Wed.Oct 12, 2022

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Why improving maternal care could be impossible without VBC

MedCity News

This dearth of maternity care providers is exacerbating the country’s less-than-stellar reputation for birth outcomes. In order to ensure better health for mothers and their newborns, OB-GYNs must identify risk factors that negatively impact pregnancy early on and work to maintain the whole picture of their pregnant patients’ health. However, OB-GYNs aren’t incentivized to do this under a fee-for-service payment model.

Patients 117
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Woman of the Week: HBA’s Nikki Jones

PharmaVoice

As the Healthcare Businesswomen’s Association’s first chief people and DEI officer, Jones is poised to tackle pay gap inequity, systemic gender bias and leadership barriers impeding women of color.

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Trending Sources

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Lewy body dementia – Do you even know what that is?

MedCity News

Too many of us and our families have been affected by dementia in one form or another. October is recognized by patients, advocates and the medical community as Lewy Body Dementia Awareness month, and perhaps this year it will mark new hope for those suffering from this disease.

Medical 109
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Eureka Institute to show what translational medicine can do for digital health

pharmaphorum

It’s no secret that the healthcare system is made up of a panoply of diverse stakeholders, each with their own priorities, incentives, and motivations. Bringing those stakeholders together is an oft-lauded goal, but it’s proved easier said than done. The Eureka Institute, a Syracuse, Italy-based non-profit, is focused on addressing this disparity by providing education, research, and advocacy around the field of translational medicine.

Medicine 101
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Unlocking Excellence: How Catalent Is Transforming Japan’s Clinical Research

Planning on running clinical trials in Japan? How can you reliably supply these studies? Discover Catalent’s clinical supply packaging facility in Shiga, Japan. Strategically located between Tokyo and Osaka, and one of largest in Japan, this 6,000 square meter facility offers comprehensive services including primary and secondary clinical packaging and labelling, comparator sourcing, cold chain storage, local and global distribution, local language support and white glove service to support stud

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Merck pays Moderna $250M to share equally in cancer vaccine for melanoma

MedCity News

Moderna and Merck have been partners in the development of messenger RNA cancer vaccines since 2016. Merck is deepening the alliance by exercising an option that enables it to share equally in further work on a partnered cancer vaccine for melanoma.

Biopharma 106
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What are E-Detailers and how can they Benefit Pharma Marketers?

Celeritas

Over the last decade, the US BioTech and Pharma industries have truly flourished, with pharma-related discoveries and innovations growing at an increasing rate. In line with this trend, there is building pressure on HCPs to adopt newer processes and prescribe advanced medication. Due to rigid FDA regulations, however, pharma financial resources are often depleted in generating drugs which fail to pass the approval process.

Pharma 98

More Trending

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Merck gets on board with Moderna cancer vaccine in $250m deal

pharmaphorum

Shares in Moderna were ticking upwards today after Merck & Co took up an option on a personalised RNA-based cancer vaccine with a payment of $250 million. It is the first time that Merck has exercised an option in its collaboration with the mRNA vaccine specialist, first agreed in 2016 and expanded two years later to include additional candidates.

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High-touch, tech-enabled patient engagement + patient activation resolve barriers to accessing care

MedCity News

The years ahead will require the ongoing enactment of meaningful policy, ongoing research and investment, and foresighted dedication to innovative solutions and technical advancements that support patient engagement and activation.

Patients 105
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Investment fuels AI-driven development of breakthrough genomic medicines

pharmaphorum

David Del Bourgo (CEO and co-founder, Whitelab Genomics) has always been passionate about introducing disruptive, innovative technologies to markets. Now, he leads Whitelab Genomics as its artificial intelligence (AI) platform powers the development of genomic therapies – an emerging field in which genetic sequences are injected into cells to target and repair damaged genes.

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CMS is proposing a national provider directory. Here’s what AHIP thinks it should look like

MedCity News

CMS is proposing a system in which it would collect information from providers that would go in a single national directory it maintains. AHIP is seeking a more collaborative directory between the government and private insurers.

Insurance 102
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How Machine Learning Drives Clinical Trial Efficiency

Clinical trial data management is increasingly challenging as studies grow in complexity. Quickly accessing and analyzing study data is vital for assessing trial progress and patient safety. In this paper, we explore real-time data access and analysis for proactive study management. We investigate using adverse event (AE) data to monitor safety and discuss a clinical analytics platform that supports collaboration and data review workflows.

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Could first anti-tau therapy be approved for Alzheimer’s?

