Recent MRNA transcripts
Associated MRNA filings
Lavina Talukdar | Head, IR |
Stéphane Bancel | CEO |
David Meline | CFO |
Stephen Hoge | President |
Paul Burton | Chief Medical Officer |
Salveen Richter | Goldman Sachs |
Gena Wang | Barclays |
Matthew Harrison | Morgan Stanley |
Michael Yee | Jefferies |
Cory Kasimov | JP Morgan |
Tyler Van Buren | Cowen |
Good morning. My name is Kevin and I’ll be your operator today. Welcome to Moderna’s Fourth Quarter and Full-Year 2021 Earnings Call. At this time, all participants are in a listen-only-mode.
Following the formal remarks, we will open the call up for questions. this being that advised be call recorded. is Please to call Investor over this at time, Lavina the like I’d of At to turn Talukdar, Moderna. Relations Head Please proceed.
us And Thank quarter fourth XXXX business you morning, Kevin. and full-year call everyone. results you, for discuss Good and joining update. on financial Moderna’s today’s to thank
are the the access be call reviewing we’ll and the issued Bancel, Investors Medical You On Chief that of Stéphane release can website. this Officer. morning our Burton, Paul Executive Meline, going to Chief slides we press as section our our Officer; President; well Officer; as Chief our our by Stephen today’s David Hoge, Financial
those Harbor Act the accompanying Before see performance these that include our conference we to turn SEC of statements differ will of slide that could please I Private X and that, call over our cause the this from or note risk Securities factors will Litigation of call for to XXXX. and provisions results the the filings statements. With expressed Please Stéphane. actual Reform implied important materially made begin, Safe presentation forward-looking forward-looking pursuant to in
then clinical where then before programs about will our heading. David financial review some or XXXX everyone. review will good Good to data. to our year Welcome back ‘XX come will Stephen close QX fiscal of results. Lavina. are you, our by a Thank you walks some conference through I real-world to evidence morning I Today, we business thoughts call. afternoon, start presents quick before share Paul
first year income the quarter GAAP average $XX.X August which and billion. of count per for time (sic) COVID, as revenues the programs received share expand during the of diluted of the proud that you have In our for full $XX.XX morning with vaccines, know, billion, advance I new Spikevax. from $XX.X U.S. history. we old translating $X very $XX.X BLA our Company we we in XX team’s development announced are We GAAP fiscal authorization following for respiratory for as billion the approval a at cash dose running today as fourth to FDA year a ability XXXX pipeline. report share plan, reduced completed study of in of FDA. for our earnings well with [$XX.XX] our We the XX billion, share this end billion the for to discussions in pleased With balance U.S. a markets XXXX years the to XX-microgram are globally, of buyback the with key adolescents net to am
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deaths On robust individuals that over in above, years viruses against populations. fact, coronaviruses the coronaviruses, between the And visits, respiratory to and flu yearly vulnerable achieve XX-year-old in RSV a do SARS-CoV-X, months X from will other SARS-CoV-X chart, cause population similar in the and of respiratory and follow XX,XXX hospitalizations pattern believe will to countries, will against endemic you be and those on and RSV leads hospitalizations an will impact XX of over that. as of protecting by XX populations our level impact XXX,XXX influenza. and to SARS-CoV-X OECD be shot highest and We ongoing years endemic Across the single and outpatient seasonal years provide strategy. update Protecting million a can estimated Hoge to such age our shortly other followed of XX disease human viruses annually. the as Stephen see with combinations critical central will come. in strategy human
protection it Moderna updates vaccines is continue mRNA to future as further and hand topic booster post of hospitalization pandemic. an in believe Dr. give our in booster real-world the boosting. fight against available that of Real continue data mRNA-XXXX dose by Omicron remarkable effectiveness world end by but globally. So, we of to a protect caused will now leaders summary, XXXX the show to data And variants will We Hoge a mRNA-XXXX. Stephen? to we that help to important titers and provide to provides booster that this XX-microgram vaccines, I on Stephen needed us this develop shows months waning believe antibody against Omicron, the six over note full will we be opportunity as pipeline.
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three evaluating in age XX different currently booster are strategies adults We plus.
