FDA can’t tackle drug shortages alone

Today's Big News

May 31, 2023

FDA warns patients about compounded versions of Novo Nordisk’s Ozempic, Wegovy


Sanofi sees midphase success in multiple sclerosis decades after safety concerns scuttled peers


FDA can't solve drug shortages on its own, agency's oncology chief says


iRhythm hit with FDA warning letter over alleged regulatory ‘nonconformities’ in heart monitor patch


Precision to aim lead off-the-shelf CAR-T at patients who relapse after cell therapy. Will FDA play ball?


Making us thinner will see fatter profits for pharma as Bloomberg’s crystal ball predicts obesity drug sales hitting $44B by 2030

 

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FDA warns patients about compounded versions of Novo Nordisk's Ozempic, Wegovy

In the rush to supply prescriptions of Novo Nordisk’s popular diabetes and weight loss meds, some pharmacies are making unauthorized versions of Ozempic and Wegovy, the FDA warned on Tuesday. Some compounding pharmacies are using unauthorized versions of semaglutide, according to the FDA.
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Top Stories

Sanofi sees midphase success in multiple sclerosis decades after safety concerns scuttled peers

More than 20 years after a pre-merger Biogen and Idec independently raised safety concerns about the mechanism, the French drugmaker has presented phase 2 data that suggest its second-generation drug candidate may be safe and effective in multiple sclerosis.

FDA can't solve drug shortages on its own, agency's oncology chief says

As drug shortages persist nationwide, the director of the FDA Oncology Center of Excellence, Richard Pazdur, M.D., talked about the root cause of the problem and the agency's response. One cause, he says, is that manufacturers haven't invested enough to build capacity.

iRhythm hit with FDA warning letter over alleged regulatory ‘nonconformities’ in heart monitor patch

A recent warning letter from the FDA may have iRhythm Technologies changing its tune.

Precision to aim lead off-the-shelf CAR-T at patients who relapse after cell therapy. Will FDA play ball?

Precision BioSciences has landed on an ideal patient population for its lead off-the-shelf cell therapy to treat blood cancer, and it’s, well, precise. 

Making us thinner will see fatter profits for pharma as Bloomberg's crystal ball predicts obesity drug sales hitting $44B by 2030

Novo Nordisk has lit the tinder of a new megablockbuster market with Saxenda and Wegovy as new, branded anti-obesity drugs are set to haul in $44 billion by this decade’s end.

The Alzheimer's pipeline is as strong as ever. Now we just need the patients

There are, at this moment, 187 clinical trials for the neurodegenerative disease underway, the highest ever on record, according to a new report from the Alzheimer’s Association.

NICE gives thumbs-up to Pfizer's migraine drug—but with lots of restrictions

The U.K.'s National Institute for Health and Care Excellence has recommended approval of Pfizer's Nurtec (Vydura) but with lots of restrictions.

Yuhan makes $325M cancer bet to challenge Boehringer, Takeda

Yuhan Corporation has bought its way into a cancer space targeted by Boehringer Ingelheim and Takeda, wagering up to $325 million to get its hands on a preclinical HER2 tyrosine kinase inhibitor.

ASCO: NeuroMetrix’s neurostim wearable eases symptoms of chemotherapy-induced nerve damage

A year after its neuromodulation device became the first non-drug treatment cleared by the FDA to relieve chronic pain associated with fibromyalgia, NeuroMetrix is one step closer to adding another first-of-its-kind indication to the technology.
 
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'Podnosis': 'Game-changing' generative AI and gender-affirming healthcare

This week on "Podnosis," we discuss why generative AI can be "game-changing" in healthcare. We also take a second look at an episode on gender-affirming healthcare
 

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.
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.
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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.
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.
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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