Fri.Oct 07, 2022

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New comments outline ways to protect patients from health plans and PBMs who profit from patient assistance

PhRMA

PhRMA submitted comments this week in response to the Department of Health & Human Services (HHS) proposed rule on the Nondiscrimination in Health Programs and Activities. As outlined in our comments, PhRMA supports many policies in the proposed rule that aim to combat discrimination in health programs and activities, including broad application of nondiscrimination provisions, promoting health equity and preventing discriminatory benefit designs.

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SingleCare Announces the Best of the Best Pharmacy Award Winners

Drug Topics

SingleCare's 4th annual celebration of the best in pharmacy, from pharmacists to pharmacy technicians and teams across the United States has been announced.

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Trending Sources

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Monkeypox Treatment and Prevention: Stopping the Latest Outbreak

Pharmacy Times

There is not yet an FDA-approved treatment available for monkeypox, but existing antiviral agents have been found to be effective in vitro and in animal studies.

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Poor Lung Function Tied to Asthma Exacerbations

Drug Topics

Early interventions might preserve lung function, particularly in younger patients with frequent asthma exacerbations, say authors.

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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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Psychedelic Medicine May Be an Effective Treatment for Alcoholism

Pharmacy Times

New research suggests that MDMA may offer promising benefits to patients with certain unmet psychological treatment needs.

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Provention and Sanofi enter deal to launch teplizumab for type 1 diabetes

Pharmaceutical Technology

Provention Bio and Sanofi US have signed a co-promotion agreement to launch the former’s lead investigational drug candidate, teplizumab for the delay in the onset of clinical type 1 diabetes (T1D). The agreement aids Provention in leveraging the capabilities and commercial resources of Sanofi to back teplizumab’s launch. The US Food and Drug Administration (FDA) is presently reviewing teplizumab for the delay of clinical T1D in people who are at risk.

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Merck’s Lagevrio ‘no better than placebo’ in COVID hospitalisations

pharmaphorum

A UK study has found that Merck & Co’s oral COVID-19 therapy Lagevrio was unable to reduce hospitalisations compared to placebo in patients at higher risk from the virus, adding fuel to assertions in some quarters that its authorisation was premature. The 25,000-subject PANORAMIC trial conducted by researchers at Oxford University looked at the addition of a five-day course of Lagevrio (molnupiravir) to standard care in people aged over 50, or adults aged 18 and over with conditions th

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A Rare Specialty Pharmacy’s Quick Response to Customized Patient Education Using QR Codes

Pharmacy Times

QR codes are currently used in various health care settings, such as in hospitals for patient verification, but more recently for health care-related education.

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STAT+: Merck’s Covid-19 pill was no better than placebo in lowering the risk of hospitalization

STAT

A Merck pill used to combat Covid-19 failed to demonstrate it can lower the risk of hospitalization compared with a placebo among adults at a higher risk from the disease, according to the results of a large study conducted in the U.K. The preliminary results of the randomized trial, which involved more than 25,000 participants, showed that taking molnupiravir did speed time to recovery by about six days, which means that patients did get some relief.

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Pharmacy Focus: Psychedelic Pharmacy - An Exploration of Psychedelic Medicines in Palliative Care

Pharmacy Times

For patients facing end-of-life care, psychedelic medicines may offer a chance to feel connected with themselves and others during such a difficult time.

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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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AZ/BenevolentAI collab achieves AI-enabled further milestones

pharmaphorum

Two additional novel AI-generated targets for chronic kidney disease (CKD) and idiopathic pulmonary fibrosis (IPF) have been discovered using the Benevolent Platform and selected for AstraZeneca’s (AZ) drug discovery portfolio. These latest discoveries bring the total number of targets selected to date for AZ’s portfolio-entry under the collaboration up to five, with potential for future development milestones and sales-based royalty revenues for London-based BenevolentAI, also.

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Clinician Discusses How To Support A Team-Based Model Between Pharmacists, Physicians

Pharmacy Times

Michael Barr, MD, MBA, MACP, FRCP, discusses the importance of physicians and pharmacists sharing skills to increase positive patient outcomes.

