Laurie Glimcher and Ansbert Gadicke (Justin Knight, Dana-Farber Cancer Institute)

Ty­ing ba­sic sci­ence to spin­outs, Dana-Far­ber de­buts sis­ter funds to­tal­ing $126M with MPM Cap­i­tal

As one of the most pres­ti­gious can­cer in­sti­tutes in the US, Dana-Far­ber has en­joyed con­sid­er­able sup­port for its en­tre­pre­neur­ial pur­suits, spin­ning out about 30 com­pa­nies in the past 12 years.

Bar­rett Rollins

“Now where we’ve al­ways strug­gled — where every can­cer cen­ter strug­gled — is sup­port of ba­sic sci­ence,” Bar­rett Rollins, chief sci­en­tif­ic of­fi­cer emer­i­tus, told End­points News.

And then two of its trustees had an idea. What if they tied phil­an­thropy to in­vest­ment in Dana-Far­ber star­tups, re­quir­ing a do­na­tion to ba­sic sci­ence as a con­di­tion for ac­cess­ing its bright­est biotech ven­ture ideas?

Eight years of in­vestor-vet­ting and mod­el-re­fin­ing lat­er, it’s raised $26 mil­lion for the phil­an­thropic fund and set­tled on a gen­er­al part­ner to man­age the “sis­ter” ven­ture fund: MPM Cap­i­tal.

The $100 mil­lion On­col­o­gy In­no­va­tion Fund will com­ple­ment the $1 bil­lion MPM has re­served for on­col­o­gy in­vest­ing, Ans­bert Gadicke, co-founder and man­ag­ing di­rec­tor, said. It in­cludes a $400 mil­lion ven­ture cap­i­tal fund and $700 mil­lion crossover fund — with on­col­o­gy sit­ting as the num­ber 1 fo­cus at the firm.

Around half of the fund will go to­ward new spin­outs from Dana-Far­ber that MPM will help launch, he added. All told, he ex­pects to back 15 star­tups with this fund, some of which could be fledg­lings from oth­er aca­d­e­m­ic in­sti­tu­tions or start­ed by fel­low VCs. Six in­vest­ments are al­ready un­der­way.

“We like to have that lev­el of di­ver­si­fi­ca­tion but what still al­lows us to be con­cen­trat­ed and make mean­ing­ful in­vest­ments in each com­pa­ny,” Gadicke said.

MPM has full con­trol over the fund, while Dana-Far­ber — led by Lau­rie Glim­ch­er — is whol­ly re­spon­si­ble for how to spend their phil­an­thropic mon­ey.

Much re­mains to be ex­plored in both ge­net­ic con­trol of can­cer and ear­ly de­tec­tion/pre­ven­tion work, ac­cord­ing to Rollins. And then there’s the re­lent­less tide of im­muno-on­col­o­gy — a field that he said Dana-Far­ber pi­o­neered 40 years ago. In fact, the in­sti­tute has pre­vi­ous­ly worked with MPM to pour Ar­lene Sharpe, Gor­don Free­man and Vi­jay Kuchroo’s find­ings in­to CoS­tim Phar­ma­ceu­ti­cals, lat­er ac­quired by No­var­tis. Tizona Ther­a­peu­tics, the Ab­b­Vie-part­nered biotech that Gadicke de­scribed as the star of the port­fo­lio, is al­so fo­cused on im­munother­a­py.

“The rea­son why that’s such a great ex­am­ple is be­cause the dis­cov­ery of PD-L1 and PD-1 ef­fect by Gor­don were the re­sult of this undi­rect­ed cu­rios­i­ty-dri­ven ba­sic sci­ence which is the tar­get of the phil­an­thropic fund,” Rollins said.

The plan is to of­fer $1 mil­lion grants to two to four such projects each year over the next four to five years, hire a new ju­nior fac­ul­ty mem­ber and pur­chase some ex­pen­sive equip­ment with the rest of the fund.

No­var­tis reshuf­fles its wild cards; Tough sell for Bio­gen? Googling pro­teins; Ken Fra­zier's new gig; and more

Welcome back to Endpoints Weekly, your review of the week’s top biopharma headlines. Want this in your inbox every Saturday morning? Current Endpoints readers can visit their reader profile to add Endpoints Weekly. New to Endpoints? Sign up here.

If you enjoy the People section in this report, you may also want to check out Peer Review, my colleagues Alex Hoffman and Kathy Wong’s comprehensive compilation of comings and goings in biopharma.

