Wed.Oct 19, 2022

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Earlier Intervention Can Decrease Hospitalizations for COVID-19

Drug Topics

Implementing mask mandates even days earlier can cause a decrease in the number of cumulative hospitalizations due to COVID-19.

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Word of the Month: What is Long COVID?

PhRMA

What is Long COVID?

Vaccines 290
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Trending Sources

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Increased HPV Knowledge Could Lead to Increased Vaccination Rates

Drug Topics

Improving vaccination rates for the most common STI in the United States could be as simple as increasing knowledge about HPV.

Vaccines 185
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CVS Health supports future of pharmacy through minority scholarship program

Drug Store News

The scholarships represent a commitment to an inclusive community and promoting diversity of thought, background, perspective and experience to advance pharmacy education and improve patient health.

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Position Your Pharmacy for Expansion

Speaker: Chris Antypas and Josh Halladay

Access to limited distribution drugs and payer contracts are key to pharmacy expansion. But how do you prepare your operations to take the next step? Meaningful data: Collect and share clinical data regarding outcomes, utilization, and more Reporting: Limited distribution models require efficient tracking and reporting systems Workflows: Align workflows with specific pharma and payer contractual requirements For in-depth, expert insights on pharmacy expansion, watch this webinar from Inovalon.

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Therapies Targeting Capsid Proteins Show Promise for HIV-1

Pharmacy Times

By targeting the viral conical core, these ARTs could disrupt the process of assembly and/or disassembly of the virus and result in its suppression.

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Could monkeypox infections have long-term consequences?

STAT

Since the world began confronting a global outbreak of monkeypox in the spring, the scientific community has had plenty of reasons to rue the fact that for decades this virus has been understudied. Here’s another one: Because of that oversight, doctors treating people who have been infected with monkeypox can’t answer with certainty whether some of them will face any long-term health consequences, referred to as sequelae in the field of medicine.

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More Trending

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Opinion: To learn lessons from pandemics, don’t listen to big pharma

STAT

Early in the Covid-19 pandemic, the leaders of wealthy countries pledged to respond with “global solidarity.” But when vaccines to prevent the disease were developed, those same leaders pushed low and middle-income countries to the back of the queue, outbidding poorer countries, as well as COVAX, a worldwide initiative developed to achieve equitable vaccine access, to secure vaccines for themselves.

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Study Shows Psoriasis Does Not Increase Heart Attack Risk in Patients with Kidney Disease

Pharmacy Times

The study confirmed that patients with psoriasis are considered to have an increased risk for both chronic kidney disease and ESRD, because inflammation plays a significant role in those conditions as well as heart disease.

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Lilly agrees to acquire gene therapy developer Akouos for $610m

Pharmaceutical Technology

Eli Lilly and Company has signed a definitive agreement for the acquisition of all outstanding shares of precision genetic medicine firm Akouos for a total deal value of up to nearly $610m or up to $15.50 for each share in cash. The deal comprises an acquisition value of $12.50 for each share in cash payable at closing along with one non-tradeable contingent value right per share (CVR) of up to another $3 in cash.

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FDA Grants Emergency Use Authorization for Novavax Adjuvanted COVID-19 Vaccine as Booster for Adults

Pharmacy Times

Neutralizing antibodies increased by 34- to 27-fold compared to pre-booster levels when administered at 8 or 11 months post-primary series.

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What the FDA's New Dosage Guidance Means for the Future of Clinical Research

Speaker: Dr. Ben Locwin - Biopharmaceutical Executive & Healthcare Futurist

What will the future hold for clinical research? A recent draft from the FDA provides valuable insight. In "Optimizing the Dosage of Human Prescription Drugs and Biological Products for the Treatment of Oncologic Diseases," the FDA notes that "targeted therapies demonstrate different dose-response relationships compared to cytotoxic chemotherapy, such that doses below the Maximum Tolerated Dose (MTD) may have similar efficacy to the MTD but with fewer toxicities.

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Frontiers Health 2022 – day 1

pharmaphorum

Frontiers Health 2022 in Milan is LIVE! Opening Day One will be Healthware Group’s CEO and founder Roberto Ascione and WTF Health’s founder and host Jessica DaMassa. The day’s keynote addresses will include ‘The H is for humanity’ by MD of Taliossa Tony Estrella and founder and trustee of Rachel’s House Lynna Chandra, as well as ‘Creative disruption in delivering novel VR solutions in pain: evidence, teamwork, and delivery’ by Christopher Eccleston, professor of medical psychology at the U

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Prepare for Impact: How the Right Technology Can Energize the Pharmacy Experience

Pharmacy Times

More than 90% of independent pharmacy customers want technology to enhance their experience. Is your pharmacy ready?

