20 most influential people in biopharma

Today's Big News

May 9, 2023

UPDATED: Novavax cuts head count by 25%, hitting hundreds of jobs, to align costs with dwindling COVID-19 market 


Takeda confirms fallout from gene therapy R&D refocus: up to 186 layoffs 


EQRx abandons low cost drug plan, slashes programs down to 1 and cuts staff in 'reset'


Roche, with HER2 franchise under pressure, pays $70M for breast cancer brain metastases prospect


The most influential people in biopharma in 2023 


Gilead picks up small PARP1 biotech to find a mate for Trodelvy and take on Lynparza 


Salarius' rare cancer drug breaks free from one FDA partial hold, but another study remains in limbo


ADC implements 'lower risk' R&D strategy with 17% layoffs, preclinical culls


Enanta makes the case for COVID-19 antiviral's mixed data in hopes of attracting a partner

 

Featured

UPDATED: Novavax cuts head count by 25%, hitting hundreds of jobs, to align costs with dwindling COVID-19 market

Novavax is reducing its head count by 25%. After trying to cut costs without laying off staff, the vaccine company has now accepted it will need to part ways with hundreds of employees to align its spending with the dwindling size of the COVID-19 opportunity.
 

Top Stories

Takeda confirms fallout from gene therapy R&D refocus: up to 186 layoffs

Last month, Fierce Biotech told you about an unknown number of layoffs due to hit Takeda employees as the Japanese pharma moves away from early-stage R&D work in adeno-associated virus-based gene therapies and rare hematology. Now, we’ve got a better sense of the workforce impact.

EQRx abandons low cost drug plan, slashes programs down to 1 and cuts staff in 'reset'

EQRx is abandoning its plan to provide drugs that are typically expensive at lower prices. The biotech is also cutting ties with two of its partners, letting go of 170 staff members and slashing all assets from its pipeline except one. 

Risk Management Processes for Cell and Gene Therapies

Cell and gene therapies hold great promise but can also carry serious risks. Applying a risk-based approach during development and manufacturing increases patient safety and product quality. Read more.

Roche, with HER2 franchise under pressure, pays $70M for breast cancer brain metastases prospect

Roche is stepping up the defense of its critical HER2 franchise, committing $70 million in upfront and near-term payments to secure global rights to Zion Pharma’s early-phase treatment of brain metastases.

Precision's President Sofia Baig on Change, Adaptation & The Future of Clinical Research from a CRO’s Perspective

Discover Sofia Baig's vision for clinical research, data-driven insights & patient centricity at Precision for Medicine!

The most influential people in biopharma in 2023

The times are changing in biopharma. We hope our selections for this year's Most Influential People in Biopharma special report reflect the trends many of our readers are seeing in the industry.

Gilead picks up small PARP1 biotech to find a mate for Trodelvy and take on Lynparza

Gilead has found a potential friend for breast cancer med Trodelvy in PARP1 and MK2 Inhibitor specialist XinThera, which will now come under the Big Pharma's wing. 

Salarius' rare cancer drug breaks free from one FDA partial hold, but another study remains in limbo

The FDA has lifted its partial clinical hold on Salarius Pharmaceuticals’ lead asset seclidemstat in a rare cancer indication, a hold that was put in place last fall after a patient death was reported.

ADC implements 'lower risk' R&D strategy with 17% layoffs, preclinical culls

Biotech may be an inherently risky business, but ADC Therapeutics is now keen to pursue a low-risk R&D strategy that will see it focus on assets it deems most likely to make it to market.

Enanta makes the case for COVID-19 antiviral's mixed data in hopes of attracting a partner

Enanta Pharmaceuticals’ COVID-19 drug reduced some symptoms of the respiratory disease but did not reduce viral load or time to improvement when compared to placebo. Executives pointed to a tighter analysis of key symptoms for signs that EDP-235 could have value on the market—so long as a partner helps them get there.

Don't trust your gut? Microbiota could hold key to why some cancer therapies fail

New research from Harvard scientists confirmed suspicions that the gut microbiome could be responsible for why checkpoint inhibitors aren't effective in some patients.

SNAPing together a universal receptor system for T cell therapies

A new universal receptor system designed by a research team from the University of Pittsburgh could make engineering custom T cell therapies far more efficient.

Post-spinoff, PerkinElmer rebrands diagnostics, life sciences business as Revvity

With the sell-off of its applied science, food and enterprise services businesses now complete, PerkinElmer is charting a new path with its remaining diagnostics and life sciences divisions.