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Okay. Thank you, Stephen.
it for marked providing today the year the Company drivers XXXX of financial fourth quarter view as transition along performance forward. key a We are and a of full was dedication the commercial stage year employees analysis of company. XXXX transformative scale-up. wanted going actual their from with to company an a our at for challenges response unprecedented thank the and to with performance, of and pleased I’m our many R&D-focused to during very Moderna this all entity results
of fourth vaccine our in international shifted COVID reflecting the Sales of QX U.S. of billion, mix geographic fourth billion manufacturing supply with on our network. sales the sales XXX by XXX doses the doses in as sales an to course the relatively and slide chain doses stable overview QX quarter, of picture of over to quarter our the quarter year, dose million to focused QX of our compared the for We rest $X.X world XX, now expectations after have doses in million to of and doses. with fourth ramp-up of QX outside in delivered Total the XXX starting sales fourth sold. XXXX terms and compares in reflecting in the in were were billion the bottlenecks million supply customers. XX successfully Sales the $X.X government million in our QX. This a to line capabilities. the U.S. increased Turning were removing in our XX% we $X.X performance. representing product quarter, And XXX billion our $X.X million to in
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Our capital remain allocation priorities unchanged.
reinvesting priority Our continue areas. investment be top across business been in will to multiple and has the base
accelerate advance we For and new to R&D, spending increase in continue programs. expect in increased this significantly pipeline, approximately And billion. area to $X our to XXXX existing our spending for have further and we to both our
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further attractive Our investment the priority expand collaboration reach technology seek external and to is opportunities to Moderna’s and second investment of capabilities.
take are disciplined attractive investments. We complement considering a approach potential and opportunities enable platform that in evaluating outside our and
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for financial to planning regarding Stéphane. we the $X.X to the turn build performance. my Finally, and capital out concerning concludes And are our further manufacturing we expenditures general company capital expenditures, the remarks as now in of billion infrastructure range billion $X.X This call over I globally.
you, Thank David, Paul. Stephen and
X. X, product Phase Let me RSV annual on now the how in share number booster. already some pleased thoughts Priority team about where is executing is to strategy. am I see our we’re heading. pan-respiratory
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continued now our $XX to APAs have to increase signed We billion. around
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ground, new markets. our those strong penetration. on of same with impact I the Moderna teams market seen greater believe phenomena will XX have drive in data, the the coupled real-world happen You evidence
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or world. have with around to service the We a governments model started create subscription
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this shared strategy the for our allocation. in past, capital As we is
in the As priority invest one number David said, Company. the remains to and is
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about respiratory on our We impact We be hospitalized a a because ability nobody have of should humanity. believe are passionate to virus. profound
short medical or We to of should term a have We term do believe technology that. because consequences long nobody have latent a virus.
the to questions. be profound beginning. a we we’ll We impact a on happy therapeutics our our just treatments have disease first is believe then with technology do to your Operator, We can take have gene-editing and This that. programs.
Salveen [Operator Richter Instructions] with Goldman from Sachs. first Our question comes
taking Good well what the disease regulatory data see rare in this vaccine going we’re of morning. just could and then, personalized cancer for to, we’re would we the speak Could proof data. Thanks as get flu to that for to sense going of my this you success get a would question. there data as to the Outside year, And whether disease, personalized of what year? be look be? cancer path like vaccine, able concept rare
Sure. Salveen. for you Thank the question,
cohort study it’s recognize moving -- forward enrolled these studies, the the is the has because, first is space, study. are the its in ago, moment PA with MMA it’s I’ll And that disease that X/X first, PA said important speak enrollment. a as rare So and Phase to mostly to both one our and I
from studies, foremost, safety looking to X/X. So, we a these in first be and at you’d Phase as are going expect
platform When study. establishing And case of on number is on the studies the to the the mRNA, diseases. usually up longer, again, they comes to early over case efficacy, to for as extension. stay important small is months ill important it repeatedly establish we of of most in in studies and dose, the an of if that continue children open-label can dosing months the part six people, these or safety LNPs are rare X is, chronic of the even very of things one both objective to to so, with And or with these unfortunately, XX
data careful the medicines we’ll outcomes. so, things too at any looking for, of from And be to in and the the the early clinical looking I reads But be we’ll about first interpreting be performance terms the of clinical of foremost, preventing have concretely.
