‘The pursuit of normal’: Pfizer launches first Covid-19 vaccine TV ads

One of Pfiz­er’s new vac­cine TV com­mer­cials nev­er men­tions its vac­cine brand Comir­naty. In fact, it doesn’t men­tion vac­cines or Covid-19 at all and doesn’t show peo­ple wear­ing masks or so­cial dis­tanc­ing. Yet it’s clear the ad is talk­ing about the phar­ma’s Covid-19 vac­cines.

The ad’s voiceover talks about the un­re­mark­able mo­ments and rou­tines that mat­ter, like get­ting a cof­fee re­fill at a din­er or Sun­day gro­cery shop­ping. The im­ages shift from those every­day mo­ments to a sci­en­tists and pur­ple lid­ded glass vials spin­ning off a pro­duc­tion line and be­ing packed in­to freez­ers.

The sign-off? ‘At Pfiz­er, pro­tect­ing the reg­u­lar rou­tine in every day, dri­ves us to reach for ex­cep­tion­al. Work­ing to im­pact hun­dreds of mil­lions of lives young and old, it’s what we call ‘the pur­suit of nor­mal.”

A sec­ond video ad is more overt, fea­tur­ing NBA Brook­lyn Nets play­er Bruce Brown who talks about how he’ll do ‘lit­er­al­ly any­thing the team needs me to do out there on the floor. So I re­al­ly can’t miss any games. When the vac­cines be­came avail­able, there was no doubt I was get­ting vac­ci­nat­ed. I was su­per ex­cit­ed be­cause my life is bas­ket­ball.’

One of the fi­nal screens shows the words ‘Don’t miss your shot,’ fol­lowed by a screen show­ing the Nets’, Pfiz­er’s and BioN­Tech’s lo­gos. Sim­i­lar to the oth­er ad, the bas­ket­ball ad is tagged ‘All rights re­served. De­cem­ber 2021.’

Pfiz­er de­clined to com­ment about the new ad, cit­ing that it does not dis­cuss its mar­ket­ing strate­gies. How­ev­er, the ads are copy­right­ed Dec. 2021 and a vac­cine cam­paign had been ex­pect­ed be­fore the end of the year.

Ac­cord­ing to me­dia re­ports, Pfiz­er hired ad agency Ogilvy to do vac­cine ad­ver­tis­ing short­ly af­ter the shot was ap­proved by the FDA in Au­gust. The new com­mer­cial how­ev­er is tagged on iS­pot.tv as cre­at­ed by a dif­fer­ent ad agency, Young & Ru­bi­cam. Pfiz­er has used both Ogilvy and VM­LY&R for its mar­ket­ing and ad­ver­tis­ing cam­paigns in the past.

No mat­ter the agency, the tim­ing of vac­cine ad­ver­tis­ing syncs with FDA guide­lines that wouldn’t al­low Pfiz­er to ad­ver­tise be­fore be­ing of­fi­cial­ly ap­proved.

This sum­mer Pfiz­er ramped up its Covid-19 vac­cine sales force, the Fi­nan­cial Times re­port­ed, and post­ed ad­ver­tis­ing on LinkedIn to find a se­nior di­rec­tor to lead the US launch as well as a se­nior man­ag­er for Covid con­sumer mar­ket­ing. The job list­ing now reads as ‘no longer ac­cept­ing ap­pli­ca­tions.’

One TV ad first aired last Sun­day, and so far has run more than 300 times, ac­cord­ing to da­ta from re­al-time TV ad track­er iS­pot.tv.

Pfiz­er ex­pects Comir­naty sales of more than $36 bil­lion in 2021. It fore­cast­ed ad­di­tion­al sales of $29 bil­lion in 2022 in No­vem­ber, based on 1.7 bil­lion dos­es sold — al­though it has the ca­pac­i­ty to pro­duce 4 bil­lion. It’s al­ready in the process of sign­ing more deals with more coun­tries for 2022.

Some may won­der with sales like that why even both­er mar­ket­ing. It may seem like a waste of re­sources, and that may be true for now when Pfiz­er is the on­ly FDA-ap­proved Covid-19 vac­cine. How­ev­er, there are at least sev­en more emer­gency use vac­cines au­tho­rized around the world that are com­ing for Pfiz­er’s mar­ket share, es­pe­cial­ly in light of emerg­ing ev­i­dence that boost­er will be need­ed for some time.

Mod­er­na’s Spike­vax, J&J’s Janssen vac­cine, Novo­vax’s Nu­vax­ovid/Cov­o­vax, As­traZeneca’s Vaxzevria and Sanofi and GSK’s vac­cine will all be com­pet­ing to be­come the boost­er of choice around the world. When and if those vac­cines are ful­ly ap­proved in the US, ex­pect more mar­ket­ing and ad­ver­tis­ing as the phar­ma com­pa­nies jock­ey for po­si­tion.

And that means not just con­sumer aware­ness or even DTC ads, but al­so mon­ey spent mar­ket­ing to physi­cians to be­come the Covid vac­cine of choice with doc­tor’s of­fices like­ly de­liv­er­ing most fu­ture boost­er shots.

