Tue.Sep 26, 2023

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Rollout of Covid vaccines is bumpy, but not unexpected, experts say

STAT

The latest rollout of Covid-19 vaccines has been messy, with people facing more challenges getting one of the updated shots than they may have experienced since the frantic start of the very first vaccination campaign in late 2020 and the first half of 2021. The issues have come as a surprise to people whose appointments have been canceled for lack of vaccine doses, who couldn’t get an appointment at their nearest pharmacy, or who learned with dismay that the place where they got previous

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Do humans have a place in pharma’s AI future?

PharmaVoice

From COTA’s large datasets and AI model assistants to a company guiding patients through cancer care, AI can help — but it’s a long way from human-free.

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Trending Sources

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Nurses and health care support workers at higher risk of suicide, study finds

STAT

Jobs in health care are known to be challenging for workers’ mental health. But the mental health toll can be especially burdensome for registered nurses, health technicians, and health care support workers, who are at a higher risk of suicide compared to the general population, according to a study published on Tuesday in the Journal of the American Medical Association that looked at a nationally representative cohort of about 1.84 million employed people (both within the health care fie

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Why Senda’s new chief medical officer says targeted delivery tech is like ‘science fiction’

PharmaVoice

The Flagship-backed biotech believes the secret to more precise drug delivery lies in the nanoparticles of plants and fungi.

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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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Women face host of disadvantages in cancer prevention and care, report finds

STAT

Patriarchy isn’t a word that Ophira Ginsburg expected to be at the center of her work as a cancer researcher but, like an infection, it was invading her everyday work as a medical oncologist. There were times when she saw people treat women’s lives and health with cruel indifference. There were times when she saw women who struggled to access care because of violence or social obligations or stigma.

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Encourage pregnant women to take up Covid jab offer, NHSE asks

The Pharmacist

Community pharmacies and other vaccination providers are being urged to make sure pregnant women know they are eligible for booster vaccinations this autumn amid concerns over the latest Covid variant. A total of 1.16 million Covid jabs were delivered in total in the first week of the programme. Some 2.8 million flu jabs were also […] The post Encourage pregnant women to take up Covid jab offer, NHSE asks appeared first on The Pharmacist.

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UKHSA reaches vaccine deal with CSL Seqirus

Pharma Times

Agreement will provide timely boost to pandemic preparedness against influenza - News - PharmaTimes

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STAT+: Just how much money do drugmakers gain from patent extensions?

STAT

Extending patent protection doesn’t just stretch a drug’s profits — in some cases, doing so can lead to its most significant revenue period, according to a recent analysis published by the Initiative for Medicines, Access & Knowledge, or I-MAK, a nonprofit advocating for drug pricing reforms. The organization looked at four blockbuster drugs — Humira, Avastin, Rituxan, and Lantus — that had biosimilars launched between 2019 and 2023.

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Intercept, after biotech rollercoaster ride, agrees to buyout by Alfasigma

BioPharma Dive

Once valued at more than $7 billion, the liver drug company couldn’t secure a long-sought FDA approval in NASH and last month said it would abandon that research.

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STAT+: Medicare Advantage plans for dual-eligible enrollees set to get Senate scrutiny

STAT

The Senate has set its eyes on regulating insurance plans for some of the most vulnerable patients in the U.S. — the 12.5 million people eligible for both Medicare and Medicaid. “They’re a complex group of people with a lot of chronic conditions — mental illness, frailty, disability,” said Jose Figueroa, an internal medicine physician and health policy expert at Brigham and Women’s Hospital.

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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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Oxford Biodynamics launches prostate screening test

Pharma Times

EpiSwitch is designed for men with prostate cancer risk in the UK and is 94% accurate - News - PharmaTimes

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STAT+: Early data are promising for autoimmune disease drug from Roivant Sciences’ Immunovant

STAT

Results released Tuesday from an early study of an autoimmune disease drug from Roivant Sciences’ Immunovant showed the treatment could reduce the levels of a key immune marker in the blood, a promising signal. The results are only from a Phase 1 trial, but were anticipated because they were the first-in-human outcomes being reported for the antibody drug, IMVT-1402.

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Immunovant data show potential for autoimmune disease drug

BioPharma Dive

Much anticipated clinical trial data for Immunovant’s experimental FcRn inhibitor could catalyze business development decisions for its parent, Roivant Sciences.

