Sat.May 17, 2025 - Fri.May 23, 2025

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Must Watch Pharmaceutical Trends

Pharma Marketing Network

Can a flashy website really move the needle for an oncology brand? Is social media too risky for pharma compliance? These questions reflect some of the biggest myths in digital marketing in pharma , an area that continues to evolve at warp speed yet remains tethered by legacy thinking. Many marketers in the pharmaceutical industry struggle to balance innovation with regulation, often falling into traps set by outdated beliefs.

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Suicide Risk Management Crucial in Dermatological Care

Drug Topics

Researchers conducted a clinical review detailing the intersection of dermatology and suicide, explaining why skin conditions lead to increased risk of poor mental health.

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FDA Grants Market Clearance to Diagnostic Blood Test for Alzheimer Disease

Pharmacy Times

The Lumipulse G pTau217/-Amyloid 1-42 Plasma Ratio is the first in vitro diagnostic device that tests blood to aid in diagnosing Alzheimer disease.

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Opinion: I study diet and chronic illness. Here’s the uncomfortable truth about seed oils

STAT

For decades, mainstream nutrition guidelines have recommended that Americans replace animal fats like butter or lard with polyunsaturated fats, especially seed oils such as soybean, corn, and sunflower oils. These oils are rich in omega-6 fatty acids and now make up a significant portion of the fat consumed in the standard American diet. But recently, the conversation has shifted.

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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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With the third round of Medicare price negotiations on the way, here’s how the policy is shifting

PharmaVoice

HHS issued guidance for the third cycle, teeing up another 15 drugs to be selected by early next year.

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Fierce Healthcare - Untitled Article

Fierce Healthcare

With most eyes on Medicaid cuts in Congress, keep a close eye on ACA enrollment over the next six months, warn health policy experts.

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STAT+: Maryland governor signs law to expand powers of the state’s prescription drug affordability board

STAT

In a notable development, Maryland Gov. Wes Moore signed a bill that will allow a state board to extend its mandate for lowering prescription drug costs to all residents, not just those employed by government agencies. The move was hailed by consumer advocates who hope the Prescription Drug Affordability Board, which is designed to function much like a state utility commission, will usher in era of lower medicine prices for everyone who lives in Maryland.

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Lilly’s former small molecule head makes the leap to a rising biotech in obesity

PharmaVoice

Utpal Singh joined the peptide-focused biotech Zealand Pharma last month after it notched a massive obesity deal with Roche.

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Fierce Healthcare - Untitled Article

Fierce Healthcare

In a briefing held by the Catholic Health Association, hospital leaders referred to the moral imperative they and Congress share to preserve the countrys safety net.

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Navigating the Impacts of “COVID Brain”: A Pharmacy Student’s Journey

Pharmacy Times

COVID-19 can reshape ones academic journey and outlook on life.

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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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Private funder HHMI pauses postdoc fellowship

STAT

Molecular biologist Chiara Masnovo spent weeks filling out an application for a research fellowship earlier this year — taking it over the finish line as she was 38 weeks pregnant and starting a new job.  The chance of getting this fellowship was well worth the toil. The Hanna Gray fellowship, created by the Howard Hughes Medical institute, supports postdoctoral researchers from diverse backgrounds in their transition to heading their own labs.

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FDA tightens heart tox warnings on mRNA COVID vaccines

pharmaphorum

The FDA has instructed Pfizer and Moderna to add stronger warnings to the labels of their COVID-19 vaccines about the risk of cardiotoxicity

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Tracking a moving target: How drugmakers should brace for a looming tariff impact

PharmaVoice

With policies in flux, companies seek to be proactive and understand their supply chain.

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FDA Approves Mepolizumab for Treatment of Patients With COPD and an Eosinophilic Phenotype

Pharmacy Times

Mepolizumab gains FDA approval as a promising add-on therapy for COPD patients with eosinophilic phenotype, reducing exacerbation rates significantly.

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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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New FDA framework on Covid vaccines leaves pediatricians confused and concerned

STAT

A new framework for Covid-19 vaccines announced by Food and Drug Administration leaders Tuesday suggests the agency will no longer approve new Covid vaccines for healthy individuals under 65, including babies, without data from new randomized clinical trials showing their benefit.  The plan — described in a commentary in the New England Journal of Medicine, followed by a live stream on YouTube — created confusion among physicians about what it means for young children.

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Japan follows UK in GSK's comeback tour for Blenrep

pharmaphorum

The revitalisation of GSK's blood cancer therapy Blenrep continues with a second approval, in Japan, as a second-line treatment for multiple myeloma

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Prescribing Red Flags: Pharmacists Be Wary of What the Doctor Orders

The FDA Law Blog

By Larry K. Houck Last month the U.S. Attorneys Office for the Northern District of Illinois announced that Walgreens agreed to pay up to $350,000,000 to resolve allegations that its pharmacies illegally filled millions of invalid prescriptions for opioids and other controlled substances in violation of the federal Controlled Substances Act, and sought payment for filling many of those prescriptions by federal health care programs, violating the False Claims Act.

