Wed.Aug 28, 2024

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STAT+: UnitedHealth pledged a hands-off approach after buying a Connecticut medical group. Then it upended how doctors practice

STAT

MIDDLETOWN, Conn. — UnitedHealth Group told the Connecticut primary care doctors everything they wanted to hear. Take our money, the company said, and together we can bring about a future where primary care leads. A future where doctors can take better care of their patients, and reap the financial rewards of improved health. We’ll handle the business side while you look after your patients.

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PQA Issues Call to Action to Improve Medication Therapy Management

Pharmacy Times

Eight areas of improvement were developed as part of national initiative with stakeholder involvement.

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Trending Sources

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NIH launches $270 million anti-overdose research program for, and led by, Native Americans

STAT

Fatal drug overdoses shot up during the peak of Covid-19 in 2020. And as the dust settled on the pandemic, it quickly became clear that one demographic group had fared far worse than any other: Native Americans.  Now, to combat the drug crisis and its disproportionate impact on indigenous people, the federal government is launching an initiative specifically meant to bolster research into addiction and overdose within native communities.

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FDA Clears Omnipod 5 Automated Insulin Delivery System for Use in Adults With Type 2 Diabetes

Pharmacy Times

Previously, the device was indicated for the management of type 1 diabetes in patients aged 2 years and older.

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From Diagnosis to Delivery: How AI is Revolutionizing the Patient Experience

Speaker: Simran Kaur, Founder & CEO at Tattva Health Inc.

The healthcare landscape is being revolutionized by AI and cutting-edge digital technologies, reshaping how patients receive care and interact with providers. In this webinar led by Simran Kaur, we will explore how AI-driven solutions are enhancing patient communication, improving care quality, and empowering preventive and predictive medicine. You'll also learn how AI is streamlining healthcare processes, helping providers offer more efficient, personalized care and enabling faster, data-driven

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After an FDA rejection, here’s what’s next in the psychedelics pipeline

PharmaVoice

By rejecting the first MDMA therapy earlier this month, the FDA signaled to the psychedelic drug sector that the road to approval isn’t clear cut.

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Activation, Preparedness Following Treatment Lacking Among Lymphoma Survivors

Pharmacy Times

In survivors of lymphoma with fragmented transition of care, preparedness and activation for the next phase of their survivorship was lacking.

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More Trending

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Opinion: Medicare’s new transitional coverage of emerging technologies program doesn’t go far enough

STAT

Included in the original law that established Medicare in 1965 was a short but consequential mandate that the program only pay for items and services that are “reasonable and necessary” for the treatment of illness and injury. Over the decades that followed, this requirement was generally viewed as excluding from coverage those medical services and products that were experimental or investigational, or for which there was still uncertainty about the benefits and harms for Medicare

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FINTOX May Improve Financial Toxicity Screening in Cancer Treatment

Pharmacy Times

Accurate, effective screening is crucial for connecting patients with needed financial resources and support.

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STAT+: Neurocrine reports mixed results on schizophrenia therapy in mid-stage trial

STAT

Neurocrine Biosciences said Wednesday that the lowest dose of an experimental pill for schizophrenia reduced psychosis reported by patients in a mid-stage study, but higher doses of the drug also tested were ineffective.  The company said the study results supported advancing the medicine into Phase 3 studies next year. Investors viewed the mixed data with more concern, sending Neurocrine’s stock down 18% in early trading.

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Novartis taps Lindy to turn biologic drugs into at-home injectables, puts nearly $1B on the line

Fierce Pharma

Novartis has formed a strategic collaboration with drug delivery specialist Lindy Biosciences to develop self-administered versions of the Swiss pharma’s innovative drugs. | Novartis has formed a strategic collaboration with drug delivery specialist Lindy Biosciences to develop self-administered versions of the Swiss pharma’s innovative drugs.

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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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FDA Grants Priory Review for Mirdametinib to Treat NF1-PN

Pharmacy Times

Mirdametinib is an oral, allosteric small molecule MEK inhibitor to treat pediatric patients with neurofibromatosis type 1-associated plexiform neurofibromas (NF1-PN).

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Drug Topics Top 10: Most Read Stories From August 2024

Drug Topics

Check out this list of our top 10 stories from August 2024.

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Pharmacists' Guide to Evolocumab for Lowering LDL-C

Pharmacy Times

Pharmacists can play a crucial role in educating patients on the proper storage and administration of evolocumab.

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Details emerge of £400m investment programme tied to VPAG

pharmaphorum

The £400m pledged by industry as part of the new VPAG voluntary scheme of pharma rebates will be used mainly to support the UK clinical research sector

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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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With phase 3 win, Novartis pads case for broader use of heart med Leqvio

Fierce Pharma

Three years after launching Leqvio in the U.S., Novartis is still steadily advancing its blockbuster ambitions for the cholesterol-lowering drug. | After a positive phase 3 readout, Novartis said it aims to apply cholesterol-lowering Leqvio across the "full spectrum" of atherosclerotic cardiovascular disease.

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AI voice assistant can spot complications in heart patients

pharmaphorum

A virtual voice assistant used to contact patients after heart procedures can make early discharge possible and spot complications

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Inclisiran Monotherapy Significantly Reduces LDL-C in ASCVD

Drug Topics

Additional data will be presented at a scientific meeting later this year.

