Eight years and $1.3B later, AstraZeneca finally unveils Cambridge R&D palace

AstraZeneca’s Cambridge R&D center

One of the biggest projects that Pas­cal So­ri­ot ini­ti­at­ed, all the way back in 2013, af­ter he first took over as As­traZeneca’s CEO is fi­nal­ly com­plete. As­traZeneca is for­mal­ly un­veil­ing its $1.34 bil­lion (£1 bil­lion) R&D cam­pus in Cam­bridge, UK, a shiny new fa­cil­i­ty span­ning 19,000 square me­ters in the south­ern part of the city. On top of 2,200 re­search sci­en­tists, it will al­so host a suite of ro­bot­ics, high-through­put screen­ing and AI-dri­ven tech­nol­o­gy.

‘I think it’s a very bold state­ment that we’ve got the new build­ing,’ Su­san Gal­braith, EVP of on­col­o­gy R&D, said in a video, ‘be­cause it’s ba­si­cal­ly say­ing that R&D is the fu­ture of the com­pa­ny, and that we want to in­vest in hav­ing the best fa­cil­i­ties pos­si­ble for peo­ple to do in­no­v­a­tive sci­ence. So that it­self I think is a state­ment of in­tent for what we want the fu­ture of the com­pa­ny to be.’ From pre­ci­sion med­i­cines to next-gen treat­ments such as nu­cleotide-based, gene-edit­ing and cell ther­a­pies, the com­pa­ny has high hopes for the site.

When As­traZeneca first an­nounced plans to build the new glob­al R&D hub and cor­po­rate head­quar­ters, the goal was to be ready for move-in by 2016 on a bud­get of $500 mil­lion. So­ri­ot’s vi­sion was for the team to be­come an in­te­gral part of the lo­cal ecosys­tem in Cam­bridge, ‘a world-renowned bio­science hotspot that ri­vals the likes of San Fran­cis­co and Boston.’

In the end, it was just like de­vel­op­ing a new drug. Fraught with high costs, dis­ap­point­ing set­backs and the source of bit­ter crit­i­cism. But the de­lays didn’t stop As­traZeneca from ink­ing over 200 col­lab­o­ra­tions in the re­gion, in­clud­ing 130-plus with the Uni­ver­si­ty of Cam­bridge, on top of more than 2,000 around the world, ac­cord­ing to Andy Williams, VP of Cam­bridge pro­gram and strat­e­gy. And the open-floor de­sign of the new build­ing will hope­ful­ly deep­en these ties while fos­ter­ing more.

The grand open­ing on Tues­day fea­tures Prince Charles as the guest of hon­or.

Lo­cat­ed with­in the Cam­bridge Bio­med­ical Cam­pus, As­traZeneca is now neigh­bors with mul­ti­ple re­search hos­pi­tals as well as Ab­cam, the re­search tool provider.

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Joan Perelló, Sanifit CEO

Joan Perelló beat all the odds with his little Spanish biotech startup Sanifit.

Working on the far perimeter of the big US/European drug development scene, he took a drug born out of his PhD work and got enough seed cash to get started. That’s one near miracle. In the second near miracle he gathered a previously unheard of venture raise in Spain — helping build an industry ecosystem from scratch — to pursue a successful search for solid human data for his drug, SNF472. And while gathering a virtual team of developers from Europe and the US, the CEO/co-founder steered it into the late-stage arena.

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In an effort to up its development of microbial-derived proteins, Swiss CDMO Lonza will invest in its manufacturing capacities in its home country.

The extension will be good to go by the end of this year, the company said. The expanded development will strengthen the upstream, downstream and process analytics support for new projects. The microbial footprint at its Visp site will be consolidated, and new high-throughput equipment and automation processes will be added to increase efficiency and project delivery. That will include three liquid handling workstations, and the upgrades will help improve data generation.

The FDA’s backlog of drug manufacturing facility inspections continues to be a sore spot for the agency, as FDA said Monday that a total of 52 new drug (but no biologics) applications still remain delayed due to the backlog from the pandemic.

And while the agency has maintained that it won’t issue a CRL for a delayed inspection, the number of delayed applications is rising as FDA said in May that 48 new drug applications have been delayed due to FDA’s inability to conduct pre-approval, pre-market, or pre-license inspections as of last March.

Most people know if they’re ‘Team Pfizer’ or ‘Team Moderna,’ but few know if they got the Comirnaty or Spikevax Covid-19 vaccine. Those are the brand names of Pfizer and Moderna vaccines, respectively, however they have yet to take hold with consumers, media or even medical professionals.

And there are others. Covid vaccine brand names also include AstraZeneca’s Vaxzevria, Novovax’s Nuvaxovid, and Sanofi and GlaxoSmithKline’s Vidprevtyn. J&J’s Janssen-developed Covid vaccine is the lone major holdout and is still yet to be named, if ever. In EMA filings approving its conditional use, the brand name is listed simply as ‘Covid-19 Vaccine Janssen.’

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Emma Walmsley, GlaxoSmithKline CEO (Fang Zhe/Xinhua/Alamy Live News)

As activist investors champ at the bit for change at drug giant GlaxoSmithKline, the pharma giant has turned over many rocks to find an R&D success to present to its detractors. In NASH, a field strewn with failures, GSK hopes a new license deal can churn out a much-needed winner.

GSK will pay $120 million in upfront cash and $910 million in downstream milestones to develop and sell ARO-HSD, Arrowhead Pharmaceuticals’ RNA interference drug targeting fatty liver disease nonalcoholic steatohepatitis (NASH), the companies said Monday.

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Michael Engsig, Nykode CEO

Vaccibody who? A little over a year after securing a $700 million-plus deal with Roche for its neoantigen cancer vaccine, the Norwegian biotech has attracted yet another Big Pharma partner with deep pockets — and with it, a new name and facelift.

Regeneron is betting nearly $1 billion on five new vaccine programs from Vaccibody, now called Nykode Therapeutics. The deal will double Nykode’s current pipeline, adding three programs in cancer and two in infectious disease.

Stephen Hahn and Donald Trump, AP Images

The House Select Subcommittee on the Coronavirus Crisis on Monday questioned former FDA commissioner Stephen Hahn on whether he acquiesced to political pressure in authorizing the use of hydroxychloroquine and convalescent plasma early in the pandemic, despite limited evidence of their effectiveness.

Hahn publicly disavowed any political interference in any of his agency’s EUA decisions, but behind the scenes, the pressure clearly caught up with him.

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Paul Hudson, Sanofi CEO (Eric Piermont/AFP via Getty Images)

Back in June, Sanofi unveiled a big project to reshape its R&D around the future of mRNA, and followed that up Monday by taking a step toward achieving that goal.

The French drugmaker signed a deal with Chinese tech giant Baidu to access its AI algorithm for mRNA-based therapeutics, Baidu said Monday morning. It’s for an undisclosed sum, but Baidu noted its platforms will be used to ‘contribute to the optimization of mRNA sequences’ in Sanofi’s drug development processes.

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