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FDA Approved Antihemophilic factor, PEGylated-Aucl For Pediatric Patients With Hemophilia A

Pharmacy Times

The approval expands the therapys indication to children as young as 7 years of age.

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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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STAT+: The UnitedHealth crash and mandatory Medicare models

STAT

This is the online version of STAT’s email newsletter Health Care Inc., delivered to your inbox every Monday.  Sign up here. I’ve always been skeptical of virtual reality headsets, and it appears my skepticism has been justified. Tell me what’s going on in your reality, virtually: bob.herman@statnews.com or bobjherman.09 on Signal.

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Regeneron swoops on genetic testing firm 23andMe

pharmaphorum

DNA testing company 23andMe looks destined to be taken over by a pharma company, as Regeneron agrees a $256 million acquisition deal

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Turning the page: Novo’s CEO transition reflects Big Pharma’s era of change

PharmaVoice

Turnover of the top execs at pharma giants like J&J, AbbVie and Merck in the last few years illustrates the seismic industry shifts that often accompany leadership changes.

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FDA to Restrict Future COVID-19 Vaccine Recommendations to Older Adults, High-Risk Groups

Pharmacy Times

In a major policy shift, officials from the FDA announced a new regulatory framework for COVID-19 vaccinations, prioritizing adults aged 65 and older and individuals with serious comorbidities putting them at high risk for severe COVID-19.

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FDA approves diagnostic tool for MET-targeted lung cancer therapy

Pharmafile

The US Food and Drug Administration (FDA) has approved Roches VENTANA MET (SP44) RxDx Assay as a diagnostic tool to identify non-squamous non-small cell lung cancer (NSQ-NSCLC) patients eligible for treatment with AbbVies targeted therapy Emrelis (telisotuzumab vedotin-tllv). The assessment detects an overexpression of the MET protein, a predictive biomarker associated with tumour progression and […] The post FDA approves diagnostic tool for MET-targeted lung cancer therapy appeared first

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Bankrupt DNA testing firm 23andMe to be purchased for $256m

The Guardian - Pharmaceutical Industry

Drugmaker Regeneron Pharmaceuticals will buy the genetic testing firm through a bankruptcy auction The drugmaker Regeneron Pharmaceuticals will buy the genetic testing firm 23andMe Holding for $256m through a bankruptcy auction, the companies said on Monday. Regeneron said it will comply with 23andMes privacy policies and applicable laws with respect to the use of customer data and that it is ready to detail its intended use of the data to a court-appointed overseer.

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STAT+: RFK Jr. meets with health tech startups, most backed by Andreessen Horowitz

STAT

Of the seven health tech companies that met with the government’s most powerful health official on Monday, all but one had something in common: Financial backing from one of Silicon Valley’s top venture capital firms. In a post on the social media platform X, the Department of Health and Human Services announced that health secretary Robert F.

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Triple-Combination Therapy Met Primary End Point in Phase 3 Trials, Providing Treatment for Individuals With Asthma

Pharmacy Times

A new triple-combination therapy shows promise in improving asthma management, offering hope for millions with uncontrolled symptoms.

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UK trumpets £1bn investment plan from BioNTech

pharmaphorum

BioNTech has said it will commit up to 1bn in investment in the UK over the next decade, in what has been described as a "template" for the sector

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Fierce Healthcare - Untitled Article

Fierce Healthcare

As Republicans in Congress push through a tax and immigration package that includes provisions that would cut Medicaid eligibility, Providence CEO Erik Wexler has a stark warning to lawmakers: the challenges facing healthcare amount to a national security issue.

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STAT+: Mental health apps can boost outcomes and lower costs, study finds

STAT

Developers of digital mental health treatments now have fresh economic data to help make the case for broader coverage of their apps. Companies selling Food and Drug Administration-cleared apps for the treatment of psychiatric and other conditions have long struggled with adoption by patients, providers, and payers for many reasons. Clinical evidence supporting these prescription digital therapeutics has gradually improved , but policymakers and insurers have been hesitant to open the path to re

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FDA Approves Roflumilast Topical Foam 0.3% for Plaque Psoriasis in Adults and Children

Pharmacy Times

This indication is for adult and pediatric patients aged 12 and older with plaque psoriasis of the scalp and body.

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O'Shaughnessy says UK clinical trials sector is on the mend

pharmaphorum

After losing ground in commercial clinical trials in recent years, the UK has now turned a corner and is once again taking a "global lead"

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Fierce Healthcare - Untitled Article

Fierce Healthcare

Vertical consolidation in healthcare has been a hot-button topic of late as regulators eye strategies to bring down healthcare costs.

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Blunt Rochester presses RFK Jr. on CDC acting director

STAT

Sen. Lisa Blunt Rochester has written a stinging letter to Health Secretary Robert F. Kennedy Jr. demanding that he clarify whether the Centers for Disease Control and Prevention has an acting director. In her three-page missive, Blunt Rochester suggested that Matthew Buzzelli, the person Kennedy said was the CDC’s acting director, cannot hold the role because he isn’t qualified under the federal Vacancies Act.

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