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WELCOME TO FIERCE LIFE SCIENCES WEEKLY DIGEST

After regulators on both sides of the Atlantic revealed probes into Johnson & Johnson’s COVID-19 vaccine, U.S. officials called for an immediate pause. Nearly 7 million shots have been delivered, and six women have been diagnosed with rare blood clots that have a tricky treatment regimen. One died and one is in critical condition. At the same time, a shortage of sterile plastic bags used to grow vaccine cells, at 2,000 liters apiece, has hampered Novavax's work to scale up its own shot—a scarcity the company’s CEO described as a threat to the global vaccine supply. Those stories, plus our top reads of the week, follow below.

Featured Story

Feds call halt to Johnson & Johnson COVID-19 vaccine rollout after 'extremely rare' blood clot cases

After drug regulators on both sides of the Atlantic revealed safety probes into Johnson & Johnson’s COVID-19 vaccine, U.S. officials have called for an immediate pause to the rollout.

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Top Stories Of The Week

MIT and UCSF researchers create CRISPR 'on-off switch' that controls gene expression without changing DNA

Researchers at the Massachusetts Institute of Technology and the University of California, San Francisco designed gene editing technology that changes gene expression without damaging DNA. They used it to silence the gene that makes the protein Tau, which has been implicated in Alzheimer’s disease.

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SPECIAL REPORT—The top 10 medtech M&A deals of 2020

Outside of unceasing demand for protective equipment, ventilator hardware and diagnostic tests, the COVID-19 pandemic brought many medical procedures to a standstill and slowed the rate of medtech mergers and acquisitions to a crawl. But last summer the dam burst, and money flowed like it could make up for lost time.

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Johnson & Johnson's COVID-19 vaccine under scrutiny at EMA after 4 'serious cases' of unusual blood clots

AstraZeneca’s COVID-19 vaccine has dominated headlines as reports of rare blood clots mounted, but, now, European drug safety regulators are investigating potential clotting risks from Johnson & Johnson’s vaccine. Like AstraZeneca's, the J&J shot is adenovirus-based.

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Sanofi pays $160M for mRNA tech to reprogram T cells in vivo

Sanofi has paid $160 million upfront to buy a preclinical biotech that is using mRNA to reprogram immune cells inside the human body. The technology could enable patients to make their own CAR-T cells, eliminating the complex cell therapy supply chain while improving safety and dosing.

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Merck posts early clinical data on subcutaneous Keytruda, setting stage for further studies 

Merck has presented early clinical data on subcutaneous formulations of its blockbuster checkpoint inhibitor Keytruda. The data drop is an early step in an ongoing effort to reformulate Keytruda ahead of the anticipated expiration of U.S. patents in 2028.

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Thermo Fisher reels in PPD for $17.4B as it looks to follow the LabCorp playbook

Thermo Fisher is spending a major $17.4 billion to buy out contract research organization PPD.

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Sanofi drops 'intriguing' data on rival to Bristol Myers' bempeg

Sanofi has posted early-phase data on its recombinant IL-2 molecule in solid tumor patients. Analysts at Jefferies called the data “intriguing” while noting it is currently hard to tell whether the drug improves on the IL-2 pathway agonist Bristol Myers Squibb is developing in partnership with Nektar Therapeutics. 

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New approaches to AI, cell biology may have uncovered a novel drug target for COVID-19: Humans themselves

By combining artificial intelligence and an extensive atlas of protein biology, Cyclica is taking new approaches to searching for old drugs that could fight COVID-19—and, now, it’s helped find what could become a first-in-class candidate.

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Plastic bag shortage a hefty problem for Novavax's COVID-19 vaccine production push

With its supply chain straining, Novavax has pushed back supply goals for its COVID-19 vaccine. The company's production push is hindered by a lack of raw materials, CEO Stan Erck said, including sterile plastic bags used to grow vaccine cells.

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Eli Lilly, riding pharma's rising digital wave, drafts Apple exec to replace Shah as CDO

Eli Lilly's new chief digital chief hails from Apple. The latest pharma to tap a consumer executive to head digital strategies, Lilly is swapping CDOs amid an accelerated shift to digital spurred by the pandemic.

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Resources

Whitepaper: COVID-19 Survey report: The Lasting Impact on Outsourcing Decisions

How has COVID-19 impacted CRO/CDMO customer (dis)satisfaction and outsourcing decisions for pharma and biotech companies in 2021 and beyond?

Whitepaper: Top 5 Benefits of a Cloud ELN

Discover the benefits of a cloud-native ELN that delivers better performance, security, connectivity, total cost of ownership PLUS sub-second search results through even the largest data volumes.

Content Hub: Emerging Biotech Resource Center

A one-stop hub for Cytiva resources to support process development and manufacturing of your novel molecule

Annual Report: Why do US pharma come to Russia for clinical trials.

Find out why more than 400 clinical trials annually are initiated in Russia by US and EU pharma in the free annual report by OCT Clinical.

Special Report: The Marketer’s Guide to Taking the Vaccine Viral

Access this guide for the latest insights into how marketers can use data, technology, and personalized messaging to build vaccine confidence and drive successful immunization efforts.

Report: New research indicates an accelerated shift to decentralized clinical trials

New research indicates an accelerated adoption of decentralized clinical trials due to COVID-19.

Content Hub: Remarque Systems Resource Hub

Remarque Systems consolidates data, then layers on visualization and automated metrics to generate consistent, actionable data insights in real-time. Click here for more info. 

Whitepaper: Overcoming the hurdles of Real-World Data Access through a federated global network

Those wishing to unlock RWD’s true value must have access to a variety of data sources/types and the technological capabilities to use the data to uncover meaningful insights. 

Report: New research indicates an accelerated shift to decentralized clinical trials

New research indicates an accelerated adoption of decentralized clinical trials due to COVID-19.

Content Hub: How to improve the virtual work you do every day

We enable virtual work — offering over-time sessions where participants are more focused, insights are more diverse and business goals are met.

Webinar: Age-Appropriate Formulation Development for Pediatric Trials-Challenges and Considerations

Hear industry experts discuss the recent advances, challenges and considerations in pediatric drug development. Real-life examples presented by the experts illustrate the impact of age-appropriate dose forms for pediatrics and highlight insights into the caregiver perspectives.

eBrief: Manufacturing Strategies to Effectively Industrialize Autologous Cell Therapies

Autologous cell therapies have seen propelled growth since 2017, with the spotlight on the first FDA approval of a chimeric antigen receptor (CAR) T cell immunotherapy, Kymriah® (tisagenlecleucel), for the treatment of relapsed/refractory B-cell acute lymphoblastic leukemia.

Q&A: Planning Successful Launches

Learn about proven strategies for a successful product launch, including cross-functional team collaboration, risk management and using the right project management tools.

Case Study: Establishing Parameters for Success

Learn about a real-world example of how clinical supply management expertise was applied to overcome inventory challenges for a complex, global study.

Fact Sheet: Forecasting to Optimize Clinical Trial Supply Management

Whether a study is simple or highly complex, forecasting and simulation reports serve as data driven communication tools to help minimize risks and keep the study on track. Learn more about forecasting solutions for informed decision making and supporting contingency planning for clinical study.