CALQUENCE is a registered trademark of the AstraZeneca group of companies.

At the 2021 American Society of Hematology (ASH) Annual Meeting & Exposition, blood cancer researchers from around the world gathered virtually to discuss the progress that has been made in the field of hematology. Over the past decade, that progress has been tremendous. We’ve seen not only breakthrough approaches to care, but also significant improvement upon existing novel treatments and exploring combinations within those medicines.1 These advances have transformed expectations of what a blood cancer diagnosis now means for patients. While we’ve come a long way, I believe the most exciting scientific discovery is yet to come, and that future advances will truly transform patient care.

Michel Vounatsos, Biogen CEO (Credit: World Economic Forum/Valeriano Di Domenico)

In a surprise move, Biogen announced Monday that it will cut the price of its controversial Alzheimer’s drug Aduhelm in half, slashing the cost from $56,000 to $28,000.

The sudden discount marks a sudden turnaround for the big biotech as it struggles to turn around a drug whose stuck-in-the-mud sales and political ramifications have sent the company into turmoil and triggered the ousting of its longtime chief scientist. Biogen’s leadership had resisted calls since June to reduce the price of the drug.

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Right as the new Omicron variant is poised to increase rapidly across the US, the federal government has effectively run out of the only monoclonal antibody treatment that works against it, and at least one major hospital system is now halting all mAb infusions.

Late last month, the federal government paused shipments of GlaxoSmithKline and Vir’s mAb treatment sotrovimab in order to conserve supplies of the only treatment that might work against the Omicron variant. Last week, however, HHS told Endpoints News that the move to hold back sotrovimab was unrelated to Omicron, and due to a surplus of Eli Lilly mAbs, which aren’t effective against Omicron.

Sen. Joe Manchin (D-WV) at the Capitol on Friday, Dec. 17 (J. Scott Applewhite/AP Images)

Sen. Joe Manchin on Sunday derailed President Biden’s trillion-dollar spending package, effectively halting the Democrats’ best chance yet to allow Medicare to negotiate drug prices, among a bevy of other health-related provisions tacked onto the Build Back Better Act.

White House press secretary Jen Psaki, stunned by Manchin’s announcement on Fox News, said in a statement: ‘Senator Manchin claims that this change of position is related to inflation, but the think tank he often cites on Build Back Better — the Penn Wharton Budget Institute — issued a report less than 48 hours ago that noted the Build Back Better Act will have virtually no impact on inflation in the short term, and, in the long run, the policies it includes will ease inflationary pressures.’

As the new year rapidly approaches, and gyms and health food stores across America prepare for a wave of people seeking weight loss, Novo Nordisk has announced that it does not expect to meet demand for Wegovy, its prescription injectable weight-loss medication for obesity, until the second half of 2022 in the US.

The shortage comes due to manufacturing issues at a contract manufacturer that was tasked with filling syringes for the pens. The news comes just days after Novo announced that it would invest roughly $2.58 billion to expand its manufacturing hub in Kalundborg, Denmark with three new facilities and the expansion of a fourth to keep up with the success of its diabetes and obesity med semaglutide, Wegovy and Rybelsus.

The AbbVie/Alvotech debacle on a Humira biosimilar has taken yet another turn — escalating tensions between the two biotechs.

The pharma giant filed a complaint with the US International Trade Commission on Friday, trying to prevent Alvotech from selling a lower cost version of AbbVie’s Humira, an anti-TNF drug that treats rheumatoid arthritis, ankylosing spondylitis and Crohn’s disease, among other ailments.

The long wait for Novavax’s promising Covid-19 vaccine will soon be over for Europeans.

The European Medicines Agency on Monday recommended granting a conditional marketing authorization for Novavax’s shot, to be known as Nuvaxovid, to prevent Covid-19 for all those over the age of 18. And later Monday morning, the European Commission granted that authorization.

Clinical trials of the two-shot vaccine, with each jab taken three weeks apart, showed it was safe and offered strong efficacy, but the EMA warned that the vaccine has not been tested against some variants of concern like Omicron.

Tom Plitz (L) and Arthur Roach, Chord Therapeutics CEO and founder

About a year after Geneva-based Chord Therapeutics emerged from stealth to see if it could repurpose an old chemotherapy agent for rare diseases, Merck KGaA is swooping in with a buyout.

While the companies are keeping mum about the financial terms of the deal, Merck KGaA is adding Chord’s lead candidate to its neurology pipeline — a small molecule oral version of the chemotherapy drug cladribine dubbed CRD1.

Brian Culley, Lineage Cell Therapeutics CEO

In a lucrative market for ocular degeneration, Roche has long sat on a gold mine with its drug Lucentis — but the times are changing. Now, Roche will bet on a regenerative approach to eye disease with a small biotech with some very early but promising data.

Genentech will pay $50 million upfront and a potential $620 million in downstream milestones for licensing rights to Lineage Cell Therapeutics’ OpRegen program, a cell therapy that aims to regenerate healthy versions of retinal pigment epithelial cells in patients’ eyes, the companies said Monday.

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