WEBVTT

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JULIE HYMAN: As we mentioned earlier,

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the JP Morgan Health Care Conference does kick off today,

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a lot of CEOs speaking there, a lot

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of deals and collaborations being

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announced in advance of that.

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Our Anjalee Khemlani is here with us

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and with a special guest, Albert Bourla,

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who is the CEO of Pfizer.

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Anjalee, take it away.

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ANJALEE KHEMLANI: Thank you, Julie, and hello to Albert.

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Thank you again for joining us today.

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I know that you and I were both looking

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forward to possibly seeing each other in person this time.

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But, unfortunately, Omicron got in the way.

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I want to start off with talking about that, actually, and just

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the impact that you're seeing.

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We know that here in the US that, you know,

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we've had discussions about boosters coming this fall.

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And we're watching the Omicron wave

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really surge in certain parts of the country as

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well as the world.

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Tell me what you're seeing in terms of the potential

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for possibly changing how we look at boosters

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and what kinds of boosters you anticipate.

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I know you're working on an Omicron-specific booster

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as well right now.

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So what's at stake for us in fall of '22?

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ALBERT BOURLA: Here the situation

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has been deteriorated because of the Omicron,

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which had a very quick ramp-up.

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It is a disease that manifests a little bit less

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in terms of mildness.

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I mean, it's more mild.

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But, you know, because of the higher infectious rates, still,

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the hospitals, in absolute numbers,

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are going much higher in terms of severe disease,

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ICUs' occupation, et cetera, et cetera.

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So-- and we know that the two doses of the vaccine

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offer very limited protection, if any.

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The three doses, with the booster,

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they offer reasonable protection against hospitalization

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and deaths--

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and, again, that's, I think, very good--

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and less protection against the infection.

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Now, we are working on a new version of our vaccine--

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the 1.1, let me put it that way--

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that will cover Omicron as well.

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And, of course, we are waiting to have the final results.

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The vaccine will be ready in March.

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And the vaccine, we'll be able to produce it massively.

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We need to see if we will need it.

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And we need to see if--

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and what place it can take in the overall fight

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against the virus, particularly now that we

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know that mutations are coming faster,

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but we have a treatment.

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So all of that needs to be taken seriously

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[? in this direction. ?] But we've never had more

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weapons on our [? box tool. ?]

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ANJALEE KHEMLANI: Absolutely, and Pfizer, of course,

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taking the lead with that.

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I know that you've expanded of course,

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your collaborations on that front,

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especially with BioNTech for mRNA.

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But I want to quickly talk about the kids' vaccine

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before we get to that.

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I know that right now, there's a lot of parents waiting for that

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under five to come out.

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And the company has said that it's going to need

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to be a three-dose vaccine.

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Do you see that to be the case for adults

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as well, especially as we see that, while you do offer really

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strong protection, the waning immunity is an issue

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because it wanes pretty quickly?

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ALBERT BOURLA: Yes.

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First of all, I don't have any doubts

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that this is also, for adults, a three-dose vaccine.

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And I think this is what basically everyone--

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every health authority in the world--

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is recommending right now.

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Now, the question is if we will need, let's say,

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annual boosters or not.

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But this is a three-doses of vaccine,

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particularly for the adults.

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What was the second question that you asked, Anjalee?

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ANJALEE KHEMLANI: Sorry, for the kids,

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the update on the timeline there,

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knowing that there are so many parents

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waiting for that under five.

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Do you have an updated timeline on when we can see that?

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ALBERT BOURLA: I think that things will move fast.

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We are collecting, right now, data from the third dose.

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We are having, already, data from the second dose

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because two doses in younger kids

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is different than in adults.

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We are in discussions with FDA, and they will submit them--

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everything to them.

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I hope that things can move very, very fast, actually,

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not in months, in a few weeks.

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ANJALEE KHEMLANI: Sure, yeah.

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We're all waiting for that, for sure.

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And when you were talking about--

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the treatments are also out there,

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but we also still need to meet global needs for vaccines.

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I know you've repeatedly said that you have

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had refusals for the vaccines.

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There's also vaccine hesitancy as an issue,

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especially in lower- and middle-income countries.

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Is that still the situation now?

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Have you found a change after you started shipping more

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towards the end of last year?

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ALBERT BOURLA: Oh, yes.

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First of all, let's put some statistic out there.

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In 2021, we had said that we would produce over 3

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billion doses, and we did.

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We released 3 billion doses, from which 2.6 billion,

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approximately, were shipped to countries.

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Among those 2.6, a billion were shipped

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to middle- and low-income countries, so 38%.

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So that's what we had promised, and this

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is what we have delivered.

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Now, what is the situation, particularly for the lower

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income of this range?

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Right now, we have more than they can absorb, unfortunately.

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And I think all the efforts of the WHO,

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of UNICEF, of philanthropic organizations like Gates,

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Doctors Without [? Medicines, ?] and us

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should be in one fighting the misinformation

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in these countries and creating a vaccine advocacy

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and support because people are hesitant to do

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it in higher numbers than in the high-income countries.

