Good morning and welcome to Moderna's Third Quarter Earnings Call. At this time, all participants are in a listen-only mode. Following the formal remarks, we will open the call up for your questions. Please be advised that the call is being recorded. At this time, I would like to turn the call over to Lavina Talukdar, Head of Investor Relations at Moderna. Please go ahead, ma'am.

Thank you, operator. Good morning, everyone, and thank you for joining us on today's call to discuss Moderna's third quarter 2021 financial results and business update. You can access the press release we issued this morning, as well as the slides that we'll be reviewing by going to the Investors section of our website. On today's call are Stéphane Bancel, our Chief Executive Officer; David Meline, our Chief Financial Officer; Stephen Hoge, our President; and Paul Burton, our Chief Medical Officer. Before we begin, please note that this conference call will include forward-looking statements made pursuant to the Safe Harbor provisions of the Private Securities Litigation Reform Act of 1995. Please see slide 2 of the accompanying presentation and our SEC filings for important risk factors that could cause our performance and results to differ materially from those expressed or implied in these forward-looking statements. On slide 3, please see the important indication and safety information for our COVID-19 vaccine, which has been authorized for emergency use in the United States and many countries around the world. I will now turn the call over to Stéphane.

Thank you, Lavina. Good morning or good afternoon, everyone. Welcome to our Q3 2021 conference call. Today, I will start by a quick business review of the quarter before David presents the key financials. Paul will then walk you through some real world evidence updates. And Stephen will provide the clinical development update. I will then come back to close to share some thoughts about where we are heading. Let's start on slide 5 with a holistic pipeline update. First, respiratory vaccines. We are pleased to have filed the BLA for our COVID-19 vaccine with the FDA and have now received a priority review designation. We received our first full approval for Spikevax batch release in Canada. We received EUA from the FDA for the 50 microgram booster and mix and match has been authorized. We also received authorization for boosters from our major geographies, EMA, UK and so on. We were informed recently that the FDA may take until January 2022 to review the EUA request for 12 to 17 years of age. Turning now to flu. mRNA-1010 is fully enrolled for Phase 1 and we expect human data soon. For RSV, mRNA-1345, after very positive data in Phase 1, with high neutralizing antibody levels after one dose, our teams are finalizing the preparation of a Phase II/III in older adults. This study should start soon. We also announced our development candidate for a COVID booster plus flu booster in a single dose, mRNA-1073, which we anticipate will be in the clinic soon. Let me now turn to vaccines against latent viruses. As many of you know, latent viruses are a major cause of health problems. Latent viruses are mainly made of DNA viruses. And once a human is infected by a latent virus, that virus will stay in the body. You are familiar with some latent viruses like HIV and HPV. There are many others that impact humans. As a company, we are committed to developing a portfolio of first-in-class vaccines and therapeutics against these latent viruses. Our first programs are CMV vaccine, EBV vaccine, and EBV therapeutic vaccine. We have also partnered to work on two HIV vaccines. Last week marked a big milestone for Moderna. We started dosing in the clinic the first participant of our Phase III pivotal registration study for the CMV vaccine mRNA-1647. This marks the second Phase III study that the company has started and brings us one step closer to getting another important vaccine to millions of people around the world. For EBV vaccine, mRNA-1189 should start dosing for its Phase I very soon. And our new development candidate on the EBV therapeutic vaccine, mRNA-1195, is moving toward the clinic. Let me now turn to therapeutics. Our personalized cancer vaccine is in Phase II in combination with KEYTRUDA; the trial is fully enrolled. And we expect data in the back end of 2022. Our rare genetic programs continue to progress well in the clinic. PA has its Phase I dose cohort fully enrolled. MMA is dosing patients in its Phase I. GSD1a has an open IND and has received orphan drug designation by the FDA. So, as you can see, we have three rare genetic disease programs in the clinic or soon to be in the clinic. We look forward to showing clinical data in the coming months. We are very proud to have found a way to get Crigler-Najjar Type 1 or CN-1 to patients through a donation of our IP and the assets to the Institute for Life Changing Medicines. CN-1 disease is an ultra-rare disease with very few patients afflicted around the world. For ultra-rare disease, just the cost of clinical development will result in a very high price for a few patients around the world that could benefit. This model is not one that we support. So instead of developing a drug and charging a very high price, we decided to give the drug away and innovate for a creative partnership. We provide the drug to the institute, we pay for clinical trial material, the institute pays for the clinical trial cost. If the drug is approved, we'll provide the medicines to the kids and their families for free. And we will not charge any royalty or milestone to the institute. We believe this is the right thing to do to continue to contribute to society for ultra-rare disease where our mRNA platform can help. One of the important news items announced today is the introduction of a new modality through our existing six modalities. We're very pleased to announce that Vertex and Moderna are now in GLP tox studies for the cystic fibrosis program, VXc-522. This marks our first inhaled pulmonary therapeutics program. I would like to congratulate and thank our scientific team as well as the Vertex team for having been able to develop a novel lipid formulation to allow inhaled pulmonary delivery. This is really exciting for patients. As we communicated previously, in addition to doing therapeutics using mRNA coding for human proteins, like the ones I just described, we want to use our mRNA plus lipid technologies to develop therapeutics using mRNA coding for gene editing enzymes. We are pleased to announce our first partnership in the field. We announced earlier this week that we entered into a licensing collaboration with Metagenomi based in California to use their next generation gene editing enzymes. We believe that that technology, coupled with our mRNA plus lipid technologies, and our manufacturing infrastructure will produce some exciting new medicines to take into the clinic. I am very pleased with the progress of the company. We are increasing depth in vaccines, and at the same time increasing breadth of applications including gene editing. On slide 5, you will find financial highlights. For Q3, we reported revenue of around $5 billion enabled by delivering 208 million doses of our COVID-19 vaccine. Net income of $3.3 billion. Our cash and cash equivalents position was $15 billion at the end of September. Since the end of the quarter, we have been working to get better visibility into those variables that will impact our full year results. We have much better visibility today than we did a month ago. For fiscal year 2021, we're updating the range of doses we plan to deliver to 700 million to 800 million doses. The key variables of this updated volume range are, first, longer lead time for exports to countries outside the US and for international shipments in general. In Q3, we shipped more deliveries to new international markets and expect Q4 to also have more international deliveries. As we deliver to these countries for the first time, we expect the process to become more routine and delivery time to shorten. However, some Q4 deliveries may still move to early 2022 as a result. Second, in Q3, we have expanded our fill-finish capacity with our manufacturing partners, which had a temporary impact on our shipments. That work is complete now. And we should see a positive impact from this expansion very soon. Third, the bottleneck of production has moved down the manufacturing line to product release. We added additional resources and skilled personnel to the release end of the manufacturing line. And we expect to increase the weekly number of doses released. We believe resolution of these factors put us in a good position heading into Q4 and 2022. Now if I turn to revenue for 2021. The updated revenue range for 2021 is $15 billion to $18 billion. This range reflects our updated delivery schedule with fewer doses delivered in 2021 as some doses are pushed into 2022. And also, the pricing impact of prioritizing delivery to COVAX and the African Union that have a lower tier pricing. On slide 7, let me start by summarizing the scale-up operational challenges that the team had to work through as we scaled from making less than 100,000 doses in 2019 to hundreds of millions of doses in 2021. Q1 scale up challenges were around drug substance, making mRNA in lipids. Q2 scale up challenges were on drug product and ensuring we could fill enough vials. In the first half of the year, we made great progress in these challenges, as you can see from the numbers on the right. We now have 901 million doses of drug substance that have been formulated into mRNA products. And we have 770 million doses of drug product already in vials. Q3 scale-up challenges were on product release as the supply chain became more complex with increased deliveries to many countries around the world. At the beginning of the year, we supplied just a few large countries. As mentioned before, we are working through these challenges. As of November 1, we achieved 566 million doses released around the world. With the progress year-to-date, we expect to be able to deliver 700 million to 800 million doses for full year 2021. We were pleased to be named last week for the seventh year in a row as one of the top 20 biotech and pharmaceutical companies in the world by Science. We continue to invest in science and the culture of our team. We aim at building the best mRNA science in the world, in the culture of boldness, collaboration, curiosity and relentlessness. On slide 9, you will find our usual summary slide, which describes some of the key high-level attributes of the company as of today. Now let me turn it over to David.

