Philips recalls 21K newly repaired ventilators

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Today's Big News

Feb 17, 2023

After 3-plus years and multiple FDA approvals, Gilead's cell therapy head Shaw leaving next month


Pfizer pulls 50% of people from phase 3 Lyme disease study for GCP violations at US trial sites


Philips recall of 21K previously recalled, repaired ventilators nets FDA Class I tag


'It's the right call': GSK expresses no regrets on abandoning cell therapy as oligo strategy heats up


Novartis, Roche avoid $475M antitrust fine in French appeals court


As HQ move nears completion, Merck finds a buyer for its sprawling Kenilworth campus

 

Featured

After 3-plus years and multiple FDA approvals, Gilead's cell therapy head Shaw leaving next month

Gilead on Friday said Shaw will be leaving as Kite Pharma's CEO at the end of March. The company didn't give a reason for her departure, but the drugmaker said she'll work closely with Gilead CEO Daniel O'Day on the transition in the coming weeks.
 

Top Stories

Pfizer pulls 50% of people from phase 3 Lyme disease study for GCP violations at US trial sites

Pfizer and Valneva’s phase 3 Lyme disease vaccine clinical trial has gone badly wrong. After discovering good clinical practice violations at some trial sites, the partners have removed around half of the enrolled participants from the study.

Philips recall of 21K previously recalled, repaired ventilators nets FDA Class I tag

Philips has identified two potential issues in some ventilators that were newly refurbished as result of the June 2021 recall of 5.5 million of the company's respiratory devices.

'It's the right call': GSK expresses no regrets on abandoning cell therapy as oligo strategy heats up

Rather than racing to get an “off-the-shelf” CAR-T into the clinic or going all-in on a solid tumor strategy, GSK executives told Fierce Biotech they believe the Big Pharma's genetics expertise will offer the smoothest path to market success.

Novartis, Roche avoid $475M antitrust fine in French appeals court

In 2020, when Novartis and Roche were fined 444 million euros ($475 million) by France’s Autorite de la Concurrence, it was the largest ever penalty levied by the country’s anti-competition watchdog. Three years later, the Swiss pharma giants are off the hook.

As HQ move nears completion, Merck finds a buyer for its sprawling Kenilworth campus

Merck has reached a deal with real estate business Onyx Equities to sell its 108-acre campus in Kenilworth, NJ, where the drug behemoth relocated its main digs back in 2015. Merck will move out of Kenilworth in phases over the next “several years” as it completes an expansion at its new headquarters in Rahway, NJ.

BD issues cybersecurity alert for hacking risk found in Alaris infusion pump software

A vulnerability found in software used to monitor some of BD’s infusion pumps could potentially give hackers access to personal data stored in the system.

Moderna checks a few boxes in phase 3 mRNA flu shot trial, but misses on B strains and safety

Moderna checked off two influenza A strains in a phase 3 clinical trial for a new flu shot candidate, but the vaccine struggled against two B strains in the same test, marking a mixed readout for the famed mRNA biotech.

Merck targets BMS' stomach cancer head start with Keytruda win, but past failure casts shadow

Merck & Co.’s Keytruda has risen from the ashes with a positive stomach cancer trial readout. But there’s some reconciliation to do with a past failure that led to the withdrawal of an accelerated approval.

Labcorp plots 2023 revenue growth despite a possible 90% drop in COVID test revenues

In a full-year earnings report published Thursday, Labcorp reported a 7.7% year-over-year drop in revenues in 2022, thanks almost entirely to a COVID diagnostics haul that weighed in at less than half the size of the previous year’s.

Madrigal’s NASH candidate looks more cost-effective than Intercept rival, ICER says

Madrigal’s resmetirom fared better than Intercept’s Ocaliva in a study by ICER assessing cost-effectiveness in non-alcoholic steatohepatitis (NASH). There are no approved treatments for the disorder which affects between 1.5% and 6.5% of adults in the United States.
 
Fierce podcasts

Don't miss an episode

'The Top Line': Moderna vs. Pfizer-BioNTech and this week's news

This week on "The Top Line," we discuss the intense patent fight between Moderna and Pfizer-BioNTech around the mRNA technology used in their COVID-19 vaccines. We also talk about negotiating vaccine contracts via text messages, one of the biggest medtech deals of the year and other top headlines from this week.

 

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

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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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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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