Andrew Hopkins, Exscientia

Black­Rock push­es Ex­sci­en­tia Se­ries C to $100M as AI biotech boom con­tin­ues

The ju­ry’s still out on whether the first wave of AI com­pa­nies can sig­nif­i­cant­ly change drug de­vel­op­ment, but in­vestors are in­creas­ing­ly buy­ing in­to the hype.

Ex­sci­en­tia, the decade-old UK ma­chine learn­ing out­fit, an­nounced Thurs­day that they’ve ex­pand­ed their Se­ries C, first an­nounced in May, from $60 mil­lion to $100 mil­lion. The ex­pan­sion most no­tably in­cludes Black­Rock, the pri­vate eq­ui­ty firm that has been wad­ing deep­er and deep­er in­to biotech. They now join No­vo Hold­ings, Bris­tol My­ers Squibb and oth­ers among the com­pa­ny’s most re­cent back­ers.

William Abecas­sis

“Ex­sci­en­tia is break­ing ground in small mol­e­cule drug de­sign, with a plat­form that rad­i­cal­ly im­proves drug dis­cov­ery” William Abecas­sis, head of Black­Rock’s biotech fund In­no­va­tion Cap­i­tal, said in a state­ment. “We are thrilled to be in­vest­ing in this world-class team, who are al­ready de­liv­er­ing re­sults with AI-de­signed drugs now en­ter­ing clin­i­cal tri­als.”

One of the first AI biotechs that emerged in the ear­ly 2010s promis­ing to ac­cel­er­ate drug de­vel­op­ment by screen­ing for mol­e­cules far faster than hu­man chemists, Ex­sci­en­tia an­nounced in 2020 that they brought the first AI-dis­cov­ered drug in­to hu­man tri­als. It was a du­bi­ous claim, de­pen­dent on pre­cise­ly what one means by AI-de­vel­oped; Re­cur­sion Phar­ma­ceu­ti­cals had claimed the same man­tle not long be­fore.

Still, Ex­sci­en­tia has emerged as a clear win­ner of the first round of AI drug de­vel­op­ers, part­ner­ing with Bay­er, Bris­tol My­ers, Sanofi, Glax­o­SmithK­line, Evotec and Sum­it­o­mo Da­nip­pon among oth­ers.

Oth­er com­pa­nies that emerged around the same time have al­so found mo­men­tum and dol­lars. Re­cur­sion land­ed a $239 mil­lion mega-round and a $1 bil­lion Bay­er part­ner­ship in Sep­tem­ber.  Atom­wise, a com­pa­ny that start­ed out at Y Com­bi­na­tor and re­ceived crit­i­cism for over­hyp­ing its ser­vices, more than tripled its to­tal ever fundrais­ing with a $123 mil­lion Se­ries B.

At the same time, oth­er com­pa­nies have popped up, most promi­nent­ly Daphne Koller’s In­sitro, which raised near­ly $250 mil­lion and scored a big-mon­ey part­ner­ship with Gilead with­in 2 years of its 2018 launch. But al­so a raft of oth­er small­er biotechs, in­clud­ing Gen­e­sis Ther­a­peu­tics and Rever­ie Labs, that have launched teamed with big biotech or Big Phar­ma and raised small to mid-sized rounds.

The pan­dem­ic al­so brought the AI field one of its first con­crete suc­cess­es: Ear­ly in the out­break, Benev­o­lent AI iden­ti­fied Eli Lil­ly’s JAK in­hibitor baric­i­tinib as a po­ten­tial treat­ment for Covid-19. Lil­ly pushed it through pre­clin­i­cal and clin­i­cal de­vel­op­ment on their sug­ges­tion, even­tu­al­ly show­ing it im­proved time-to-re­cov­ery in hos­pi­tal­ized pa­tients and land­ing an EUA from the FDA.

Ex­sci­en­tia will use the cash to keep scal­ing the ma­chine learn­ing plat­form they’ve used to iden­ti­fy can­di­dates for Big Phar­ma but al­so to ex­pand their abil­i­ty to de­vel­op their own pipeline of drugs. It’s a piv­ot sev­er­al of the first AI biotechs have made as they raise more cap­i­tal and ex­pand op­er­a­tions. Ex­sci­en­tia said they’ve dou­bled in size over the past year and now em­ploy over 100 peo­ple.

“We are de­light­ed that Black­Rock shares our vi­sion for rev­o­lu­tion­is­ing how drugs are dis­cov­ered,” CEO An­drew Hop­kins said in a state­ment. “Black­Rock’s in­vest­ment is an im­por­tant step in our vi­sion that all drugs will be de­signed by AI. I be­lieve that our com­pa­ny’s reimag­ined ap­proach to drug dis­cov­ery will be­come the new de fac­to stan­dard.”

Image courtesy of The Janssen Pharmaceutical Companies of Johnson & Johnson.

Pro­tect­ing the glob­al phar­ma­ceu­ti­cal in­no­va­tion ecosys­tem – what’s at stake?

We are living in a new era of healthcare that is rapidly advancing progress impacting patient outcomes and experiences. We’ve seen a remarkable pace of transformational innovation, applied research, and advanced clinical development over the last decade.

Despite this tremendous progress, there is much more work to be done, and patients are counting on us – now more than ever – to continue that momentum. At the heart of our industry is a focus on developing and delivering medicines for some of the world’s most challenging diseases, including those that have few or no effective treatments today.