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But, also, there is a lack of infrastructure.

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Sometimes, it's difficult even to carry the vaccine

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to a vaccination center.

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We use-- we worked with a project

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to carry them with drones.

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It was very successful.

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The drones could carry, in these low temperatures, the vaccines.

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But we didn't have where to take them, eventually, because they

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are not operating vaccination centers in the rural parts

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of the country.

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So all of these are issues that needs to be addressed.

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And that should be the focus of everyone right now.

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ANJALEE KHEMLANI: Definitely.

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ALBERT BOURLA: [? The ?] [? supply's ?] [? not ?]

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[INAUDIBLE].

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ANJALEE KHEMLANI: And, to that point--

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absolutely.

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And, to that point, the mRNA really being a newer

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technology, for these countries to absorb that

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has been part of the issue.

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I know that you created that agreement with South

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Africa, the Biovac Institute.

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And, with the sort of investment that you're

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making in mRNA right now, expanding that agreement

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with BioNTech, that partnership, and moving into other vaccines,

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do you see this as more of a long-term plan?

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And do you see maybe resolving some of those transportation

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and logistical issues as part of your work there?

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ALBERT BOURLA: Yes.

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I think the transportation and logistical issues has--

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that are related to the nature of our vaccine,

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[INAUDIBLE] have been addressed.

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Right now, we are able to produce a new formulation that

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can stay two and 1/2 months in normal refrigeration,

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so like every other vaccine.

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So I don't think this is the issue.

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The issue, it is that there are not people to inject.

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There's no health care practitioners.

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There is not a [? sender ?] to receive

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it so that people can come.

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And, very importantly, people are not

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queuing outside to get the vaccine, because they

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don't believe in that.

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So these are the issues, mainly, that needs to be addressed.

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As regards to the investment we are doing in the area,

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it's not only on the COVID vaccine.

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But, clearly, we are investing a lot

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to make sure that we make better vaccines, the Omicron

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one, a vaccine that can cover Omicron in addition

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to everything else is, for example, a good example.

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But we are also working--

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we just announced three new deals today.

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One is with [? Beam ?] [? Therapeutics ?]

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that is trying to harness the power of mRNA in gene editing.

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The other is with Codex, which will potentially allow us

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to reduce the time in manufacturing of RNA from one

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month, which is the [? part ?] [? it ?] takes now to make

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the DNA, to maybe a few days--

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very, very important.

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And the other is licenses from Acuitas's

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LMP, 10 targets of LMP.

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LMP is the technology that uses lipid nanoparticles

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to transfer RNA to our tissues.

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So we truly believe that the mRNA

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technology is very powerful.

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It's not the holy grail, but it is very powerful.

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We are just scratching the surface.

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And we are very, very well positioned to put together

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capabilities of others and ourselves

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to produce medicines that the world needs.

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ANJALEE KHEMLANI: Absolutely.

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And, speaking of medicines that the world needs,

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we also see the antiviral, you know, making its way

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throughout the world, production of that still ramping

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up and deliveries as well.

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So, while supplies are constrained for right now,

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do you see that impacting, really, the pandemic in sort

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of the way that people have been anticipating,

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especially because it's coming a little bit

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after this Omicron spread?

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ALBERT BOURLA: I think it's coming--

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I wish we had it in larger quantities,

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but it came exactly the moment that you needed.

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I think it's a game changer.

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It is a game changer because we know that the people

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are getting way more sick--

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first of all, they are unvaccinated people that they

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are getting hospitalizations.

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They are people that new variants don't protect.

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And, clearly, Omicron is not going to be the only variant

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that exists there.

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And this wave is not going to be the only wave that we

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are facing, unfortunately.

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But this is the reality.

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The virus is endemic almost all over the world.

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And, also, both the natural infection

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and vaccinations, they don't produce lasting immunity

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against this virus.

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It's not that the vaccines that they have--

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it is the virus that has these characteristics.

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As I said, even the natural infection

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produces even smaller, less durable immune responses.

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And so the virus will be here for many, many years.

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And we are lucky that we have pills and vaccines

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of high, high, high effectiveness

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so that we can control it and go back to normal lives,

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which is the given right now--

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ANJALEE KHEMLANI: Right, absolutely.

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ALBERT BOURLA: --which is [INAUDIBLE]----

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ANJALEE KHEMLANI: We're all looking forward to that.

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ALBERT BOURLA: --right now.

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This is what everybody is asking.

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Go back to normal life.

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ANJALEE KHEMLANI: Certainly.

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And it certainly has set the stage

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for you to be able to expand, like you mentioned, in mRNA.

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So I believe that we're gonna be hearing a lot more about this.

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Unfortunately, we have to leave it there.

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But Albert Bourla, CEO of Pfizer,

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thank you so much again for your time

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and helping us with our coverage for JPM this year.

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All the best, and look forward to speaking to you again soon.

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Julie, back to you.

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JULIE HYMAN: Thanks, Anjalee.

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Appreciate it, and yes, indeed, back to normal

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is what we are all hoping for.