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Demis Hassabis, DeepMind CEO (Qianlong/Imaginechina via AP Images)

Google's Deep­Mind opens its pro­tein data­base to sci­ence — po­ten­tial­ly crack­ing drug R&D wide open

Nearly a year ago, Google’s AI outfit DeepMind announced they had cracked one of the oldest problems in biology: predicting a protein’s structure from its sequence alone. Now they’ve turned that software on nearly every human protein and hundreds of thousands of additional proteins from organisms important to medical research, such as fruit flies, mice and malaria parasite.

The new database of roughly 350,000 protein sequences and structures represents a potentially monumental achievement for the life sciences, one that could hasten new biological insights and the development of new drugs. DeepMind said it will be free and accessible to all researchers and companies.

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In­side Bio­gen's scram­ble to sell Aduhelm: Pro­ject 'Javelin' and pres­sure to ID as many pa­tients as pos­si­ble

In anticipation of Aduhelm’s approval for Alzheimer’s in June, Biogen employees were directed to identify and guarantee treatment centers would administer the drug through a program called “Javelin,” a senior Biogen employee told Endpoints News.

The program identified about 800 centers for use, he said, and Biogen now pays for the use of bioassays to identify beta amyloid in potential patients having undergone a lumbar puncture procedure, the employee said — and one center preparing to administer the drug confirmed its participation in the bioassay program.

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Vas Narasimhan, Novartis CEO (Jason Alden/Bloomberg via Getty Images)

No­var­tis dis­cards one of its ‘wild card’ drugs af­ter it flops in key study. But it takes one more for the hand

Always remember just how risky it is to gamble big on small studies.

A little more than 4 years ago, Novartis reportedly put up a package worth up to $1 billion for the dry eye drug ECF843 after a small biotech called Lubris put it through its paces in a tiny study of 40 moderate to severe patients, tracking some statistically significant markers of efficacy.

By last fall, the program had risen up to become one of CEO Vas Narasimhan’s top “wild card” programs in line for a potential breakthrough year in 2021. These drugs were all considered high-risk, high-reward efforts. And in this case, risk won.

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UP­DAT­ED: Three biotechs price hefty IPOs just be­fore the week­end, while a fourth and a SPAC seek spots on Wall Street

Editor’s note: Interested in following biopharma’s fast-paced IPO market? You can bookmark our IPO Tracker here.

A handful of biotechs are hitting Wall Street just before the start of the weekend, with three companies — Caribou Biosciences, Sophia Genetics and Absci — all pricing big raises Wednesday and Thursday. Gamma delta T cell-focused IN8bio relaunched its IPO campaign months after postponing it last November, seeking a slightly lower raise. And another SPAC has filed for a public debut.

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Victor Perlroth, Kodiak Sciences CEO

Ko­di­ak turns down $125M pay­ment from Bak­er Bros. deal, slash­es roy­al­ty cap by 55%

Following a massive public raise last November, Kodiak Sciences has re-worked a royalty sale agreement with an old partner — and declined new funds in the process.

Kodiak is turning down a planned $125 million payment from Baker Bros. Advisors, according to an SEC filing, cutting short an agreement that saw the biotech hand over a 4.5% stream of royalty sales on its experimental anti-VEGF therapy KSI-301 for retinal vascular diseases. In conjunction with the move, Kodiak is shrinking the royalty cap from just over $1 billion to $450 million.

EMA re­jects FDA-ap­proved Parkin­son's drug, signs off on Mod­er­na vac­cine use in ado­les­cents ahead of FDA

The European Medicines Agency on Friday rejected Kyowa Kirin’s Parkinson’s disease drug Nouryant (istradefylline), which the US FDA approved in 2019 under the brand name Nourianz.

EMA said it considered that the results of the clinical studies used to support the application “were inconsistent and did not satisfactorily show that Nouryant was effective at reducing the ‘off’ time. Only four out of the eight studies showed a reduction in ‘off’ time, and the effect did not increase with an increased dose of Nouryant.”

6 top drug­mak­ers of­fer per­spec­tives on FDA's new co­vari­ates in RCTs guid­ance

Back in May, the FDA revised and expanded a 2019 draft guidance that spells out how to adjust for covariates in the statistical analysis of randomized controlled trials.

Building on the ICH’s E9 guideline on the statistical principles for clinical trials, the 3-page draft was transformed into an 8-page draft, with more detailed recommendations on linear and nonlinear models to analyze the efficacy endpoints in RCTs.

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Mol­e­c­u­lar Di­ag­nos­tics Can Trans­form Can­cer Care. Let’s Make It Hap­pen.

Like so many people around the world, my life has been profoundly shaped by cancer. Those personal experiences, along with a deep love of clinical laboratory science and a passion to apply the power of genomics in medicine, motivated me to launch a company that would improve cancer care through better diagnostics. Thirteen years later, I am proud that we are delivering more accurate information at multiple points along the patient journey, with a focus on eight of the 10 cancers that are most commonly diagnosed in the United States.