Rethinking Clinical Trials

JULY 27, 2022

ACTIV-6 is testing medication doses approved by the FDA for other purposes, i.e., repurposed drugs. Participants test positive for COVID-19 with a FDA-authorized test, register from home, are randomized remotely, receive study medication through the central pharmacy, and follow instruction until their clinical symptoms improve.

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Rethinking Clinical Trials

NOVEMBER 1, 2022

Vanderbilt University Medical Center. Important issues early on included COVID-19’s effects on the workplace, vaccine access and willingness, and impact on home life. Department of Population Health Sciences. Russell Rothman, MD, MPP. Senior Vice President, Population and Public Health. Key Points. pctGR, @Collaboratory1.

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Trials Clinical Research Vaccination Vaccine 130

pharmaphorum

DECEMBER 17, 2020

Another is Dr Austin Chiang , a gastroenterologist and the chief medical social media officer at Jefferson Health in Philadelphia, who said in an interview with the New York Times that covering vaccine-related topics on TikTok can be a minefield. Dr Austin Chiang.

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Scientist Vaccination Vaccine Medicine 97

Rethinking Clinical Trials

JANUARY 17, 2024

The COVID Therapeutics Committee worked with the state health department to develop a policy for fair allocation of scarce medications to treat COVID-19. Tags #pctGR, @Collaboratory1 The post Grand Rounds January 12, 2024: Design and Implementation of a Weighted Lottery to Equitably Allocate Scarce Covid-19 Resources (Erin K.

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Clinical Trials Clinical Trials Antibody Trials 173

Rethinking Clinical Trials

OCTOBER 27, 2022

Perakslis said his definition of digital health is any time you mix medical information and the internet. How can we do research in states that are restricting access to reproductive health and keep patients safe? We don’t want to create a disparity like that and have these women lose access to research. pctGR, @Collaboratory1.

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Clinical Research Research Clinical Trials Clinical Trials 130

Rethinking Clinical Trials

FEBRUARY 7, 2024

The spread of misinformation has accelerated, in part because more people than ever are accessing health information on the internet and via social media. The primary finding is that clear consistent communication both to consumers directly and via medical channels is critical to the FDA’s mission to protect and promote public health.

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Intouch Solutions

APRIL 11, 2024

Offering the physician support from a virtual assistant during the differential diagnosis process where they have access to a more extensive knowledge and experience base. but others must be external such as: electronic health records, prescription data, medical literature, social media, and more.

Compliance 52

Compliance Marketing Drugs Pharma Companies 52

pharmaphorum

JANUARY 21, 2022

Access to medicines is “one of the most challenging policy areas in every country in the European region” – it’s time to develop a solution that works for everyone. Balancing the incentivisation of innovation against affordable access to revolutionary new medicines is an age-old conundrum in the biopharmaceutical industry.

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Medicine Marketing Manufacturing Production 52

Rethinking Clinical Trials

JULY 9, 2023

Many of these communities are served by federally qualified health centers that often lack options to provide accessible nonpharmacologic alternatives. Researchers must also be prepared to consider the question of sustaining a service that many clinics in the study have come to rely on, even before the results are available.

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Clinical Trials Clinical Trials Trials Research 130

Rethinking Clinical Trials

FEBRUARY 28, 2024

But there are concerns to developing DCTs including lack of standardization and validation, regulatory and ethical uncertainties, engagement vs. coercion, data security and privacy issues, technological literacy and access, resistance to change and adoption, and lack of “safe” sharing.

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Clinical Trials Clinical Trials Trials Clinical Research 143

Drug Discovery World

MAY 22, 2023

But are these price tags a barrier to access? The fact remains that the science behind the drugs is sound, there is direct patient need, and the medical benefits are pertinent. Biotech and pharma are actively working with payers and insurers to deliver on equitable pricing models that ensure access. million per dose.

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Gene Therapy Gene Drugs Contamination 52

Rethinking Clinical Trials

MAY 19, 2023

The data visualization started with a basic list of information needed, including systolic and diastolic data; clinic and home data; raw data numbers, effect of medications on blood pressure; goal ranges; out of range values; customizable goal ranges; patient burden of entry; data variability relative to control, and contextual life event data. .

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Trials Clinical Trials Clinical Trials Medicine 130

Rethinking Clinical Trials

AUGUST 18, 2022

Vanderbilt University Medical Center. The recruitment plan needs to include study materials that are tailored and accessible to the research population. Consuelo H. Wilkins, MD, MSCI. Senior Vice President and Senior Associate Dean. for Health Equity and Inclusive Excellence. Professor of Medicine. Equity, Diversity, Recruitment.

