To view this email as a web page, click here

WELCOME TO FIERCE LIFE SCIENCES WEEKLY DIGEST

After stepping down as head of Merck’s R&D late last year, Roger Perlmutter has returned to take the helm of the new biotech Eikon Therapeutics, which raised $148 million to discover new drugs by using super-resolution microscopes to observe proteins in motion. Meanwhile, AstraZeneca’s Farxiga blockbuster gained a new landmark approval in chronic kidney disease—after nabbing a first-in-class heart failure nod just last year. It’s a pill that could one day make it to our annual list of top 20 drugs by global sales, with its ups-and-downs illustrating the trends in a changing international landscape.

Featured Story

AstraZeneca's diabetes drug Farxiga nabs coveted kidney disease nod, way ahead of rival Jardiance

AstraZeneca's diabetes med Farxiga stormed the heart failure market with a first-in-class approval last year—and in chronic kidney disease, it just left would-be rival Jardiance in the dust. 

read more

Top Stories Of The Week

Perlmutter named CEO of Eikon, a biotech with $148M to apply Nobel-winning tech to undruggable targets

Roger Perlmutter has taken up the CEO post at Eikon Therapeutics. The startup disclosed the hiring of the former president of Merck Research Laboratories alongside news that it has raised a $148 million series A round to apply live-cell super-resolution microscopy to drug discovery.

read more

The top 20 drugs by worldwide sales in 2020

While the global sales rankings of Big Pharma's superstar drugs naturally feature the biggest names in the business, new meds often pop up or old drugs exit the scene. And the moves within the list from year to year illustrate many of the trends shaping pharma on a daily basis. 

read more

Pfizer halts BCMA trial amid safety woes, hit by DMD delay

Pfizer has paused enrollment in a pivotal trial of its anti-BCMA bispecific antibody after seeing three cases of peripheral neuropathy in an earlier-stage study. The Big Pharma shared the news alongside details of a delay to the start of the U.S. part of its Duchenne muscular dystrophy (DMD) phase 3.

read more

Ahead of potential semaglutide approval in chronic obesity, Novo hits 'full go mode' for launch, exec says

Novo Nordisk has started the year on solid footing, thanks in no small part to its GLP-1 portfolio in Type 2 diabetes. With top earner semaglutide (approved in diabetes as Ozempic) due for a decision in obesity this June, the company is gearing up for a busy second half to the year.

read more

Novavax handed an extra $147M from legacy Warp Speed program as spotlight shines brighter

A biotech with a long and often troubled past is hoping 2021 will be its year, and it’s just been handed a major tranche of cash to help make that happen.

read more

With supply timelines more certain, Novavax closes in on a COVID-19 vaccine deal with Europe: report

Novavax has told the European Union that it will be ready to send COVID-19 vaccine shipments to Europe before the end of the year. That could help the biotech strike a supply agreement for hundreds of millions of doses.

read more

Apple Watch could gain long-sought glucose tracking with Rockley Photonics deal: report

While the Apple Watch has evolved from a fashionable phone accessory to a high-tech health monitor—capable of scanning for heart conditions and calling for help after injuries—future generations may tap into a deeper set of features to track the body’s inner workings.

read more

Glass half-full? Embattled AstraZeneca CEO Soriot defends COVID-19 vaccine

As the weeks turn to months on AstraZeneca’s COVID-19 vaccine filing in the U.S., the big question is when? Its answer remains the same—soon. But with so many other shots available, why bother?

read more

How new 'lung-on-a-chip' models from Harvard are advancing COVID-19 drug discovery

Pitting COVID-19 drug candidates against the virus in cell cultures doesn’t accurately predict how effective they’ll be in the human respiratory tract. Now more accurate models of the human lung airway are uncovering new treatment candidates. They include the antimalarial drug amodiaquine, which reduced viral load in animal models of the virus by 70%.

read more

Bristol Myers sees automation, virtual reality on the horizon for pair of new CAR-T manufacturing plants

With two new cell therapy factories on the way, Bristol Myers Squibb is looking to take its CAR-T manufacturing into the future. On one side, the company is plotting increased automation; on the other, virtual reality training that could eventually be used to work through production hitches remotely.

read more

Resources

Guide: How to Establish a Successful Clinical Data Standards Program

Learn how to develop a standards program that has your full team’s buy-in and improves the efficiency and quality of your clinical trials.

Whitepaper: The Journey to a Global Modular Content Strategy

One top 10 pharma outlines three key steps to launching a modular content strategy to generate localized content faster.

E-Book: 7 Keys to Success in Europe

This 77-page e-book explores 7 keys to success that any biopharma company needs to keep in mind as it enters Europe.

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

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.