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Community Pharmacist Training Program Enhances Care for Patients With Epilepsy

Pharmacy Times

Community pharmacists can participate in continuing education epilepsy programs, but they are usually not specific to pharmacy practice.

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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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Investigational Acute Pain Therapy to be Evaluated in Pivotal Phase 3 Trials

Drug Topics

Tris Pharma will examine the efficacy and safety of cebranopadol in the ALLEVIATE-1 and ALLEVIATE-2 studies.

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In key win for GSK, Delaware court will review decision to allow expert testimony in Zantac cases

Fierce Pharma

Delaware's Supreme Court has upheld a GSK appeal, deciding to review the state’s Superior Court decision to allow expert testimony in Zantac lawsuits.

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We like to think UK health services aren’t influenced by big money. That’s just not true | Margaret McCartney

The Guardian - Pharmaceutical Industry

There must be transparency over funding to medics from the pharmaceutical industry – and that’s only the start Shouldn’t we be able to trust doctors to give us independent advice? Earlier this year, there was an outcry when it appeared that a doctor who often appeared on TV to speak about Covid vaccines had been paid a significant sum by the pharmaceutical company AstraZeneca.

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Novartis collaboration to innovate subcutaneous drug delivery

European Pharmaceutical Review

Novartis Pharma AG and biotech Lindy Biosciences have agreed to collaborate to advance subcutaneous biologic injectables. As part of a worldwide licensing agreement and collaboration, some of Novartis’ medicines will be developed into the injections via Lindy Biosciences’ proprietary microglassification suspension technology. This platform enables high concentrations of biologics to be delivered in a single dose, improving the convenience of administration and patient and treatment compliance, a

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HDA 2024 Traceability Seminar: DSCSA Implementation and Readiness

Pharmaceutical Commerce

Session uncovers distributors’ experiences with the Waiver, Exception, or Exemption request process, and how these affect the overall supply chain.

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Type 2 diabetes drug associated with 35% lower risk of dementia, study finds

The Guardian - Pharmaceutical Industry

Large Korean study suggests sodium-glucose cotransporter-2 inhibitors may prevent dementia A drug used to treat type 2 diabetes is associated with a 35% lower risk of dementia, according to research. The number of people with dementia globally is expected to nearly triple to 153 million by 2050. The health and social costs linked to dementia already exceed $1tn (£780bn) a year , research shows.

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Pharma Pulse 8/28/24: AI Regulation Is Coming, A Case for Payer Engagement/Participation in Clinical Research & more

Pharmaceutical Commerce

The latest news for pharma industry insiders.

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Hims takes a blow from Lilly’s vial news

STAT

Good morning. As a treat for Labor Day weekend, we’re running a deal for STAT+ subscriptions. If you use the code LABORDAY at checkout, you can get 25% off your first year. Learn more here. Now onto the biotech news of the day.

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ICYMI: Drug Topics July/August 2024 Issue

Drug Topics

Don’t miss out on the latest pharmacy insights in the Drug Topics July/August issue.

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Our investigation of UnitedHealth, explainer on Oropouche and news on maternal health

STAT

Want to stay on top of health news?  Sign up  to get our Morning Rounds newsletter in your inbox. Good morning! Amid today’s news, two items on pregnancy that are interesting and eerie to read in tandem. And on top of that, two itchy pieces of mosquito-related news from STAT’s Helen Branswell.

Insurance 101
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Rivaroxaban Clinical Pearls – 4 Big Ones

Med Ed 101

Rivaroxaban is classified as a direct oral anticoagulant. It is one of the most commonly used anticoagulants within this class (in addition to apixaban). In this blog post, I’ll share the 5 most important rivaroxaban clinical pearls that may appear in practice or on a board exam! Dosing of Rivaroxaban There are a couple of […] The post Rivaroxaban Clinical Pearls – 4 Big Ones appeared first on Med Ed 101.

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Germany's Stada reports rosy earnings as CEO tempers expectations around possible sale, IPO

Fierce Pharma

As Stada Arzneimittel’s private equity owners continue to weigh their options around a potential sale or public offering, the German drugmaker gave a good indication Wednesday of exactly what it ca | As Stada Arzneimittel’s private equity owners continue to weigh their options around a potential sale or public offering, the German drugmaker gave a good indication Wednesday of exactly what it can bring to the table.

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STAT+: Pharmalittle: We’re reading about Zantac court cases, a Neurocrine schizophrenia pill, and more

STAT

Hello, everyone, and how are you today? We are doing just fine, thank you, especially since the middle of the week is upon us. After all, we have made it this far, so we are determined to hang on for another couple of days. And why not? The alternatives — at least those we can identify — are not so appetizing. And what better way to make the time fly than to keep busy.

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Changing Faces – Board of Directors appointments from July 2024

pharmaphorum

Changing Faces announces new board of directors appointments from July 2024 for Immatics, Memo Therapeutics, Scancell, Abcuro and more. Stay updated on the latest developments in the biotech industry.

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HHS Releases Campaign to Promote Vaccine Recommendations for RSV, COVID-19, and Flu

Pharmacy Times

"Risk Less. Do More." plans to partner with national, state, and local organizations to provide resources to families and communities on how to protect themselves from RSV, influenza, and COVID-19.