Let's make a deal: Conditions are right for biopharma M&A to break out, analysts say

Pfizer’s proposed $43 billion acquisition of Seagen two months ago was the largest deal in biopharma since 2019 but it came during a period when M&A activity has been limited. Analysts from EY and West Monroe however believe that the M&A market is about to grow because of a confluence of factors.
 
Fierce podcasts

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'Podnosis': Healthcare’s relationship to climate change

This week on "Podnosis," we discuss how the healthcare industry is addressing its role in climate change.
 

Resources

Whitepaper

ChatGPT in Drug Discovery: Rise of Large Language Models

ChatGPT shows promise in drug discovery for information extraction, scientific text authoring, hypothesis prediction, and chemical entity prediction. This whitepaper explores its potential to streamline research, delving into its technology, applications, and limitations.
Whitepaper

Discovering High-Affinity, Functional Anti-GLP-1R Antibodies

Learn how a GPCR-focused library with a cell-based biopanning strategy led to the discovery of 13 high-affinity and selective anti-GLP-1R antibodies with highly developable therapeutic properties.
eBook

Decentralized Clinical Trials: The Complete Guide for 2023

Discover a game-changing approach to clinical research with Hybrid and Decentralized Clinical Trials (DCTs). Learn about the benefits, challenges, and key elements for success.
Research

How Lilly’s Legal and Library Services Empower Teams Across the Drug Development Pipeline

What role do the Library and Legal teams play in the drug development pipeline at Lilly? An import one – find out how.

Whitepaper

Medical Affairs Metamorphosis VI: The Changing Face of Stakeholder Engagement

This paper focuses on stakeholder engagement and how Medical Affairs teams’ responsibilities, goals, tools, and techniques are changing.
Research

Maximizing Clinical Trial Success

Strategies for Optimal Site Selection and Feasibility Research in Novel Therapies and Geographies
Whitepaper

eConsent: Flexible Consent Through Enabling Technologies

How can eConsent provide a more flexible approach to informed consent?

Whitepaper

Plan for scalable process liquid and buffer preparation

Preparation of critical process liquids and buffer components shifts resources away from core activities and can be filled with inefficiencies and risks that can increase time and costs across your workflow. Learn about the framework to help reduce your total costs beyond capital and operational expenditures and set a solid foundation for successful scale-up of buffer preparation.

Whitepaper

Running Decentralized Trials at Scale

Explore how clinical supply can be scaled up as decentralized programs progress, and how technological solutions can accelerate trial deployment.
Whitepaper

Key Clinical Supply Issues Sponsors Should Consider with their CRO

As sponsors increasingly look to CROs to support their clinical studies, making and addressing certain clinical supply considerations at the outset of the relationship can reduce the risk of potentially unforeseen impact to budget and time later. Discover key issues sponsors should consider to help their CRO or partner of choice better understand their clinical supply needs.

Whitepaper

Specialized Expertise for Management of Clinical Supply Budgets

For sponsors, cost is a key concern when it comes to managing the supply of their clinical trials. A financial project analyst (FPA) is a specialized expert who can help control clinical supply costs and keep the project within budget. Explore the critical role that a Financial Project Analyst plays in clinical trial supply and budget management.
Whitepaper

Clinical Supply Solutions for the Asia-Pacific Region

Learn how Catalent’s extensive network across APAC can meet a wide range of clinical supply needs for sponsors conducting trials within the region.
Whitepaper

Designing an Optimal APAC Clinical Supply Chain

Discover key considerations that every trial sponsor should know when navigating the complex clinical supply distribution landscape across Asia-Pacific.
Whitepaper

Roles and Responsibilities of Specialized Clinical Supply Experts

How can specialized expertise help you optimize your clinical supply chain? Learn about the roles and responsibilities of unique experts such as clinical supply management, project management, and financial project analysis.
Whitepaper

Supply Services to Support Clinical Trials in Japan & Beyond

Explore Catalent’s newest clinical supply facility in Japan, including the comprehensive services & solutions it offers to help support trials both in-country & around the world.
Whitepaper

Questions You Need to Ask Your CRO About Clinical Supply

Planning on using a CRO to support your next clinical study? This infographic outlines critical areas to address at the start of the relationship in order to ensure that budget and timelines keep on track for the duration of the trial.
 

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