in and of the validated therapeutic preclinical not to therapeutics a some will happen these space, with are extent, yet of correlated in disease, not, things interventions across so, been the biomarkers, also metabolic have and these to looking do it’s diseases there important for or or like lesser be unfortunately, that acidemia, some of major PA. will note in transplant-based that regularity, they approved. with that from But, decompensation who rare perhaps diseases. the so specifically, hospitalizations these events suffer these at existing we propionic And all case And folks unfortunately, biomarkers diseases have disease with biomarkers be these those because biomarker for
a it and individuals. outcomes, of And across signals be so, looking a number at biomarkers potential looking will between signals in be improvements clinical fair, to relatively balance efficacy of small early, at
and performance. And will there heterogeneous so, of be their genetically terms disease, in both
the second we’ll able hospitalizations, decompensation and matter studies Our we that so, that to will then clinical hospitalization are have study will outcomes with of although continue part discussions discussion we about present and if is is we outcomes, believe that major and a small matter patient pivotal most even prevention hope that when and and forward. of death. perhaps regulators, of your things question, events have be the the that’s data composite get ultimately number, potential and But a do the what in clear, which most be obviously, for
So, those But looking studies. based how we early updates sorts we’ll when be regulatory be as recognize, we ago, forward a said small want consultations I circumspect to have those from we’ll it’s be and those into for it. number, those we’ll our of in relatively important data, move on are And studies. signals provide to moment efficacy and these will
a -- obviously X that we And enrollment reminder, KEYTRUDA we that head-to-head Phase PCV. the completed a survival randomized approximately quarter going vaccine. KEYTRUDA plus personalized and as On would comparison based the data a come when of study, decide could proceed the fourth regulators potential it’s on PCV of And on completement KEYTRUDA relapse-free fourth obviously we have positive. year. And if that consult complete enrollment at would this versus expect of the data, would which year. in announce emerge signal That vaccines as standard is versus based expect study it And program, to forward I a said, and That is is because that the looking to the a you that benefit of year. with clear alone we data, we’re we in in alone, of in we’re for. provide cancer how this PCV head-to-head quarter
next with comes Barclays. Our question Wang from Gena
have questions. I two
What regarding is XX. primary need not benefit provide the the question press concluded data think would trial So, with risk XXX-microgram be efficacy outcome? additional XXXX. data has the the second early be of the without you little on you specific that data, XXXX, you a data timing? XX bit in provide? more And approval? the fileable release, XX-microgram could X you need to on series. of kind need The in X Can Phase the to In to what regarding FDA first of order said age Phase will is And one flu profile you a data U.S., receive to
you, both questions. Thank for Great. those Gena,
data the demonstrate that we an back happened have of X X consultations are we expect to data on independent with approximately of think will need efficacy whether a Moderna. sufficient filing. Phase based efficacy Phase fileable. Phase but on will alone data. not prior efficacy Phase do that are with not approval. yet the in the question believe which to clarification or regulatory possible be guidance first, on to have safety for would X hundred, X is, that accelerated we those you study -- We regulators, flu immunogenicity not study based just a thousand published And on study, specific up ultimately, approvals and guidance, what be previously But efficacy sorts always shortly. approval few X So safety not follow from filing important don’t of then And whether It’s flu alone, based that’s would accelerated which Phase a necessary an a note immunogenicity is on perhaps post study to that or immunogenicity several perspective, on and and an precedents there for an The But studies are Phase just immunogenicity is to safety is filing. that study, X in people. a
viable. Phase previously current don’t and the as whether we those the X summary, And an before, some studies, efficacy study do we efficacy expect a Phase is year. said immunogenicity I they’re Phase X we with after that or question study safety X whether X accelerated to on approval so, study be We and try this or That before point. Phase safety alone study, not start said flu think study in would to and in would Phase immunogenicity intend, at The follow as to have study. and is do it X
we the been globally -- XX that up markets, approved to been dose to of the And to XXXX series. evaluate of believe the X them question its adolescents series filing not we XXX-microgram the over in on with quite in note provided XXX-microgram series primary primary decided adolescent -- perhaps On a XX FDA broadly, has has to It’s consultation and the have in to adolescent so and has XX primary lower not adolescent completed U.S., XX. of important globally. a has the many adolescents administered dose, review other XX-microgram million
data when of as And for appropriate, continue their series. evaluation the to so the FDA submit observational well monitoring the And XXX-microgram data studies. from we’ll as our that that continued collect to and as primary real-world
interim for are -- efficacy given seen strong Spikevax particularly the we’ve the data population. that We in in XXXX, on real-world immune-compromised
with is been it. We which more benefit why submit that that that evaluate strategies we and other U.S. we’ll micrograms FDA believe the XXX broadly, it’s population. the provides as dose-sparing potential develop XXX do and data in to globally. micrograms the in to a work United an for risk risk efficacy the profile clear mRNA-XXXX compromised because in of we are micrograms those disease severe States a We adolescents or EUA the immune benefit at provides think outcomes from of interim at preparing high for But strong authorized continue filing XXX
Matthew Harrison Stanley. Morgan from comes question next with Our
two a then clarifications have and I question.