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Black Death may have influenced evolution of genes involved in immune responses, study finds

STAT

The phrase “Black Death mass burial site” tends to evoke images of haphazard piles of diseased deceased like the “bring out your dead” Monty Python scene. But Hendrik Poinar, anthropology professor at McMaster University, said the East Smithfield graveyard in London, a mass burial site that dates back to the height of the bubonic plague pandemic, is the exact opposite.

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Technicians Play Key Roles in Health Systems

Pharmacy Times

Seventeen percent work in hospital settings, including compounding, inpatient, medication reconciliation, and outpatient areas.

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5 Reasons to Upgrade Your Pharmacy Management Software

Are you still using workarounds to manage your daily operations? To achieve peak performance, it's time to explore other options for specialty and infusion pharmacy software. Streamline pharmacy operations and improve clinical performance with automated processing, real-time data exchange, and electronic decision support. Download this helpful infographic to: Drive efficiency and patient adherence from referral receipt to delivery and ongoing care – all with our Pharmacy Cloud.

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FDA authorizes booster shot for Novavax’s Covid-19 vaccine

STAT

The Food and Drug Administration announced Wednesday that it has authorized a booster shot for Novavax’s Covid-19 vaccine. Unlike the latest boosters from Pfizer-BioNTech and Moderna, which target both the original strain of SARS-CoV-2 and the Omicron BA.4/5 variants, the Novavax booster only targets the original strain. The company announced in late May that it was studying an Omicron-targeting strain, as well as a bivalent booster.

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Tip of the Week: Prescribing Medicines Must Be Done With Confidence and Competence

Pharmacy Times

If pharmacists increasingly take up the prescribing mantle, then they must see to their competence to exercise that authority.

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STAT+: Large insurer’s decision to cover some prescription digital therapies may be a milestone for app makers

STAT

A large commercial insurer’s decision to cover a controversial class of software-based treatments for psychiatric and other conditions could prove to be a landmark moment in the development of these so-called prescription digital therapeutics, which until now had been unable to secure coverage from insurers skeptical that the new technologies are as effective as their makers claim.

Insurance 101
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New PCR Test May Detect COVID-19, 2 Other Respiratory Viruses With Near 100% Efficacy

Pharmacy Times

The TaqMan SARS-CoV-2, Flu A/B, RSV RT-PCR multiplex assay can differentiate between 3 different viral infections (including COVID-19), making it highly cost-effective.

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Opinion: STAT+: How digital health innovators can successfully navigate evolving FDA regulations

STAT

In the rapidly changing landscape of digital health, innovation has often outpaced regulations , especially for novel technologies and emerging industries. To narrow the gap, the Food and Drug Administration has acknowledged that new regulatory policies and frameworks are necessary. To this end, the FDA has been testing new regulatory paradigms , modernizing submission approaches , updating policies , and urging legislative actions to keep up with new developments.

FDA 101
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Top 5 Travel Healthcare Myths

Aureus Medical Group

Traveling. The word itself has so many stereotypes and misconceptions, especially when it comes to healthcare traveling. I want to bring light to a few of those misconceptions so more people fall in love with traveling. Read on for the top six myths that I believe are most common in the traveling industry. Myth #1: “It’s too hard to travel with kids or family.” Many clinicians travel with partners, children, relatives, pets, and even friends!

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STAT+: FDA panel votes that a controversial premature birth medication should be withdrawn

STAT

After an extraordinary three-day hearing, an expert panel of advisers to the U.S. Food and Drug Administration voted on Wednesday to uphold an effort by the regulator to withdraw a controversial drug for preventing premature births. The 14-to-1 vote came after the agency and Covis Pharma, the manufacturer of the drug, offered highly contrasting views of reams of clinical evidence — which they parsed in excruciating detail — in order to settle the fate of the treatment, known as Mak

FDA 101
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How the Digital Patient Experience is Shaping the Future of Pharma

pharmaphorum

From diagnosis to treatment and ongoing condition management, the patient journey is becoming an increasingly digitised one – a process which has been massively accelerated by the Covid pandemic and has significant implications for pharma & their patients vs. their customers. Join us on Monday 7 th November at 12:30 GMT / 13:30 CET / 7:30 am EDT as panellists focus on how this new paradigm is shaping both the industry’s omnichannel engagement and the patient care journey, from patient identi