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STAT+: Medicare Advantage quality ratings plunge as government resets to pre-pandemic standards

STAT

Federal officials significantly reduced the quality scores of next year’s Medicare Advantage plans, a move that was widely expected but will still affect millions of older adults and people with disabilities who have migrated to the growing program. The lower scores also will drain billions of dollars in bonuses that flow to health insurers that get high marks.

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Rucaparib Trial Achieves Primary Endpoint in Metastatic Castration-Resistant Prostate Cancer With BRCA, ATM Mutations

Pharmacy Times

Rucaparib is the only PARP inhibitor demonstrated to have better outcomes than a docetaxel-containing control arm, according to researchers.

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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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To boost rural vaccination rates, health officials head for NASCAR

STAT

WASHINGTON — The federal government, which has long struggled to increase Covid-19 vaccinations in rural areas, is starting to take its shots to where the people are: NASCAR races. A vaccination tent at the NASCAR Cup Series in Arizona next month — attended by roughly 100,000 people — is the latest effort devised by Health and Human Services officials and advisers keen to reinvigorate booster rates that have stalled amid public fatigue and skepticism.

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USP Expert: A Pharmacist Saved My Father’s Life as We Emigrated From Iraq, ‘That's Why I Became a Pharmacist’

Pharmacy Times

Farah Towfic, PharmD, MBA, RPh, director, CEO Operations, US Pharmacopeia, details some of the moments that led her to the pharmacy field and the important role that mentorship played in that process.

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Another potential roadblock to wider telemedicine abortion: state medical boards

STAT

In the post-Roe landscape, advocates for abortion rights are pinning hopes on telehealth as one way to provide access in states with newly imposed limits. Startups like Abortion on Demand and Hey Jane  have expanded their capacity to offer telemedicine services, prescribing abortion pills by mail in early pregnancy. Pro-access states, including Massachusetts last month, have enacted measures to protect providers of abortion care from legal penalties.

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Frontiers Health Steering Committee spotlight – Fredrik Debong

pharmaphorum

As we enter October and the Frontiers Health 2022 conference in Milan, we’re shining a spotlight on some of the Steering Committee members who have helped make the event what it is. Here we talk to Fredrik Debong, who cofounded MySugr in 2012 and sold it to Roche Diabetes Care five years later in an eight- to nine-figure deal. A cooling off in digital health investment.

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Opinion: Certified nursing assistants do important work. They deserve to be paid a living wage for it

STAT

In mid-April 2020, as Covid-19 shutdowns and lockdowns were being put in place across the U.S., my grandmother’s health started to decline. With so many unknowns , the assisted living facility where she lived, like most others, had a strict no-visitors policy. When it became clear that my grandmother was in her last hours of life, the facility figured out how to safely allow my aunt into the building for my grandmother’s last breaths.

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Betting the House on Orphan Drugs

Pharmaceutical Commerce

While all drug development efforts are fraught with peril, a growing number of biopharma companies—large and small—are staking a claim in the rare disease treatment space, chasing odds that could yield clinical and financial rewards.

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Opinion: FDA’s plan to define “healthy” for food packaging: Better than the existing labeling anarchy, but do we really need it?

STAT

The FDA has announced the set of rules it proposes to enforce for manufacturers to claim that a food product is “healthy.” The proposed rules are a lot better than the labeling anarchy that currently exists. But here’s my bottom line: health claims are not about health. They are about selling food products. The FDA says that a “healthy” product must meet two requirements: It must contain a meaningful amount of food, and it must not contain more than certain upp

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NICE recommends first oral S1P receptor modulator for ulcerative colitis

European Pharmaceutical Review

The National Institute of Health and Care Excellence (NICE) has recommended Bristol Myers Squibb’s Zeposia ® (ozanimod) for use in England and Wales to treat moderate to severe ulcerative colitis (UC) cases in adults who are intolerant of, or unresponsive to biologics or conventional therapies. UC is an Inflammatory Bowel Disease (IBD) that makes immune system attack the gastrointestinal (GI) tract.

