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March 20, 2019

Today's Rundown

Featured Story

Pfizer eyes Fierce 15 winner Vivet buy as gene therapy fever heats up

Vivet is in the crosshairs of Big Pharma Pfizer as the U.S. giant looks to get in on the new industry craze of buying up small gene therapy biotechs.

Top Stories

NGM Bio gains Genentech, Lilly veteran as new R&D chief

It’s a pretty good news day for NGM Bio: Merck doubled down on its R&D pact, and it’s nabbed a Genentech executive to help run its trials.

Merck doubles down on NGM Bio pact, but culls obesity drug

Back in 2015, Merck penned a $450 million R&D pact with little NGM Bio for a broad range of early-stage assets. Today, Merck is extending this pact, although it’s also tidying up shop with the culling of one particular therapy that didn’t work out.

Flagship Pioneering adds a new $824M biotech growth fund

Flagship Pioneering has raised $824 million for a new fund to support biotech and health companies that have come up through its Flagship Labs foundry. The new fund, dubbed the Special Opportunities Fund II, eclipsed its predecessor, the Special Opportunities Fund I, which raised $285 million in 2016.

ACC: Merck anacetrapib reveal bodes neutral at best for DalCor’s dalcetrapib

At the annual meeting of the American College of Cardiology this week, a new analysis of data for Merck’s anacetrapib cast a shadow on DalCor’s hypothesis—that CETP inhibitors, a class that has failed in broad heart disease populations, may prove useful in patients with certain genetic variants.

Alexion strikes another anti-FcRn deal, bagging Affibody drug

Alexion has paid Affibody $25 million (€22 million) to codevelop a treatment for rare IgG-mediated autoimmune diseases. The deal gives Alexion rights to an anti-FcRn drug designed to have a longer half-life than rival assets in development at Argenx, UCB and other companies.

WHO panel pushes for genome editing research registry

A WHO advisory committee has spoken out against clinical applications of human germline genome editing. The panel, which formed in the wake of China’s germline modification scandal, wants WHO to create a central registry on human genome editing research as part of an effort to boost global governance of the field.

A liquid biopsy that combines Illumina’s ‘ultradeep’ sequencing with Grail’s machine learning

Scientists have been working on new ways to increase the sensitivity of blood tests for detecting cancer, known as liquid biopsies. Now, a consortium of scientists from three top U.S. cancer research institutions, along with Illumina and Grail, have developed a new assay that could detect multiple targetable cancer mutations with a high degree of accuracy.

Sage wins OK for depression drug Zulresso. Up next? Major marketing challenges

Sage Therapeutics has the first-ever approval for a postpartum depression drug, thanks to the FDA’s Tuesday green light for Zulresso. But it also faces some big challenges in launching the new drug: its 60-hour infusion time, for instance.

Resources

[Article] Are you ready for 2008 Microsoft SQL and Windows Servers end of life?

Software end of life puts you at risk for data breaches, business disruption and liability. Support for Microsoft SQL Server 2008/2008 R2 and Windows Server 2008/2008 R2 ends on July 9, 2019 and January 14, 2020, respectively. Learn how you can turn these risks into a strategic business advantage.

[Case Study] TriCore Reference Laboratories Transforms to Clinical Lab 2.0 Model

Analytics using patients’ real-time longitudinal laboratory results, and claims data, yielded higher value information and new revenue streams for TriCore reference laboratories.

[Whitepaper] Accelerating Clinical Trials through Access to Real-World Patient Data

Whitepaper on leveraging normalized real-world patient data to streamline clinical trials, reduce delays and lower costs.

[Whitepaper] The Right Partner Can Improve Flexibility and Mitigate Risks from Forecast Inaccuracy in Biomanufacturing

The Right Partner Can Improve Flexibility and Mitigate Risks from Forecast Inaccuracy in Biomanufacturing.

[Whitepaper] How changes in drug substance processes can affect formulation

Download this whitepaper to learn more.

[Research] Maximize Pharma Marketing ROI with Digital HCP Engagement

Which HCP Touchpoints and channels are yielding the best results in today’s digital world?

[Whitepaper] Cell-Based Cancer Immunotherapies: Commercial Risk, Curative Reward

White paper outlining the key types of cell-based immunotherapies in oncology, as well as the development and commercial outlook for each.

[Whitepaper] Better Market Intelligence With Smart Search

It’s never been more challenging to stay on top of trends and innovation shaping the future of healthcare. Discover how AI can help competitive intelligence teams achieve more proactive strategies.

[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.

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