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Opinion: STAT+: The problem with potential changes to the biosimilar regulatory framework

STAT

Biosimilars are no longer a new and untested class of medicines. Today, they provide critical treatment options across multiple therapeutic areas. Since the Biologics Price Competition and Innovation Act of 2009 created a regulatory pathway for biosimilar medicine review in the U.S.,  37 biosimilars  have come to market offering the potential to increase patient choice and cost savings.

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Lilavati Hospital promoter family launches Lilavati Pharmacy

Express Pharma

The Mehta family, the promoter of the Lilavati Hospital, is establishing a chain of Lilavati Pharmacy stores across the country. The Lilavati Pharmacy project is being driven by Prashant Mehta, the promoter and MD. The Lilavati Pharmacy chain will also commence a wellness programme for community members. Customers will be able to consult a doctor at the pharmacy itself and seek an appropriate line of treatment.

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STAT+: Intercept, once a biotech trailblazer, sells itself for less than $1 billion

STAT

Intercept Pharmaceuticals, a firm whose treatment for a prevalent liver disease once made it the hottest stock in biotech, said Tuesday it would sell the company for less than $1 billion. Alfasigma, an Italian pharmaceutical firm, will pay $19 a share for Intercept , in a roughly $800 million cash deal that represents an 80% premium to the company’s recent trading price.

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Queens University Belfast study reveals strong economic case for precision oncology medicine

Express Pharma

Queen’s University Belfast conducted a comprehensive study of the initial wave of precision oncology medicines. This was conducted in collaboration with a team of precision healthcare economists and researchers from Salutem Insights, Diaceutics PLC and King’s College London. The study examined the economic impact of precision oncology medicines compared to traditional oncology medicines.

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STAT+: Ionis inches toward first solo drug launch with late-stage trial success for rare genetic disease therapy

STAT

Ionis Pharmaceuticals, a California biotech that has spearheaded the development of RNA-targeting medicines, announced on Tuesday that its drug against familial chylomicronemia syndrome, a rare and serious disease that prevents the body from breaking down fats, succeeded in a late-stage clinical trial. The Phase 3 trial, dubbed Balance, enrolled 66 adults who were randomly divided into three groups and given a monthly injection of placebo or one of two doses of olezarsen, the company’s ex

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IIT Mandi researchers propose a protein-based vaccine against pork tapeworm

Express Pharma

Indian Institute of Technology Mandi researchers, led by Dr Amit Prasad, Associate Professor, School of Biosciences and Bioengineering, has made strides in the development of vaccines against the pork tapeworm (T. solium). This tapeworm is responsible for both intestinal infections and the more severe brain infection that leads to seizures. Their research, conducted in collaboration with scientists from Dayanand Medical College and Hospital in Punjab and the CSIR-Institute for Himalayan Bioresou

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STAT+: Elevance’s embattled bid to buy Louisiana’s Blues plan was a stretch to begin with

STAT

If you’re surprised Elevance Health is having trouble buying a not-for-profit Blues plan, you haven’t been paying attention. The insurance behemoth hasn’t pulled off such a deal in almost 20 years. Elevance’s announcement that it’s pausing its $2.5 billion bid to buy Blue Cross and Blue Shield of Louisiana follows strong pushback amid concerns about higher prices, fairness to members, and uncertainty over what would happen with the billions in proceeds.

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Sanofi gets Japanese authorisation for factor VIII therapy for hemophilia A

Pharmaceutical Business Review

ALTUVIIIO, also known as efanesoctocog alfa, is an antihemophilic factor (recombinant), Fc-VWF-XTEN fusion protein used for perioperative management of bleeding, controlling bleeding episodes, and routine prophylaxis. The recommended dosage of ALTUVIIIO for all patients, and when used under different clinical scenarios is 50 IU/kg. The company claimed that ALTUVIIIO is the first and only hemophilia A treatment that can deliver normal to near-normal factor activity levels (over 40%) for most of t

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STAT+: Pharmalittle: FDA to furlough one-fifth of staff if government shuts down; FDA cites ‘grossly deficient’ data for ALS drug

STAT

Hello, everyone, and nice to see you again after we engaged in an extended respite. We took the opportunity to recharge and reflect, but now, of course, have returned to the usual routine of deadlines and calls and the like. So time to fire up the coffee kettle and quaff a few cups of stimulation. We are starting today with glazed doughnut, since one can never be too sweet, yes?

