next question is coming from Umer Raffat of Evercore ISI. Umer, your line is live. Speaker 700:44:34Hi. This is Chen Zhang on for Umer. Thanks for taking our questions. Two questions, if I may. So first, in the scenario that Norwich loses the patent appeal, will they reunite their APA loss case appeal? Speaker 700:44:45And if that if so, what would be the angle? And secondly, can we get more colors on the SG and A increase in the Q4 and your expectation in 2024? Thank you. Could Speaker 500:44:56you just on the first part of your question, what specifically we are asking on Novoix? Just Speaker 200:45:03could you I'm trying to Speaker 500:45:04understand what you're actually asking there. Speaker 700:45:08Let me repeat. So if in a scenario that Norrish loses the patent appeal case, will they reignite their APA against FDA case? If so, what will be the angle? Speaker 500:45:21Yes. I can't comment on what they would do on their litigation if they were to lose. So I mean, again, I can't comment on the call of what their steps would be. But again, we feel confident in our appeal and in our intellectual property. Next question? Operator00:45:45Thank you very much. Your next question is coming from Jason Gerberry of Bank of America. Jason, your line is live. Speaker 800:45:55Hi, this is Chi on for Jason. Thanks for taking our questions. A couple from us. So regarding the SYFAXAN acute decision that you expect later in Q1, early Q2, Say let's say if the appeal is favorable to Bausch, how does the favorable appeal ruling impact your thinking on the separation of Belco? Would you look to move quickly once that particular legal matter is resolved? Speaker 800:46:27Or are there other settlements in legal matters contingent? And my second question is on emisalomod. You ran a Phase II in mild to moderate and it sounds like you are moving thinking about moving Phase III to in the moderate to severe population. So I'm curious what prompt that change and given there are multiple other S1Ps already approved for in development in the moderate or moderate to severe population? Thanks. Speaker 500:47:01Okay. On your first part of the question regarding XIFAXAN, what I would say is this is, as you know, we had the appeal that was heard, the oral arguments were heard in January. We believe it went well. What I would say is, is we believe that the if we were to win, there are still factors that we need to consider. We believe that the separation continues to make strategic sense. Speaker 500:47:31And there are many factors that will go into the timing of any potential data and the positive data that we saw, as you know, we ran the trial mild to moderate, we think that amiselimod has the potential to be very broad in what the data shows. So we did when the trial was running, we did have mild to moderate. But as we look at it, we could move it more into moderate to severe on a Phase 3 program. And as I said in my prepared remarks, probably treat all, but that's still under discussion. Operator, next question. Operator00:48:18Thank you very much. Your next question is coming from Douglas Meem of RBC Capital Markets. Douglas, your line is live. Speaker 900:48:27Great. Thank you. Question has to do with Q4 of XIFAXAN and TRULANCE where it looked like it was all flat. And forgive me if you spoke about this already. Just curious as to why that occurred given the strong prescription strength during the quarter and also the pricing increase you took at the beginning of the year? Speaker 900:48:48And then perhaps related to that, you can expand on the commentary that was made around prescription growth in the guidance 2024 and how that could be impacted by, I think it was managed care that you talked about? Thank you. Speaker 500:49:07Yes. So let me just overall, when we look at XIFAXAN and the TRx growth, if you look at the product for the full year, we had an increase of 8%, 3% on price, 5% on volume and we talked about some of the inventory channels, the inventory channel that we had. But overall the TRx growth that we looked at it for the year was strong. And when we looked at the Q4 on the IBS D side, we were exiting at much higher than what the full year looked like. And when we look at HE in the long term care space that was over 6%. Speaker 500:49:50So the product as the performance as we ramped up the investments, okay, in and launched different activities during the year, you could see it benefited from the second half. I'll let John talk specifically about the second part of the question. Speaker 300:50:09Yes. On the revenue trends, if you remember in the Q3, Salix was plus 13%, I believe, for the Q3. And we saw at this time, we spoke about some pull forward of the demand increase that we'd normally see in Q4 into the later stages of Q3. And so that I think is the biggest driver of the difference between revenue growth and TRx growth for Q4 on the XIFAXAN and the TRULANCE side. And then on the question of the Q4 guidance, I think what we had said was, we expect expansion of the growth of TRx. Speaker 300:50:49However, we did end 2023 a little bit higher in the wholesale channel than we ended 2022. And so we had a little bit of a build there. And it's possible, right? The wholesalers have their own algorithms for how and when they buy, but it's possible that if we see that revert back a little, that it could temper some of the benefit from a revenue standpoint of the underlying demand growth. Okay. Speaker 300:51:15Great. Speaker 200:51:16Lastly, when we just take Speaker 500:51:18a look at it, we could frame it. When we look at IBS D, there's 2,200,000 patients that are diagnosed, but only about 100 and 20,000 received treatment. So again, with a second line medication like XIFAXAN. So clearly still a large unmet need and some of the investments that we have made this year and last year and we will continue to make in 2024 to capture that. On the HE side, if you look at the analytics that we look at, there's about 190,000 patients that potentially have HE and only that we're going to continue to invest behind. Speaker 500:52:16Operator, next question. Operator00:52:18Thank you very much. And your next question is coming from Michael Nedelkovich of TD Cowen. Michael, your line is live. Speaker 1000:52:27Thank you for the question. I have 2. For the first, if you could transport us to late May, let's assume that you had a wildly favorable ruling in the case against Norwich such that XIFAXAN's exclusivity out to 2028 is all but certain. I know that as it relates to the Bausch and Lomb full separation, there are multiple additional factors to consider. But what is item number 2 on your checklist? Speaker 1000:52:55So the XIFAXAN ruling is done and its outlook is certain. What's item number 2 when you move toward full separation? And then my second question relates to amicelimod. As has already been noted, there are 2 other S1P receptor modulators approved for UC, but their market reception so far has been lukewarm. Do you think that imicelimod has better commercial prospects than the agents already approved? Speaker 1000:53:20And if so, why is that? Speaker 500:53:24Yes. So let's take the first part of the question. I can't speculate on what number 2 would be. There as I said, there's still many factors that go into the timing of the potential distribution. And clearly, again, we believe in our intellectual property and hoping for a favorable outcome. Speaker 500:53:46But there are a multitude of steps. So I