And would had one, you not expect initial to first terms Phase you discussions you data, us in And can potential or of may present just second PA, see of weighting Should and that’s had Phase switched. And talked able what those believe the the you revenues about or of or I’ve COVID studies would helpful be Thanks. then, many to timing for cohorts we half X a flu. couple first the else you talk second, And of I something So, just like before data? about need? steps have when to of weighting it to more able think there in of scope half clarify. weighting. now boosters on seems at on third, regulatory questions this us gotten then, how sense that next give fall, revenues? terms X you’ll that year, the on of you be Is happening because a whether need targeting that is you’re here you be thought provide I JPM, the to that mainly
Matthew. I’ll two first questions. thanks, So, the take
hands in it’s flu, obviously on first, alone. So our not
connect feedback get the able whether -- be FDA with would to will we back. We and
As but in are agency now. we agency the all right the on -- also a have know, lot the States, globally, United going agencies
some And getting may in that be so, delays feedback. there
we we get data, rapidly back agencies, it’s And that share will will moving is possible from share are have not and response that with something we’ll forward. that more as agencies we it. the obviously, that -- we before data X at negate Phase our share So, quickly, will be but But, to we plans time. if on probably will obviously hearing consult not it
that we’ll it’s quickly. crossed our short feedback, agencies level can perhaps the So being dose able it, I wouldn’t more it’s to number that but around a fingers expect possible, so keep PA, have On of version, turn cohorts. that the agency and of
two the to or are level important of objective say how major we’re frequency cohorts looking to also, duration dose study? of there of we’ll cohorts, it’s the think intervention metabolic looking prevent the particularly here that of features level I is the dose be at. But that Obviously, many sort dose that different that then so on at because the the time that program decompensations. in primary study PA
whether is that time can so, changed within requires And so accrue, rate the to of you’ve recurring understand patient, also an individual those you that that something events.
data whether dose a level not and and obviously, tolerability, will we’ve the or allow and that dose all safety mean, you and we for if composite that it determination level And clear two expect. combination, enrollment, year what with I we whether to move early chronic given of things. of data we next for many we us recipients. a make expect the think to we’re three the to escalation allow and the will seeing as two would think right to feels while dose And see would we’ve so, that whether clinical But who’ve mix on probably then indication a got cohorts. can I probably as to which got have benefit, on consultation approximately also, regulatory that to also of it’s we in a been drug studies, and be will accrue that achieve of perhaps will on well step the clear, And information. obviously, those a us seeing update biomarkers, rate
David level third So, question. think, And a that concrete dose number more a data early it I’ll on perhaps dose function turn clarity. cohorts, with over, level I cohort third drug for or will of but for both the second not us and of that time the a cohorts of provide
Yes.
bit secondly, now half a second the emerging is then we product we think to strong I half as second that at, second the receiving refined to half. that the we to the in the the as first we quarter, the therefore, half, countries a going looked at lot outlook that indicated booster versus timing looked second particular, first of So, having And see? be, all timing, as absorb we see be donations. in And to do challenge quarter as of will half sales quite move terms of into half, ‘XX, there’s that we’ve described, have third half. than -- certainly, be first second higher as mentioned, cause they’re We that Stéphane market what COVAX through they’re the
Michael Your Yee question with Jefferies. next from comes
you able two-part remember to pick strategy strategy was to bivalent, decide approved is great. thinking be and and and a you Can had just question. We COVID including which point boost One your the would about whatever you would that laid that be to you’re about different I confident presumably ready would to think know talked fall talk the for color XXXX and strategies or which what by three that the that the previously would for what the the be distribute that And But FDA at XXXX? out, be, actually relates USA that USA XXXX options just boosting you. in or can’t purchases. question I are for And season, speak the guidance that if we actually and is XXXX. market. second had where the about to USA. be product I for maybe for about booster that Thank you
Michael. Great,
to perhaps over second. the take I’ll turn and the So Stéphane question it first on
strategy, as maybe the already start to XXXX thing of is with most booster so exists. So, that terms important in the a
booster And so, that is candidate. a
Although and real-world we’ve evidence relatively of evaluating seen that to fourth mRNA-XXXX. in strong have data, quickly data safety dose, the we’d we’re immunogenicity expect a
that’s markets is available known quite and well obviously And something candidate so booster be quickly. that to could
and the in evaluating XXX two studies that or right bivalent now. We’re Omicron-containing ongoing Omicron-specific the are