Okay. Thank you, Stéphane. We're providing today the analysis of actual 2021 third quarter results, along with an updated view of key drivers of financial performance going forward. Turning now to slide 11, starting with an overview of our sales performance before commenting more broadly on our financial results. Total product sales in the third quarter were $4.8 billion, representing 208 million doses delivered to our customers. This compares to sales of $4.2 billion and 199 million doses in Q2 and sales of $1.7 billion and 102 million doses in Q1 of this year. Sales to the US government were $1.2 billion in the third quarter, reflecting 73 million doses delivered, compared to $2.1 billion and 126 million doses in Q2 and sales of $1.4 billion and 88 million doses in Q1. Sales to the rest of the world were $3.6 billion in the third quarter, reflecting 136 million doses delivered, compared to sales of $2.1 billion and 73 million doses in Q2 and $0.4 billion of sales and 14 million doses in Q1. This reflects the significant manufacturing ramp up outside the US over the last two quarters. The relatively modest increase of delivered doses in Q3 versus Q2 was driven by the factors that Stéphane just explained. We continue to scale our production network and are working to achieve an increased quarter-over-quarter improvement starting in Q4. Turning to slide 12. The transformation of Moderna from an R&D-focused biotech to a commercial company continues to be very apparent when reviewing our financial results. The comparison of the third quarter of 2021 to prior year is not meaningful due to our significant growth, which is why we will primarily focus on the quarter-over-quarter comparison relative to Q2 on the slide. Total revenue was $5 billion in the third quarter of 2021 compared to $4.4 billion in the second quarter and $0.2 billion in the prior-year period. The increase of total revenue is driven by the sale of the company's COVID-19 vaccine. Product sales in Q3 were $4.8 billion compared to $4.2 billion in the second quarter, an increase of 15%. Cost of sales was $722 million or 15% of the company's product sales in the third quarter compared to $750 million or 18% of product sales in the second quarter. The quarter-over-quarter percentage improvement is driven by higher average selling price as a result of shifts in our customer mix and, to a smaller extent, by favorable manufacturing costs. Research and development expenses were $521 million in the third quarter, up from $421 million in Q2 and $344 million in the same period in 2020. The higher spend versus prior quarter and prior year was driven by increased COVID-19 vaccine clinical development activities, including our announced efforts around booster variant-specific and multivalent vaccine candidates. Headcount increases as well as external costs to support our growing and maturing development pipeline beyond the COVID-19 vaccine activities also contributed to the expense increase. Selling, general and administrative expenses were $168 million for Q3 compared to $121 million in the prior quarter and $48 million for the same period in the prior year. The growth in spending was driven by the commercialization of our COVID-19 vaccine globally with continued investments in personnel and outside services in support of the accelerated company build-out. Provision for income taxes was $219 million in the third quarter, following $283 million in Q2 and an insignificant amount in the prior year. Our effective tax rate for the third quarter was 6%. Let me remind you of the fact that we had a net operating loss carryforward of $2.3 billion at the end of 2020. This year, we started to release the valuation allowance against the related deferred tax assets, which results in an estimated non-recurring full-year benefit to our effective tax rates of about 5 percentage points. Our Q3 effective tax rate was lower than the US statutory rate, primarily due to the just-described benefit related to the release of the valuation allowance, the foreign derived intangible income deduction and an excess tax deduction related to stock-based compensation. This last item drove the quarter-over-quarter reduction due to the increase in our share price in Q3 versus Q2. We recorded net income of $3.3 billion in Q3 compared to $2.8 billion in Q2, an increase of 20%. This compares to a loss of $0.2 billion in Q3 of last year. Diluted earnings per share for Q3 2021 were $7.70. Turning now to year-to-date financial results compared to prior year on slide 13. Total revenue was $11.3 billion for the first nine months of this year compared to $0.2 billion for the same period in 2020. The significant growth was driven by the sales of 510 million doses of the company's COVID-19 vaccine. Grant revenue of $473 million in the first nine months of 2021, an increase of $286 million compared to the prior year, was primarily driven by increases in revenue from BARDA related to the company's COVID-19 vaccine development. Cost of sales was $1.7 billion or 16% of the company's product sales for the year-to-date period as of September 30, including third-party royalties of $400 million. A portion of the inventory costs associated with this year's product sales was expensed as prelaunch inventory costs in 2020. If inventories sold for the first nine months of this year was valued at cost, our cost of sales for the period would have been 17% of the product sales. Research and development expenses were $1.3 billion for the nine months ended September 30 of this year compared to $0.6 billion for the same period in 2020. The growth in spending in 2021 was mainly due to increase in clinical trial expenses and, to a lesser extent, personnel-related costs, manufacturing expenses, and consulting and outside services, primarily driven by increased mRNA-1273 clinical development activities. Selling, general and administrative expenses were $0.4 billion for the first nine months of this year compared to $0.1 billion for the same period in 2020. The growth in spending in 2021 was mainly due to increases in consulting and outside services, personnel-related costs, and marketing expenses primarily attributable to the company's COVID-19 vaccine commercialization-related activities and increased headcount. For the nine months ended September 30, we recorded a provision for income taxes of $541 million compared to insignificant amounts in the same period in 2020. Our effective tax rate for the first nine months of this year was 7%. It was lower than the US statutory rate primarily due to non-recurring benefits related to the release of the valuation allowance, the ongoing benefit of the foreign-derived intangible income deduction, as well as a discrete item for excess tax deductions related to stock-based compensation. Net income was $7.3 billion for the nine months ended September 30 of this year compared to a net loss of $0.5 billion for the same period in 2020. Diluted earnings per share were $17 for the first nine months of 2021. Turning to cash and selected cash flow information on slide 14. We ended Q3 2021 with cash and investments of $15.3 billion compared to $12.2 billion at the end of Q2. The increase is driven by our commercial sales and additional customer deposits received in the third quarter for future purchases of our COVID-19 vaccine. Net cash provided by operating activities was $3.3 billion in Q3 after $4.1 billion in Q2. The quarter-over-quarter reduction is driven by a lower amount of cash deposits for future product supply received in Q3 compared to Q2. On a year-to-date basis, net cash provided by operating activities was $10.3 billion compared to $0.8 billion in the prior year. Cash used for purchases of property and equipment was $164 million for the nine months ended September 30 compared to $44 million for the same period in 2020, reflecting continuous investments in our manufacturing infrastructure. Now turning to slide 15. Let me briefly expand further on our cash and investment position and the net balance of cash deposits for future product supply as this is an important point when modeling future cash flows. The cash and investment balance reported as of September 30 was $15.3 billion, up from $12.2 billion as of June 30. The increase is driven by our commercial activities, including cash receipts from product sales and customer deposits for future product supply. The net balance of cash deposits for future product supply was $6.7 billion at the end of Q3, at a similar level to the balance in Q2 of this year. Turning now to the 2021 updated financial framework on slide 16. For the full-year 2021, we expect a product sales range of $15 billion to $18 billion. We now expect to be able to deliver 700 million to 800 million doses at the 100 microgram dose level to our customers. This compares to the prior outlook of 800 million to 1 billion doses. Our total cost of sales includes the cost of goods manufactured, third-party royalties as well as logistics and warehousing costs. Given the favorability we have observed in the year-to-date period, we now expect total cost of sales as a percent of product sales between 16% to 17% for the full year 2021. This compares to our previous outlook of 18% to 20% of product sales. For 2022, we currently expect the cost of sales ratio to exceed 20%, driven by customer mix and multiple presentation types. On the R&D and SG&A expense side, we continue to plan for an increase on a quarter-over-quarter basis and expect this trend to continue for the remainder of 2021 and beyond, driven by a maturing development portfolio and the scale-up of our commercial activities. Based on further increased visibility of the utilization of our accumulated net operating loss carryforward, expected global sales mix and the mentioned discrete benefits in the first nine months of this year, we now expect our all-in 2021 tax rate to be in the high single-digit range. This compares to our previous forecast of approximately 10%. Since we won't have a material benefit from our valuation allowance in future years, we expect our reported 2022 effective tax rate will increase relative to our 2021 rate. It's also too early to further comment on impacts from a potential tax reform. Finally, regarding capital investments. We are now planning for approximately $0.4 billion of capital investment to fall into the 2021 calendar year compared to our previous range of $450 million to $550 million. We are strongly committed to a further build-out of our manufacturing and general company infrastructure, and hence predict capital investment in 2022 will be meaningfully above 2021 levels. This concludes my remarks concerning the financial performance. And I now turn the call over to Paul Burton.