European Pharmaceutical Review

A Phase III trial evaluating TauRx Therapeutics’ oral drug hydromethylthionine mesylate (HMTM), a tau aggression inhibitor, showed the medication continued to improve cognition over a pre-treatment baseline in patients with early Alzheimer’s for the first time. It has potential to become the first DMT targeting tau to be approved for the condition, stated Pippa Salter, Senior Neurology Analyst at GlobalData.

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Telehealth benefits need extension with 2 key guardrails, policy expert says

MedCity News

If telehealth flexibilities are not protected once the public health emergency expires, many Americans will lose their access to virtual care. To prevent this, the healthcare industry must advocate for the extension of these benefits for at least two years following the end of the emergency, with guardrails placed around two key areas — the prescription of addictive medications and audio-only visits.

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Where the CEO of ADC Therapeutics sees ‘huge potential’ in the tech beyond oncology

PharmaVoice

The “magic bullet” approach of ADCs has been a breakthrough in cancer care — but this excitement could be just the beginning.

98
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CA physicians’ union nears strike as working conditions continue to suffer

MedCity News

The strike authorization vote comes after survey results earlier this month that showed 68 percent of respondents reported they are contemplating leaving public employment with the county in the next three years.

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Roles and Responsibilities of Specialized Clinical Supply Experts

When selecting a clinical supply provider, consideration often focuses upon the manufacturing, packaging, storage and distribution capabilities available that will, at face-value, be sufficient to meet the needs of the sponsor and their trial. However, there are human-based and knowledge-driven factors that are often overlooked that go beyond these basic physical capabilities and are integral to the development and delivery of high performing clinical supply chains.

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The criticality of compliance

pharmaphorum

Remaining compliant is imperative to the life sciences industry, so adhering to regulatory requirements is mandatory. Prior to selling drugs or medical products in any country, pharmaceutical companies must prove compliance and gain the regulatory approval required by the country in which the goods will be distributed in. By remaining compliant, medicines are manufactured in line with their pre-defined and approved specifications, in order to ensure the delivery of safe and effective products to

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Brave Health lands $40M to support mental health services for Medicaid beneficiaries

MedCity News

The funding round was led by Town Hall Ventures. Brave Health is primarily focused on providing mental health services for those on Medicaid, a rarity for mental health providers.

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Aptar launches digital disease management platform

pharmaphorum

Aptar Pharma has added another element to its suite of digital support tools for patients as they make their journey through the healthcare system. The new disease management platform will allow for better patient treatment adherence tracking, according to the company, which says it will create an “end-to-end” digital health programme that will support patients “from the prevention and diagnosis phases, to disease management, and more, across multiple therapeutic areas.”

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Folx rakes in $30M to enhance direct-to-consumer LGBTQ health platform

MedCity News

LGBTQ virtual care platform Folx Health recently closed a $30 million Series B financing round, bringing the startup’s total funding to date to roughly $60 million. The company will use the money to expand its services, including the addition of clinician-led support groups. The first of these support groups will focus on queer fertility and family planning.

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Deliver Fast, Flexible Clinical Trial Insights with Spotfire

Clinical research has entered a new era, one that requires real-time analytics and visualization to allow trial leaders to work collaboratively and to develop, at the click of a mouse, deep insights that enable proactive study management. Learn how Revvity Signals helps drug developers deliver clinical trial data insights in real-time using a fast and flexible data and analytics platform to empower data-driven decision-making.

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CSafe and BioLife Collaborate on CGT Delivery

Pharmaceutical Commerce

Partnership looks to provide supply chain support for products in this sector, ranging from early clinical phase to commercial scale.

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Sea creature-inspired biotech Ascidian surfaces with $50M and a new way to edit RNA

MedCity News

Ascidian Therapeutics is developing therapies for inherited disorders that work by editing RNA with an approach that could offer advantages over currently available genetic medicines. The biotech’s lead program is in preclinical development for Stargardt disease, a rare eye disorder caused by multiple genetic mutations.

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Novo Nordisk submitting once-weekly insulin to FDA following Phase III success

Pharmaceutical Technology

Novo Nordisk has recently completed its six-part ONWARDS Phase III trial, as ONWARDS 5 reached its primary endpoint with Icodec demonstrating non-inferiority in reducing hemoglobin A1C (HbA1c) in patients with type 2 diabetes (T2D) at week 52 in comparison to once-daily basal insulin analogs. This successful outcome for insulin icodec increases the likelihood of achieving Food and Drug Administration (FDA) approval next year, which will establish Novo Nordisk’s dominance in the basal insulin mar

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Liverpool city region wins government status for vaccine discovery

PharmaTimes

DIT to showcase Liverpool city region’s life sciences expertise which will also include manufacturing

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Accelerating Clinical Supply Through Integrated Drug Development

As the development pipeline for new drugs continues to grow, biopharmaceutical companies are re-evaluating how to best manage and balance resources across an increasing number of development projects and complex clinical trials. There are two approaches that can be used to speed a drug from development to clinic faster: timeline compression and parallel processing, but only one that considers the benefits of integrating clinical supply into the overall drug development process.

