Greetings. Welcome to Kamada Ltd.'s Fourth Quarter and Full Year 2023 Earnings Conference Call. 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. At this time, I'll turn the conference over to Brian Ritchie with LifeSci Advisors. Mr. Ritchie, you may now begin.

Thank you. This is Brian Ritchie with LifeSci Advisors. Thank you all for participating in today's call. Joining me from Kamada are Amir London, Chief Executive Officer, and Chaime Orlev, Chief Financial Officer. Earlier today, Kamada announced its financial results for the three and twelve months ended December 31, 2023. If you have not received this news release, please go to the Investors page of the company's website www.kamada.com. Before we begin, I would like to caution that comments made during this conference call by management will contain forward-looking statements that involve risks and uncertainties regarding the operations and future results of Kamada. I encourage you to review the company's filings with the Securities and Exchange Commission, including, without limitation, the company's Forms 20-F and 6-K, which identify specific factors that may cause actual results or events to differ materially from those described in the forward-looking statements. Furthermore, the content of this conference call contains time-sensitive information that is accurate only as of the date of the live broadcast – Wednesday, March 6, 2024. Kamada undertakes no obligation to revise or update any of the statements to reflect events or circumstances after the date of this conference call. With that said, it is my pleasure to turn the call over to Amir London, CEO. Amir?