Thank you, David. And good morning, good afternoon, everyone. With more than 150 million people worldwide now having received two doses of our vaccine, we are humbled to be able to see the positive impact it is having on people's lives around the world. We are reminded of the fact that almost 250 million people have been infected with COVID-19 globally and 5 million people have lost their lives. Our profound thanks, as always, go out to those on the front lines, working tirelessly to keep us safe in this ongoing fight. Through numerous independent studies, time and time again, we see consistent findings showing that mRNA-1273 is highly effective in saving lives, reducing hospitalizations and reducing the risk of COVID-19 infection. I will highlight a few of these independently conducted studies this morning. In slide 18, I will begin with some of the data from the United States government. These data come from the CDC and show through September of this year the difference in COVID-19 cases between fully vaccinated and unvaccinated populations. An unvaccinated person has an 11-fold greater risk of dying from COVID-19, underscoring the important role that getting vaccinated plays in our protection and ending this pandemic. The data show that vaccination with mRNA-1273 provides the greatest protection, not only against COVID-19 infection, but also death due to COVID-19. In fact, even during the surge of the Delta virus variant during the summer months this year, Moderna's vaccine had the lowest reported deaths associated with breakthrough infection as the CDC data demonstrate. Approximately 160 million doses of the Moderna vaccine have been administered in the United States. And in the next slide, I want to show you some further government-generated data in a country where the Moderna vaccine has also had extensive use, and that country is Switzerland. You can see here exposure data on the left. Approximately 3.6 million people have been fully vaccinated with the Moderna vaccine and 1.9 million people have been fully vaccinated with the Pfizer/BioNTech vaccine. These government-generated data from the Federal Office of Public Health in Switzerland, again, are clear and show that vaccination with the Moderna vaccine is highly effective at reducing infections, hospitalizations and deaths due to COVID-19 infection. For every 1 million people vaccinated, use of mRNA-1273 would be expected to result in 643 fewer COVID-19 breakthrough infections, 78 hospitalizations and 38 fewer deaths. Next, in slide 20, our data from two other recent independent studies that build on the results I just showed you from Switzerland. The first study on the left side of this slide followed 38 million vaccinated people in the United States, Iceland and South Korea and again found that those people vaccinated with mRNA-1273 were at 53% reduced risk of a COVID-19 infection and 33% reduced risk of a COVID-19 hospitalization compared to those vaccinated with the alternate mRNA vaccine. The data on the right side of the slide are from a recent publication by Nordstrom and colleagues in Sweden and Norway, showing that mRNA-1273 delivered 87% vaccine effectiveness during a time of high Delta variant circulation in those countries. The data I've shared so far are all from the general population. Let me turn now to the effectiveness of the Moderna vaccine in particularly vulnerable populations, the immunocompromised. These data were published just two days ago, again, by the United States CDC VISION network and examine vaccine effectiveness at preventing COVID-19 hospitalization, which is so critically important in individuals with a variety of immunocompromised medical conditions between January and September of this year. As the authors of this study note, with the exception of those individuals with rheumatic disorders, vaccine effectiveness point estimates were generally higher for the Moderna vaccine than for the Pfizer/BioNTech vaccine. And the difference in effectiveness in these hard-to-immunize populations is shown in the column on the right. I want to turn now to the topic of myocarditis and to put it in the context of the clinical benefits of vaccination that I've just described with mRNA-1273. It is important to recognize that the cases of myocarditis reported to occur following mRNA vaccination are rare, generally mild, typically respond to conservative treatment and are self-limiting. Health authorities have reviewed many data sets and the US CDC and WHO have concluded that there is a risk of myocarditis and pericarditis after receiving any mRNA vaccine. The WHO's Advisory Committee on Vaccine Safety notes that myocarditis can occur following SARS-CoV-2 infection or COVID-19 disease and that mRNA vaccines have a clear benefit in preventing hospitalization and death from COVID-19. Analyses from our global safety database show that the events of myocarditis are very rare. Overall, we observe 9.5 cases of myocarditis per million vaccinated individuals compared to an expected rate of 21 cases per million individuals. Now, in common with other reports of mRNA vaccines in individuals aged 18 to 24, we see an increased rate of myocarditis of 40 cases versus 17 expected cases per million individuals. These data from our own safety database are consistent with the findings from safety databases evaluated by the CDC and other global health authorities. Moderna's global safety database has information on an estimated 1.5 million adolescents, providing us an opportunity to look at the rate of myocarditis in those individuals, and those data are shown in this table. We see the small, absolute, well-described risk of increased myocarditis rates in males aged 18 to 24 that I just described to you. But we do not see an increased risk in adolescents, neither in boys nor in girls. These data are reassuring and important as we continue to offer mRNA-1273 to adults, adolescents and as we file for authorization in children. So, in summary, the data I've shared with you today from independent government reports in the United States and in Switzerland, countries with high vaccination rates of Moderna's vaccine, show that mRNA-1273 is associated with low breakthrough infections, hospitalizations and deaths due to COVID-19. Other independent studies in millions of individuals continue to show that mRNA-1273 is highly effective in reducing the risk of breakthrough COVID-19 as well as hospitalizations and death. And importantly, this is also true in those vulnerable and hard-to-vaccinate immunocompromised patient populations. Moderna's global safety database of 151 million vaccinated individuals shows a rate of myocarditis in males aged 18 to 24 that is consistent with analyses by CDC and others. Moderna's global safety database does not show an increased risk of myocarditis in 1.5 million individuals below the age of 18 and vaccinated with Spikevax. So, this concludes my quick overview of some recent analyses of mRNA-1273 effectiveness data and review of data from our global safety database. And I will now turn the call over to Stephen.

