Marrying precision med and AI, Groupon co-founder Eric Lefkofsky takes total haul for his analytics firm over the $1B line

Amber Tong

Senior Editor

The pandemic has taken Tempus — the company Groupon co-founder Eric Lefkofsky launched to bring artificial intelligence to physicians and researchers focused on precision medicine — in quite a few unexpected turns.

Not only did it launch efforts to help doctors in their core field of cancer adapt to new ways of working, it also made a decision to expand into infectious diseases (starting with Covid-19), while doubling down on depression and cardiology.

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Marrying precision med and AI, Groupon co-founder Eric Lefkofsky takes total haul for his analytics firm over the $1B line

Amber Tong

Senior Editor

Unlock this article instantly by becoming a free subscriber.

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Mar­ry­ing pre­ci­sion med and AI, Groupon co-founder Er­ic Lefkof­sky takes to­tal haul for his an­a­lyt­ics firm over the $1B line

Amber Tong

Senior Editor

Unlock this article instantly by becoming a free subscriber.

Ab­b­Vie makes sec­ond deal in a week, bet­ting $8.7B in cash on CNS biotech Cerev­el

Pfiz­er plans to pull out of BIO, fol­low­ing moves by oth­er large drug­mak­ers to re­duce lob­by­ing foot­print

Aviv Regev leads Genen­tech's next rev­o­lu­tion with AI

FDA ap­proves No­var­tis drug for rare blood dis­or­der

FDA sends let­ter to No­var­tis over Kym­ri­ah man­u­fac­tur­ing safe­ty con­cerns

Ear­ly pre­dic­tion of out­comes in DL­B­CL clin­i­cal tri­als through MRD test­ing

Marrying precision med and AI, Groupon co-founder Eric Lefkofsky takes total haul for his analytics firm over the $1B line

AbbVie makes second deal in a week, betting $8.7B in cash on CNS biotech Cerevel

Pfizer plans to pull out of BIO, following moves by other large drugmakers to reduce lobbying footprint

Aviv Regev leads Genentech's next revolution with AI

FDA approves Novartis drug for rare blood disorder

FDA sends letter to Novartis over Kymriah manufacturing safety concerns

Early prediction of outcomes in DLBCL clinical trials through MRD testing