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STAT+: Biogen CEO search focuses on scientists, with former J&J exec as a leading candidate

STAT

A senior researcher who was most recently at Johnson & Johnson has emerged as a top candidate to be Biogen’s CEO, according to people familiar with the discussions. The selection of the researcher, Mathai Mammen, until recently the head of R&D at pharmaceutical giant Johnson & Johnson, would be a major departure for Biogen, which has tended to hire corporate operators rather than credentialed scientists to serve as CEO.

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Is Stevia Good or Bad for Hashimoto’s Disease?

The Thyroid Pharmacist

When I began my health journey with nutrition, I was skeptical. Could giving up gluten, dairy, and sugar really make a difference? If these foods were that problematic, I would have certainly learned about them in pharmacy school, right? Well, much to my surprise, within three days of giving up these three foods, my bloating, acid reflux, and irritable bowel syndrome vanished!

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STAT+: Up and down the ladder: The latest comings and goings

STAT

Hired someone new and exciting? Promoted a rising star? Finally solved that hard-to-fill spot? Share the news with us, and we’ll share it with others.  That’s right. Send us your changes, and we’ll find a home for them. Don’t be shy. Everyone wants to know who is coming and going. And here is our regular feature in which we highlight a different person each week.

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Is the launch environment really more competitive now?

pharmaphorum

It’s often stated – mostly without reference to data – that the environment for innovative launches is more competitive now than it ever has been. Is this true? IQVIA has the long term market data, from World Reviews back to 1978, to investigate, and analysed nearly 30 years of launches into leading therapy classes, from multiple eras in the development of the pharmaceutical industry.

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STAT+: Health plans say texting could help reach underserved patients. But a federal rule is getting in their way

STAT

Health plans trying to reach low-income and underserved customers say they’re being stymied by a decades-old federal rule limiting texting — and they’re framing it as a health equity issue in their bid to change it.  Low-income and underserved patients, they say, are more likely to see and respond to texts about their health than they are to answer calls from unknown numbers or to receive mailed notices, especially if they’re at work or move frequently.

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OSD contract manufacturing market valued at $54.7 billion by 2030

European Pharmaceutical Review

A market report has projected that the global oral solid dosage (OSD) contract manufacturing market is expected to be worth $54.7 billion by 2030, displaying a compound annual growth rate (CAGR) of 6.0 percent. Data showed that worldwide, oral solids are the most popular mode of drug delivery due to being highly cost-effective and offering simple manufacturing processes.

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STAT+: Pharmalittle: Medicare can still penalize drugmakers for hiking prices to privately insured patients; FDA explains push to withdraw premature-birth drug

STAT

And so, another working week will soon draw to a close. Not a moment too soon, yes? This is, you may recall, our treasured signal to daydream about weekend plans. Our agenda calls for manicuring the Pharmalot campus, hanging with our shortest short person, indulging in still more ancient rituals and, otherwise, simply lounging about. And what about you?

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TauRx sees path to FDA filing for tau-targeting Alzheimer’s drug

pharmaphorum

TauRx Pharma’s effort to bring a tau-targeting drug for Alzheimer’s disease (AD) to market has been a marathon, with a number of setbacks over the years, but the company reckons it may finally be getting closer to the finishing line. The phase 3 LUCIDITY trial of tau aggregation inhibitor hydromethylthionine mesylate (HMTM, formerly known as LMTM or LMTX) showed improvements in cognition in patients compared to their performance and baseline, and also seemed to reduce brain atrophy t

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Medical Debt Pushed by More Than Cancer, Diabetes

Drug Topics

Pre-pandemic survey examines effects of heart disease, asthma, and more.

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Acetazolamide Found to Improve Decongestion in Patients With Acute Decompensated Heart Failure

Pharmacy Times

New research suggests that acetazolamide and standard loop-diuretic therapy may decrease congestion and prevent future hospitalizations in patients with acute decompensated heart failure.

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News Roundup: October 3 to October 7

Drug Topics

Your weekly roundup of the latest news from Drug Topics®.

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Are you a bad boss?

PharmaVoice

Pharma execs share their tips for being a better leader.

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