Thank you, Paul. And good morning or good afternoon, everyone. Today, I'll review the progress we've made across our vaccines and therapeutics pipeline. Let me start with our COVID-19 vaccine, mRNA-1273, for adults ages 18 and above where there are a number of important regulatory updates. First, we have announced that the FDA granted priority review to Moderna's COVID-19 vaccine BLA. In October, we also received an EUA from the FDA and the European Commission's approval for a booster dose of our COVID-19 vaccine at the 50-microgram dose level for the adult cohort ages 18 and above. Turning to the adolescents and pediatric settings. As a reminder, there are two clinical trials for each of these groups: TeenCOVE is our study in the adolescent population, 12 to 17 year olds, and KidCOVE is the study in the pediatric population, age 11 and younger. For the adolescent population, 12 to 17 years old, our vaccine is authorized in a number of countries worldwide, including the United Kingdom, the European Union, Canada, Switzerland, Japan, Thailand, Taiwan, Saudi Arabia, and Argentina, to name a few. We've submitted data from our Kid/TeenCOVE study to the FDA in the United States as well as to other countries. We were recently notified by the FDA that the agency will require additional time to evaluate our proposed amendment due to recent analysis of the risk of myocarditis after vaccination in some populations. The agency expects this evaluation may extend until January 2022. As Paul noted, Moderna's global safety database includes an estimated 1.5 million adolescents, who've received the Moderna COVID-19 vaccine, most outside of the United States. To date, we have not observed a rate of myocarditis from those younger than 18 years in our safety database that points to an increased risk of myocarditis in that population. We continue to believe the benefits of vaccination significantly outweigh the risks. In the pediatric setting, our study known as KidCOVE is ongoing and is focused in three age groups, a group with children 6 to 11 years of age, a group of 2 to less than 6, and a group of children 6 months to less than 2. The trial consists of a dose escalation phase for each group, followed by an expansion phase once the dose has been selected. Last week, we shared positive top line data from the oldest of the age groups in KidCOVE, the 6 to 11-year-old cohort, showing the two 50-microgram doses of mRNA-1273 were generally well tolerated and that the primary immunogenicity endpoints were met. We will submit our results soon to the EMA and other global regulatory agencies. For the other two age groups in KidCOVE, the 2 to less than 6 years old group and the 6-month to less than 2-year old group, our dose selection studies are ongoing. On the next slide, let me share with you some of the data we have in children ages 6 to less than 12 years of age. This data is after dose one as we are waiting for additional follow-up time to share the post-dose two data. As a reminder, the study was randomized two to one for vaccine versus placebo. Based on the case definition of COVID-19 that we used in the Phase III adult study, the observed interim vaccine efficacy was 100% in this analysis, starting two weeks after the first dose and using that case definition. Vaccine efficacy against SARS-CoV-2 infection was also high at 80% and vaccine efficacy against asymptomatic SARS-CoV-2 infection was 65%. Both endpoints are incredibly important as we seek to end the pandemic. Turning now to our booster and next-generation COVID-19 vaccine programs on slide 28. As a reminder, we are evaluating multiple COVID-19 vaccines as potential boosters to provide the broadest range of countermeasures to the virus as it continues to evolve. We were granted EUA for the 50-microgram dose of our current vaccine as a booster, as mentioned previously. And we are currently evaluating two variant-specific vaccines and two multivalent vaccine candidates, which are combinations of different variants of concern in an effort to stay ahead of the evolving virus. In addition, we're also evaluating mRNA-1283 as a next-generation refrigerator-stable vaccine, which is in a Phase I study. The interim analysis of that Phase I data has been completed at three different dose levels and indicates that a lower dose of mRNA-1283 can achieve similar neutralizing antibody responses in primary series as our authorized vaccine mRNA-1273. mRNA-1283 also had an acceptable safety and tolerability profile and we're moving forward toward a Phase II booster study for that candidate. This will also evaluate even lower doses of mRNA-1283, given the strong boosting performance seen in Phase I. While the start of our booster strategy in late January of this year was in response to the threat of newly identified variants at that time, our booster strategy has continued to evolve as the pandemic unfolds. Slide 29 is a slide we shared at our Vaccines Day in April of this year. At the time, the graph on the left was illustrative of our view of the likely path for the pandemic based on our perspective on respiratory virus evolution and epidemiology, including prior coronavirus pandemics. Today, it's becoming clear that the SARS-CoV-2 virus is following the footsteps of other respiratory viruses and is on its way to becoming a seasonal epidemic/endemic threat. So, where are we now? With Delta and the potential for other variants, the winter of 2021-2022 still looks to be a time of moderating, but persistent, variant epidemic waves. Infection and reinfection continue to cause morbidity and mortality during this phase, but hopefully in fewer people. The focus will remain on suppressing the rate of viral evolution and emergence. Primary vaccination is critical. But given the high rate of background transmission, booster vaccines will also be important in all countries. Looking ahead, we expect 2022 will be the beginning of the seasonal endemic phase. Reinfections in individuals who are at high risk, including older adults, the immunocompromised or healthy adults with more rapidly waning immunity due to under-vaccination with potentially less effective vaccines will be at the greatest risk for severe outcomes. As with the recent Delta wave, this will include some risk of hospitalization and, unfortunately, some risk of death as well as social disruption. We believe this will become the primary population for whom seasonal boosting will provide a significant and enduring benefit. In summary, as we described earlier this year, we believe SARS-CoV-2 is following a familiar path that will ultimately become a seasonal threat to a large population of higher risk adults. Perhaps the biggest unknown in the near term is the extent to which further viral evolution in the coming Northern Hemisphere winter and Southern Hemisphere winter in 2022 will create fertile ground for newly transmissible and immune-evading variants to emerge. If so, rapid boosting may become necessary. We will need to remain vigilant throughout this time as we fight the pandemic, and we are ready to advance updated boosters rapidly if they become needed. Now moving from COVID on to slide 30. We announced in September that the Phase I portion of our quadrivalent seasonal flu vaccine, mRNA-1010, is fully enrolled and we look forward to sharing data from that trial and moving to Phase II soon. We also announced positive Phase I interim data from our RSV vaccine in older adults in September, and we plan to start a pivotal Phase II/III RSV vaccine trial before the end of 2021. Separately, the pediatric RSV program continues to move forward with cohorts enrolling well in our Phase I study. Our hMPV/PIV3 study in pediatrics is also currently enrolling in toddlers. We were very excited to announce last week that our Phase III CMV vaccine trial has dosed its first participants. The start of the Phase III trial, CMVictory, is an important step in evaluating our CMV vaccine against congenital CMV. As a reminder, CMV is the number one cause of birth defects in the United States, and we are evaluating the safety and efficacy of mRNA-1647 in women ages 16 to 40 at the 100-microgram dose level. The trial is starting in the US and will include approximately 150 sites globally, and will enroll approximately 6,900 women of child-bearing age. Importantly, the inclusion criteria of the trial include women at high risk of CMV exposure through direct exposure in the home, socially or occupationally to children under five years of age. Diversity in our clinical trials is also extremely important to us, and we're proud to continue our commitment from last year on clinical trial diversity. We believe setting targets and measuring ourselves against them remains one of the most important ways we can work to address healthcare inequity in clinical research. For the CMVictory Phase III study, our goal is to have 42% of the trial participants in the United States come from communities of color, many of which are disproportionately impacted by the CMV virus. Moving on from vaccines. This slide highlights our mRNA therapeutics pipeline. At R&D Day, we described how our modalities and therapeutic areas overlap. In oncology, our PCV Phase II trial is now fully enrolled and we expect to readout for that as early as the fourth quarter of next year. Separately, an expansion cohort in head and neck cancer in our Phase I trial is ongoing. We also have Phase I trials ongoing for our KRAS vaccine, which is partnered with Merck, the triplet program, and the IL-12 intratumoral program, which is partnered with AstraZeneca. In cardiovascular, our VEGF program, also partnered with AstraZeneca, has completed the enrollment of a low-dose cohort in its Phase II study and AZ will be providing updates at a presentation of the data at the American Heart Association meeting in two weeks. Within autoimmune, our IL-2 program is in a Phase I trial in dosing. And within rare diseases, our PA and MMA trials are ongoing in Phase I and our GSD1a program has an open IND and is expected to start a Phase I study soon. I'm also very excited to announce that our first cystic fibrosis program has moved into preclinical development with IND-enabling studies now underway. We and our partners at Vertex are pleased to announce that development candidate, VXc-522. This program marks our first program in a brand-new modality, inhaled therapeutics. As a reminder, our Moderna modality encompasses a new method for utilizing our proprietary lipid nanoparticle technologies and mRNA technologies to bring forward medicines. Now double-clicking for a moment on the CF programs in research, recall that we have two partnerships with Vertex. Our first collaboration targets the CFTR protein and trying to produce it using mRNA and LNP technologies. This is where we are advancing our candidate, VXc-522. We also have a collaboration with Vertex using mRNA for gene editing and gene therapy. Both collaborations are focused on treating this 10% of CF patients with disease that unfortunately is not addressable with current CFTR modulators. For this 10% of the CF population, alternative approaches are absolutely necessary. And the exciting update today, as I said a moment ago, is that we're announcing the first development candidate to move into development from that collaboration described on the left-hand side of this slide. In this collaboration, we're delivering messenger RNA that encodes for CFTR protein that is missing or non-functional in patients who suffer from cystic fibrosis. We plan to target that 10% that I mentioned a moment ago. We've been working incredibly hard with Vertex to advance the candidate, and we are very excited that that has now moved into IND-enabling studies. As Vertex announced recently, they expect to submit an IND in 2022, paving the path for clinical studies in these patients. In the close, I'd like to just highlight our pipeline on the following three slides, starting on slide 35, which includes our respiratory vaccines in development. Slide 36 summarizes our large portfolio of latent virus vaccines and vaccines against other viruses. And on slide 37, you will see the extensive mRNA therapeutics pipeline that we have in development. With that, I'll hand it back to Stéphane to close.

