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WELCOME TO FIERCE LIFE SCIENCES WEEKLY DIGEST

After Regeneron established its position in the COVID-19 fight last year with one of the few antibody treatments to win the FDA’s blessing, stock awards led to massive, nine-figure paydays for both the company’s CEO and scientific chief. With that amount of money at play—and an unrelenting international spotlight on infectious disease research—many hope one pandemic silver lining will be progress against other persistent bugs. For example: AstraZeneca and Sanofi’s antibody, which protected healthy babies from respiratory syncytial virus in a phase 3 study—something Sanofi’s CEO described as a “massive opportunity.” Those stories, plus our list of the most sought-after biopharma assets of the past year, follow below.

 

Featured Story

AstraZeneca and Sanofi's antibody prevents RSV in phase 3, accelerating path to market

AstraZeneca and Sanofi’s nirsevimab has protected healthy babies against respiratory syncytial virus disease in a phase 3 clinical trial. The earlier-than-expected readout will enable a 2022 filing for a monoclonal antibody Sanofi CEO Paul Hudson has hailed as a “massive opportunity.”

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Top Stories Of The Week

Regeneron CEO Schleifer, chief scientist Yancopoulos bag massive $270M payday

Regeneron chief Len Schleifer earned a whopping $135 million in 2020 as the company opted to give its top execs years of front-loaded equity awards. Meanwhile, chief scientist George Yancopoulos made $134.38 million for the year.

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Special Report—The top 15 biopharma licensing deals of 2020

Oncology, specifically immuno-oncology, was the dominant theme in biopharma licensing last year, as cancer drugs accounted for half of the top deals.

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What are Merck, Bristol Myers and Roche planning for the big FDA cancer approval review? Here's our rundown

In a three-day meeting starting Tuesday, a panel of experts convened by the FDA will discuss whether the agency should revoke accelerated approvals from three cancer drugs that later failed confirmatory trials. Here's what the drugmakers—and the agency—are saying ahead of the meeting.

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Lilly scraps IL-23 psoriasis program despite phase 3 success, focuses on IBD race against AbbVie, J&J

Eli Lilly has scrapped plans to seek approval for mirikizumab in psoriasis. Lilly chose not to enter the crowded market despite the anti-IL-23p19 antibody outperforming Novartis' Cosentyx in a phase 3 trial last year.

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Pfizer weighs sale of Philly-area campus—where 2,000 once worked—as company mulls when and how to bring employees back

Pfizer said it’s considering the sale of its 1.89-million-square-foot office and laboratory space in Collegeville, Pennsylvania, as the company searches for a more “modern and flexible” workspace for returning employees.

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Inovio's COVID-19 vaccine funding axed as U.S. says thanks, but no thanks

U.S. officials have pulled the plug on funding a phase 3 trial for Inovio’s COVID-19 vaccine, telling the biotech that another vaccine is no longer needed as inoculations pick up around the country.

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Regeneron looks to inject another $330M into long-running manufacturing expansion plan: report

Regeneron first unveiled plans to build a $150 million facility at its Tarrytown campus in 2015, but the company is now planning to spend another $330 million for the project, a local news outlet reports.

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Could unclogging the brain's drainage system improve the efficacy of Biogen's aducanumab in Alzheimer's?

Scientists have proposed a possible explanation for the disappointing clinical trial results from Biogen's anti-amyloid Alzheimer's drug aducanumab. The team pointed to the brain’s newly discovered drainage system, suggesting drugs could be developed to enhance its function, in turn improving the efficacy of drugs like aducanumab.

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Big innovation shift to small pharma? Rookies grab lead in annual poll—and look to stay put

Pharma innovation is shifting from larger players to smaller companies, according to IDEA Pharma's annual tally—and it may not be temporary. Regeneron, Seagen and Incyte all landed in the top five, with the latter two joining after never before cracking the top 30.

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Illumina to move its oncology assay into blood-based cancers with companion diagnostic partnership

Following the launch of multiple tumor diagnostic partnerships with Big Pharma earlier this year for its TruSight Oncology 500 assay, Illumina now aims to expand the use of its genomic profiling test to blood-based cancers.

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Resources

Executive Brief: Seven Secrets to Patient Experience Breakthroughs: Improving the Patient Experience and Study Retention

The average clinical trial spends $40,000 per patient. Yet despite these high costs, most trials struggle to retain patients.

Article: Make the right move at every step of the drug commercialization process

Developing a quality product and getting it approved for distribution is not enough to guarantee commercial success.

eBook: The New Standard: Virtual Study Training in Clinical Trials

The new standards in study training help sponsors and CROs reduce costs by 60%, cut training time by 50%, and start enrollment 55 days faster – learn more today.

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: Process Intensification Resource Center

A one-stop hub for Cytiva resources to support process intesification

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?

Content Hub: Emerging Biotech Resource Center

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

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.

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.

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.