Har­vard biotech wiz Greg Ver­dine grabs a $55M A round to build a ground­break­ing biotech

It’s hard not to en­joy talk­ing with Greg Ver­dine about the new biotech com­pa­nies he sets up. Years of teach­ing at Har­vard have honed his skill for trans­lat­ing sci­ence in­to a pithy set of sto­ries that every­one can un­der­stand and get a kick out of.

“What I am re­al­ly pas­sion­ate about is dis­cov­er­ing new types of mol­e­cules that do things that can’t be done by stan­dard small mol­e­cules and an­ti­bod­ies,” he told me in the lead-up to to­day’s for­mal launch of LifeM­ine Ther­a­peu­tics with a $55 mil­lion A round. “I want to go af­ter un­drug­gable tar­gets, get drugs that peo­ple con­sid­er now aren’t doable. The ques­tion is where you go look­ing for this.”

Greg Ver­dine

The an­swer for Ver­dine, this time, is fun­gi.

“Fun­gi have been duk­ing it out with their neigh­bors in the soil for a bil­lion years,” says Ver­dine, “steal­ing the lunch of their cowork­ers, com­pet­ing, and fend­ing off in­vaders us­ing small mol­e­cules as com­pet­i­tive sub­stances.” And it all fits very close­ly with hu­man pro­teins, giv­ing it a good shot at work­ing in hu­mans.

It helps that evo­lu­tion doesn’t obey the same rules that guide med­i­c­i­nal chemists, and now Ver­dine’s new com­pa­ny will re­ly on se­quenc­ing to fol­low this strange path in search of some rad­i­cal new break­throughs in can­cer — a field that has at­tract­ed bil­lions of dol­lars to back a new gen­er­a­tion of ther­a­pies.

To do this, he says, the team has to “grow up fun­gi in­di­vid­u­al­ly, iso­late DNA and se­quence the DNA. Take the DNA and an­a­lyze it for biosyn­thet­ic gene clus­ters; an in­struc­tion set to make a nat­ur­al prod­uct.”

Ver­dine blends mul­ti­ple roles in biotech: Pro­fes­sor, ven­ture part­ner at WuXi Health­care Ven­tures — which seed­ed this new start­up — and now a dou­ble CEO, with his dual role run­ning Fog Phar­ma made eas­i­er by hav­ing both com­pa­nies housed in the same build­ing in Cam­bridge, MA.

Over the years Ver­dine has been one of the most pro­lif­ic start­up artists in the busi­ness, a go-to fig­ure in the in­dus­try who’s helped kick a slate of biotechs in­to ex­is­tence, rang­ing from Enan­ta to Tokai, Aileron and Warp Dri­ve Bio, which he al­so helmed for a time.

Right now the team at LifeM­ine is made up of a dozen sci­en­tists and five DNA spe­cial­ists, where they are fo­cus­ing on pro­grams and tar­gets for the pipeline as they build the plat­form along the way. By mid-2019, Ver­dine ex­pects the crew to ex­pand to about 40 staffers.

It’s still ear­ly days, though.

“We’ve left our­selves 3.5 years to en­ter the clin­ic,” says Ver­dine.

That re­quires some very pa­tient mon­ey, which Ver­dine lined up from WuXi Health­care Ven­tures with a syn­di­cate that in­cludes Fore­site Cap­i­tal, Google Ven­tures (or GV, with Kr­ish­na Yesh­want join­ing the board), Arch Ven­ture Part­ners, Boyu Cap­i­tal, Blue Pool Cap­i­tal, MRL Ven­tures Fund, and Alexan­dria Ven­ture In­vest­ments.

Those blue chip VC names are mix­ing with some mon­ey out of two promi­nent Chi­nese in­vestors, aside from the transpa­cif­ic WuXi op­er­a­tion: Boyu — an in­flu­en­tial pri­vate eq­ui­ty group led by co-founder and part­ner Sean Tong — and Blue Pool.

At this stage of his life, Ver­dine is po­si­tioned at ex­act­ly the right place, and ex­act­ly the right time, for a pricey space shot in­to the biotech uni­verse. The stars have aligned — again.

De­vel­op­ment of the Next Gen­er­a­tion NKG2D CAR T-cell Man­u­fac­tur­ing Process

Celyad’s view on developing and delivering a CAR T-cell therapy with multi-tumor specificity combined with cell manufacturing success
Overview
Transitioning potential therapeutic assets from academia into the commercial environment is an exercise that is largely underappreciated by stakeholders, except for drug developers themselves. The promise of preclinical or early clinical results drives enthusiasm, but the pragmatic delivery of a therapy outside of small, local testing is most often a major challenge for drug developers especially, including among other things, the manufacturing challenges that surround the production of just-in-time and personalized autologous cell therapy products.

Paul Hudson, Getty Images

UP­DAT­ED: Sanofi CEO Hud­son lays out new R&D fo­cus — chop­ping di­a­betes, car­dio and slash­ing $2B-plus costs in sur­gi­cal dis­sec­tion

Earlier on Monday, new Sanofi CEO Paul Hudson baited the hook on his upcoming strategy presentation Tuesday with a tell-tale deal to buy Synthorx for $2.5 billion. That fits squarely with hints that he’s pointing the company to a bigger future in oncology, which also squares with a major industry tilt.