Thank you, Stephen. Slide 39 is from our September 9 R&D Day and summarizes the product franchise we focus on at Moderna. Priority number 1 is our pan-respiratory annual booster franchise. Priority number 2 is our first-in-class vaccines for latent viruses. Priority number 3 is our therapeutics based on mRNA-encoded proteins. And priority number 4 is the therapeutic space on mRNA-encoded gene editing enzymes. As we have said for several quarters now, SARS-CoV-2 is here to stay and will evolve from a pandemic to endemic setting. We believe that 2022 will see pandemic in low-income countries throughout the year, but in high-income countries, the year will be of two halves: pandemic priming for children and boosting for others with an endemic boosting campaign in the fall of 2022. On slide 42, you can see the revenue drivers that we anticipate will play out in 2022. We believe there are three components that will drive our COVID-19 vaccine revenues for next year. First, signed APAs. We have already signed around $17 billion of advanced purchase agreements, or APAs, for delivery in 2022. Second, APA options. There are up to $3 billion of APAs that are in options. Some options have been converted in Q3 from options to firm order. Third, the fall of 2022 commercial market. We also believe that the fall of 2022, assuming that a BLA is granted for boosters, will drive the commercial booster market of up to $2 billion. So, in total, at this point, we believe that 2022 revenues could be between $17 billion and $22 billion. We, of course, continue to have discussions around APAs with governments and international organizations, including COVAX, the Pan American Health Organization or PAHO, and the African Union. For this pan-respiratory franchise, our goal is to evolve the COVID-19 vaccine primary series into fall of 2021 boosters, which is happening as we speak, and then fall of 2022 boosters and then add to a COVID booster a flu booster in a single dose, and then add to COVID and flu an allergy booster in a single dose. Our flu vaccine human data should be out soon. And the team is already preparing the Phase II/III for flu. And RSV is moving fast to Phase II/III. If you look at the health damage of latent viruses, it is profound. EBV is a major cause of infectious mononucleosis. EBV has been reported to increase risk of multiple sclerosis. EBV is associated with certain cancers and autoimmune diseases and EBV is associated with a higher risk of long COVID. CMV associated will be the leading cause of birth defects. CMV is a major driver of immune dysfunctions with aging. CMV is associated with cardiovascular diseases. CMV is associated with cancer and cognitive impairments. For now, our focus is CMV, EBV and HIV, but we are developing in the labs vaccines against other latent viruses that impact human health. Our goal is to eliminate these viruses. As we discussed earlier, several cancer and rare genetic programs are in the clinic and will provide clinical results soon. On November 15, AstraZeneca will present Phase II data in patients from the VEGF program at the American Heart Association. And we are pleased to announce the new modality with inhaled pulmonary therapeutics. Moderna Therapeutics is our effort to expand the use of our platform to create more innovative drugs to help patients. Our strategy is to invest internally under the leadership of Dr. Eric Huang with a dedicated team and to set up license agreements with next-generation gene editing companies. The Metagenomi partnership is a first step in that direction. The strategic path of the company is very clear and exciting. We want to stop people getting hospitalized from respiratory infection. We won't stop until this goal is achieved. We want to stop our fellow human beings from suffering from these latent viruses. We want to bring to market mRNA encoded protein therapeutics in oncology, cardiology, rare genetic disease, autoimmune. We want to bring therapeutics using gene-editing enzymes. We believe Moderna could become the most impactful drug company in the world. As we scale, we realize that we needed to go further in setting the right framework for our team to understand what has made Moderna. So, we worked through Q2 and Q3 to articulate our mindset, how we behave, and make decisions at Moderna. There is more information on our website and we'll be happy to spend time with those of you who want to learn more about them. Let me just summarize them at a high level. At Moderna, we act with urgency. Action today compounds the life saved tomorrow. We pursue options in parallel to make the best choice later. We accept risk as the only path to impact. We're obsessed over learning. We don't have to be the smartest. We have to run the fastest. We pivot fearlessly in the face of new data. We question convention because proven models don't always fuel the future. We push past possible. We behave like owners. The solutions we are building go beyond any job description. We act with dynamic range, driving strategy and execution at the same time and at every step of the way. We remove viscosity to encourage collective action. We prioritize our platform over any single product. We digitalize everything possible using the power of digital information to maximize our impact on patients. We want to be the most impactful drug company in the world. We care deeply about doing it the right way. It means being a great company to work for, as exemplified by our seventh consecutive year ranked as the best company to work for by Science. But it also means building a company that is responsible in minimizing our impact on the planet. We are proud to have announced earlier this week that we will work to achieve net zero carbon emissions for our operations globally by 2030. I want to thank the Moderna team for their commitment to our mission, and their relentless work to build the best version of Moderna over the next 20 years. Before we jump into Q&A, we wanted to share the dates of our annual investor event for 2022; Vaccine Day on March 24; Science Day on May 17; and R&D Day on September 8. Operator, we'll now be happy to take any questions.