The Modulo Bio team with CEO Michael Horowitz (fourth from right in semicircle)

Ex­clu­sive: With $8M, neu­ro start­up Mod­u­lo Bio emerges to test small mol­e­cules for ALS, de­men­tia in CEO’s per­son­al mis­sion

Embarking on a personal mission after his best friend’s mother was diagnosed with a mutation-driven case of frontotemporal dementia, Michael Horowitz has pulled together $8 million in venture funding at Modulo Bio to create small molecules for neurodegenerative diseases.

The San Diego and Bay Area biotech will select its lead development candidate and some backup options within six months and then raise a Series A to investigate therapeutics for C9orf72 mutation-driven cases of ALS and frontotemporal dementia, Horowitz told Endpoints News.

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Roger Perlmutter, Eikon Therapeutics CEO

Roger Perl­mut­ter builds Eikon's pipeline with deal-mak­ing flur­ry, rais­ing $106M more

Eikon Therapeutics announced three business development deals on Thursday, effectively dropping in a pipeline of cancer drugs alongside more than $100 million in fresh funding.

The Hayward, CA-based company has become one of biotech’s richest startups since its 2019 founding, having raised nearly $775 million. It’s developing a massive, automated research approach built around Nobel Prize-winning microscope science to peer inside cells and watch proteins in action. After its Series B last year, PitchBook reported a $3.02 billion valuation. And while CEO Roger Perlmutter declined to comment on that figure, he said its first tranche of nearly $106 million in Series C funding is a “meaningful step-up to our Series B valuation.”

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Eu­ro­pean Par­lia­ment calls mem­ber states to ac­tion on an­timi­cro­bial re­sis­tance

Members of the European Parliament have called on EU countries to develop national action plans against antimicrobial resistance (AMR), calling it a top-three priority health threat.

Parliament on Thursday announced recommendations for the fight against AMR, including national action plans that must be updated at least every two years, an EU-level database tracking AMR and antimicrobial use and increased partnership between the pharma industry, patient groups and academia.

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Roche plans to di­vest from lega­cy Genen­tech man­u­fac­tur­ing fa­cil­i­ty in Cal­i­for­nia

Roche is planning to make some changes to its subsidiary’s manufacturing network in California.

The Swiss pharma announced Wednesday that it plans to divest from Genentech’s manufacturing facility in Vacaville, CA, around 58 miles northeast of San Francisco. According to a statement from Roche, the move is part of a “broader strategy” to bring its manufacturing capabilities in line with its future pipeline. Roche is starting the process of finding a buyer for the site but has not named any candidates yet.

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Peter van de Sande, Synaffix CEO

Lon­za shells out $107M cash to snap up Synaf­fix and its ADC plat­form

After lining up a string of partnerships over the years, Dutch antibody-drug conjugate specialist Synaffix has found a new home: Lonza, the contract development and manufacturing giant.

Lonza is paying about $107 million (€100 million) in cash to acquire Synaffix, with up to $64 million (€60 million) in “additional performance-based consideration” on the table. Synaffix’s ADC tech platform will now become part of Lonza’s offering for biopharma clients, lending its bioconjugate technologies to not just ADCs but also targeted gene therapy, immune cell engagers and other applications.

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Who's con­fi­dent­ly in­vest­ing in biotech star­tups dur­ing these tense days? We've got some an­swers

We’ve got a changeup to our event schedule in Boston next week, where we’ll be doing a mix of live/streaming events at our base at The Seaport Hotel as part of a two-day lineup of webinars, virtual firesides and a cocktail hour Q&A with a veteran of the biotech financing scene.

The 9:30-10:30 am ET live slot on Tuesday, June 6, will now feature a panel conversation on the current state of affairs for VC investing in biotech, focusing on what startups are getting cash — and how. Alaa Halawa, head of US ventures at Mubadala, is confirmed, along with Brian Goodman at MPM and Geoff von Maltzahn, a general partner at Moderna-buoyed Flagship. I have a couple of other invites out and will let you know how that plays out.

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Albert Bourla, Pfizer CEO (Michel Euler/AP Images, Pool)

FDA ap­proves Pfiz­er’s RSV shot for old­er adults, tee­ing up a com­pet­i­tive $17B vac­cine mar­ket

The FDA approved Pfizer’s RSV vaccine called Abrysvo for older adults on Wednesday, placing another Big Pharma onto the commercial stage ahead of the next RSV season.

Pfizer’s approval comes weeks after GSK won approval for its rival shot, Arexvy. Those two vaccines are both approved for use in adults 60 years and older and will be reviewed by a CDC panel in June before they’re expected to commercially launch this fall. Wall Street analysts see RSV as the next multibillion-dollar vaccine market, with Jefferies analysts recently forecasting the RSV market will grow to $17 billion over the next decade.

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Richard Pazdur, FDA's OCE director (Flatiron Health via YouTube)

FDA's can­cer chief weighs in on com­mon chemo short­ages — re­port

Richard Pazdur, director of the FDA’s Oncology Center of Excellence, attributes the current shortage of two cancer drugs to drug companies that haven’t invested in building out their production capacity.

In an interview with The Cancer Letter, a weekly cancer publication, Pazdur said that the current shortages of cisplatin and carboplatin, a pair of drugs used to treat a wide range of cancer patients, are the result of two problems: manufacturers not investing in enhancing production capacity, and drug companies being dependent on one supplier of raw ingredients. The cisplatin shortage followed an inspection that revealed quality issues at a manufacturing facility, which then led to the shutdown of production. This led to a surge in carboplatin demand, creating a secondary shortage.

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