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pharmaphorum

SEPTEMBER 15, 2020

“Digitally native brands are typically agile businesses from the ground up, and agility and flexibility are part of their core makeup,” says Joe Holmes, vice president, marketing services, US at Tag. Jeremy Richter, Tag. Build on the rapid responses to COVID-19. The mindset that accomplished this needs to be retained,” Jeremy says.

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Branding Marketing Pharma Companies Life Science 130

The Pharma Data

NOVEMBER 29, 2021

1.1.529 a variant of concern, named Omicron, on the advice of WHO’s Technical Advisory Group on Virus Evolution (TAG-VE). WHO’s TAG-VE will continue to monitor and evaluate the data as it becomes available and assess how mutations in Omicron alter the behaviour of the virus. Recommended actions for countries.

Vaccination 52

Vaccination Vaccine Genome Genomics 52

XTalks

JUNE 28, 2023

It is indicated for patients who do not have a pre-existing medical reason preventing treatment with the therapy. In its approval, the FDA said it considered the potential risks associated with the drug, the life-threatening and debilitating nature of the disease for these children and the urgent unmet medical need.

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Gene Therapy Gene Protein FDA Approval 98

The Pharma Data

DECEMBER 3, 2020

The manuscript describing the detailed results will be accessible on an online preprint server shortly. We and our collaborators are steadfast in our commitment to the development of safe, effective and accessible COVID-19 vaccines for the global population.”. About Trimer-Tag © Technology. About COVID-19 S-Trimer Vaccine.

Vaccination 52

Vaccination Vaccine Immune Response Protein 52

Roots Analysis

JANUARY 28, 2024

The concept of big data is often described using three key characteristics, known as the 3 V’s, as coined by Doug Laney in the early 2000s: Volume: Big data is collected from a wide range of sources, like transactions, Internet of Medical Things (IoMT), industrial equipment, videos, images, audio, and social media.

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Big Data Medicine Marketing Clinical Trials 40

pharmaphorum

NOVEMBER 24, 2021

reSET-A is still in development and has not yet been approved by the FDA, but could help “bring effective, evidence-based treatments for alcohol use disorder to many more people,” according to the digital health company’s chief medical officer Yuri Maricich. Photo by thom masat on Unsplash.

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Production Development Trials 59

pharmaphorum

AUGUST 17, 2020

In this article Joanna Carlish, managing director of financial services at Tag Americas , and Robb DeFilippis, Tag Americas’ managing director, life sciences, go head-to-head to discuss marketing within a regulated industry. Joanna Carlish, managing director, financial services, Tag Americas. Virtual connections.

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Regulation Marketing Sales Branding 97

World of DTC Marketing

DECEMBER 13, 2021

As cancer survival rates rise, so do the price tags of life-saving treatments. Monthly drugs costs may reach $100,000, causing many Americans to struggle with the physical and emotional effects of high out-of-pocket medical costs. billion included out-of-pocket costs of $16.22 billion and patient time costs of $4.87

Drugs 55

Drugs FDA Approval Medicine Containment 55

Rethinking Clinical Trials

AUGUST 28, 2023

 Speakers Prof Sir Martin Landray, FMedSci Professor of Medicine & Epidemiology University of Oxford Chief Executive, Protas Khair ElZarrad, PhD, MPH Director, Office of Medical Policy Center for Drug Evaluation and Research (CDER) U.S. While E6(R3) provides a foundation for GCP expectations, guidelines alone are not adequate.

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Clinical Trials Clinical Trials Trials Development 130

Rethinking Clinical Trials

AUGUST 28, 2023

 Speakers Prof Sir Martin Landray, FMedSci Professor of Medicine & Epidemiology University of Oxford Chief Executive, Protas Khair ElZarrad, PhD, MPH Director, Office of Medical Policy Center for Drug Evaluation and Research (CDER) U.S. While E6(R3) provides a foundation for GCP expectations, guidelines alone are not adequate.

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Clinical Trials Clinical Trials Trials Development 130

Pharmaceutical Technology

MARCH 22, 2023

The pharmaceutical industry began using radio frequency identification (RFID) tags in the early 2000s. Pfizer was the first to use the tech, adding RFID tags to track a Viagra (sildenafil) shipment circa 2006. Twenty years ago, the cost of implementing RFID tags and the ecosystem (software) was much more expensive than today.

