Deep tech, round 2: DCVC Bio bags $350M fund to chase the tip of the life sci­ence spear

It took one trip from San Fran­cis­co to Van­cou­ver for Kier­sten Stead and her DCVC Bio crew to feel con­fi­dent about throw­ing their weight — and cash — be­hind Ab­Cellera.

Kier­sten Stead

CEO Carl Hansen’s aca­d­e­m­ic back­ground and the po­ten­tial of the plat­form, which com­bined ma­chine vi­sion and ro­bot­ics with mi­croflu­idics, were promis­ing. But the site vis­it sealed the Se­ries A deal, where DCVC was the lead and on­ly in­vestor.

“We saw a com­pa­ny that had a high­ly ad­van­taged method for ba­si­cal­ly turn­ing an­ti­body de­vel­op­ment in­to a deep search mech­a­nism, sim­i­lar to what Google might do,” she said.

As Ab­Cellera bur­nish­es its pro­file through an Eli Lil­ly-part­nered an­ti­body de­signed to help end the pan­dem­ic, Stead and John Hamer, the oth­er man­ag­ing part­ner of DCVC Bio, have closed $350 mil­lion to bet on com­pa­nies that sim­i­lar­ly sit at the in­ter­sec­tion of “deep tech” and life sci­ences.

DCVC Bio II, just like its pre­de­ces­sor, will look for ear­ly-stage com­pa­nies. Se­ries A, seed rounds should com­prise the ma­jor­i­ty of the port­fo­lio, but they al­so don’t mind rolling up their sleeves to help spin out a start­up if the op­por­tu­ni­ty aris­es.

John Hamer

The way Stead de­scribes it, these are places where com­pu­ta­tion is an “ab­solute core com­pe­ten­cy” rather than an af­ter­thought or sim­ply a sup­port­ing func­tion.

“Gen­er­al­ly speak­ing, our com­pa­nies gen­er­ate their own da­ta, they have their own de­vel­op­ers and they’re build­ing nov­el AI, nov­el al­go­rithms on their pro­pri­etary da­ta to ad­dress re­cal­ci­trant prob­lems across the life sci­ences,” she said.

The team — most of whom worked to­geth­er at Mon­san­to Growth Ven­tures be­fore mov­ing un­der DCVC — is think­ing big. Cit­ing “the triple threat of cli­mate change, an in­creas­ing glob­al pop­u­la­tion and frag­ile glob­al sup­ply chains,” they al­so want to tap in­to agri­cul­ture and in­dus­tri­al biotech­nol­o­gy.

When it comes to ther­a­peu­tics, Stead is be­gin­ning to see the con­flu­ence of dif­fer­ent modal­i­ties from pro­tein degra­da­tion to cell ther­a­pies and gene edit­ing.

Chas­ing those emerg­ing arcs of com­pu­ta­tion and bi­ol­o­gy has brought DCVC Bio to new in­ven­tions in ro­bot­ics and au­toma­tion — think Or­ca Bio’s au­to­mat­ed sys­tem for man­u­fac­tur­ing cell grafts — as well as liv­ing med­i­cines, such as the ge­net­i­cal­ly en­gi­neered mi­crobes at Novome. Phys­i­cal in­tel­li­gent sys­tems will loom large to com­ple­ment soft­ware break­throughs, she pre­dict­ed, while things like re­in­force­ment learn­ing (al­go­rithms that can gen­er­ate their own da­ta) could work around some of the cur­rent con­straints in bi­o­log­i­cal re­search.

Even though phar­ma these days is clear­ly cog­nizant of the need to in­te­grate new com­pu­ta­tion­al tech­nolo­gies, Stead said they face the re­al chal­lenge of re­cruit­ing peo­ple who have ex­pe­ri­ence set­ting up com­mer­cial AI. That’s not to say they don’t play a key role in bring­ing the com­pounds gen­er­at­ed on new plat­forms to­ward the mar­ket; they may just come in lat­er in the process.

“A com­mon thread of en­tre­pre­neurs that we in­vest in and build com­pa­nies with is that they ran X com­pu­ta­tion­al group at X phar­ma­ceu­ti­cal com­pa­ny but re­al­ized that they couldn’t start from scratch and build it from the ground up,” she said, “and and they were re­al­ly pro­found­ly lim­it­ed by that, and want­ed to start a start­up so that they could do X right, what­ev­er their par­tic­u­lar area of in­ter­est is.”

DCVC man­ag­ing part­ners Matt Ocko and Zachary Bogue said on their blog re­cent­ly the fact that the new fund was raised en­tire­ly dur­ing the pan­dem­ic high­lights the ap­petite for even more. Their first fund has backed some ef­forts to ad­dress the cur­rent health­care cri­sis; it’s time to find “the next set of so­lu­tions to the next set of prob­lems.”

Scoop: Boehringer qui­et­ly shut­ters a PhII for one of its top drugs — now un­der re­view

Boehringer Ingelheim has quietly shut down a small Phase II study for one of its lead drugs.

The private pharma player confirmed to Endpoints News that it had shuttered a study testing spesolimab as a therapy for Crohn’s patients suffering from bowel obstructions.

A spokesperson for the company tells Endpoints:

Taking into consideration the current therapeutic landscape and ongoing clinical development programs, Boehringer Ingelheim decided to discontinue our program in Crohn’s disease. It is important to note that this decision is not based on any safety findings in the clinical trials.