can't speculate on what number 2 would be, but clearly looking to a favorable outcome on the XIFAXAN case. When it comes to amicilimod, we've had a lot of discussions on this internally. Yes, the 2 that are out there are as you use lukewarm. We believe based on our data that we have a competitive product, a once a day treatment and oral. Speaker 500:54:21So clearly, as we continue to look at it and build the Phase 3 program, I can give you more information as we move forward on the program and see what we think going forward. But if we look at our data, again, we think it's positive and we think we have a really interesting product here. Operator, next question. Operator00:54:49Thank you very much. Well, that appears to be the last of our questions. I will now hand back over to Tom for any closing comments. Speaker 500:54:57Okay. Well, since there's no further comments, I want to say thank you to all who joined the call today. As we discussed on this call, we had a solid Q4 2023. We grew our company and delivered or exceeded our guidance. I would like to thank my over 7,000 colleagues around the world for their relentless drive to deliver better health outcomes and continue to build a company that is trusted and valued by patients, healthcare professionals and investors. Speaker 500:55:30We entered 2024 with strong momentum and look forward to executing on our strategic objectives, delivering on our commitments as we continue transforming Bausch Health, positioning our company for the long term. Thank you for your interest in and the support of Bausch Health.Read morePowered by Conference Call Audio Live Call not available Earnings Conference CallBausch Health Companies Q4 202300:00 / 00:00Speed:1x1.25x1.5x2x Earnings DocumentsSlide DeckInterim reportAnnual report Bausch Health Companies Earnings HeadlinesIs Bausch Health Companies (BHC) the Ridiculously Cheap Stock to Invest in?April 19 at 5:00 PM | insidermonkey.comBausch says court grants summary judgment in favor of FDA, Salix, and TevaApril 18 at 5:41 AM | markets.businessinsider.comCrypto’s crashing…but we’re still profitingMost traders are panicking right now. Bitcoin’s dropping. Altcoins are bleeding. The stock market’s a mess. The news is screaming fear. But while most traders watch their portfolios tank…April 19, 2025 | Crypto Swap Profits (Ad)Bausch Health shares jump on favorable court rulingApril 17 at 7:39 PM | investing.comFitch raises Bausch Health rating to CCC+ amid refinancingApril 17 at 2:38 PM | investing.comBausch Health Adopts Shareholder Rights Plan to Ensure Fair TreatmentApril 14, 2025 | tipranks.comSee More Bausch Health Companies Headlines Get Earnings Announcements in your inboxWant to stay updated on the latest earnings announcements and upcoming reports for companies like Bausch Health Companies? Sign up for Earnings360's daily newsletter to receive timely earnings updates on Bausch Health Companies and other key companies, straight to your email. Email Address About Bausch Health CompaniesBausch Health Companies (NYSE:BHC) operates as a diversified specialty pharmaceutical and medical device company in the United States and internationally. It develops, manufactures, and markets a range of products primarily in gastroenterology, hepatology, neurology, dermatology, international pharmaceuticals, over-the-counter (OTC) products, aesthetic medical devices, and eye health. The company operates through five segments: Salix, International, Solta Medical, Diversified, and Bausch + Lomb. The Salix segment provides gastroenterology products in the United States. The International segment sells aesthetic medical devices, branded pharmaceuticals, generic pharmaceuticals, and OTC products internationally. The Solta Medical segment engages in the sale of aesthetic medical devices. The Diversified segment offers pharmaceutical products in the areas of neurology and certain other therapeutic classes; generic products; ortho dermatologic; and dentistry products in the United States. The Bausch + Lomb segment offers products in the areas of vision care, surgical, and ophthalmic pharmaceuticals products. The company was formerly known as Valeant Pharmaceuticals International, Inc. and changed its name to Bausch Health Companies Inc. in July 2018. Bausch Health Companies Inc. is headquartered in Laval, Canada.View Bausch Health Companies ProfileRead more More Earnings Resources from MarketBeat Earnings Tools Today's Earnings Tomorrow's Earnings Next Week's Earnings Upcoming Earnings Calls Earnings Newsletter Earnings Call Transcripts Earnings Beats & Misses Corporate Guidance Earnings Screener Earnings By Country U.S. Earnings Reports Canadian Earnings Reports U.K. Earnings Reports Latest Articles Archer Aviation Unveils NYC Network Ahead of Key Earnings Report3 Reasons to Like the Look of Amazon Ahead of EarningsTesla Stock Eyes Breakout With Earnings on DeckJohnson & Johnson Earnings Were More Good Than Bad—Time to Buy? 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There are 11 speakers on the call. Operator00:00:00Greetings. Welcome to the Bausch Health Fourth Quarter and Full Year 2023 Earnings Call. At this time, all participants are in a listen only mode. A question and answer session will follow the formal presentation. Please note this conference is being recorded. Operator00:00:17I would now like to turn the conference over to your host, Maria Lycouris. You may begin. Speaker 100:00:23Good morning, and welcome to Bausch Health's 4th quarter 2023 earnings conference call. Participating in today's call are Thomas Ophio, Chief Executive Officer of Bausch Health and John Bareesi, Interim Chief Financial Officer. Before we begin, I'd like to remind you that our presentation today contains forward looking information. We ask you to take a moment to read the forward looking statements disclaimer at the beginning of the slides that accompany this presentation as it contains important information. Our actual results may vary materially from those expressed or implied in our forward looking statements, and you should not place undue reliance on any forward looking statements. Speaker 100:01:00Please refer to our SEC filings and filings with the Canadian Securities Administrators for a list of some of the risk factors that could cause our actual results to differ materially from our expectations. We use non GAAP financial measures to help investors understand our ongoing business performance. Non GAAP financial measures may not be comparable to similarly titled measures used by other companies and should not be considered along with, but not as an alternative to, measures calculated in accordance with GAAP. You will find reconciliations to our non GAAP measures in the appendix of the slides that accompany this presentation, which are available on Bausch Health's Investor Relations website. Finally, the financial guidance in this presentation is effective as of today only. Speaker 100:01:46We do not undertake any obligation to update guidance. Our discussion today will focus on Bausch Health, excluding Bausch and Lomb. However, we will briefly comment on Bausch and Lomb's results announced yesterday. We will refer to year over year comparisons with the same period last year unless otherwise noted. For the benefit of those who may be listening to the replay or archived webcast, this call was held on and recorded on February 22, 2024. Speaker 100:02:12With that, it is my pleasure to turn the call over to our CEO, Thomas