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Production Pharma Production Pharma Companies Drugs 264

Delveinsight

JULY 22, 2020

The method of services delivery and design has transformed to the extent that people can access healthcare services from thousands of miles away with just a smartphone. Now the user can easily access the information through various user interfaces for their personal, commercial or industrial decision making as required. Emergency Care.

Doctors 59

Doctors Doctor Marketing Production 59

pharmaphorum

AUGUST 28, 2020

Giving the Joseph Leiter lecture at this year’s virtual Medical Library Association (MLA) conference Harvard Medical School’s Professor John Brownstein spoke about embracing non-traditional data streams in public health. Many other industries have exploded because they’ve been able to access data,” he said. “If

Medicine 71

Medicine Research 71

Delveinsight

FEBRUARY 25, 2021

once Galleri becomes accessible in the second quarter of 2021. Earlier, the prescription-only blood test will only be available through partner health systems, medical practices, and self-insured employers. Working with Quest will help them support convenient access to blood collection for patients and healthcare providers.

DNA 52

DNA In-Vivo Genetics Medicine 52

pharmaphorum

NOVEMBER 16, 2022

However, with a price tag of €1.58 However, a recently released report from the organisation could blow the price tag of Zolgensma out of the water. Equity of access. million, the company could not find government and payers ready to meet the cost and chose to withdraw from the European market , rather than lower the price.

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Gene Therapy Gene Marketing Development 131

XTalks

AUGUST 23, 2021

But these aims must be balanced with the third principle of protecting study participants from unnecessary risks, like those that may result from preventing patients from accessing available therapies to maintain the integrity of the treatment and placebo arms of the trial.

Clinical Trials 52

Clinical Trials Clinical Trials Trials Drugs 52

pharmaphorum

NOVEMBER 28, 2022

Innovation thrives in collaboration, not in isolation – and the open sourcing of Substra is a landmark moment in the use of collaborative AI in medical research,” Ibrahim Haddad, general manager of the LF AI & Data Foundation, said in a statement. Open source is undoubtedly the future of AI research.”.

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Pharma Companies Life Science Research Development 72

XTalks

FEBRUARY 27, 2024

Despite high price tags of a couple of million dollars, gene therapy makers say they are working to ensure patients are able to access the treatments through patient assistance programs developed in conjunction with the support of governments. Sarepta hopes to clarify Elvidys’ effectiveness in older children in a confirmatory trial.

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Research Drugs Gene Therapy Clinical Trials 59

XTalks

DECEMBER 21, 2022

The past year has been a strong one for life sciences industries, from pivotal gene therapy approvals to continued innovations in the biotech and medical device spaces. As of October 5, 2022, the list includes 178 AI/ML-enabled medical devices, 91 of which were granted clearance in 2022 alone. million for a single infusion.

Life Science 52

Life Science Gene Therapy Gene Clinical Trials 52

Intouch Solutions

JULY 27, 2021

And 17%, or 56 million Americans, can be considered “medically disenfranchised,” with inadequate access to a primary care doctor. The first recent event was covered in our May article “ $ To Switch ,” where we explained how Cigna was offering patients $500 incentives to switch medications. What’s happening?

Drugs 52

Drugs Marketing Vaccination Vaccine 52

Delveinsight

DECEMBER 3, 2020

There are presently no medical treatments, which can regenerate retinal cells that have atrophied, though gene therapies and stem cell therapies are the leading R&D hopes in this arena. Zimmer Biomet buys chest surgery toolmaker A&E Medical. It has already succeeded in a phase 1 test, with a second in patients with wet AMD.

Gene Therapy 52

Gene Therapy Gene Antibody Research 52

The Pharma Data

MAY 15, 2021

While this was unfortunate for the soldiers as they lost access to an excellent tool that helped them lose weight and stay fit… This is fortunate for you because it’s allowed us to create our PentagonFit tracker – and give them away– for just the cost of shipping. Most people don’t know it, but U.S

Production 52

Production Containment Medicine Vaccination 52

XTalks

MARCH 22, 2023

And make sure you’re registered for our free online community for instant access to thousands of on-demand webinars. There’s been a 20 percent increase in the average launch price for new drugs every year since 2008, according to a research letter published in the Journal of the American Medical Association ( JAMA ).

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XTalks

FEBRUARY 11, 2021

In 1951, Franklin joined the Biophysical Laboratory at King’s College, London as a research associate in the Medical Research Council’s (MRC) Biophysics Unit headed by John Randall, where she was made to take up work on DNA after her stints in coal research.

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Genetics DNA Genome Genomics 119