Please follow the operator instructions. Our first question comes from the line of Salveen Richter from Goldman Sachs.

For 2022, can you walk through the supply aspects. Are you still guiding to up to 3 billion doses here? And can you also speak to demand dynamics? Is there upside to the guidance that you've commented on today for future signed APAs? And then secondly, how confident are you that you can fix these supply issues and over what time frame?

Let me take those different questions. Let me start with the short term. Yes, we really believe we can fix those short-term supply issues. As I tried to explain in my remarks, those are what I would qualify as teething problems of scaling up so fast. In Q1, it was all about making enough drug substance and we are literally now waiting to have enough drug substance to fill vials. And as the teams scaled very nicely, in Q2, the challenge we had internally was all about filling vials. And the complexity of Q3 has really moved to, I would say, the back end of the supply chain, which is releasing product and shipping products. And the complexity has been around just a number of markets we have to serve. Beginning of the year, it was mostly shipping to CDC in the US and Europe, and that was it. But then as we increased the number of countries to many dozens by now, the complexity is just increasing and it's even further now that we are serving COVAX. We need to go country by country. So, that's just the type of teething problems that we are experiencing right now. We have increased personnel. We have invested in digital to help the teams. So, I already expect this to be resolved like we resolved the drug substance challenges in Q1 and the drug product challenges in Q2. In terms of drug substance, yes, we could see making up to 3 billion doses in terms of material. As you know, that number was really depending on the booster dose. And now that we're on the other side of that decision with 50-microgram dose, we confirm we could make up to 3 billion doses, if there was a need for it. The challenge in 2022 is going to really be around product form because, as the market moves to an endemic market, you're going to need basically vials to be able to go to a smaller number of doses per vial. Again, in a pandemic setting, as you know, we launched with 10-dose vials, which we think was really appropriate. In low-income countries, we even add more into vials now. But as we think about the endemic market and we're trying to serve pandemic and endemic at the same time, we just need to keep adding presentations to be relevant to healthcare workers and to healthcare systems around the world. So drug substance will not be an issue. There's, of course, as I described, potential upside to those numbers. We still have quite a number of APAs being discussed with countries around the world. We don't know what will happen in terms of epidemiology. Is there a new variant coming? Is it a variant where the current vaccines are still helpful or do we need, as Stephen described, a new booster. There is, of course, a big question mark here that we're all following epidemiology literally on a daily basis. And then, there's so many for boosting people around the world that have had non-mRNA vaccines. As everybody knows, there is a problem of waning immunity over time. So, time is not our friend as people see the level of antibody going down and as we have new variants like Delta or potentially others. But we should not forget that most people around the planet have not had an mRNA vaccine injected in their body to date. And so, we believe there is an important need to boost people with mRNA vaccines. And as Paul showed the real world evidence including the data from CDC and Switzerland, the more we get data and the more time we have been to see, we see a net differentiation between products. And this doesn't go unnoticed by governments around the world who are working really hard to prevent hospitalization and death. And so, there is upside to that. Again, it's a very unpredictable environment. None of us has worked through a pandemic before thankfully. But you will be assured that we will keep scaling up manufacturing, we'll keep engaging with governments, so that we can maximize how we can help people and the revenue should follow from that.

Your next question is from Matthew Harrison with Morgan Stanley.

Two for me this morning. So, first, can we just spend a moment on myocarditis. And I think the overlying question here is, why do you think the regulator is more concerned with your vaccine in younger age groups compared to Pfizer, which has obviously already been approved in younger age groups. And then related to that, how much of an impact is this having on uptake and distribution of your vaccine given that we see Pfizer continue to highlight potential differences and bringing that to governments' attention? And then secondly, on flu, can you just comment on how you're going to interpret these results? Obviously, we're just going to get titer results. But I think it's your premise that you can achieve a much higher efficacy flu vaccine compared to traditional flu vaccines. So do you think there is a clear correlation in titers to efficacy? And what level of titers would demonstrate very high efficacy?

This is Stephen. I'll try and take those questions. So, first, look, I think it's most important to say that what we communicated and desired to be maximally transparent last week was that the FDA, unlike other regulators, has asked for some more time to review emerging recent data. And that might take until January. I think your question is how is that different vis-à-vis what happened with the Pfizer vaccine. I think the most important thing to recognize is that the Pfizer adolescent vaccine was authorized prior to any substantial discussion about myocarditis as a benefit or as a risk. In fact, the signal emerged a few weeks later just before we made our filing. And I think a prudent approach there was to — there was a VRBPAC conducted, there were ongoing discussions. But what we've continued to see over the last four or five months is that for both mRNA vaccines, there's a question of whether there's an increased rate of myocarditis above background in 18 to 24-year-old males, a relatively small population, but an important one. And I think it's in the face of those continuing emerging questions that the FDA has been diligent and appropriately conservative in their approach and making sure they have the time to review those. And they have continued to come out over time. And so, I think, principally, what we're seeing here as the difference is a function of timing, which is that the other vaccine had been authorized prior to this concern and there has been continued emerging data around that. We are very grateful to the FDA for that diligence. I would note that the same information is available to other regulators. And as I have said before, we are authorized for that population internationally. And fortunately, as Paul characterized, we have not seen an increased rate of myocarditis in 12 to 17-year-olds. And we think, over time, the substantial benefits of our vaccine will ultimately win out here. And so, we look forward to continuing to work with the FDA. So, that's my best version of what I think we heard from them last week. The question about how we see that evolving over time. Obviously, internationally, we are participating in the market. In the United States, adolescent vaccinations have substantially tailed off, as we all would note. And so, the extent that there is an ongoing need in the United States for vaccination, it is a diminishing market for sure. Again, this is a primary series vaccine. And so, we do hope that most people in the world will seroconvert and not need a primary series moving forward. The question then of what is that endemic market going forward that is of greatest import. I've tried to summarize that in our view of the evolution of this virus and what that need will be. It is, we believe, in the future, a booster market. And the booster market, targeted at those populations that are at higher risk of respiratory disease. Those populations tend to be older adults and immune-compromised. Places where we think mRNA-1273 is demonstrating really remarkable efficacy, differentiated perhaps. But publicly reported data is really encouraging on that dimension. I would note that is not a population that's associated to date with any of the vaccines that have an increased rate of myocarditis. And so, the benefit risk there, we think, even swings more favorably to 1273, but we'll allow data to continue to develop and ultimately drive this behavior. We are quite encouraged by the performance of the vaccine in a population that we think is going to be most important in the years ahead. The last question was on flu, which is what do we think about that data. Obviously, as you pointed to, there are correlates of protection that have been used previously with HAI titers in influenza vaccine. We will be looking at that, as I'm sure everybody will, as well as other responses in the immune system as we continue to try and identify the optimal dose. I'm not going to put out there a view of what I think our view of success will look like. I would just say that we have very high expectations for our platform. We do believe that our performance in older adults, including with the COVID vaccine, but also more recently with the RSV booster study in Phase I demonstrates that our platform does incredibly well in those at highest risk of these respiratory viral diseases. And so, we're optimistic that we will continue to show strong performance, hopefully strongest performance in those populations. But I won't give you a specific titer number today.