Appiah. Tom? Speaker 200:02:18Thank you, and welcome to those of you joining the call this morning. I want to start today's call by highlighting the strategic priorities we set out to achieve this past year: growth, performance, focus and unlocking value. These priorities help support our ambition of being a globally integrated healthcare company trusted and valued by patients, healthcare providers, employees and investors as we relentlessly drive to deliver better health outcomes. We made significant progress on these priorities in 2023, reinforcing our strong global foundation, which consists of a large portfolio of products across a diverse set of therapeutic areas and geographies. Our significant presence in gastroenterology, hepatology, neurology, dermatology, medical aesthetic devices and international pharmaceuticals across the branded, generic and branded generic markets give us a solid platform for growth as we are excited about the opportunities in each of these areas. Speaker 200:03:27From a financial perspective, I am pleased to report we achieved or exceeded our February 2023 guidance. For Bausch Health, excluding BNL, full year revenue was $4,610,000,000 and organic revenue growth was 6%, both slightly above our February 2023 guidance range and in line with our guidance update in November. For Bausch Health, excluding BNL, full year adjusted EBITDA was $2,360,000,000 in line with our guidance while funding incremental spend on R and D to support our Red Sea and amicillimod programs. Importantly, we ended the year on a strong note as the 4th quarter represented our 3rd consecutive quarter of year over year growth in adjusted EBITDA and we delivered adjusted operating cash flow of $708,000,000 above our guidance. For the Q4, revenues for Bausch Health excluding BNL were $1,240,000,000 up $38,000,000 or 3 percent on a reported basis and 2% on an organic basis. Speaker 200:04:45Adjusted EBITDA was $663,000,000 an increase of approximately 1% compared to the prior year. We made significant progress across our key R and D initiatives during the quarter. 1st, we received a positive top line data from our large global Phase 2 trial for amisolimod. 2nd, we completed enrollment for 1 of our 2 global Phase 3 trials for Red Sea with the second trial expected to complete enrollment in the first half of this year. And 3rd, in January, we received approval by the National Medical Products Administration or NMPA for Thermage FLX and the TR-four return pad in China. Speaker 200:05:34I will touch on these in more detail shortly. I am pleased with the continued momentum in our pipeline. Strengthening our balance sheet also remains a priority as we are focusing on managing our liquidity position. During 2023, we reduced debt net of cash for Bausch Health excluding BNL by 670,000,000 and in January 2024, we retired an additional $250,000,000 in principal value of debt through an open market repurchase program. We continue to defend our intellectual property rights for XIFAXAN. Speaker 200:06:13As discussed on our Q3 2023 earnings call, on October 6, 2023, the DC District Court held a hearing in Norwich's lawsuit against the FDA, where Norwich was seeking immediate approval of their ANDA. On November 1, the court denied Norwich's motion and granted summary judgment in favor of the FDA and Salix. In December, Norwich appealed the District Court's decision to the U. S. Court of Appeals for the DC Circuit. Speaker 200:06:47The DC Circuit has stayed the appeal until the Federal Circuit renders the decision in our XIFAXAN litigation. The consolidated appeals from the Delaware District Court are pending at the U. S. Court of Appeals for the Federal Circuit. On January 8, the Federal Circuit heard oral arguments. Speaker 200:07:07We expect a decision to follow late in Q1 or early in Q2. We are committed to vigorously defending our intellectual property and providing healthcare providers and patients with safe and effective treatments. You will recall that in January of 2023, we reached a tentative settlement with the IRS to resolve the Granite Trust matter. We continue to expect this settlement to be finalized in the coming months as we have previously said. The anticipated outcome of the settlement does not have a material impact on the company's results or cash flows. Speaker 200:07:46Turning now to the potential full separation of Bausch and Lomb. We continue to believe the separation of Bausch and Lomb makes strategic sense and we continue to evaluate strategies regarding the potential full separation with the objective of ensuring that this transaction results in 2 appropriately capitalized companies. Any decision regarding if and when a separation occurs or its structure will be based on and subject to an assessment of all relevant factors and circumstances. Any potential separation will also be subject to shareholder and other applicable approvals. And in the meantime, we are focused on managing our balance sheet. Speaker 200:08:31We ended the quarter with more than 1 $500,000,000 of liquidity. We repurchased a small amount of debt in the Q4 and in January 2024 repurchased approximately $250,000,000 in principal value of our debt. Finally, we are introducing our 20 24 guidance for Bausch Health excluding BNL, which reflects our confidence that we can deliver top and bottom line growth again in 2024. John will speak in more detail to this later in the call. Turning now to an overview of our segment performance for the quarter. Speaker 200:09:07In Salix, we continued to see strong demand in Q4 for our key products, including XIFAXAN. For XIFAXAN, we saw approximately 3% TRx growth in Q4 over the prior year with a strengthening trend in the back half of the quarter. This was led by strong growth for IBS D with a return to growth for HE driven by long term care channel. Putting this all together, we believe we are starting to see the benefits our investments in AI enabled sales force tools and DTC advertising to spread awareness of the underlying medical conditions and the options that are available to treat them. For 2024, we anticipate maintaining our current level of investment in these areas to drive further growth in this important franchise. Speaker 200:09:57Finally, TRULANCE and RELISTOR continued to deliver double digit TRx growth in the quarter. Turning to international, we saw strong year over year revenue growth on both a reported and organic basis. In all regions during the Q4, continued growth in our promoted brand portfolios in key markets including Poland, Mexico and Canada More than offset the impact of the MRADE recall earlier in 2023 and increased generic competition for certain products particularly in Canada. Our focus in 2024 will be continuing to invest in our promoted product portfolio, while looking for business development opportunities to drive long term growth. In Sultum Medical, revenues increased by 4% on a reported and 5% on an organic basis, reflecting solid growth in China as well as growth in the broader Asia Pacific region. Speaker 200:10:59Revenues in the U. S. Declined slightly in the quarter. Highly focused on maintaining our momentum in Asia, including driving Thermage FLX performance in China. And in 2024, we'll also be focused on growing our U. Speaker 200:11:14S. And EMEA markets, where we believe there is meaningful opportunity to expand our presence. To support these efforts, we have added talented key leadership to the Solta business to advance our leading