Bayer braces for another year of eroding Eylea sales

Today's Big News

Feb 28, 2023

FDA flags Guillain-Barré risks for GSK, Pfizer RSV shots, but just one will need safety trial 


120 jobs on the line as Boston Scientific slims down Texas facility acquired in Preventice buyout


Bayer grapples with Eylea sales slowdown, sees trend continuing in 2023


AstraZeneca grows Canadian snowshoe print with 500 new jobs and rare disease hub


Novartis halts Pluvicto new patient starts, struggles with radiotherapy's supply amid manufacturing expansion

 

Featured

FDA flags Guillain-Barré risks for GSK, Pfizer RSV shots, but just one will need safety trial

Both Pfizer and GSK’s upcoming respiratory syncytial virus vaccines had instances of Guillain-Barré syndrome in clinical trials. And yet the FDA is only recommending that one of them conduct a new post-marketing study to assess the risk.
 

Top Stories

120 jobs on the line as Boston Scientific slims down Texas facility acquired in Preventice buyout

Amid Boston Scientific’s decision to transfer some work out of a facility in Houston in the coming months, more than 100 jobs are hanging in the balance.

Bayer grapples with Eylea sales slowdown, sees trend continuing in 2023

Eylea's sales growth is slowing down, Bayer reported on Tuesday, chalking it up to "pricing pressures," while not addressing competition from Roche's Vabysmo. The company expects the trend to continue in 2023 but sees a rebound after a potential high-dose approval.

AstraZeneca grows Canadian snowshoe print with 500 new jobs and rare disease hub

AstraZeneca is bucking the biopharma layoff trend, instead expanding its Canadian footprint with the creation of 500 new jobs and a new rare disease research hub.

Novartis halts Pluvicto new patient starts, struggles with radiotherapy's supply amid manufacturing expansion

Novartis has been experiencing challenges meeting the demand for Pluvicto. And as demand climbs, the company has decided to pause accepting new patients until it has “more clarity on the FDA’s approval” of a manufacturing site in New Jersey.

Abbott, FDA warn that replacement aortic valves could deteriorate faster than expected

Typically, bioprosthetic aortic valves begin deteriorating about a decade after they're implanted—but two of Abbott’s replacement valves may be much less durable than that.

Big-sellers from Merck, Novo and Lilly likely to face Medicare price negotiations: report

Between 2026 and 2028, Medicare could parley on pricing for some 38 Part D drugs and 2 Part B drugs under the Inflation Reduction Act. Many well-known pharma brands are among those expected to face negotiations.

Latest biotech-on-biotech merger sees aimless Adamis snapped up by DMK

It’s an increasingly common story in 2023—a biotech searching for strategic options after a tough set of clinical data is snapped up by a private company that sees an opportunity in the clinical expertise and Nasdaq listing.

Pandemic-era insider trading scheme netted ex-Phlow exec and his cousin $1.5M, SEC says

The U.S. Justice Department and the SEC have charged former Phlow Vice President Andrew Stiles with insider training, alleging that he and his cousin, Gray Stiles, netted more than $1.5 million on purchases of stock made using nonpublic information about a government pandemic preparedness contract awarded to Eastman Kodak.

Getinge life support systems temporarily lose CE marks due to issues with sterile packaging

Several years into the process of rectifying potential breaches in the sterile packaging of its life support systems—a process that has been littered with field correction notices and FDA-rated recalls—Getinge has been hit with a particularly serious penalty.

A Kafka-esque transformation and the story of MS through 'The Metamorphosis': book review

In Franz Kafka’s 1915 novella "The Metamorphosis," we see the grim reality of a sudden change that turns protagonist Gregor Samsa overnight into a giant, unwieldy insect and the struggles he has from basic movement to the failing empathy from his family and neighbors, who eventually and quite literally throw him away like garbage.
 
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'The Top Line': A checklist for immuno-oncology combo phase 3 trials

This week on "The Top Line," we discuss a checklist that the Society for Immunotherapy of Cancer released last October. The guidelines are designed to maximize the value of phase 3 immuno-oncology combination trials. We also cover the top headlines from this week.

 

Resources

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Discover the Power of Small with NanoplasmidTM – the next-generation plasmid for manufacturing today’s cell and gene therapies.

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Leveraging Archetypes for Effective Launch Strategy

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Writing the Future of Antibody Discovery Solutions

See how high-throughput DNA synthesis combined with antibody engineering expertise provides end-to-end antibody discovery solutions.

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Intranasal Drug Product Development: Formulation to Manufacturing

What are key considerations for intranasal delivery in the treatment of acute and chronic conditions?
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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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Step-wise strategy to address process characterization and late phase development

Learn more on Catalent’s step-wise approach for the definition and execution of Process Characterization for the production of a monoclonal antibody for late phase process characterization and development.

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A Strategy to Standardize Process Characterization & Late Phase Development

Learn more on an approach for process characterization for the production of a monoclonal antibody, which will improve the efficiency and effectiveness of the process by targeting the right design and number of experiments.

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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.

Research

A Strategy to Standardize Process Characterization & Late Phase Development

Learn more on an approach for process characterization for the production of a monoclonal antibody, which will improve the efficiency and effectiveness of the process by targeting the right design and number of experiments.

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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.
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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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