Maybe just to add to Stephen's point, Matthew, I think we should not forget the company's strategy, which is on combination. We believe that combining flu and COVID boosters in a single dose and then adding allergy is the critical central part of our strategy. We think it has tremendous value for compliance, for protection. It has tremendous value in terms of convenience to the consumers. I do not believe that most people will want the flu shot and a COVID shot and an allergy shot every fall. And as we heard from the payer and healthcare workers, that's the value of our product. So we believe the combination is really a critical success factor.

Next question is from Ted Tenthoff with Piper Sandler.

My question has to do with the emerging orphan disease pipeline. I've been really impressed by the progress that you guys are making there in these important patients. I think the mRNA technology just suits ideally here. So, what do you see as the plans over the next couple of years? Take us forward a little bit. What could this pipeline look like? Maybe give us a sense of where you think Moderna will be in the orphan disease setting in a couple of years.

I'll take that. We're very excited about the programs that are already in the clinical space, either already dosing patients or about to start. I think the most important thing is looking forward to next year, the demonstration, we would hope, of proof of concept in that rare disease modality. As you know, we are dosing quite a number of folks in propionic acidemia and we've been dosing in methylmalonic acidemia. With the opening of the GSD1a IND, we'd hope to be following in short order there. So, all three of those are potentials for us to demonstrate the real proof that this technology can be used to correct inborn errors of metabolism in these populations. I'll also note that there's quite a wide range of disease going down to as young as two years of age in some of the organic acidemias and also the older adults in some of the GSD1a program. So, we're going to be demonstrating quite a lot there. Crigler-Najjar presents another opportunity for that proof-of-concept as well as the PKU program when that moves forward, but those are still in preclinical. So the question is what do we do on the back of that proof-of-concept from any one or all of those programs. What you've seen us do in respiratory vaccines and in vaccines generally is probably the best predictor of how we will respond, which is, as you know, there are a very, very large number of metabolic diseases that could be addressed to deliver through mRNA therapy. We could list off large groups, the urea cycle disorders, other organic acidemias, so many beyond that. And even in moving into more broadly present metabolic diseases. So, what we would do is we would define that systemic intracellular therapeutic modality as a core modality, just like we did with vaccines a couple of years ago. And that would cause us to dramatically expand that pipeline. I can assure you we're looking at those programs in research right now, but we have held back on moving them into preclinical development and putting them on our pipeline until we've seen the modalities perform. So that is probably the most important thing for me, looking at the rare and orphan disease space over the course of the coming year, is when do we cross that threshold and then, ultimately, when do we expand dramatically that pipeline of programs.

We have a question from Michael Yee from Jefferies.

Two questions. One is trying to clarify guidance. I think there's some confusion around guidance. So I would love to understand some clarification. You lowered 2021 a little bit, I think, by about $5 billion, but raised 2022 by about $5 billion. Is that a timing shift of deliveries? And how much of that is just option contracts as you think about 2022 because you've talked about APAs as firm commitments. I'm just trying to understand how much are commitments versus options and how to think about those two. And then on flu. Following up on the flu question, I think people are looking at labels and looking at fold increases and seroconversion rates of four to seven times and 50 to 60% seroconversion rates. Are those accurate numbers? Are those numbers we should be looking at and comparing to? Maybe you could just help us qualify that because I think that's what people are trying to do.

I'll take the first one and give it through to Stephen. So, I think you already highlighted some of the other drivers. So on 2021, there are two things I think that are driving. First is, of course, the lower volume. And the second one is price. As you know, we are working very hard with several governments to send products that they have bought for high-income countries like the US to low-income countries this side of Christmas. And so, when you think about just the US, the US we see that publicly. When we announced our African Union partnership, the US decided to delay some deliveries to Q2 of next year. That volume is going to the African Union at a low tier price. So, you have an impact on the turnover just by doing the math of a lower price on the same volume right there. And some orders that are moving from December to January on the supply volume side of things. So, on to 2022 where you have the increase of volume moved from December to January, that is one. We've signed new APAs since the last numbers. And as I said, some options have been exercised. One of them was a COVAX option that was exercised at the end of Q3. That is now counted as a full APA because of the firm commitment and some prepayments and so on. Those are the dynamics that are happening. The team also is starting to spend a lot of time, the commercial team, on focusing on the fall of 2022 because we think that's going to be an important moment. The mix and match, we think, is critical. That is now allowed in most places. In some countries, they've been doing mix and match for a long time. But the US market, of course, is allowing mix and match. As Paul just shared, we believe that as time goes, the data will show that we have a longer duration efficacy vaccine on the market. Today, if you look at data and market research, very few consumers in the US know that. People that are listening to this call know that because you read papers on a daily basis, a few people in the US. We believe there is an opportunity for us between now and, let's say, next summer to make sure that people understand the facts, understand the real-world evidence, so that they can make an informed decision and that includes the healthcare workers, the pharmacies, the doctors, the nurses, and the consumers directly. This is why, as we're starting to sharpen our pencils, everybody is spending a lot of time working toward the fall of 2022; we believe that's another piece that was not fully baked into prior numbers. Stephen, on flu?

I'll try and clarify that answer on seroconversion rates. It is a Phase I study. And so we are looking at a range of doses and I have not got access to the full data. I don't want to presuppose the specific answer yet. As soon as we have the data, we will provide our thorough interpretation of it. However, generally seroconversion is defined as a fourfold rise in titers above baseline, and we've used that in some of our other studies. We will be looking at that from the percentage of people who've achieved that seroconversion. Most important to me, we'll be looking at consistency of that percentage across ages, in particular the older adults where you often don't achieve the same level of immunogenicity. We will also be looking at seroprotection defined as absolute titers, again with 40 often accepted as a threshold. We will look at how high that goes because that can also be reassuring. But I don't think right now we're ready to guide on a specific target that we will declare success other than looking again at that fourfold rise for measuring seroconversion across the range of antigens that we'll be studying in the study.

Next question is from Gena Wang from Barclays. Your line is open.

I have two regarding the COVID vaccine. First, given the supply restraints, do you see 100-microgram doses being used as 250-microgram doses? And then also, any hesitance due to safety concerns? We did see a few countries put a cautionary action on Moderna vaccine. Second, in the US, if we do the math, you completed delivery of 300 million doses and then the US exercised total doses of 410 million for 2021 and the 90 million doses in first quarter 2022. So, just wondering how much of the remaining 110 million doses in Q4 2021 will flow through next year.