portfolio of products and have invested in the expansion of the U. S. Field force. Speaker 200:11:31We are also focusing our R and D organization on our pipeline of new market authorizations and next generation products as we continue to build upon this world class durable aesthetics business. In Diversified, we saw another quarter of healthy performance, particularly in neurology as we continue to capitalize on opportunities in the market created by competitor supply constraints. We remain focused on managing this mature portfolio of products for profitability and cash generation in a challenging competitive and pricing environment and continue to look for opportunities to make targeted investments where appropriate. Dentistry revenues were in line with a strong Q4 in the prior year and in the coming year we are looking to accelerate growth with a focus on the sales force and new marketing tools. In dermatology, CabTrio is now launched and available for patients in the U. Speaker 200:12:30S. At the end of January 2024 and we are excited to be able to provide this new once a day triple combination topical acne treatment for patients. We continue to expect that Cabtrillo will be launched in Canada in the second half of twenty twenty four. Turning to the latest developments in our R and D pipeline, starting with our GI pipeline. In December, we announced positive top line results from our Phase 2 study evaluating amicilimod, an S1P antagonist in the treatment of ulcerative colitis or UC. Speaker 200:13:09We are very pleased that the study met the primary and key secondary endpoints including clinical remission and endoscopic improvement during the double blind period of the study with no unexpected adverse events. We are preparing for our next steps to progress this program, including presenting the detailed results at upcoming scientific conferences and planning to meet with the FDA for an end of Phase 2 meeting. We are planning to advance into Phase 3 in moderate to severe UC patient and could possibly target all UC patients based on our results. We anticipate a step up in R and D spend to support these Phase 3 efforts as well as exploring opportunities to expand into other therapeutic areas, primarily Crohn's disease with a Phase 2 program. We expect to initiate our global Phase 3 program for UC in late 2024. Speaker 200:14:09Our Red Sea program for rifaximin for reduction of early decompensation in cirrhosis continues to advance. The global program is focused on delivering a novel formulation and assessing the efficacy of rifaximin SSD formulation versus placebo to delay the occurrence of HE related hospitalizations. We completed enrollment for 1 of 2 large global Phase 3 trials as of the end of the year with enrollment for the second trial expected to be completed during the first half of twenty twenty four. Together, these studies are expected to include approximately 1,000 patients across the major markets of North America, Europe and Asia Pacific. Turning now to our aesthetics pipeline. Speaker 200:14:57We are very pleased to have received approval for Thermage FLX and TR-four return pad from the NMPA in China in January. We are excited about the opportunities in this market and we see a runway for growth. We expect to start realizing the benefits of this starting in the Q2 of this year. We plan an FDA submission for our next generation Fraxel, a fractionated laser device for skin resurfacing in the Q2 of 2024, we expect approval could be received in the second half of this year. Finally, our program for clear and brilliant touch, a fractionated laser device for skin rejuvenation continues to advance with regulatory submission still on track for 2024 in Europe, Canada and Asia Pacific markets. Speaker 200:15:50As a leadership team, we remain committed to driving growth by leveraging our existing assets, making targeted investments and executing with commercial excellence, while continuing to progress our pipeline all with a patient centered mentality. With that, I will turn the call over to John Barresi who will provide further details on our Q4 performance and financial outlook for 2024. John? Thanks, Tom. Hello, everyone, and thanks for joining us. Speaker 300:16:23We closed the 4th quarter with consolidated revenues for Bausch Health of $2,410,000,000 up 10% on a reported basis and 4% on an organic basis over the same quarter last year. On a consolidated basis, revenue increased 8% for the full year on a reported basis and 7% on an organic basis. 4th quarter revenues for Bausch Health excluding BNL were $1,240,000,000 up 3% on a reported basis and up 2% on an organic basis over the same quarter last year with growth in our international, diversified and Solta segments, while Salix was in line with last year. Bausch Health excluding B plus L ended the year with revenues of $4,610,000,000 up $255,000,000 or 6% on both a reported and organic basis compared to 2022. Let's dive into the revenue performance for each segment in more detail starting on Slide 13 with Salix. Speaker 300:17:204th quarter Salix revenues increased $2,000,000 on both an organic and reported basis to $583,000,000 driven by TRx growth in our key products, including XIFAXAN, RELISTOR and TRULANCE. Comparisons to the prior year's quarter were impacted by changes in the timing of wholesaler buying patterns. As you will recall, sales reported 13% growth in the Q3 of 2023 compared to the Q3 of 2022. As we noted then, we saw an increase in wholesale channel inventory in Q3 earlier than we had anticipated. And this quarter, we saw inventory in the wholesale channel decline compared to a build in Q4 of 2022. Speaker 300:18:02For the full year, Salix reported revenues of $2,250,000,000 an increase of approximately 8% over 2022 on a reported basis. We realized an approximately 3% increase in net price along with an approximately 5% increase in volume with the volume increase split roughly equally between underlying demand and the impact of higher overall wholesale inventory levels year over year. While inventory in the channel declined relative to Q3, we did end the year higher than we ended 2022. XIFAXAN continued to represent approximately 80% of Salix segment revenues this year and saw strong growth in underlying demand. Retail prescriptions grew 3.1% in Q4 versus the prior quarter. Speaker 300:18:47We saw growth in TRx for IBS D and importantly, we also saw solid growth of approximately 6% year over year in Q4 in TRx for the long term care channel as well as strong growth in non retail units attributable to outpatient clinics. For the quarter, XIFAXAN revenues were in line with the prior year as this TRx growth was offset by the timing of wholesaler buying patterns discussed earlier. For the quarter, RELISTOR delivered 44% growth over the prior year due to both higher demand and improved net pricing, while TRULANCE revenues were flat as TRx growth was offset by lower net pricing and shifts in wholesale inventory. International revenues were $290,000,000 during the quarter, an increase of 11% on a reported basis and 6% on an organic basis compared to the prior year period, with strong performances across the EMEA, Canada and Latin America regions. For the full year, international revenues were $1,070,000,000 for 2023 compared to $988,000,000 for 2022, an increase of $83,000,000 or 8% on a reported basis and 6% on an organic basis. Speaker 300:20:01This year's international segment performance was driven mainly by an