Thank you, Brian. My thanks also to our investors and analysts for your interest in Kamada and for participating in today's call. We are extremely pleased with the strong financial and operational momentum we experienced throughout our business during 2023, which allowed us to achieve our full-year guidance. Importantly, we are well positioned for further top and bottom line growth this year. I will begin with a high-level review of our robust financial results for full-year 2023. With total revenues of $142.5 million, which represented year-over-year growth of 10%, and EBITDA of $24.1 million, an increase of 35% as compared to the 12 months ended December 31, 2022, we achieved the top and bottom line growth anticipated in our business during 2023. We continue to effectively leverage the growth drivers in our business, focusing on the significant increase in KEDRAB US market share and the promotion of CYTOGAM in the US market. Looking ahead, we expect the momentum generated last year to extend through 2024, with full-year revenue and profitability to be meaningfully increased as compared to 2023. As such, we are introducing full-year 2024 revenue guidance of $156 million to $160 million and adjusted EBITDA guidance of $27 million to $30 million. The midpoint of these ranges would represent top line and profitability growth of approximately 11% and 18%, respectively, over 2023. To reiterate what we have said previously, we anticipate annual double-digit revenue and profitability growth in the foreseeable years beyond 2024, with significant upside potential and limited downside risk. Additionally, I would like to highlight our strong balance sheet. We ended the year with over $55 million in cash, and we continue to have the financial flexibility to both accelerate the growth of our existing business and pursue compelling business development opportunities, a process we are actively engaged in. In 2023, KEDRAB, our anti-rabies immunoglobulin, was especially impactful. And throughout the year, we experienced a significant increase in demand for the product in the US. Following the recent amendment and extension of our distribution agreement with Kedrion, we fully expect this trend to continue in 2024 and beyond. The substantial market share growth demonstrated by KEDRAB is being driven by Kedrion's extensive market coverage and robust commercial activity as well as FDA approval for label expansion for the product obtained in 2021 that has differentiated it as the first and only human rabies immunoglobulin available in the US to be clinically studied in children. In 2023, Kamada generated approximately $32.8 million in revenues from sales of KEDRAB to Kedrion for distribution in the US market, which more than doubled our sales compared to 2022. Based on the new distribution agreement, further growth is expected in 2024. Looking ahead with KEDRAB, the amended and extended distribution agreement is a tremendous milestone for Kamada. In fact, this strategic agreement with Kedrion represents the largest commercial agreement since Kamada's inception. Specifically, within the first four years of the eight-year term, which began this past January, Kedrion will purchase minimum quantities of KEDRAB with revenues to Kamada of approximately $180 million. The revised financial terms affect KEDRAB's significant US market share and focus its continued growth throughout the eight-year term, as well as the potential expansion of KEDRAB distribution by Kedrion to other territories beyond the US. We believe the continuation of this partnership maximizes the future growth and value potential of this important product. Moreover, this agreement most effectively exploits the US business by allowing us to focus on our own internal sales effort on the commercialization of our other specialized FDA-approved immunoglobulin products, primarily in transplant centers where Kedrion continues to promote KEDRAB in numerous hospitals and medical centers across the US. Moving on, our US team, established in 2022, continues to achieve steady progress in promoting our specialty IgG portfolio to physicians and other healthcare practitioners through direct engagement and opportunities at medical meetings. As we have said previously, our activities promoting these important therapies, primarily CYTOGAM and VARIZIG, represent the first time in over a decade that these high premium specialty products are being supported by field-based activity in the US. Each of these products made important contributions to our financial results in 2023, and we expect further impact this year. Importantly, in October 2023, results from an investigator-initiated five-year retrospective study consisting of 325 lung transplant patients evaluating the real-world use of CYTOGAM in combination with antiviral agents for the prevention of CMV disease in high-risk CMV mismatch lung transplant recipients were published by Dr. Fernando Torres, the Clinical Chief, Division of Pulmonary and Critical Care at the University of Texas Southwestern Medical Center, and the results were also presented at IDWeek 2023 in Boston, Massachusetts. The high-risk mismatched patients are CMV seronegative patients receiving a lung from a seropositive donor. Dr. Torres concluded that the use of proactive multimodality CMV prophylactic consisting of antivirals and immune augmentation with CMV immunoglobulin may improve outcomes among high-risk CMV mismatch lung transplant recipients. We are in the process of sharing this result with physicians and transplantation experts promoting the advantages of CYTOGAM. We have already been notified that two additional studies related to the benefit of CYTOGAM conducted by leading US transplantation experts were accepted for presentation at transplantation-related medical meetings during this year. Of note, our CYTOGAM Scientific Advisory Board, which was established last year and consists of eight US-based world-renowned thought leaders in the solid organ transplantation field, continues to evaluate new opportunities and future research and development possibilities for this important product. Moving on, looking further ahead at future catalysts, enrollment continues in the ongoing pivotal Phase 3 InnovAATe clinical trial for the inhaled alpha-1 antitrypsin therapy for the treatment of alpha-1 deficiency. Of significance, we recently received positive feedback from the FDA in the meeting conducted with the agency. The FDA reconfirmed the overall design of our ongoing clinical program and endorsed the Data and Safety Monitoring Board's unblinded positive safety assessment. The FDA also accepted our plan to conduct an open-label extension study, which is expected to be initiated in mid-2024. The agency also expressed its willingness to potentially accept a p-value smaller than 0.1 alpha level in evaluating InnovAATe for meeting the study efficacy primary endpoint for registration, which may allow for the acceleration of the program. As a result, we plan to present a revised statistical analysis plan, standard operating procedure, and study protocol for the InnovAATe study and seek FDA feedback by mid-2024. As a reminder, the European Medicines Agency, the EMA, previously also reconfirmed the overall design of the ongoing InnovAATe study and acknowledged the statistically and clinically meaningful improvement in lung function measured by FEV1 demonstrated in our prior Phase 2/3 European study. In parallel to the clinical and regulatory progress recently achieved, we also continue to have active discussions related to potential partnering of this promising late-stage product candidate. To reiterate what we have said previously, Kamada's investigation on inhaled AAT treatment is a non-invasive, at-home treatment with expected better ease of use and quality of life for alpha-1 patients compared to current IV standard of care. The inhaled product is a leading new innovative alpha-1 treatment in advanced clinical stages and it represents a substantial opportunity to be a transformational product in a market that is already over $1 billion in annual sales in the US and the EU. We also continue to be pleased with the progress achieved at Kamada Plasma, our US-based plasma collection company. Our 2021 acquisition of a plasma collection center in Houston, Texas represented Kamada's entry into the US plasma collection market and supported our strategic goal of becoming a fully integrated specialty plasma product company. We continue to successfully expand the high premium plasma collection capacity at our first center, and construction is nearly completed at our second plasma collection center, located in Houston, Texas, expected to be open during the second half of this year. Finally, I would like to note our new logo launched a few weeks ago, which, if you're currently viewing the webcast, you've hopefully noticed by now. This new logo represents the transformation Kamada is going through as a leading innovative, vertically integrated, profitable specialty plasma company. With that, I now turn the call over to Chaime for a detailed discussion of our financial results for the fourth quarter and the full year 2023. Chaime, please go ahead.

