Roche bags full con­trol of Foun­da­tion Med­i­cine in $2.4B fol­low-up buy­out

What­ev­er Foun­da­tion Med­i­cine has been do­ing since Roche threw its weight be­hind an R&D col­lab­o­ra­tion three years ago, both part­ners are lik­ing it. And now, Roche wants all of it, putting $2.4 bil­lion more on the ta­ble.

The val­u­a­tion of Cam­bridge, MA-based Foun­da­tion has grown quite a bit since Roche ac­quired a ma­jor­i­ty stake in Jan­u­ary 2015 at $50 a share — a hefty pre­mi­um then — with each share now cost­ing the Swiss phar­ma gi­ant $137. That’s 29% more than its clos­ing price on Mon­day. Roche’s as­sess­ment of the com­pa­ny val­ue: $5.3 bil­lion.

Daniel O’Day

With per­son­al­ized med­i­cine writ­ten all over it, this ac­qui­si­tion fol­lows that of Flat­iron, a tech start­up build­ing an elec­tron­ic health record sys­tem used by on­col­o­gists. There, Roche al­so bought a stake in the com­pa­ny and cul­ti­vat­ed a re­la­tion­ship be­fore swoop­ing in for a buy­out. And last De­cem­ber they swooped in to buy Igny­ta $RXDX for $1.7 bil­lion, putting the phar­ma gi­ant in di­rect com­pe­ti­tion with Loxo On­col­o­gy $LOXO, with its work in ROS1 and NTRK fu­sion-pos­i­tive tu­mors.

While Foun­da­tion Med­i­cine does have an FDA-ap­proved di­ag­nos­tic called Foun­da­tionOne CDx, Roche is choos­ing to high­light its broad­er po­ten­tial in com­pre­hen­sive ge­nom­ic pro­fil­ing of can­cers, which can both guide de­vel­op­ment of treat­ments and match pa­tients with the ap­pro­pri­ate ther­a­pies. Mean­while, Roche has carved out a place for it­self in di­ag­nos­tics, in­vest­ing 12% of its en­tire R&D bud­get on the area.

“We will pre­serve FMI’s au­ton­o­my while sup­port­ing them in ac­cel­er­at­ing their progress,” said Daniel O’Day, CEO of Roche Phar­ma­ceu­ti­cals and for­mer di­ag­nos­tics chief, in a state­ment.

It’s a big win for Foun­da­tion Med­i­cine ex­ecs, who now get to op­er­ate as a “sep­a­rate and au­tonomous” unit.

Troy Cox

“Join­ing forces with Roche as an in­de­pen­dent op­er­at­ing com­pa­ny al­lows Foun­da­tion Med­i­cine to con­tin­ue its col­lab­o­ra­tion with Roche, as well as our bio­phar­ma part­ners, to dri­ve ubiq­ui­tous ac­cess to CGP test­ing and in­no­v­a­tive da­ta ser­vices,” said Foun­da­tion Med­i­cine CEO Troy Cox.

The deal is ex­pect­ed to close in sec­ond half of 2018. Citi and Davis Polk & Ward­well are the fi­nan­cial ad­vis­ers and le­gal coun­sel to Roche, re­spec­tive­ly, while Gold­man Sachs and Good­win Proc­ter ad­vised and coun­seled for Foun­da­tion Med­i­cine.

Health­care Dis­par­i­ties and Sick­le Cell Dis­ease

In the complicated U.S. healthcare system, navigating a serious illness such as cancer or heart disease can be remarkably challenging for patients and caregivers. When that illness is classified as a rare disease, those challenges can become even more acute. And when that rare disease occurs in a population that experiences health disparities, such as people with sickle cell disease (SCD) who are primarily Black and Latino, challenges can become almost insurmountable.

The End­points 11: They've got mad mon­ey and huge am­bi­tions. It's time to go big or go home

These days, selecting a group of private biotechs for the Endpoints 11 spotlight begins with a sprint to get ahead of IPOs and the M&A teams at Big Pharma. I’ve had a couple of faceplants earlier this year, watching some of the biotechs on my short list choose a quick leap onto Nasdaq or into the arms of a buyer.

Vividion, you would have been a great pick for the Endpoints 11. I’m sorry I missed you.

