Biotech uni­corn's 'brain' at­tracts a $115M mega-round as in­vestors em­brace AI up­start

Ar­ti­fi­cial in­tel­li­gence in drug de­vel­op­ment is still gain­ing mo­men­tum. Just ask Benev­o­len­tAI, which has brought in a new $115 mil­lion round for its tech­nol­o­gy that promis­es to process vast amounts of bio­science in­for­ma­tion and churn out new dis­cov­er­ies.

Ken Mul­vany

Backed by new, undis­closed in­vestors from the Unit­ed States as well as ex­ist­ing sup­port­ers like Wood­ford In­vest­ment Man­age­ment, the round puts Lon­don-based Benev­o­len­tAI at a pre-mon­ey val­u­a­tion of $2 bil­lion. The syn­di­cate fea­tures a mix of fam­i­ly of­fices and some strate­gic back­ers but not “more tra­di­tion­al VCs,” TechCrunch re­ports.

Since its found­ing in 2013, the biotech has raised more than $200 mil­lion. The new cash will go in­to scal­ing its drug de­vel­op­ment ac­tiv­i­ties, broad­en­ing fo­cus dis­ease area, and ex­tend its plat­form ca­pa­bil­i­ties — not just in phar­ma­ceu­ti­cals but al­so in ma­te­r­i­al sci­ence, en­er­gy and agri­cul­ture.

De­spite con­tin­ued skep­ti­cism and scruti­ny as to how much AI can shave off the painful­ly lengthy drug de­vel­op­ment process and in­crease suc­cess rates, it con­tin­ues to in­spire en­thu­si­asm es­pe­cial­ly in Big Phar­ma, where ex­ecs are al­ways look­ing for ways to trim spend­ing. In fact, J&J hand­ed some clin­i­cal-stage drug can­di­dates for Benev­o­len­tAI to guide de­vel­op­ment back in 2016 with plans to start Phase IIb tri­als last year.

Jack­ie Hunter

The core of Benev­o­len­tAI’s promise is an AI “brain” that now holds “50 bil­lion bi­o­log­i­cal da­ta points and com­plex bi­o­log­i­cal con­cepts – the world’s largest most so­phis­ti­cat­ed bio­science knowl­edge graph,” founder and chair­man Ken Mul­vany writes in a blog post. “The tech­nol­o­gy that sits on this knowl­edge is able to gen­er­ate new in­sights in­to the cause of dis­ease at a scale not pos­si­ble for hu­man be­ings.”

Un­der the lead­er­ship of GSK vet Jack­ie Hunter, Benev­o­len­tAI is work­ing on 22 pro­grams across ar­eas span­ning Parkin­son’s dis­ease, mo­tor neu­ron dis­ease, glioblas­toma and sar­cope­nia, though on­ly two are in ad­vanced stages.

Re­cent­ly, the com­pa­ny ac­quired a drug dis­cov­ery and de­vel­op­ment fa­cil­i­ty on the Babra­ham Re­search Cam­pus in Cam­bridge, UK, bring­ing a new sci­en­tif­ic team and late-stage clin­i­cal test­ing ca­pa­bil­i­ties in­to its fold. Mul­vany told TechCrunch that he hopes to al­most dou­ble the size of the team by the end of the year, from 155 to 300.

“We have come a very long way since we found­ed the busi­ness in 2013. The ca­pa­bil­i­ties of our tech­nol­o­gy didn’t ex­ist 6 years ago,” he said in a state­ment.

Chas­ing Roche's ag­ing block­buster fran­chise, Am­gen/Al­ler­gan roll out Avastin, Her­ceptin knock­offs at dis­count

Let the long battle for biosimilars in the cancer space begin.

Amgen has launched its Avastin and Herceptin copycats — licensed from the predecessors of Allergan — almost two years after the FDA had stamped its approval on Mvasi (bevacizumab-awwb) and three months after the Kanjinti OK (trastuzumab-anns). While the biotech had been fielding biosimilars in Europe, this marks their first foray in the US — and the first oncology biosimilars in the country.

Seer adds ex-FDA chief Mark Mc­Clel­lan to the board; Her­cules Cap­i­tal makes it of­fi­cial for new CEO Scott Bluestein

→ On the same day it announced a $17.5 million Series C, life sciences and health data company Seer unveiled that it had lured former FDA commissioner and ex-CMS administrator Mark McClellan on to its board. “Mark’s deep understanding of the health care ecosystem and visionary insights on policy reform will be crucial in informing our thinking as we work to bring our liquid biopsy and life sciences products to market,” said Seer chief and founder Omid Farokhzad in a statement.

Norbert Bischofberger. Kronos

Backed by some of the biggest names in biotech, Nor­bert Bischof­berg­er gets his megaround for plat­form tech out of MIT

A little over a year ago when I reported on Norbert Bischofberger’s jump from the CSO job at giant Gilead to a tiny upstart called Kronos, I noted that with his connections in biotech finance, that $18 million launch round he was starting off with could just as easily have been $100 million or more.

