Cel­gene hands over $101M in cash to launch a re­search col­lab­o­ra­tion with pro­tein play­er Vi­vid­ion

Diego Mi­ralles

A year af­ter Vi­vid­ion Ther­a­peu­tics de­buted with a $50 mil­lion launch round and a plat­form tech cen­tered on drug­ging a whole slate of un­drug­gable pro­teins, the San Diego-based biotech has picked up its first big bio­phar­ma col­lab­o­ra­tion with Cel­gene.

Cel­gene is pay­ing a hefty $101 mil­lion up­front in a fee plus eq­ui­ty deal to see how Vi­vid­ion’s R&D en­gine can work for them in on­col­o­gy, in­flam­ma­tion and neu­rode­gen­er­a­tion — a nascent field for them.

Cel­gene has been knocked around re­peat­ed­ly in re­cent months, watch­ing mon­gersen go down in flames, ex­as­per­at­ing an­a­lysts with weak num­bers and then be­ing em­bar­rassed by an FDA refuse-to-file for its all-im­por­tant ozan­i­mod ap­pli­ca­tion. But the com­pa­ny, which just paid $9 bil­lion to buy Juno, still has one of the busiest BD teams scour­ing the biotech field for new deals. And once again, they’re not afraid to pay an un­usu­al­ly large amount of cash to get a dis­cov­ery deal start­ed with a com­pa­ny that is not yet in the clin­ic.

Why is that?

“We can drug the en­tire pro­teome in its na­tive state,” Vi­vid­ion CEO Diego Mi­ralles tells me, “and that is the trans­for­ma­tion­al po­ten­tial of Vi­vid­ion.”

The plat­form tech­nol­o­gy, he adds, of­fers a view of the “re­al life of a cell that gives you a very dif­fer­en­ti­at­ed and unique in­sight in­to how those pro­teins are be­hav­ing and how they are vul­ner­a­ble to be­ing drugged.”

One as­pect of that are in­sights in­to “pro­tein degra­da­tion around pro­teins that to­day are un­touch­able.”

Mi­ralles — a J&J vet who es­tab­lished the John­son & John­son In­no­va­tion Cen­ters and JLABS — joined the com­pa­ny last fall in a process that saw Cel­gene vet Tom Daniel trade the hands-on ex­ec­u­tive chair­man’s role for the chair­man’s ti­tle. And se­r­i­al biotech en­tre­pre­neur Rich Hey­man, who knows a thing or two about pro­tein degra­da­tion, stepped in to sit on the board.

Ben Cra­vatt

Mi­ralles cred­its sci­en­tif­ic founder Ben Cra­vatt — based in Scripps — with the ear­ly talks that ini­tial­ly at­tract­ed Cel­gene’s at­ten­tion. At Cra­vatt’s Scripps lab re­searchers used frag­ment lig­ands at­tached to a class of chap­er­one mol­e­cules that re­acts with cys­teine amino-acids on pro­teins, lock­ing the lig­ands to the pro­teins with co­va­lent bonds.

Not so un­usu­al­ly there are things that Mi­ralles ei­ther can’t or won’t say about the deal and their own re­search plans.

The split be­tween an up­front fee and eq­ui­ty in the Cel­gene deal? Can’t say.

What kind of tar­gets are they go­ing af­ter here? Can’t say.

Time­line for get­ting pro­grams in­to the clin­ic? Won’t say.

On the oth­er hand the com­pa­ny now has a grow­ing staff of 45 and an in­ter­est in pur­su­ing part­ner­ships like this to lever­age its reach.

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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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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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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(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.

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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Scoop: Roche scraps one of two schiz­o­phre­nia PhII tri­als af­ter fail­ing the pri­ma­ry end­point

Roche has terminated one of two Phase II trials testing its drug ralmitaront in patients with schizophrenia, the Big Pharma confirmed to Endpoints News.

The study was terminated last month, according to a June 22 update to the registry on clinicaltrials.gov. Begun in September 2020, the trial was looking at ralmitaront in patients with acute schizophrenia. The trial enrolled 286 patients out of an originally planned 308.

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