In a big reveal later in the day, though, Hudson offered a slate of stunners on his plans to surgically dissect and reassemble the portfoloio, saying that the company is dropping cardio and diabetes research — which covers two of its biggest franchise arenas. Sanofi missed the boat on developing new diabetes drugs, and now it’s pulling out entirely. As part of the pullback, it’s dropping efpeglenatide, their once-weekly GLP-1 injection for diabetes.

“To be out of cardiovascular and diabetes is not easy for a company like ours with an incredibly proud history,” Hudson said on a call with reporters, according to the Wall Street Journal. “As tough a choice as that is, we’re making that choice.”

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Roger Perlmutter, Merck

#ASH19: Here’s why Mer­ck is pay­ing $2.7B to­day to grab Ar­Qule and its next-gen BTK drug, lin­ing up Eli Lil­ly ri­val­ry

Just a few months after making a splash at the European Hematology Association scientific confab with an early snapshot of positive data for their BTK inhibitor ARQ 531, ArQule has won a $2.7 billion buyout deal from Merck.

Merck is scooping up a next-gen BTK drug — which is making a splash at ASH today — from ArQule in an M&A pact set at $20 a share $ARQL. That’s more than twice Friday’s $9.66 close. And Merck R&D chief Roger Perlmutter heralded a deal that nets “multiple clinical-stage oral kinase inhibitors.”

This is the second biotech buyout pact today, marking a brisk tempo of M&A deals in the lead-up to the big JP Morgan gathering in mid-January. It’s no surprise the acquisitions are both for cancer drugs, where Sanofi will try to make its mark while Merck beefs up a stellar oncology franchise. And bolt-ons are all the rage at the major pharma players, which you could also see in Novartis’ recent $9.7 billion MedCo buyout.

ArQule — which comes out on top after their original lead drug foundered in Phase III — highlighted early data on ‘531 at EHA from a group of 6 chronic lymphocytic leukemia patients who got the 65 mg dose. Four of them experienced a partial response — a big advance for a company that failed with earlier attempts.

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Paul Hudson, Sanofi

Paul Hud­son promis­es a bright new fu­ture at Sanofi, kick­ing loose me-too drugs and fo­cus­ing on land­mark ad­vances. But can he de­liv­er?

Paul Hudson was on a mission Tuesday morning as he stood up to address Sanofi’s new R&D and business strategy.

Still fresh into the job, the new CEO set out to convince his audience — including the legions of nervous staffers inevitably devoting much of their day to listening in — that the pharma giant is shedding the layers of bureaucracy that had held them back from making progress in the past, dropping the duds in the pipeline and reprioritizing a more narrow set of experimental drugs that were promised as first-in-class or best-in-class.  The company, he added, is now positioned to “go after other opportunities” that could offer a transformational approach to treating its core diseases.

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Am­gen puts its foot down in shiny new South San Fran­cis­co hub as it re­or­ga­nizes R&D ops

Amgen has signed up to be AbbVie’s neighbor in South San Francisco as it moves into a nine-story R&D facility in the booming biotech hub.

The arrangement gives Amgen 240,000 square feet of space on the Gateway of Pacific Campus, just a few minutes drive from its current digs at Oyster Point. The new hub will open in 2022 and house the big biotech’s Bay Area employees working on cardiometabolic, inflammation and oncology research.

Ab­b­Vie, Scripps ex­pand part­ner­ship, for­ti­fy fo­cus on can­cer drugs

Scripps and AbbVie go way back. Research conducted in the lab of Scripps scientist Richard Lerner led to the discovery of Humira. The antibody, approved by the FDA in 2002 and sold by AbbVie, went on to become the world’s bestselling treatment. In 2018, the drugmaker and the non-profit organization signed a pact focused on developing cancer treatments — and now, the scope of that partnership has broadened to encompass a range of diseases, including immunological and neurological conditions.

South Ko­rea jails 3 Sam­sung ex­ecs for de­stroy­ing ev­i­dence in Bi­o­Log­ics probe

Three Samsung executives in Korea are going to jail.

The convictions came in what prosecutors had billed as “biggest crime of evidence destruction in the history of South Korea”: a case of alleged corporate intrigue that was thrown open when investigators found what was hidden beneath the floor of a Samsung BioLogics plant. Eight employees in total were found guilty of evidence tampering and the three executives were each sentenced to up to two years in prison.

Nick Plugis, Avak Kahvejian, Cristina Rondinone, Milind Kamkolkar and Chad Nusbaum. (Cellarity)

Cel­lar­i­ty, Flag­ship's $50M bet on net­work bi­ol­o­gy, mar­ries ma­chine learn­ing and sin­gle-cell tech for drug dis­cov­ery

Cellarity started with a simple — but far from easy — idea that Avak Kahvejian and his team were floating around at Flagship Pioneering: to digitally encode a cell.

As he and his senior associate Nick Plugis dug deeper into the concept, they found that most of the models others have developed take a bottom-up approach, where they assemble the molecules inside cells and the connections between them from scratch. What if they opt for a top-down approach, aided by single-cell transcriptomics and machine learning, to gauge the behavior of the entire cellular network?

Sanofi’s big week in­cludes a promis­ing PhI­II for an or­phan dis­ease drug, with plans for a pitch to the FDA

The biopharma R&D food chain is paying off with a plan at Sanofi to pitch regulators on a new drug for an orphan disease called cold agglutinin disease.

The pharma giant ushered out a statement Tuesday morning — after it spelled out plans to radically restructure the company, abandoning cardio and diabetes research altogether — saying that their C1s inhibitor sutimlimab had cleared the pivotal study.