I can try and take the first question, although invite Paul as well. In terms of the more recent communications that happened from public health officials, for instance, in the Nordics and elsewhere, I would note that those same communications often include reference to the fact that there's very strong efficacy for the Moderna COVID-19 vaccine. In fact, some of those communications include reference to the fact that it looks to be potentially greater in terms of protection, which is emphasized as a reason the vaccine is still recommended in many of those jurisdictions. Those communications often state that the vaccine provides very favorable benefit-risk. We continue to believe that whole picture looking at the benefit and quantifying that benefit, which we think is substantial and larger than any risks contemplated here, is really important. Again, we look to those communications that clearly state that. Paul, anything you would add to that?

Only, Stephen, that recently, the WHO gave updated guidance continuing to endorse mRNA vaccines including ours. As they analyze these data sets, they consider potential biases that occur in general practice, looking at primary vaccination schedules and differences in timing. We know vaccines are used differently sometimes, and that may account for some observations. But I think the WHO statement and other guidance continue to stand behind the data supporting the vaccines' use.

Maybe just to add a bit of color. I've had a chance to speak with a couple of health ministers across the world in the last week or two. People are very clear that the risk is low and it's very manageable, and it's focused primarily in males aged 18 to 24. Those health ministers were clear about going back to the risk profile that Stephen just mentioned. They care about having a winter where they don't have hospitals overloaded again. This is driven by older populations where they know the vaccine, as Paul mentioned, with the data from the US or Switzerland or many other countries, seems to provide lasting protection, and that's what they care about. I think people are getting educated and looking at the data. They're trying to look at the facts and figure out, in a very practical way, how do they keep the economies running and keep people out of hospitals. Many countries are focusing on the older population for boosters. On the US government, Gena, we don't comment on volume specifics. But indeed, there are some shifts from Q4 to next year, both Q1 and Q2.

Next question is from Cory Kasimov with J.P. Morgan.

Two for me. First, in terms of the 2022 APAs that you outlined, are the $17 billion worth of existing contracts constructed as firm commitments or do countries have optionality embedded in them wherein countries don't necessarily have to take the full amount depending on the evolution of the pandemic? Second, given your comments about potentially moving into the endemic phase by the second half of next year, should we think about 2022 revenue as being weighted towards the first half of the year?

Thank you, Cory. So let me take this apart. The APAs do not have options. When we say $17 billion of APAs, those are firm orders, signed orders and all our APAs have upfront payments. It's one of the ways that we are conducting our business. We want customers to be committed and to have a material upfront of the total value of a deal when they sign. The options components that we characterize as up to $3 billion as of today are true options, meaning customers are reserving capacity. Sometimes it's for financing rhythm because, as I said, we do not do APAs without upfront. One of the best examples that's public is COVAX. We had to do quarterly options with COVAX. They exercised a Q2 option at the end of Q3. But Q3 2022 and Q4 2022 COVAX volumes are still options mostly because of funding timing. They receive funds from multiple donors over time, so we did that to help COVAX and to do the right thing to help the planet. We expect, if they want their Q3 volume, that they will exercise the options in the earlier part of next year. On whether 2022 revenue will be weighted first half or second half, I would caution that it is too early to make a definitive timing judgment. There are a number of variables: volume, pricing, mix (for example, COVAX and African Union are lower-priced), and commercial timing, including fall booster campaigns. So it's premature to declare a specific intra-year weighting.

Next question is from Geoff Meacham from Bank of America.

One on the flu program for Stephen. It's highly likely that you'll see an increase in antibody titers. For the combo study with 1273, what other factors do you need to address to de-risk that study? I'm trying to determine how to optimize the regimen by things like dose titration or selecting the population by more urgent need for the COVID booster side of things.

What we'll be looking at in the combinations are exactly those factors. We believe the most of the near-term value of respiratory vaccination for boosting will be in older adults, 50-plus or 60-plus depending on jurisdictions. Very similar to the RSV population and recommendations globally. We think COVID moves that direction as well. As we optimize ratios of antigens in combinations, we will index toward those higher risk populations. Optimization will be driven primarily by immunogenicity and tolerability. Fortunately, these vaccines have been very safe to date in older adult populations. The myocarditis concerns are not really present in the 50-plus, 60-plus groups. We'll want to make sure there's no antigenic interference and that we achieve balanced immunity across the four flu strains plus the COVID antigen. There are precedents for high-dose flu vaccines that have differentiated on efficacy and price, and we will consider similar approaches especially for older adults. We will evaluate a range of dose ratios in early clinical studies and let the data guide the optimal regimen.

We have a question from Joseph Stringer from Needham.

Two from us. Curious on the guidance for the $2 billion US fall 2022 booster market. Can you help us understand what assumptions are built into that number? Is that based on your internal expectations around a relative percentage of fully vaccinated individuals that would get a booster? And second, for CMV, can you give us a sense for the relative timelines for enrollment of the Phase III trial and when we could see initial data?

On the fall of 2022 commercial opportunity, the commercial team modeled various assumptions including uptake rates, market share and pricing to arrive at the estimate; I can't provide more detailed public breakdowns of pricing or exact uptake assumptions at this time for competitive reasons. We have been preparing commercially for that season and think it can be a meaningful market assuming regulatory pathways and epidemiology support it. Stephen, on CMV timeline?

For CMV, our aim is to enroll as fast as possible because it's a high unmet need. However, it won't be as rapid as a pandemic vaccine enrollment because we need to enroll women of childbearing age at heightened risk, often those exposed to young children. It's a case-driven study, so the timing of interim analyses depends on accrual of cases. We will seek to enrich the population for higher exposure to accelerate accrual. We plan to work very hard to enroll quickly, but I can't give a firm interim readout date right now because it's driven by the number of cases observed.

Next question is from Emmanuel Papadakis from Deutsche Bank. (No question audio provided.) Next is Mani Foroohar with SVB Leerink.

A couple of quick ones. Can you give a sense of when we might see the impact of pricing shifts due to increased deliveries to low- and middle-income countries that Stéphane mentioned? Is that something we'd start to see early next year? Also, the $6.7 billion in deposits on slide 15 — are those deposits generally for APAs for 2021 or 2022, or do some of those apply to contracts for 2023? Third, your CapEx guidance is a little lower than last quarter. Is the $50 million to $150 million reduction absolute savings or will it just be pushed into next year? Fourth, how much opportunity do you see for capturing more share in the EU given existing contracts from competitors? And lastly, any update on potential access to the China market, such as via a joint venture?

On Q4 and COVAX/African Union timing: we have already allocated COVAX product and African Union deliveries will be in December with a ramp into next year. On Europe, recall we had a later and slower launch in Europe because we lacked manufacturing capacity in Europe initially. As we build more capacity and teams on the ground in key European markets, we expect to be more active and have an opportunity to increase share. We already have contracts for 2022 in Europe and continue to engage country by country as data evolve. On China, nothing to announce today regarding a joint venture, but discussions continue.

In terms of the deposits, the $6.7 billion in hand is largely for deliveries in 2021 and 2022. There may be small amounts for 2023 but it's early to have material amounts for 2023. Regarding CapEx, yes you should expect a notable increase in CapEx next year. The reduction this year reflects some shifts into next year and us running below some estimated requirements; part of it will move into 2022 and part is timing of spend.

There are no further questions at this time. I would now like to turn the conference back to Mr. Stéphane Bancel.

Well, thank you very much, everybody, for joining us. If you have any further questions, you know where to reach Lavina and the team. Have a great day. Bye.

This concludes today's conference call. Thank you for joining. You may now disconnect.