Thank you, Amir. As previously highlighted, our business performed extremely well in 2023. Total revenues for the full year were approximately $142.5 million, a 10% increase from the $129.3 million recorded in fiscal year 2022. The year-over-year growth was primarily driven by increased sales of Kamada to Kedrion due to increased demand for the product in the US markets. While our CYTOGAM sales during 2023 were temporarily impacted by the short-dated inventory we initially purchased as part of the product acquisition in 2021, the technology transfer approval and fresh product batches available since October 2023 ensure continuous long-term supply of the product to the US and Canadian markets without interruption. We believe that our promotion of the product will support revenue growth during 2024. Total gross profit for 2023 was $55.5 million, representing a 39% margin, up 19% compared to the $46.7 million or a 36% margin in 2022. As previously discussed, the company is accounting for amortization expenses associated with intangible assets that were generated through the late 2021 acquisition of our IgG product. The company's cost of goods sold and sales and marketing included approximately $5.4 million and $1.7 million, respectively, of such amortization expenses for the full year 2023. Operating expenses, including R&D, sales and marketing, G&A, and other expenses, totaled $45.4 million, an increase of approximately 8% over the prior year. The increase as compared to 2022 was below our original anticipation and was related to the advancement of our commercial activities, as well as our ongoing Phase 3 InnovAATe trial. We expect our overall operating expenses, including R&D, sales and marketing, and G&A, to increase between 10% to 15% during 2024 compared to 2023 as we continue to advance our commercial activities, as well as our Phase 3 InnovAATe trial. As we did throughout 2023 and 2022, we continue to account for financing expenses with respect to revaluation of contingent consideration and long-term assumed liabilities, all of which are related to the acquisition completed in 2021. Revaluation of contingent consideration and the long-term assumed liabilities totaled $1 million during 2023, significantly lower than in 2022. Such decrease was associated with a temporary reduction of CYTOGAM sales during 2023. Net income for the fiscal year 2023 was $8.3 million or $0.15 per diluted share as compared to the net loss of $2.3 million or a loss of $0.05 per share recorded in 2022. Adjusted EBITDA for the 12 months ended December 31, 2023, was $24.1 million, up 35% compared to the $17.8 million in the prior year. As Amir highlighted earlier, we anticipate continued momentum through 2024 with double-digit top and bottom line growth. Specifically, we're introducing full-year 2024 revenue guidance of between $156 million to $160 million and adjusted EBITDA guidance of $27 million to $30 million. Finally, cash provided by operating activities was $4.3 million for the full year 2023, with total cash and cash equivalents of $55.6 million by the end of 2023. We maintain the financial strength and flexibility to accelerate the growth and profitability of our existing business beyond 2024 at double-digit rates and pursue compelling new business development opportunities. That concludes our prepared remarks, and we will now open the call for questions.

Our first question is from Annabel Samimy with Stifel.

I have a few questions, actually. So, first on CYTOGAM, what would the normalized growth rate have been for CYTOGAM without the interruption? And what type of CYTOGAM studies do you expect will be presented? If you could just give a little clarity on that. Second, I was wondering if we could dig a little deeper on the potential changes to the AAT program, the accelerated program. What are some of the changes you propose to ensure that p-value would this also hold with the EU authorities? While we're on that topic, I'd love your thoughts on Sanofi's acquisition of Inhibrx and its implications for the AAT program in the market.

I'm not sure I understood the last question. Let me start with the first two and then if you can just repeat it. In regards to CYTOGAM, if it wasn't for the short-dated inventory, if I'm looking at end-user sales, the end-user usage in 2023 numbers were similar to 2022, meaning that there is around a $5 million gap between the two years in terms of our sales to the channel, the wholesalers. So this is approximately the different gap between the years. Moving into 2024, of course, with the fresh batches now available, we expect this to go back to at least where it was in 2022 and even beyond because we do a lot of medical affairs and promotional activities in the market. We expect the in-market sales and in-market usage to start increasing. I hope this answers your question regarding if we try to isolate the impact of the short-dated inventory on our sales.

What type of studies are the investigators proposing and how do they plan on expanding this market? How do they think that they can expand the market?

The two studies have already been accepted for presentation in 2024 in two different transplantation-related medical conferences. Those conference agendas, I believe, were not yet disclosed. So I cannot give the exact details of those two abstracts, but they have to do with the benefit of using CYTOGAM in addition to the standard of care in the reduction of the viral load of the patients and improve the transplantation outcome.

