To view this email as a web page, click here

WELCOME TO FIERCE LIFE SCIENCES WEEKLY DIGEST

David Sabatini, MIT professor and founder of several biotechs, has been ousted from his lab after a sexual harassment investigation. The cell signaling and cancer metabolism scientist, credited with co-discovering the mTOR pathway, is “no longer associated” with either the Whitehead Institute or the Howard Hughes Medical Institute. Details of the specific allegations are yet to emerge. That story, plus our other top reads of the week, follow below.

Featured Story

Sabatini, biotech founder and mTOR pioneer, ousted after sexual harassment investigation

David Sabatini, the scientific founder of several biotechs, has been ousted from his lab after a sexual harassment investigation. The high-profile cell signaling and cancer metabolism scientist is “no longer associated” with either the Whitehead Institute or the Howard Hughes Medical Institute. 

read more

Top Stories Of The Week

Moderna probes reports of COVID-19 vaccine contamination in Japan

It's been a relatively smooth ride for Moderna's global COVID-19 vaccine roll out. But on Wednesday, the company said it's investigating the possible contamination of one batch sent to Japan. Moderna said it is focusing its probe on its manufacturing partner in Spain, CDMO Rovi.

read more

SPECIAL REPORT—Who's getting the most out of their R&D engine? Pharma's top 11, ranked

Drugmakers have myriad tools in their arsenal when looking to grow sales, but it's new drug approvals that reign supreme and ultimately prove the worth of a company's development engine. See how 11 of the world's top drugmakers are faring.

read more

Merck KGaA's $4.2B bintrafusp alfa nabs a 3rd strike. Is the GSK-partnered cancer hopeful out?

Merck KGaA’s biliary cancer hopeful bintrafusp alfa—the immunotherapy at the heart of a $4.2 billion deal with GlaxoSmithKline—has nabbed its third strike. The German pharmaceutical company announced Monday that a phase 2 clinical trial of bintrafusp alfa has been discontinued as the therapy is unlikely to improve overall survival.

read more

Pfizer, BioNTech score FDA's first full COVID-19 vaccine nod, quickly triggering stricter mandates

The U.S. FDA awarded Pfizer and its German partner BioNTech its first full approval for a COVID-19 vaccine, a historic decision that could spark a wave of new vaccine mandates among businesses and universities awaiting the agency's final nod.

read more

Abbott destroyed millions of COVID test cards when demand plummeted. Now, it's scrambling to ramp back up

While facing sharp declines in public demand for rapid COVID-19 screening over the spring and first half of this summer, Abbott directed its workers to shred millions of paper testing cards that it felt had no chance of selling, according to a report by The New York Times.

read more

J&J CEO Gorsky to step aside, handing reins of world's largest pharma to COVID-19 navigator Duato

Johnson & Johnson is switching captain to lead the world’s largest pharma company by 2020 revenue. Nine-year CEO Alex Gorsky will hand the helm to vice chairman of executive committee and leader of its COVID-19 response group, Joaquin Duato, early 2022.

read more

After Aduhelm fallout, FDA veteran Woodcock out of running for commish job: report

Janet Woodcock, M.D., has spent more than three decades at the FDA, but her time running the agency as its interim leader is looking less likely to materialize into a full-time gig.

read more

Samsung plots $205B investment, massive hiring spree to ramp up CDMO, biosimilars and more

With a self-proclaimed “Super Plant” already on the way in South Korea, Samsung Biologics CEO John Rim said in January that the CDMO’s expansion was just getting started. He wasn’t kidding. The manufacturer’s parent company Samsung Group is investing an eye-popping 240 trillion won ($205 billion) across its biopharmaceutical, semiconductor and telecommunications businesses, among others.

read more

CRISPR pinpoints new leukemia target and a 'pocket' that could make it druggable

Using CRISPR, a team at Penn’s medical school discovered that an epigenetic regulatory protein called ZMYND8 governs the expression of genes that are critical for the growth and survival of AML cells. They uncovered a way to target it with drugs and to predict which patients are likely to respond to ZMYND8 inhibition.

read more

Pharma's reputation drops again. Could it foreshadow a return to the bottom?

Pharma's reputation continues to slide, now down to 53% of consumers who still hold a positive view. The decline began after a February high of 62% approval, down to 60% in May and then 56% in June—and now down three more percentage points, according to The Harris Poll.

read more

Resources

eBook: Accelerate recruitment with a decentralized clinical trial strategy

Learn how a decentralized clinical trial strategy improves patient recruitment, reduces drop-out rates, and ultimately streamlines the path to the next trial phase.

Whitepaper: How to build a robust packaging strategy for rapid commercialization

Learn how to build a robust packaging strategy and the key technical considerations in packaging design and operational planning to enable rapid commercialization of pharmaceuticals.

Whitepaper: Understanding the CMC regulatory landscape for cell and gene therapy products

Learn how regulations are changing and key considerations for commercializing cell and gene therapies without sacrificing quality.

Whitepaper: Navigating the Digital Transformation Journey

Uncover the real impact of “digital transformation” with practical advice to help you plan your own transformative journey to a harmonized digital ecosystem.

eBook: Get solutions to market faster

Read Get to Know Cloud Content Management for Life Sciences and learn how to eliminate silos across all workflows, from R&D to commercialization.

Content Hub: Process Intensification Resource Center

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

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. 

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.