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Opinion: What the Makena vote means about accelerated approval, trust, and the FDA

STAT

On Wednesday, the FDA advisory committee that oversees obstetrics, reproductive, and urologic drugs voted 14-1 that the drug Makena was not effective at reducing the risk of preterm birth, and that it should be removed from the market. We’ve been here before. In 2011, the same year that Makena received accelerated approval from the FDA, I was a member of a similar FDA advisory committee hearing in which we considered withdrawing the breast cancer indication for the drug Avastin.

FDA 101
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Every scientific message has a story. Medical communications must adapt to effectively bring these to life.

pharmaphorum

Medical communications are in a state of transition. Due to the combined impact of emerging technologies, changing provider preferences, and an evolving post-pandemic world, pharma must navigate new ways to engage providers with relevant, science-driven, digital content. Delivering these materials in the proper format, however, requires a keen understanding of providers’ educational needs, learning science, and creative storytelling.

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STAT+: Pharmalittle: Merck KGaA probed by French court for misleading info; former Genentech scientists given prison terms over trade-secret theft

STAT

Good morning, everyone, and welcome to the middle of the week. Congratulations on making it this far and remember there are only a few more days until the weekend arrives. So keep plugging away. After all, what are the alternatives? While you ponder the possibilities, we invite you to join us for a delightful cup of stimulation. Our choice today is green apple caramel — a new addition to our pantry.

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Indegene Acquires CultHealth, a Full Service, Healthcare Marketing Agency to Elevate Brand Experience

PharmExec

The acquisition by ILSL Inc., a subsidiary of Indegene Private Limited, augments Indegene’s commercialization portfolio spanning drug discovery and development to marketing and sales, adding brand strategy, market development capabilities, and patient engagement platforms.

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Listen: What makes food ‘healthy’ and why we don’t prioritize nutrition

STAT

After years of deliberation, the FDA recently announced a new set of rules it proposes to regulate claims on food packaging that a product is “healthy.” The most basic rule: the product must actually contain food, not just ingredients. This may seem intuitive, but as professor and nutrition policy expert Marion Nestle points out, the food industry works hard to sell their products.

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Lannett sells discontinued generics, inks private label deal for others

Drug Store News

Lannett's deal call for another pharmaceutical company to purchase and distribute under a private label a limited number of certain other Lannett owned generic drug products.

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Amplifying HCP engagement using modular content

pharmaphorum

Emma Hyland, VP strategy, commercial content at Veeva Systems, tells us modular content is the most significant wave of innovation hitting the content world in life sciences, and rightly so because HCPs’ needs and expectations have changed. As the world moves back to a form of normality after the last couple of years, the way in which we engage with HCPs has changed.

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Ayala Pharmaceuticals reports promising data from Desmoid Tumors trial

Outsourcing Pharma

Updated interim results from Part A the RINGSIDE pivotal Phase 2/3 study of the companyâs AL102 new drug showed consistent early tumor shrinkage with measures deepening over time, plus good tolerability at all doses.

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High Levels of Biomarker suPAR May Predict Risk of Heart Failure, Death

Pharmacy Times

New research suggests that high levels of an immune protein in kidney disease might be able to predict risk of heart failure or death by reflecting the upstream process of stress.

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U.S. Senators, industry orgs oppose proposed Kroger-Albertsons merger

Drug Store News

U.S. Sen. Amy Klobuchar (D-Minn.) and U.S. Sen. Mike Lee (R-Utah) announced they will hold a hearing in November to examine the proposed merger.

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Existing and Novel Treatments of Migraine Show Favorable Efficacy

Pharmacy Times

Case studies highlight recent developments and trends in pharmacologic treatments for migraine.

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$38 million will fund rare disease research over four-year period

European Pharmaceutical Review

The US Food and Drug Administration (FDA) has awarded a total of $38 million in the form of 19 new grants and two new contracts, to facilitate the upcoming four years of clinical trials and regulatory tools for rare diseases. Sandra Retzky, Director of the FDA’s Office of Orphan Products Development (OOPD) explained: “The contracts aim to help inform regulatory decision making and promote diversity, equity and inclusion in clinical research.”.

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