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‘Click’ chemistry used to tag proteins made by cancer cells 

Drug Discovery World

In their study, published in Nature Communications, the team developed a new method that identifies proteins released by a specific type of cell, even if the cells are in a complex environment with lots of other cell types. . The new method involves adding chemical tags to sugar molecules which are added to cells. Click’ chemistry .

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Grand Rounds February 2, 2024: Strategies for Improving Public Understanding of FDA and the Products It Regulates…Why Should We Care, and What Might We Do? (Susan C. Winckler, RPh, Esq)

Rethinking Clinical Trials

This work is important because the digital health information environment and limited public trust in government institutions represent pressing challenges for FDA. The research yielded a report that provides 5 observations, 16 potential strategies, and more than 40 potential tactics for the FDA to consider.

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Orphan drugs and where to launch them: The keys to Europe’s forgotten territories

Pharmaceutical Technology

Due to the high price tags associated with these speciality medicines, innovators have naturally favoured big markets with high GDP such as the US and EU-5 (Germany, France, Spain, Italy, and the UK). “The Go-to-market strategies. The choice of where to launch an orphan drug is an important and difficult decision.

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3 ways pharma marketers can draw inspiration from digitally-native brands

pharmaphorum

Companies like prescription glasses firm Warby Parker, shoe brand Rothy’s and tele-dentistry’s SmileDirectClub have grown up in today’s digitally native environment and can offer some key pointers for pharma. They also employ exceptionally high levels of ‘test and learn’ activities to understand which campaigns work and should be upscaled.

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What can pharma marketing learn from other regulated industries?

pharmaphorum

The financial world, like the pharmaceutical industry, must operate within a tightly-defined regulatory environment, and in doing so has proved adept at connecting with its customers. The key is adapting existing legacy and traditional printed material for the digital environment.”. Virtual connections.

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Grand Rounds August 12, 2022: Equitably Including Diverse Participants in Pragmatic Clinical Trials (Consuelo H. Wilkins, MD, MSCI)

Rethinking Clinical Trials

How do we adjust, repair, bring in resources to recruit and work with these populations? When you live in an environment where you have been minoritized and are experiencing discrimination, it has an impact on your biology. There is plenty of data that shows that. The social circumstances affect health outcomes. New Ideas study.

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Q&A: A decade on, what’s next for CAR-T therapies?

Pharmaceutical Technology

But access to these treatments continues to remain limited due to high price tags and variable availability across regions. BL: [It is] distressing as a scientist to work on something that patients cannot access. Currently, all approved CAR-T therapies are autologous, where T cells taken from patients are modified and then re-infused.