If we can move over to the AAT program, what are some of the changes you propose to satisfy or accelerate the program? And is that going to be accepted by the EU as well?

In general, I just want to start by saying that we were very pleased with the positive feedback from the FDA. As mentioned during the call, the agency reconfirmed the overall study design, endorsed the safety data which was reviewed by the Data and Safety Monitoring Board and found it to be robust. So we presented the DSMB data up to date in terms of the number of patients in the study who have completed a significant treatment duration. We have robust safety data, which really satisfied the agency and waived additional requirements for safety evaluation. They also accepted our open-label extension study, which is about to start with the upcoming renewal. We approached both agencies, the EMA and the FDA, with discussion questions related to potential ways to shorten the study duration and accelerate the program. We found the FDA team highly supportive and cooperative in the direction we're evaluating. The agency is willing to potentially accept the p-value as 0.1, which will be sufficient to prove a frequency of FEV1 instead of the traditional 0.05. We're preparing the revised statistical plan, which may show that we need less than 220 patients to be recruited for the study. If this will indeed be the case, and which we believe will be the situation, then we'll be able to shorten the study duration due to quicker recruitment. With that information, we will go back to the EU – to the EMA, sorry, to get their consent to basically have the same path forward.

I just want to know if you had any comments about the Sanofi acquisition of Inhibrx and their AAT program. Any thoughts around that?

Yes, absolutely. So, the Sanofi acquisition of Inhibrx program, which is a recombinant AAT, we think it's a very important trend, a very important transaction. It puts a lot of focus on alpha-1 deficiency in general. We believe that if the product makes it to the market, Sanofi, with their significant marketing and promotional power, will create better awareness and greater awareness of alpha-1 deficiency. As you may know, the majority of alpha-1 patients are still misdiagnosed or undiagnosed. So, like a powerhouse like Sanofi being active in the alpha-1 space will definitely lead to a significant market increase by better diagnostics and better coverage. So this is a very positive sign. In terms of inhaled, we believe inhaled has significant advantages in general. It's a non-invasive at-home treatment with a different mechanism of action. We believe that if it makes it to the market, it's going to be a transformational product that will compete very well in the markets. The Inhibrx/Sanofi product, although it has advantages, is still an IV treatment, while we come with inhaled non-invasive and we come with a frequency study. We believe we have sufficient advantages, significant advantages in the market which will lead to a highly competitive product. Also, the inhaled product, because we go directly into the lines versus IV treatment, we give one-eighth of the dose compared to the current standard of care and approximately one-fifth of the dose compared with the Inhibrx treatment. So, in terms of cost of goods and potential competitiveness, we also have a significant advantage.

At this time, I'll turn the call over to Brian Ritchie to see if we have any questions from the web.

Just a couple here, Amir and Chaime. First, what could a potential partnership for an inhaled AAT look like?

Building on what I just answered Annabel on the previous question, we believe that inhaled alpha-1 has significant advantages. We believe that in order to compete well in the market, especially with a powerhouse like Sanofi, it would be a good move for Kamada to partner the program with a strategic partner that has significant market and commercial capabilities and resources. And we're looking for such a type of partnership that will allow us to bring the product to market in the fastest way and to compete well with the superior product.

Maybe an update on the BD, product acquisition, and opportunities and what might be available?

We are proactively looking for products in the plasma space, as well as in transplantation. This is a specialty we're covering to be very highly synergistic with our expertise and staff. Our business development team is working proactively, evaluating some opportunities. Once we have the news to update the market, we'll be happy to do so.

That's all the questions that have come in over the web. I ask you to maybe make some closing comments.

Yes. So in closing, we're very pleased with our exceptional performance during 2023, and excited about the potential opportunities that lie ahead based on the amended KEDRAB agreement, existing ongoing late-stage inhaled alpha-1 clinical program, and the strength of our commercial portfolio and balance sheet. We look forward to continuing to support clinicians and patients with important life-saving products that we develop, manufacture, and commercialize. We thank you all for your support and remain committed to creating long-term shareholder value. We hope you stay safe and healthy. Thank you very much.

Thank you. This will conclude today's conference. We disconnect your lines at this time. Thank you for your participation.