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Considerations for safety data migration methods

European Pharmaceutical Review

Pharmaceutical companies regularly transfer databases as they shift to new systems or change service providers in pursuit of higher quality and increased efficiency. These database transfer activities must follow industry standards and pharmacovigilance regulation, which has become increasingly stringent over the last decade. The concept of good pharmacovigilance practice (GVP) has been implemented in multiple regions across the globe to ensure these migrations are validated and data integrity i

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Dr Mansukh Mandaviya launches national R&D and Innovation Policy and PRIP scheme

Express Pharma

Dr Mansukh Mandaviya, Union Minister of Chemicals and Fertilizers and Minister of Health & Family Welfare, Government of India launched of National Policy on Research and Development and Innovation in pharma-medtech sector in India and Scheme for promotion of Research and Innovation in Pharma MedTech Sector (PRIP). Dr V K Paul, Member, NITI Aayog, S Aparna, Secretary (Pharma), Ministry of Chemicals and Fertilizers and Dr Rajiv Bahl, Director General, ICMR were also present at the event.

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Lymphoma maintenance therapy delivers promise in CTCL

European Pharmaceutical Review

Resminostat (Kinselby) has been clinically proven to postpone disease progression, new data from one of the largest clinical trials in cutaneous T-cell lymphoma (CTCL) to date has revealed. The treatment is an oral small molecule class I, IIb and IV histone deacetylase (HDAC) inhibitor. Data from the RESMAIN resminostat study Findings from the RESMAIN study of the maintenance therapy could significantly change clinical practice in advanced CTCL, according to the company.

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Pharmacies must be ‘part of the primary care offer’, says Labour

The Pharmacist

Pharmacies should be part of the primary care offer and do more for their communities, the shadow minister for primary care and public health, Preet Kaur Gill, has said. The comments were made in a video filmed during a visit to an independent community pharmacy in Staffordshire last week. Ms Gill, who is the Labour […] The post Pharmacies must be ‘part of the primary care offer’, says Labour appeared first on The Pharmacist.

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Embracing AI: Q&A with Shalu Chadha

PharmExec

Accenture’s global life sciences technology lead discusses how the life sciences industry has embraced artificial intelligence.

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Medicine reimbursement system ‘in significant peril’ as £100m write-off ends

The Pharmacist

The drug reimbursement system in England is in ‘significant peril’, Community Pharmacy England’s director of pharmacy funding Mike Dent has said. This comes as the £100m in additional margin allowance that was granted back to the sector last April has been phased out. In the new drug tariff, the government has also made a downward […] The post Medicine reimbursement system ‘in significant peril’ as £100m write-off ends appeared first on The Pharmacist.

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Hires and retires: key appointments in pharma

Outsourcing Pharma

BioPharma Reporter and Outsourcing Pharma is keeping you in the know with our most recent round-up of important appointments in the pharma industry - including Veranova, Matica Bio and Aldevron.

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Post-pandemic reality hits digital health hard

pharmaphorum

Post-pandemic reality hits digital health hard Mike.

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Novartis' ruxolitinab to treat rare blood cancer recommended for approval by NICE

Outsourcing Pharma

A rare and incurable blood cancer, associated with an overproduction of blood cells, that can lead to stroke or heart attack, will soon have access to a small molecule Novartis treatment for the condition.

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Regeneron and Sanofi’s sBLA for Dupixent accepted by FDA for priority review

Pharmafile

Regeneron Pharmaceuticals and Sanofi have announced that the US Food and Drug Administration (FDA) has accepted their supplemental Biologics License Application (sBLA) for Dupixent (dupilumab) for the treatment of children between one and 11 years old with eosinophilic esophagitis (EoE). The target action date for an FDA decision is 31 January 2024.

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New tool enables target discovery for new class of diseases not yet mechanically understood

Outsourcing Pharma

A new approach to discovering targets for Alzheimerâs and other neurodegenerative diseases has been presented by Insilico Medicine with the University of Cambridge, UK.

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New study finds blocking histones using antibodies alleviated lung fibrosis

World Pharma News

Lung fibrosis is a debilitating disease affecting nearly 250,000 people in the U.S. alone with 50,000 new cases reported each year. There is currently no cure and limited available treatment options, underscoring the pressing need to better understand why people get this disease. In a new study, Boston University Chobanian & Avedisian School of Medicine researchers have identified that abnormal interactions between different cell types, particularly platelets and lung immune cells, promote l

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Opportunity Pharma and OpenEye join forces to develop AI expert for drug discovery

Outsourcing Pharma

Drug discovery will benefit from a virtual artificial intelligence (AI) expert thanks to Opportunity Pharma and OpenEye, Cadence Molecular Sciences joining forces.

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