To view this email as a web page, click here

Today's Rundown

Featured Story

Sana snags $587.5M IPO to catapult cell therapies into the clinic

Massive private raise? Check. Preclinical pipeline? Check. Now, Sana Biotechnology is raising $587.5 million in a mammoth IPO that will bankroll the development of its cell engineering platforms and complete preclinical work for each of its early-stage, off-the-shelf cell therapies.

read more

Top Stories

Roche chucks out phase 3 ipatasertib combo tests, midstage IL-33 asthma, BTKi arthritis trials in Q4 clear-out

Swiss major Roche is dumping a series of cancer, autoimmune and respiratory drugs in mid- to late-stage tests.

read more

Pfizer bags rheumatoid arthritis rights to new immunotherapy class through deal with Imcyse

Pfizer has teamed up with Imcyse to develop treatments for rheumatoid arthritis. The agreement will give Pfizer the chance to access modified peptides designed to induce cytolytic T cells and thereby eliminate the disease pathway without affecting the rest of the immune system.

read more

In Partnership: Meeting the commercialization challenge of a surging gene and cell therapy market

Undaunted by the challenges the COVID-19 pandemic unleashed on the world the expected surge of cell and gene therapies already in the pipeline and on the horizon will continue to materialize, and with them the complexity of riding that wave of innovation.

read more

Shih, fresh from selling Disarm to Lilly, takes up CEO post at CAR-NK specialist Catamaran

Catamaran Bio has named Alvin Shih as CEO. Shih arrives at the allogeneic CAR-NK cell specialist fresh from leading Disarm Therapeutics to a takeover by Eli Lilly.

read more

Sensei clinches $133M IPO to usher personalized cancer meds through the clinic

Months after banking a $28.5 million venture round, Sensei Biotherapeutics is hitting Wall Street with a $133 million IPO. The proceeds will fund a trio of personalized cancer medicines into and through the clinic, including vaccines for a rare skin cancer and head and neck cancer as well as treatments designed to boost the immune response in the tumor microenvironment.

read more

Veracyte drops $600M to acquire cancer tester Decipher Biosciences

Genomic cancer testing company Veracyte is moving to acquire Decipher Biosciences in a $600 million deal, with the goal of broadening its diagnostic reach to seven of the 10 most common tumor types affecting over 1 million new patients per year.

read more

Ken Frazier to retire as Merck CEO after 10-year run, handing the baton to CFO Robert Davis

Ken Frazier, who has been Merck & Co.’s chief executive since 2011, will retire June 30, handing the reins to Robert Davis, currently Merck’s CFO. Frazier will continue to serve as executive chairman for a transition period that’s yet to be determined.

read more

Enrollment Showcase

Specialize Your Career in Pharmaceutical Outcomes

Learn about the Top 5-Ranked UF College of Pharmacy’s online graduate programs in pharmaceutical outcomes & policy. Select from five specializations, including the new pharmaceutical value assessment & communication option. Over half of graduates progress to a new role within one year. Register now.

Resources

eBook: Your Path to Virtualization: Eight parameters to accelerate and optimize your technology strategy

8 parameters to optimize your “Path to Virtualization” across site- and patient-centric capabilities in this Sponsor Edition eBook.

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.

Whitepaper: A Single Source of Truth: Acorn AI's Commercial Data Model

Acorn AI has developed a flexible and scalable Commercial Data Model that provides pharmaceutical companies with the data-driven insights required to respond to the industry’s ever-changing landscape. Download the whitepaper to learn how Acorn AI’s intuitive data model enables launch success and more. 

Sponsored: Lessons Learned: Best IT Practices to Secure Your Remote Workforce Now

Criminals Are Actively Exploiting The CV-19 Pandemic To Gain Entry To Enterprise Networks. Don’t Let Your Company Become A Cybercrime Statistic -- Make These Cost-Effective IT Changes Now!

Content Hub: Access resources to guide your molecule from lab to clinic

It’s an exciting time to pioneer what could be a life-changing medicine. Clear the path to the clinic with pro tips and expert insights from industry leaders.

Webinar: Using SPOT™ & CHO-BC® During Cell Line Development for Titers up to 9 g/L

Innovative cell lines and early process development are critical to generate a high producing cell lines alongside a USP strategy to meet high quality standards.

Content Hub: Emerging Biotech Resource Center

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

Executive Summary: 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.

Research: Premier Research Resource Hub

Browse the latest learnings and insights from our clinical development professionals.

eBrief: Drug Product Process Development: Ensuring a Consistent, High-quality Biologic

Learn about drug product process development challenges and risks, the difference between innovator and biosimilar drug product process development, and more during the drug product process development phase.

Whitepaper: Achieving a Successful Drug Product Technology Transfer

Get insights on key considerations for a successful tech transfer process for manufacturing a biologic drug product, including a case study on overcoming challenges in a process transfer for a sterile diluent.

Whitepaper: The Art of Recognizing Clinical Supply Risk Factors

In a BioPharma Dive industry survey, planning and forecasting were identified as top concerns for trial sponsors. In response to this need, the CSM team at Catalent has developed a methodology for identifying, evaluating, and proactively managing the inherent risks involved in clinical trial supply chain management.

eBook: Expecting the Unexpected: Strategies for Efficient Clinical Supply Management and Forecasting

Learn how to drive excellence within the forecasting process and utilize forecasting throughout the clinical study to better plan clinical supply budgets and project timelines. Explore how to identify potential supply-related issues before they can negatively impact your study.

Events