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May 24, 2019

Welcome to FierceLifeSci Weekly Digest, your roundup of the biggest and most popular stories from each of our publications.


As the definition of a medical device has begun to stretch, so has the definition of a medical device company. Prescription software and at-home DNA tests have begun to fit the bill, as have previously consumer-focused companies making their first moves into healthcare. But in our special report on 2018’s top 11 medtech approvals, it’s clear that the devices most likely to change a patient’s life are the ones designed to change their routines the least.

Featured Story

AbbVie's discounting Humira to aid Skyrizi's launch—and a price war could follow: analyst

AbbVie has big plans to grow sales for Humira follow-ups Skyrizi and upadacitinib. Early into its Skyrizi launch for psoriasis, the company has offered discounts on its megablockbuster Humira to secure favorable formulary coverage for its new drug, an analyst writes. 

Top Stories Of The Week

Merck boosts late-phase cancer pipeline with $1.1B Peloton buy

Merck has struck a deal to buy Peloton Therapeutics for $1.1 billion upfront days before the biotech was due to list on Nasdaq. The deal will give Merck control of an experimental oral HIF-2α inhibitor that could challenge Keytruda for the metastatic renal cell carcinoma market.

Special Report—The top 11 medtech approvals of 2018

The once-straightforward definition of a medical device has begun to stretch. And for that matter, so has the definition of a medical devices company. But 2018’s top FDA green lights made one thing clear: The devices most likely to change a patient's life were designed to change their routines the least.

Novartis CEO calls for new drug payment model ahead of Zolgensma launch

Novartis is looking to launch spinal muscular atrophy gene therapy Zolgensma this year. But the possibility of it being a $5 million drug has already sparked controversy. To prepare for the pricey rollout, CEO Vas Narasimhan now calls for changes to the U.S. drug payment system.

Glioblastoma claims another pharma victim as AbbVie's ADC fails to boost survival

Alongside pancreatic cancer, the aggressive brain cancer glioblastoma is one of the toughest cancers out there. Now, AbbVie is yet another biopharma learning that lesson firsthand.

Editor's Choice—Novartis, Otsuka, Pfizer, Sanofi join Verily's Project Baseline

Novartis, Otsuka, Pfizer and Sanofi have signed onto Verily’s Project Baseline, a program aimed at mapping out a baseline for human health.

Editor's Choice—Merck's powerhouse Keytruda whiffs breast cancer trial, delaying hopes for new use

Right now, Roche’s Tecentriq is the only immuno-oncology drug approved in triple negative breast cancer. And thanks to a rare trial miss for Merck's superstar Keytruda, it looks like it’ll stay that way for awhile.

FBI investigating J&J, Siemens, GE and Philips’ roles in Brazilian corruption probe: Reuters

The FBI has launched its own investigation into a handful of the world’s largest medtech companies, stemming from claims of illegal kickbacks being paid to Brazilian government officials over the past 20 years—in return for contracts through the country’s public health programs that administer over 210 million people, according to a report from Reuters.

CSL Behring poaches top manufacturing executive from struggling Biogen

When Biogen recently announced its top dog for manufacturing and supply chain operations was leaving to become chief operating officer for another company, the question was, which one? The question has now been answered with the announcement that Paul McKenzie has taken that post at CSL Behring, the drug and plasma unit of Australia's CSL Ltd.

Seattle Genetics taps pharma oncology veteran as first-ever chief commercial officer

Now well on its way to becoming a multiproduct oncology company, Seattle Genetics has decided the time is right to bring in its first chief commercial officer.

New insight into a struggling AstraZeneca anti-VEGF drug could expand its use in cancer

AstraZeneca’s experimental cancer drug cediranib was originally developed to inhibit the growth of the blood vessels tumors need to survive, but it hasn’t proven to be all that effective. Now Yale University researchers have discovered that cediranib has a second function that could improve its prospects for treating cancer.

Resources

[Executive Summary] Achieving a Successful Drug Product Tech Transfer

Download the executive summary to learn key considerations for a successful technology transfer for manufacturing drug products, including a case study on overcoming challenges in a process transfer for a sterile diluent.

[Whitepaper] Choosing the Best Sterile Dosage Form for Phase I Clinical Supply Needs

Choosing the Best Sterile Dosage Form for Your Phase I Clinical Supply Needs.

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[Whitepaper] Agile Competitive Intelligence: A 3-Step Mobile Research Strategy

What is agile competitive intelligence, and how can help healthcare researchers stay ahead of the curve?

[eBook] 2018 Weekly Compendium

The Biopharma industry is moving at lightning speed and it can be a challenge to keep pace. Here at Biotech Primer we spend hours each week researching, writing, and editing original content for the Biotech Primer WEEKLY with one goal in mind: to help everyone better understand the latest science and technology driving today’s healthcare industry.