With his first anniversary now behind him, Bischofberger has that mega-round in the bank.

Endpoints News

Basic subscription required

Unlock this story instantly and join 55,000+ biopharma pros reading Endpoints daily — and it's free.

Francesco De Rubertis

Medicxi is rolling out its biggest fund ever to back Eu­rope's top 'sci­en­tists with strange ideas'

Francesco De Rubertis built Medicxi to be the kind of biotech venture player he would have liked to have known back when he was a full time scientist.

“When I was a scientist 20 years ago I would have loved Medicxi,’ the co-founder tells me. It’s the kind of place run by and for investigators, what the Medicxi partner calls “scientists with strange ideas — a platform for the drug hunter and scientific entrepreneur. That’s what I wanted when I was a scientist.”

Endpoints News

Basic subscription required

Unlock this story instantly and join 55,000+ biopharma pros reading Endpoints daily — and it's free.

Af­ter a decade, Vi­iV CSO John Pot­tage says it's time to step down — and he's hand­ing the job to long­time col­league Kim Smith

ViiV Healthcare has always been something unique in the global drug industry.

Owned by GlaxoSmithKline and Pfizer — with GSK in the lead as majority owner — it was created 10 years ago in a time of deep turmoil for the field as something independent of the pharma giants, but with access to lots of infrastructural support on demand. While R&D at the mother ship inside GSK was souring, a razor-focused ViiV provided a rare bright spot, challenging Gilead on a lucrative front in delivering new combinations that require fewer therapies with a more easily tolerated regimen.

They kept a massive number of people alive who would otherwise have been facing a death sentence. And they made money.

And throughout, John Pottage has been the chief scientific and chief medical officer.

Until now.

Endpoints News

Basic subscription required

Unlock this story instantly and join 55,000+ biopharma pros reading Endpoints daily — and it's free.

Daniel O'Day

No­var­tis hands off 3 pre­clin­i­cal pro­grams to the an­tivi­ral R&D mas­ters at Gilead

Gilead CEO Daniel O’Day’s new task hunting up a CSO for the company isn’t stopping the industry’s dominant antiviral player from doing pipeline deals.

The big biotech today snapped up 3 preclinical antiviral programs from pharma giant Novartis, with drugs promising to treat human rhinovirus, influenza and herpes viruses. We don’t know what the upfront is, but the back end has $291 million in milestones baked in.

Vas Narasimhan, AP Images

On a hot streak, No­var­tis ex­ecs run the odds on their two most im­por­tant PhI­II read­outs. Which is 0.01% more like­ly to suc­ceed?

Novartis CEO Vas Narasimhan is living in the sweet spot right now.

The numbers are running a bit better than expected, the pipeline — which he assembled as development chief — is performing and the stock popped more than 4% on Thursday as the executive team ran through their assessment of Q2 performance.

Year-to-date the stock is up 28%, so the investors will be beaming. Anyone looking for chinks in their armor — and there are plenty giving it a shot — right now focus on payer acceptance of their $2.1 million gene therapy Zolgensma, where it’s early days. And CAR-T continues to underperform, but Novartis doesn’t appear to be suffering from it.

So what could go wrong?

Actually, not much. But Tim Anderson at Wolfe pressed Narasimhan and his development chief John Tsai to pick which of two looming Phase III readouts with blockbuster implication had the better odds of success.

Endpoints News

Basic subscription required

Unlock this story instantly and join 55,000+ biopharma pros reading Endpoints daily — and it's free.

On a glob­al romp, Boehringer BD team picks up its third R&D al­liance for Ju­ly — this time fo­cused on IPF with $50M up­front

Boehringer Ingelheim’s BD team is on a global deal spree. The German pharma company just wrapped its third deal in 3 weeks, going back to Korea for its latest pipeline pact — this time focused on idiopathic pulmonary fibrosis.

They’re handing over $50 million to get their hands on BBT-877, an ATX inhibitor from Korea’s Bridge Biotherapeutics that was on display at a science conference in Dallas recently. There’s not a whole lot of data to evaluate the prospects here.

Endpoints News

Basic subscription required

Unlock this story instantly and join 55,000+ biopharma pros reading Endpoints daily — and it's free.

Servi­er scoots out of an­oth­er col­lab­o­ra­tion with Macro­Gen­ics, writ­ing off their $40M

Servier is walking out on a partnership with MacroGenics $MGNX — for the second time.

After the market closed on Wednesday MacroGenics put out word that Servier is severing a deal — inked close to 7 years ago — to collaborate on the development of flotetuzumab and other Dual-Affinity Re-Targeting (DART) drugs in its pipeline.

MacroGenics CEO Scott Koenig shrugged off the departure of Servier, which paid $20 million to kick off the alliance and $20 million to option flotetuzumab — putting a heavily back-ended $1 billion-plus in additional biobuck money on the table for the anti-CD123/CD3 bispecific and its companion therapies.