increase in net realized pricing as growth in our portfolio of promoted products was offset by the impact of increased generic competition and the effects of the MRADE recall in the 2nd quarter. Ulta Medical revenues were $103,000,000 for the 4th quarter, an increase of 4% on a reported basis and 5% on an organic basis over the prior year period. Growth in the quarter was led by China and to a lesser degree the remainder of Asia Pacific, while sales in the U. S. Slightly declined compared to the prior year. Speaker 300:20:38Ulta Medical ended the year with revenues of $347,000,000 an increase of 16% on a reported basis and 18% on an organic basis compared to 2022. Revenue growth was driven by strong demand in China, including the effect of comparison to 2022 when China and to a lesser degree the rest of the Pacific region were affected by COVID related lockdowns. With approximately 80% of the revenue for this business coming from consumables, the recent Thermage FLX approval in China and possible untapped potential in the U. S. And EMEA, we believe Solta Medical is positioned for continued near and long term growth globally. Speaker 300:21:18Diversified revenues were $259,000,000 during the 4th quarter, an increase of 1% on a reported basis and 2% on an organic basis compared to the prior year period. Neurology delivered year over year growth as we continued to capitalize on opportunities in the market created by supply constraints among competing products in the Q4. In dermatology, revenue declined by 12% for the quarter relative to the prior year as volume increases for JUVIA and ERASLO were offset by continued net pricing pressures and continued pressure on our non promoted products. And as Tom mentioned, Captrio is launched and available for patients as of late January 2024. And in addition to the important benefits this product is expected to bring patients, we view this as an opportunity to return the dermatology business to growth. Speaker 300:22:09The generics business continues to be a profitable, cash generative business. However, it also faces a highly competitive environment from both pricing and volume standpoint. While it plays a role with our LOE products, with the timeline of many of those LOEs and the competitive environment we expect to face for the long term, we have revised our expectations for this business and recorded an impairment of goodwill of $91,000,000 in the quarter. Dentistry revenue of $29,000,000 was in line with a strong Q4 in 2022. We continue to invest in the dentistry business for the long term and are looking to accelerate growth in 2024. Speaker 300:22:48For the year, Diversified segment revenues declined 4% on a reported basis and 3% on an organic basis relative to the prior year with varying degrees of declines in neurology, dermatology and generics reflecting the pressures we've discussed throughout the year. As shown on Slide 18, Bausch and loan revenues were $1,170,000,000 during the 4th quarter, up 18% on a reported basis and 7% on an organic basis compared to the prior year with growth across all Bausch and loan segments. Similarly, Bausch and Loan revenues for the year increased by $378,000,000 on a reported basis or 10% and 8% on an organic basis compared 2. Turning to the 4th quarter P and L on slides 2020 gross margin was 71.6%, 130 basis points higher compared with the prior year. Full year consolidated adjusted gross margin was 71%, 10 basis points higher than last year. Speaker 300:23:53For Bausch Health, excluding BNL, adjusted gross margin for the Q4 was 80.2%, approximately 30 basis points lower than last year's Q4. For the full year, adjusted gross margin was 80.1%, a decline of 50 basis points, which included the impact of the Emerald A recall earlier in the year. At B and L, adjusted gross margin was 62.5 percent for Q4 of 2023 compared to 57.9% for Q4 of 2022, driven primarily by product mix including Xiidra. Consolidated adjusted operating expenses for the Q4 were $891,000,000 an increase of $121,000,000 For Bausch Health excluding V and L, adjusted operating expenses increased by approximately $16,000,000 during the quarter as higher A and P was driven by investments in the Salix segment. D expenses also increased primarily related to our Salix initiatives. Speaker 300:24:51Adjusted G and A for Bausch Health excluding B and L was slightly favorable to the prior year as we annualized stabilization of the post IPO structure and focused on cost containment. B and L reported an increase of $105,000,000 in adjusted operating expenses due primarily to increased selling in A and P driven by product launches. Consolidated adjusted R and D expense for the quarter was $151,000,000 an increase of 6% compared to the prior year and represented 6.3% of product sales compared with 6.5% for the prior year period. For Bausch Health excluding BNL, R and D expenses of $72,000,000 increased by approximately $8,000,000 for the Q4 as compared to the same quarter last year. As Tom mentioned, we expect another meaningful step up in R and D expense throughout 2024 to support the next phase of development for amicilimod. Speaker 300:25:47We also will continue to progress our 2 global Red Sea Phase 3 clinical trials. 4th quarter consolidated adjusted EBITDA was $897,000,000 an increase of $56,000,000 or 7% on a reported basis. Adjusted EBITDA for Bausch Health excluding BNL was $663,000,000 for the quarter, a slight increase from $659,000,000 in the 4th quarter of 2022. For the full year, consolidated adjusted EBITDA was $3,110,000,000 and for Bausch Health excluding B plus L was $2,360,000,000 both slight increases from 2022. Turning to cash flow. Speaker 300:26:29On a consolidated basis, Bausch Health generated $390,000,000 of operating cash flow and $305,000,000 of adjusted operating cash flow in 4th quarter. Full year cash flow from operations on a consolidated basis was $1,030,000,000 adjusted cash flow from operations on a consolidated basis was $763,000,000 For Bausch Health excluding BNL, adjusted operating cash flow was $278,000,000 for the 4th quarter $708,000,000 for the full year compared to adjusted operating cash flow of $340,000,000 for the Q4 of 2022 $637,000,000 for the full year 2022, with the changes primarily reflecting the timing of working capital movements and for Q4 the timing of interest payments. The full year 2023 also exceeded our guidance of $625,000,000 driven by our focus on expense management as well as by the timing of cash collections based on the wholesaler buying patterns I discussed earlier. As we've discussed in prior quarters, as a result of the accounting treatment for the senior notes issued as part of our 2022 debt exchange, a portion of our cash interest payments are classified as financing cash flows. Adjusted cash flow includes payments of the full contractual interest as well as adjustments for the payment of separation costs, business transformation costs and litigation and other matters net of insurance proceeds. Speaker 300:28:00Now let's turn to our balance sheet on Slide 22. We continue to prioritize liquidity management and the delevering of our balance sheet. In the Q4 of 2023, we reduced our debt net of cash for Bausch Health excluding BNL by approximately $250,000,000 We continue to evaluate alternatives to reduce our overall leverage while also focusing on our maturity profile. Despite only retiring a small amount of debt in Q4, in January 2024, we retired $250,000,000 in principal value of 2025 and 