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Vas Narasimhan (Photographer: Jason Alden/Bloomberg via Getty Images)

No­var­tis de­tails plans to axe 8,000 staffers as Narasimhan be­gins sec­ond phase of a glob­al re­org

We now know the number of jobs coming under the axe at Novartis, and it isn’t small.

The pharma giant is confirming a report from Swiss newspaper Tages-Anzeiger that it is chopping 8,000 jobs out of its 108,000 global staffers. A large segment will hit right at company headquarters in Basel, as CEO Vas Narasimhan axes some 1,400 of a little more than 11,000  jobs in Switzerland.

The first phase of the work is almost done, the company says in a statement to Endpoints News. Now it’s on to phase two. In the statement, Novartis says:

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Lina Gugucheva, NewAmsterdam Pharma CBO

Phar­ma group bets up to $1B-plus on the PhI­II res­ur­rec­tion of a once dead-and-buried LDL drug

Close to 5 years after then-Amgen R&D chief Sean Harper tamped the last spade of dirt on the last broadly focused CETP cholesterol drug — burying their $300 million upfront and the few remaining hopes for the class with it — the therapy has been fully resurrected. And today, the NewAmsterdam Pharma crew that did the Lazarus treatment on obicetrapib is taking another big step on the comeback trail with a €1 billion-plus regional licensing deal, complete with close to $150 million in upfront cash.

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How pre­pared is bio­phar­ma for the cy­ber dooms­day?

One of the largest cyberattacks in history happened on a Friday, Eric Perakslis distinctly remembers.

Perakslis, who was head of Takeda’s R&D Data Sciences Institute and visiting faculty at Harvard Medical School at the time, had spent that morning completing a review on cybersecurity for the British Medical Journal. Moments after he turned it in, he heard back from the editor: “Have you heard what’s going on right now?”

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(AP Photo/Gemunu Amarasinghe)

Some phar­ma com­pa­nies promise to cov­er abor­tion-re­lat­ed trav­el costs — while oth­ers won't go that far yet

As the US Department of Health and Human Services promises to support the millions of women who would now need to cross state lines to receive a legal abortion, a handful of pharma companies have said they will pick up employees’ travel expenses.

GSK, Sanofi, Johnson & Johnson, BeiGene, Alnylam and Gilead have all committed to covering abortion-related travel expenses just four days after the Supreme Court overturned Roe v. Wade and revoked women’s constitutional right to an abortion.

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Aurobindo Pharma co-founders P. V. Ram Prasad Reddy (L) and K. Nityananda Reddy

Au­robindo Phar­ma re­ceives warn­ing let­ter from In­di­a's SEC fol­low­ing more FDA ques­tion marks

Indian-based generics manufacturer Aurobindo Pharma has been in the crosshairs of the FDA for several years now, but the company is also attracting attention from regulators within the subcontinent.

According to the Indian business news site Business Standard, a warning letter was sent to the company from the Securities Exchange Board of India, or SEBI.

The letter is related to disclosures made by the company on an ongoing FDA audit of the company’s Unit-1 API facility in Hyderabad, India as well as observations made by the US regulator between 2019 and 2022.

New Charles River Laboratories High Quality (HQ) Plasmid DNA Centre of Excellence at Bruntwood SciTech’s Alderley Park in Cheshire, United Kingdom. (Charles River)

Charles Riv­er Lab­o­ra­to­ries to start cell and gene ther­a­py man­u­fac­tur­ing at UK site in Sep­tem­ber

While Massachusetts-based Charles River Laboratories has been on an acquisition spree, they are not against planting their flag. The latest move by the company sees them crossing the pond to establish a manufacturing site in the UK.

The company on Tuesday opened its cell and gene therapy manufacturing center at Bruntwood SciTech’s Alderley Park in Cheshire, United Kingdom. The expansion follows Charles River’s acquisition of Cognate BioServices and Cobra Biologics in 2021 for $875 million. Cognate is a plasmid DNA, viral vector and cell therapy CDMO.

Bristol Myers Squibb (Alamy)

CVS re­sumes cov­er­age of block­buster blood thin­ner af­ter price drop fol­lows Jan­u­ary ex­clu­sion

Following some backlash from the American College of Cardiology and patients, Bristol Myers Squibb and Pfizer lowered the price of their blockbuster blood thinner Eliquis, thus ensuring that CVS Caremark would cover the drug after 6 months of it being off the major PBM’s formulary.

“Because we secured lower net costs for patients from negotiations with the drug manufacturer, Eliquis will be added back to our template formularies for the commercial segment effective July 1, 2022, and patient choices will be expanded,” CVS Health said in an emailed statement. “Anti-coagulant therapies are among the non-specialty products where we are seeing the fastest cost increases from drug manufacturers and we will continue to push back on unwarranted price increases.”

#Can­nes­Lions2022: Con­sumer health ex­ecs call on agen­cies to in­volve pa­tients in cre­ative process

CANNES — When Tamara Rogers joined GSK back in 2018, “science was king and R&D were the gods.” Now the global chief marketing officer of consumer healthcare wants to make room for another supreme being: the consumer.

As health and wellness becomes more relevant to consumers amid the pandemic, four health-focused executives called on marketers to involve patients in their creative process in a panel discussion at the Cannes Lions advertising creativity festival.

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