your the I think trying a evaluate that, you’re time. difference durability, where in question durability, Now, that it’s to is all going, challenge when and of that with is takes
half is months those benefit of and achieve first more that to before while be both would year, safety be would this believe, around The potential compelling. hard very that that And in studies, boosters. challenge it’s going we’re we be continue expect so, one of would time. the the and and we and running these we we just the bivalent, month data bivalent a to Omicron establish, durability the hope the to of and six to And of post data even have QX. could that’s function turn Omicron-containing boost, And
get it boost that already started day show to you we’ve that with our take If six-month people data will to durability now, vaccines. bivalent XXX or time
bivalent the of do we evaluate durability. And data vaccines. have benefit do are becomes, this have a for now. follow-up use from start we are do XXXX? having that we’re six-month And better benefit filing of so, aiming if question ongoing to tested potential the to those And how to fall the being at previous the with the for We perspective regulators proceed then there multiple able consultations
part time, concerns the the And vaccine known the could variants And the a proceed existing on over one-month of contain that that with Omicron. so, fall, mRNA-XXX non-inferiority the improvement of bivalent And the where certain we fact including safety data up vaccine durability world previous perhaps the bivalent in same of some including data early our in variants, you some we the perhaps previous imagine and then, in confirm would we showing would shown that like rely that against mutations that with benefit Omicron. against as of variants perhaps follow the had durability. on of concern, seen
timing and we because we mutations it we’ve time that improve believe, challenge picture into said, to complicated are relatively run circulating of against new -- a all variants is the it’s concern. so, do against But it of the as filings. durability of update the to does those vaccine currently those that the And
pandemic. likely provide as prepare can those which advance they vaccines to even which the wave the past governments a filings so, fall it than we with during from the public quite of regulatory them we’ll align That’s on health in did want booster in stockpile as to original as And updates in forward. are of season, all as first regulators has proceed it without parallel the the the different with decision consultations going. to And may path
I’ll with about in turn the to to Stéphane the that, fall maybe So, over talk U.S. it
Michael. you, Stephen. Thank morning, Good
So, two maybe let talk angles. me in about it
one first announced we’ve government. U.S. $XX we this is, there no APA for as and between signed Moderna -- is The said in at morning, APAs, billion, the these increased
number -- because U.S. previous option And So, contract that the government no currently. the either no a the government has the option from there is there’s in zero. from U.S. has
we decide and seen from what both dose. first, not buy Will they’ve and private or $X will not is could a the bit private options So billion that it available today third sell markets, there manufacturers U.S. and probabilized. you of the what second of can for to in want a the in procure vaccine of where mix What is if do would away XXXX. be and fall done see vaccines. is private government free, market ‘XX, and there’s give clear. them a the that’s clear be might the to vaccines the private We’ve for ‘XX for to are, free that $X because companies even the networks we is And
did manner, or have because conservative why we it’s we of numbers. zero, signed options, so the So in U.S. not those a very communicated because and what far any include APAs are government has
additional Kevin, you. we questions. Thank have time two for
Okay.
Our comes Morgan. Kasimov JP question Cory from next with
phase plus, like how for or should you’re priorities reason future? Europe many follow And you into Recognize selling we or kind be In being your of your to and the countries, structure? And sheet one, capital things nearly to this XX% think think as or though. world, Thank the marketplace of into have any think what want markets? larger buyback? on same an this the an APAs XX% is were this is be of moving with balance kind do development, you And appropriate with anywhere But you and just First endemic evolving, of cash new you. latest secondly, in in range just opening how do XX% about looking beyond and about allocation. shift that kind thinking discussing XX on away of number enough about I we APA to simultaneously. year-end up the your to from regarding just dedicated then here. just outlook priorities words, be commercial remain thinking capital the to to programs U.S. Is the you clearly, around else, do more private XXXX expect it you’ll other for there doing fall not subsidiaries
for turn let to the buyback first question, Cory, I’ll take So, David me question. the and
markets, in, governments are are at outside let’s direct non-pandemic with they So, mostly if the contract the anywhere. look say, they you countries U.S.,
is not So, of shape to is in very it going look like terms form what and clear.
case, seasonal for Europe example, purchased together not say, is For let’s has which pandemic, the example. vaccines the for flu, the for
that countries a So, basically be a like system continue But national other move will all seen. vaccines model to so or COVID to Japan, they for model go on and for single that to is Canada they and back are buyer will market.