2026 maturities through open market repurchases, capturing approximately $12,000,000 of discount in the process. At the end of the Q4, Bausch Health excluding BNL had $350,000,000 outstanding under our accounts receivable facility and had no outstanding borrowings and approximately $950,000,000 of availability under our revolving credit facility. Speaker 300:28:59As shown on Slides 2324, total debt for Bausch Health excluding Bausch and Lomb at the end of the quarter was $16,400,000,000 which consisted of approximately $15,000,000,000 of restricted debt issued by Bausch Health excluding BNL and approximately $1,400,000,000 of unrestricted debt, which includes the $1,000,000,000 of senior secured notes issued by the unrestricted subsidiary created in the Q3 of 2022 and the $350,000,000 drawn under our accounts receivable facility. Excluding B plus L debt, approximately 85% of our debt is fixed and approximately 70% of the company's debt on a consolidated basis is fixed. Debt net of cash for Bausch Health excluding BNL is down approximately $670,000,000 since the beginning of 2023. We ended the year with over $1,500,000,000 of liquidity, including approximately $616,000,000 of cash and $950,000,000 of availability under our revolving credit facility. We will continue to evaluate the best uses of that liquidity, including focus on our maturity profile and our overall leverage. Speaker 300:30:12Overall, we are pleased that revenues, adjusted EBITDA and adjusted operating cash flow for 2023 for Bausch Health excluding BNL met or exceeded expectations. With that as the backdrop, I'll now discuss our guidance for 2024, which you can find on Slide 26. In 2024, we expect revenues of $4,700,000,000 to $4,850,000,000 with growth of 2% to 5% on an organic basis. For 2024, we expect foreign exchange impact to be a slight tailwind. Full year adjusted EBITDA for Bausch Health excluding BNL is expected to be $2,360,000,000 to $2,460,000,000 For Salix, we expect to see mid single digit revenue growth. Speaker 300:31:00Based on the investments we've made, we expect volume growth from a TRx and extended units perspective to expand relative to what we saw in 2023, although changes in wholesale or purchasing dynamics may temper how that growth translates into revenue growth. We also intend to maintain our investments in selling and A and P consistent with 2023 levels. Lastly, as we've noted in the past, we typically see a seasonal step up in sales in the second half, particularly in XIFAXAN, primarily due to wholesaler inventory dynamics as well as patient level patterns related to insurance deductible activity. For international, we expect mid single digit organic revenue growth led by the EMEA and Latin America regions. We are excited by the potential for new product launches in these regions. Speaker 300:31:48In Canada, we plan to further grow the recently launched products Realtris and UCERIS and continue to focus on obtaining approval of Kebtrio. We're also making targeted investments in sales teams and promotion across the different regions. For Solta, we anticipate strong double digit organic revenue growth across all major geographies. We have new leaders in key positions in this business and have invested in expansion of the U. S. Speaker 300:32:13Sales team. Therefore, we anticipate growth led by China and Asia Pacific as well as double digit growth in the U. S. And EMEA regions. For Diversified, we expect an overall mid single digit decline in organic revenue. Speaker 300:32:28We expect growth in dermatology led by the introduction of CabTrio and in dentistry driven by continued investment in the sales force and related tools with continued pressures in our neurology and generics businesses. From a gross margin perspective, we expect to continue to mitigate the impact of inflation on our cost of goods sold and we expect our gross margin to remain comparable to last year at approximately 80%. On the expense side, we anticipate that selling and A and P will grow in line with sales growth as we maintain the base we established in 2023 and make targeted investments to drive growth in businesses including Solta and dentistry. Additionally, as we've discussed previously, there will be a meaningful increase in R and D spend throughout the year as we invest for the future in our GI and aesthetics pipeline programs. We think it is critical to continue to allocate capital to this area for the long term as it will benefit patients and healthcare providers while positioning our business to deliver stakeholder value. Speaker 300:33:29Lastly, we expect adjusted operating cash flow for Bausch Health excluding BNL in a range of approximately $775,000,000 to $825,000,000 for 2024. And as I said earlier, adjusted cash flow includes adjustments for the payment of separation costs, the payment of the full contractual interest on our existing debt and also includes lower tax payments in 2024 relative to 2023 inclusive of the impact of the tentative Granite Trust settlement. I'll now hand the call back to Tom. Speaker 200:34:02Thank you, John. In summary, as you heard today, we made significant progress against our 2023 strategic priorities and we enter 2024 with strong momentum and a clear set of objectives. We are excited about the potential of our Salix business led by XIFAXAN and we will continue to advance our pipeline with Red Sea and amicilimod. We believe Solta is poised for long term growth with Thermage FLX in China and untapped potential in the U. S. Speaker 200:34:36And EMEA. The broad portfolio of products and geographies in our international business will continue to provide balanced growth. And in our diversified business, we believe dermatology with the launch of Cabrio and dentistry will deliver growth with the remainder of the portfolio remaining profitable and cash generative in a challenging competitive and regulatory environment. With the year ahead, we are focused on building on the foundation we have set across our diverse global business by driving a results oriented culture of accountability delivering on our revenue, adjusted EBITDA and adjusted operating cash flow commitments executing with operational excellence and cost focused mindset across the enterprise, intensifying our focus and operating rigor behind R and D and business development and continuing to evaluate strategic alternatives. We will execute against these objectives with a focus on operational excellence with a patient centered mentality. Speaker 200:35:54I am thankful for and proud of our Bausch Health team for their achievements this year. They have worked tirelessly and are all in to position our business for the long term. Life won't wait, neither can wait. Every patient deserves better health and the chance to make the most of life. This drives us on with urgency and efficiency to deliver the products patients need most to enrich their lives. Speaker 200:36:25On behalf of our entire Bausch Health team, I thank you for your interest in and support of our company. With that, we will now take questions. Operator, please open the line for Q and A. Operator00:36:38Thank you very much. At this time, we will be conducting our question and answer Thank you. Your first question is coming from Glenn Santangelo of Jefferies. Glenn, your line is Speaker 400:37:17live. Yes. Thanks for taking my question. Hey, Tom, I just had two quick ones. I appreciate all the details on the 2 pipeline programs. Speaker 400:37:25But as we think