Highest paid R&D execs

Today's Big News

May 30, 2023

Theranos’ Elizabeth Holmes reports to Texas prison to begin 11-year sentence


Alnylam sticks with aggressive litigation strategy against Pfizer and Moderna, filing yet another patent lawsuit


Top 5 highest paid biopharma R&D executives in 2022


Lexicon finally scores FDA nod for heart failure drug Inpefa


Pfizer's hemophilia drug hits in phase 3, giving it a chance to leapfrog Novo Nordisk

 

Featured

Theranos' Elizabeth Holmes reports to Texas prison to begin 11-year sentence

Despite multiple attempts to put off the start of her 135-month prison sentence after being found guilty on four counts of defrauding investors in blood-testing startup Theranos, the time has come for Elizabeth Holmes to report to prison.
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Jun
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Top Stories

Alnylam sticks with aggressive litigation strategy against Pfizer and Moderna, filing yet another patent lawsuit

The company is accusing Pfizer and Moderna of stepping on its lipid particle delivery tech with their lucrative COVID-19 vaccines.

Top 5 highest paid biopharma R&D executives in 2022

The departures of 2021's three highest paid R&D executives from Big Pharma threw a curveball at our annual list, prompting us to trim the feature down to five leaders.

Lexicon finally scores FDA nod for heart failure drug Inpefa

It’s been a winding road, but Lexicon has reached its destination, gaining an FDA approval for Inpefa (sotagliflozin). The once-daily pill becomes the first SGLT1/SGLT2 inhibitor to reach the market. It has been sanctioned to reduce the risk of heart failure.

Pfizer's hemophilia drug hits in phase 3, giving it a chance to leapfrog Novo Nordisk

Pfizer is looming large in Novo Nordisk’s rearview mirror. Weeks after seeing its rival for the hemophilia market stumble, Pfizer has reported phase 3 data that suggest its candidate is competitive and position it to file for approval in the coming months.

Eli Lilly, XtalPi ink $250M deal for AI-powered drug discovery

XtalPi’s artificial intelligence- and robotics-powered technologies have helped its pharmaceutical partners pinpoint dozens of small-molecule compounds that could potentially be further developed into novel therapeutics—and Eli Lilly wants a piece of the AI drug development pie.

After price cuts, Eli Lilly inks $13.5M settlement in long-running insulin lawsuit

Eli Lilly has agreed to pay $13.5 million to end a six-year, class-action lawsuit that alleged the company overpriced its insulin. As part of the settlement, Lilly has agreed to cap out-of-pocket cost its insulin at $35 per month for four years.

Can Rain ride the storm out? Cancer biotech lays off 65% of workforce after phase 3 fail

When it rains, it pours, an old adage that Rain Oncology hasn’t been able to shelter from. After a phase 3 fail, the precision oncology biotech is saying farewell to its chief medical officer, halting programs and laying off 65% of its workforce.   

Titan Medical licenses robotic surgery tech to Intuitive, shuffles C-suite amid ‘strategic transition’

After its precarious financial situation led Titan Medical to seek out a sale—without success—lay off nearly all of its employees and, as of this March, be delisted from the Nasdaq, the surgical robotics maker is taking a different tack.

Belgium's UCB Pharma hit with FDA Form 483 after April inspection

UCB Pharma, a Belgium-based biopharma company, has been slapped with a Form 483 from the FDA following an inspection that uncovered issues with its quality control unit and product storage.

SPAC to the drawing board: GreenLight returns to private market in $46M deal after taste of Wall Street

GreenLight Biosciences will seek its dream off Wall Street in a go-private deal less than two years after taking the SPAC route there. 
 
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'The Top Line': Most influential people, plus the headlines

This week on "The Top Line," we discuss the 20 most influential people in biopharma, plus a topical gene therapy, a new opioid overdose medication, and the rest of the week's headlines.

 

Resources

Whitepaper

Commercializing Gene Therapies, Part 4 – Market Entry

This paper outlines various market archetypes and key considerations leaders must address when prioritizing new potential markets for gene therapies.
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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.
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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.
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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
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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.
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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.
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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.

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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.
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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.
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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.
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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.
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.
 

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