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FDA Expands Oversight of Cell and Gene Therapies

PharmaTech

CBER maps modernization plan to handle surge in research and applications.

FDA 109
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Mission Street and BentallGreenOak to create 23-acre ‘science district’

PharmaTimes

Development will boost life sciences sector by delivering significant lab space in Cambridge

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AstraZeneca builds its AI capabilities again with Illumina tie-up

pharmaphorum

AstraZeneca has teamed up with DNA sequencing giant Illumina on a new programme that will use artificial intelligence to find new targets for drug discovery by sifting through vast arrays of data generated from “omics” studies. Overall, the aim is to improve the efficiency of drug discovery by identifying genetic variants that contribute to human disease in omics data – a broad category that includes DNA profiles, gene transcripts, and protein expression.

Pharma 64
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Neumora raises funds for precision neuro therapies development

Pharmaceutical Technology

Neumora Therapeutics has raised $112m in a Series B financing round to advance its new precision medicine candidates pipeline for neuropsychiatric disorders and neurodegenerative diseases. New and existing investors including F-Prime Capital, Altitude Life Science Ventures, Mubadala Capital, Amgen, Exor Ventures, ARCH Venture Partners, Invus, Abu Dhabi Growth Fund (ADG), Newpath Partners, Polaris Partners, as well as other undisclosed investors have participated in the financing round.

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Clinical Data Like You´ve Never Seen It Before: Why Spotfire Is the Leading Tool for Clinical Analytics

Clinical development organizations face a wide array of challenges when it comes to data, many of which can impact the operational effectiveness of their clinical trials. In this whitepaper, experts from Revvity Signals explore how solutions like TIBCO® Spotfire® enable better, more streamlined studies. The whitepaper also features a success story from Ambrx, a leading biopharmaceutical company, detailing how it has leveraged Spotfire to tackle data quality and collaboration challenges in clinic

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Walmart follows CVS, Walgreens into clinical trial sector

pharmaphorum

Walmart is the latest US retail pharmacy giant to announce its intention of disrupting the clinical trials category, with the launch of a new institute that pledges to increase and diversify community access to healthcare research. The Walmart Healthcare Research Institute (WHRI) won’t be running trials itself, but will spearhead Walmart’s efforts to connect patients who visit its massive, nationwide chain of health centres with organisations running clinical trials.

Retail 64
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Fireside Chat with Brad Womble, Senior Director of Strategy, Marketing and Mergers & Acquisitions at Jabil Healthcare

Impetus Digital

Register for Impetus’ upcoming live webinar on October 26, 2 – 3 PM ET: A Fireside Chat with Brad Womble, Senior Director of Strategy, Marketing and Mergers & Acquisitions, at Jabil Healthcare. About the webinar. Brad Womble , Senior Director of Strategy, Marketing and Mergers & Acquisitions, at Jabil Healthcare , will sit down with Natalie Yeadon , Co-founder & CEO of Impetus Digital , in this live episode of Healthcare Goes Digital.

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Mankind Pharma Limited- Openings for Engineering – Water System & Electrical Process Area – Sterile Injectable– Apply Now

Pharma Pathway

Mankind Pharma Limited- Openings for Engineering – Water System & Electrical Process Area – Sterile Injectable– Apply Now. Job Description. Openings for Engineering – Water System & Electrical Process Area – Sterile Injectable @ Mankind Pharma Limited. Engineering – Water System & Electrical Process Area – Sterile Injectable.

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Nimbus and Lilly partner for metabolic disease therapies development

Pharmaceutical Technology

Nimbus Therapeutics and Eli Lilly and Company (Lilly) have signed a research partnership and licence agreement to develop and market new therapies that activate a specific AMPK isoform to treat metabolic diseases. Under the collaboration deal, Nimbus will develop isoform-selective small molecule AMPK activators to potentially treat several metabolic diseases using its computational drug discovery engine and structure-based drug design knowledge.

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The New Clinical Trial Supply Chain: Resilient, Flexible, and Patient-Centric

The global landscape of clinical trials is rapidly changing as studies become more complex. An increasing number of sponsors are seeking enhanced flexibility in their supply chains to address a variety of clinical supply challenges, including patient demand and reducing delays. Demand-led supply and direct-to-patient distribution are next-generation solutions that are helping to meet these growing needs, allowing for more streamlined processes and patient-centric studies.