about doing some long term modeling, I was wondering if you could maybe help us think about broad timelines for both these programs as we think about the path to approval? And then maybe secondly, in recent quarters, I mean, the company has talked about a number of different recapitalization opportunities. And in your prepared remarks, you talked about how you retired $250,000,000 of debt in January. And I'm just sort of wondering, given where the debt trading, where BLCO is trading, given that Salt is doing much better, without getting specific, do you see any meaningful opportunities for further recapitalization efforts in 2024? And I'll stop there. Speaker 400:38:07Thanks. Speaker 500:38:10Hi, Glenn. Thanks. Appreciate the question. So overall when we take a look at these two programs, clearly if we take a look at Red Sea, we think this is a great opportunity. Clearly, the patient pool here is large, much bigger than today's patient pool that we're looking at because this is a prevention trial. Speaker 500:38:33So as we one of the things that we did this year was really energized and put more money behind those studies to make sure we got the recruitment. As I said in my prepared remarks, we had the first the one study completely recruited and then the second study we're expecting that in the first half. So trying to really accelerate that program, So we have a launch probably in sometime in 2027. This is going to be again a large pool. It is prevention. Speaker 500:39:10So clearly there is a good really good opportunity for us. On the amicilimod side, of course we are really pleased with the data on the Phase 2 program. This was a very large Phase 2 program. We're working right now to see what the timing will be of the Phase 3 program. We're expecting at the end of the decade to be able to launch the product in UC. Speaker 500:39:38As I said in my prepared remarks, there is an opportunity here to continue to expand as if we looked at Crohn's and running a Phase 2 program and then if the data is good, clearly running a Phase 3 program, which would push approval something into the first half of the next decade. So I really think these two programs give us a really good momentum on our R and D programs as we Speaker 300:40:10look forward. I'll turn off turn the call over to the question over to John to talk about the debt. Yes. Thanks, Glenn. Yes, as we've said, we're always looking at the options that we have to manage our balance sheet, manage our debt. Speaker 300:40:26We're not going to comment on any specific strategies or actions that we may undertake at any point in the future. But what I will say is if you think about where we sit today, we have over $1,500,000,000 of liquidity between our cash and the revolver flexibility. We're guiding to $775,000,000 to $825,000,000 of adjusted operating cash flow and we typically use a fair amount of that manage our debt. As you noted, we do have the flexibility on the roughly 8% of BLCO that we still own that we have the option to monetize at some point. And we are focused on reducing debt. Speaker 300:41:03So we're always looking at all the tools and all the options, but we're not going to comment on anything specifically at this point. Speaker 400:41:09Appreciate all the detail. Speaker 200:41:10Thanks. Thanks. Operator, next question. Operator00:41:14Thank you very much. Your next question is coming from David Amsellem of Piper Sandler. David, your line is live. Speaker 600:41:23Hi. This is Skyler on for David. So first, what are your thoughts on how amicelimod could fit into the UC space in the context of existing approved S-1Ps and a pretty competitive pipeline? And then separately, could you also talk about the extent to which you will further invest in XIFAXAN as it moves through the later part of its commercial life? Thanks. Speaker 500:41:45Yes. What I would say is on amiselimod, clearly among S1Ps, the positive top line data suggests it could be a promising therapy in terms of efficacy and safety in the space. There are a few others in the space. When we look at the data, we think we have a real competitive product here. So as we continue to really look at the data and build our Phase 3 program, we'll see where that fits. Speaker 500:42:17But we think again on the positive top line data, it looks really good. What I would say is on XIFAXAN, we have multiple formulations on XIFAXAN. We're always looking from an R and D perspective of where we could use these new formulations as the Red Sea program. Clearly, we're using one of our new formulations, but we're always looking for and looking at the link between the gut and the brain. And then clearly that is a focus for the team. Speaker 500:42:53If you want to talk about investing in XIFAXAN on the commercial life side of it, I still think even though XIFAXAN is late in its life cycle, as you saw the results for 2023, They are strong. We believe we can continue to grow our franchise, the investments we have put behind AI for the field force and that has been rolled out to the entire the field force on both the primary care and specialty care side. If you look at the data that we saw in the Q4 as we exited the year, the data was strong. And so that those tools are really going to help us move forward with XIFAXAN. The other thing also is, is when I take a look at XIFAXAN, clearly there's a lot of unmet needs still there and I think we can tap that with the programs and the investments that we're making between AI and DTC as I said in my prepared remarks. Speaker 500:44:01So I really the team has really done a really great job this year with XIFAXAN and getting the growth on it and then the unmet need that is still there in both the IBS D side of the business and the HE side of the business, there's still an unmet need that we can treat more patients. Operator, next question. Operator00:44:25Thank you very much. Your next question is coming from Umer Raffat of Evercore ISI. Umer, your line is live. Speaker 700:44:34Hi. This is Chen Zhang on for Umer. Thanks for taking our questions. Two questions, if I may. So first, in the scenario that Norwich loses the patent appeal, will they reunite their APA loss case appeal? Speaker 700:44:45And if that if so, what would be the angle? And secondly, can we get more colors on the SG and A increase in the Q4 and your expectation in 2024? Thank you. Could Speaker 500:44:56you just on the first part of your question, what specifically we are asking on Novoix? Just Speaker 200:45:03could you I'm trying to Speaker 500:45:04understand what you're actually asking there. Speaker 700:45:08Let me repeat. So if in a scenario that Norrish loses the patent appeal case, will they reignite their APA against FDA case? If so, what will be the angle? Speaker 500:45:21Yes. I can't comment on what they would do on their litigation if they were to lose. So I mean, again, I can't comment on the call of what their steps would be. But again, we feel confident in our appeal and in our intellectual property. Next question? Operator00:45:45Thank you very much. Your next question is coming from Jason Gerberry of Bank of America. Jason, your line is live. Speaker 800:45:55Hi, this is Chi on for Jason. Thanks for taking our questions. A couple from us. So regarding the SYFAXAN acute decision that you expect later in Q1, early Q2, Say let's say if the appeal is favorable to Bausch, how does the favorable appeal ruling impact your thinking on the separation of Belco? Would you look