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Dave Lennon, former president of Novartis Gene Therapies

So what hap­pened with No­var­tis Gene Ther­a­pies? Here's your an­swer

Over the last couple of days it’s become clear that the gene therapy division at Novartis has quietly undergone a major reorganization. We learned on Monday that Dave Lennon, who had pursued a high-profile role as president of the unit with 1,500 people, had left the pharma giant to take over as CEO of a startup.

Like a lot of the majors, Novartis is an open highway for head hunters, or anyone looking to staff a startup. So that was news but not completely unexpected.

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Jacob Van Naarden (Eli Lilly)

Ex­clu­sives: Eli Lil­ly out to crash the megablock­buster PD-(L)1 par­ty with 'dis­rup­tive' pric­ing; re­veals can­cer biotech buy­out

It’s taken 7 years, but Eli Lilly is promising to finally start hammering the small and affluent PD-(L)1 club with a “disruptive” pricing strategy for their checkpoint therapy allied with China’s Innovent.

Lilly in-licensed global rights to sintilimab a year ago, building on the China alliance they have with Innovent. That cost the pharma giant $200 million in cash upfront, which they plan to capitalize on now with a long-awaited plan to bust up the high-price market in lung cancer and other cancers that have created a market worth tens of billions of dollars.

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Who are the women su­per­charg­ing bio­phar­ma R&D? Nom­i­nate them for this year's spe­cial re­port

The biotech industry has faced repeated calls to diversify its workforce — and in the last year, those calls got a lot louder. Though women account for just under half of all biotech employees around the world, they occupy very few places in C-suites, and even fewer make it to the helm.

Some companies are listening, according to a recent BIO survey which showed that this year’s companies were 2.5 times more likely to have a diversity and inclusion program compared to last year’s sample. But we still have a long way to go. Women represent just 31% of biotech executives, BIO reported. And those numbers are even more stark for women of color.

FDA+ roundup: Bs­U­FA III ready for show­time, court tells FDA to re-work com­pound­ing plan, new guid­ance up­dates and more

The FDA has now spelled out what exactly will be included in the third iteration of Biosimilar User Fee Act (BsUFA) from 2023 through 2027, which similarly to the prescription drug deal, sets fees that industry has to pay for submitting applications, in exchange for firm timelines that the agency must meet.

This latest deal includes several sweeteners for the biosimilar industry, which has yet to make great strides in the US market, with shorter review timelines for safety labeling updates and updates to add or remove an indication that does not contain efficacy data.

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Paul Hudson, Sanofi CEO (Raphael Lafargue/Abaca/Sipa USA; Sipa via AP Images)

In­side look: How a po­ten­tial part­ner­ship turned in­to a $1.9B buy­out for Sanofi

A couple of months before the FDA was set to make a decision on Kadmon’s so-called “knock-your-socks-off kind of results” for its chronic graft-versus-host disease drug, Sanofi put out feelers for a potential collaboration. But an early approval triggered an offer to buy the company outright — and Sanofi didn’t win without a fight, according to an inside look.

Sanofi’s head of business development and licensing Matthieu Merlin reached out to Kadmon on June 26 with a simple request: He wanted to introduce himself and explore potential partnerships, according to an SEC filing. It had been several months since Kadmon’s belumosudil arrived on the FDA’s doorstep, and after delaying their decision once, regulators said they’d have an answer by Aug. 30. But Sanofi wasn’t the only company interested in getting to know the execs over at Kadmon.

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Jean Bennett (Brent N. Clarke/Invision/AP Images)

Lux­tur­na in­ven­tor Jean Ben­nett starts a new gene ther­a­py com­pa­ny to tack­le rare dis­eases left be­hind by phar­ma, VCs

A few years ago Jean Bennett found herself in a surprising place for a woman who invented the first gene therapy ever approved in the United States: No one, it seemed, wanted her work.

Bennett, who designed and co-developed Luxturna, approved in 2018 for a rare form of blindness, had kept building new gene therapies for eye diseases at her University of Pennsylvania lab. But although the results in animals looked promising, pharma companies and investors kept turning down the pedigreed ophthalmology professor.

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Maureen Hillenmeyer, Hexagon Bio CEO

Hexa­gon Bio rais­es $61M to con­tin­ue ef­forts to turn fun­gi in­to drugs

A year after raising a $47 million launch round, the fungi-loving drug hunters at Hexagon Bio have more than doubled their coffers.

Hexagon announced today that it raised another $61 million for its efforts to design cancer and infectious disease drugs based on insights mined from the DNA in millions of species of fungi. The new financing brings Hexagon’s committed funding to over $108 million.