government Some countries know you of markets, as small orders. it’s mostly product but kind
And so, we are in discussions with governments about ‘XX.
they signed boosters. believe because annual UK endemic deeply for contracts that already the supply will very we’ve some the ‘XX saw, require countries secure you to As others wanted because and like market
saw we say, build model the They size. on with the to year, countries in be able setting a let’s a similar million-dose, the what to commit want. vaccines basically to several subscription-like just we respiratory agreements. million, market so, XXX And with of with And is and where secure, the want countries Australia, of ahead I think partnership, what as of we discussion are are XX-year get interesting new we about And service-based model trying we depending reserve the very Canada And to volume to we is it. is for them as XX million-dose, they believe more plant. we’re said, what kind you given XX which customize doing in a then, they
do of from Paul’s not knew a so of, even saw there’s respiratory stable. Look are together vaccine of public with that is what for all to experts Well, most PIE vaccine they coronaviruses there in were creating are So, Australia. and people as they aware circulating much lot hospitalization virus their Canada and discuss and health people or an that presentation, bring and want there annual you those local on at our components names. basis, their for vision
North picks say, HX Asia, that As then we the on a strain let’s discussed it’s America, on. between, strain fall, the winter Japan Europe flu sometimes, or flu a is -- like in call so the like different WHO and/or and flu that and
a because authorities, we public want, to unique work really combined because customize ability the And every think they local also this so, of vaccine platform of and feature components. it’s this health customize to with a speed,
at very-customized in to very more have I trying very-complex not just the to because this we’re are here, trying to teams to head. wait are actively agreements. see what very you quite in more of do And of because to to in of they really aware and discussions. XX this I’m can exactly the having other wait And we think there David, a months are lot discussion already to do do is that’s type working coming, We But a have done countries long-term companies thing pharma. we’re there, also. where so, cannot we few establish do. We’ll And same that’s partnerships. but about buybacks? is want time talk something
I think as Yes. need we think Sure, announcement you mean, what is a did. what things I’d yes. I about guess, few I say the about to today,
It allow plenty that. So, why we of we internally that as said, and have billion, to firepower why $X do is, things. us now? externally One ensuring with a starts and to few investing
enter XXXX, So good opportunities position we a clearly, they’re all the compelling. very of to we’re think fund have, that we in where and we
is, Two we certainly, enter levels. cash at additional certainly again, what visibility And very levels. that of we the this company. these attractive at the think one. about we that’s valuation And thirdly, generation we So good at as is XXXX. for quite have we look then And looking feel
adds question. and let’s see how the the right bit just us that on very encourage prospects we to continue a good for for on think I’d of basis? So, combination of comment $X an to now I your evolves. you the this wait that And in ongoing all to it’s for model early should that business. announcement filling up feel an question, billion. To to But I little be about
Company. we of I today the the is think that one out for the can a that statement set we’ve objectives confidence all of strong achieve
Our Van last question with Tyler from comes Cowen. Buren
on just you relative pricing topic your the similar thoughts contracts Spikevax? normalized Do of U.S. countries? latest has future future for to On ex-U.S. provide to a pricing you have expect new the conversation, that point on do wave vast billion emerging a maybe you in majority to of to that believe $X variant a the just is necessary second clarify, year-end APA options? And could record by
So, let me start.
reasons governments. of for the the pricing because I U.S. not with on our will comment obvious discussions So,
I standpoint. think of once think value the billion, there -- doesn’t I waiting fully price before, are $X the this pharmacoeconomic funding to -- And so just be move governments reflect a some do a just options, APAs. vaccine into vaccine from not normal as expect the we sorry, we private We a pricing are different to the goes the from mean, stage signed said market, into higher. does the reflect
with are as Some things for place COVAX future needs. that has or a
they to and need of pandemic managed transition and to endemic. plus, I we for new top never from that. don’t So, to some be through it through on the pandemic U.S. of a a a happen, again, variant think But have
chunk, to So, a I variant APAs. think we But and be doesn’t want it move to prudent. into billion, new cautious need signed for a material over $X
to call portion remarks. gentlemen, of any like concludes today’s the back for and turn Ladies closing this conference. to Stéphane the I’d Q&A
at I very and to everybody in you March. for thank talking days you. welcome the coming which forward Well, to joining. you in our much look Day, Thank Vaccine especially exciting, be weeks, to you and will
Ladies this presentation. conclude and gentlemen, does today’s
You a wonderful day. may now disconnect, and have
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