to move quickly once that particular legal matter is resolved? Speaker 800:46:27Or are there other settlements in legal matters contingent? And my second question is on emisalomod. You ran a Phase II in mild to moderate and it sounds like you are moving thinking about moving Phase III to in the moderate to severe population. So I'm curious what prompt that change and given there are multiple other S1Ps already approved for in development in the moderate or moderate to severe population? Thanks. Speaker 500:47:01Okay. On your first part of the question regarding XIFAXAN, what I would say is this is, as you know, we had the appeal that was heard, the oral arguments were heard in January. We believe it went well. What I would say is, is we believe that the if we were to win, there are still factors that we need to consider. We believe that the separation continues to make strategic sense. Speaker 500:47:31And there are many factors that will go into the timing of any potential data and the positive data that we saw, as you know, we ran the trial mild to moderate, we think that amiselimod has the potential to be very broad in what the data shows. So we did when the trial was running, we did have mild to moderate. But as we look at it, we could move it more into moderate to severe on a Phase 3 program. And as I said in my prepared remarks, probably treat all, but that's still under discussion. Operator, next question. Operator00:48:18Thank you very much. Your next question is coming from Douglas Meem of RBC Capital Markets. Douglas, your line is live. Speaker 900:48:27Great. Thank you. Question has to do with Q4 of XIFAXAN and TRULANCE where it looked like it was all flat. And forgive me if you spoke about this already. Just curious as to why that occurred given the strong prescription strength during the quarter and also the pricing increase you took at the beginning of the year? Speaker 900:48:48And then perhaps related to that, you can expand on the commentary that was made around prescription growth in the guidance 2024 and how that could be impacted by, I think it was managed care that you talked about? Thank you. Speaker 500:49:07Yes. So let me just overall, when we look at XIFAXAN and the TRx growth, if you look at the product for the full year, we had an increase of 8%, 3% on price, 5% on volume and we talked about some of the inventory channels, the inventory channel that we had. But overall the TRx growth that we looked at it for the year was strong. And when we looked at the Q4 on the IBS D side, we were exiting at much higher than what the full year looked like. And when we look at HE in the long term care space that was over 6%. Speaker 500:49:50So the product as the performance as we ramped up the investments, okay, in and launched different activities during the year, you could see it benefited from the second half. I'll let John talk specifically about the second part of the question. Speaker 300:50:09Yes. On the revenue trends, if you remember in the Q3, Salix was plus 13%, I believe, for the Q3. And we saw at this time, we spoke about some pull forward of the demand increase that we'd normally see in Q4 into the later stages of Q3. And so that I think is the biggest driver of the difference between revenue growth and TRx growth for Q4 on the XIFAXAN and the TRULANCE side. And then on the question of the Q4 guidance, I think what we had said was, we expect expansion of the growth of TRx. Speaker 300:50:49However, we did end 2023 a little bit higher in the wholesale channel than we ended 2022. And so we had a little bit of a build there. And it's possible, right? The wholesalers have their own algorithms for how and when they buy, but it's possible that if we see that revert back a little, that it could temper some of the benefit from a revenue standpoint of the underlying demand growth. Okay. Speaker 300:51:15Great. Speaker 200:51:16Lastly, when we just take Speaker 500:51:18a look at it, we could frame it. When we look at IBS D, there's 2,200,000 patients that are diagnosed, but only about 100 and 20,000 received treatment. So again, with a second line medication like XIFAXAN. So clearly still a large unmet need and some of the investments that we have made this year and last year and we will continue to make in 2024 to capture that. On the HE side, if you look at the analytics that we look at, there's about 190,000 patients that potentially have HE and only that we're going to continue to invest behind. Speaker 500:52:16Operator, next question. Operator00:52:18Thank you very much. And your next question is coming from Michael Nedelkovich of TD Cowen. Michael, your line is live. Speaker 1000:52:27Thank you for the question. I have 2. For the first, if you could transport us to late May, let's assume that you had a wildly favorable ruling in the case against Norwich such that XIFAXAN's exclusivity out to 2028 is all but certain. I know that as it relates to the Bausch and Lomb full separation, there are multiple additional factors to consider. But what is item number 2 on your checklist? Speaker 1000:52:55So the XIFAXAN ruling is done and its outlook is certain. What's item number 2 when you move toward full separation? And then my second question relates to amicelimod. As has already been noted, there are 2 other S1P receptor modulators approved for UC, but their market reception so far has been lukewarm. Do you think that imicelimod has better commercial prospects than the agents already approved? Speaker 1000:53:20And if so, why is that? Speaker 500:53:24Yes. So let's take the first part of the question. I can't speculate on what number 2 would be. There as I said, there's still many factors that go into the timing of the potential distribution. And clearly, again, we believe in our intellectual property and hoping for a favorable outcome. Speaker 500:53:46But there are a multitude of steps. So I can't speculate on what number 2 would be, but clearly looking to a favorable outcome on the XIFAXAN case. When it comes to amicilimod, we've had a lot of discussions on this internally. Yes, the 2 that are out there are as you use lukewarm. We believe based on our data that we have a competitive product, a once a day treatment and oral. Speaker 500:54:21So clearly, as we continue to look at it and build the Phase 3 program, I can give you more information as we move forward on the program and see what we think going forward. But if we look at our data, again, we think it's positive and we think we have a really interesting product here. Operator, next question. Operator00:54:49Thank you very much. Well, that appears to be the last of our questions. I will now hand back over to Tom for any closing comments. Speaker 500:54:57Okay. Well, since there's no further comments, I want to say thank you to all who joined the call today. As we discussed on this call, we had a solid Q4 2023. We grew our company and delivered or exceeded our guidance. I would like to thank my over 7,000 colleagues around the world for their relentless drive to deliver better health outcomes and continue to build a company that is trusted and valued by patients, healthcare professionals and investors. Speaker 500:55:30We entered 2024 with strong momentum and look forward to executing on our strategic objectives, delivering on our commitments as we continue transforming Bausch Health, positioning our company for the long term. Thank you for your interest in and the support of Bausch Health.Read morePowered by