Tue.Mar 25, 2025

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Character Biosciences raises $93M with an eye on vision loss drugs

Bio Pharma Dive

The startup is bringing into Phase 1 testing an experimental treatment it says could be more effective than marketed geographic atrophy medicines.

Medicine 195
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GSK and UK researchers plan to study Shingrix and dementia risk reduction link

Pharmaceutical Technology

The study will analyse electronic health records of 65- and 66-year olds from the UKs National Health Service (NHS).

Research 147
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Merck bets $200M on a new type of heart pill

Bio Pharma Dive

A licensing deal with Jiangsu Hengrui Pharmaceuticals puts Merck in a competitive race to develop a medicine that targets a genetic risk factor called lipoprotein(a).

Licensing 187
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WuXi AppTec sells UK-US units, but annual results show foreign contracts continue despite China tensions

Pharmaceutical Technology

WuXi AppTec (Shanghai, China) has sold off two US/UK businesses in February and March, it revealed in its annual results on 18 March 2025.

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Bridging Innovation & Patient Care: The Growing Role of AI

Speaker: Simran Kaur, Co-founder & CEO at Tattva.Health

AI is transforming clinical trials—accelerating drug discovery, optimizing patient recruitment, and improving data analysis. But its impact goes far beyond research. As AI-driven innovation reshapes the clinical trial process, it’s also influencing broader healthcare trends, from personalized medicine to patient outcomes. Join this new webinar featuring Simran Kaur for an insightful discussion on what all of this means for the future of healthcare!

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Medical Device Notification Warns of Continued Data Integrity Concerns

FDA Law Blog

By Adrienne R. Lenz, Principal Medical Device Regulation Expert Last year, FDA issued a letter to the medical device industry warning medical device firms of concerns related to fraudulent and unreliable laboratory testing data in premarket submissions, which we blogged about here. This was followed last September with warning letters issued to two Chinese firms performing biocompatibility testing, citing violations of 21 C.F.R.

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Novo Nordisk earmarks $2bn for Chinese “triple G” weight loss shot

Pharmaceutical Technology

Novo Nordisk has acquired the global rights to United Laboratories triple-agonist weight-loss and diabetes drug in a deal worth up to $2bn.

Drugs 130

More Trending

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Overcoming regulatory challenges in sterile manufacturing

Pharmaceutical Technology

Evolving regulations in sterile manufacturing requires innovation, market knowledge, and investment. How can drug manufacturers respond?

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UK weight loss market: M&A opportunities

pharmaphorum

Explore the latest M&A opportunities in the UK weight loss market, including market access for products like Wegovy and Mounjaro. Stay informed about key trends and opportunities in the industry.

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Alumis and Kaken sign agreement in Japan to develop ESK-001

Pharmaceutical Technology

Alumis and Kaken Pharmaceutical have entered a partnership and licensing agreement for the development of the formers ESK-001.

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GSK taps into UK health data for dementia study

pharmaphorum

GSK joins with two UK research organisations to explore a possible link between its shingles vaccine Shingrix and a reduced risk of dementia.

Vaccine 64
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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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EMA to review GSK’s Nucala for COPD treatment expansion

Pharmaceutical Technology

The EMA has agreed to review GSKs application to expand Nucalas use as an add-on maintenance for individuals with COPD.

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AbbVie sues Genmab, claiming trade secrets theft

pharmaphorum

A multibillion-dollar partnership between AbbVie and Genmab risks being soured by a lawsuit claiming misappropriation of trade secrets

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UKHSA unveils high-risk pathogen list to drive innovation

Pharmaceutical Technology

The agency has published a list of 24 high-risk infectious diseases as a reference tool for funders and researchers.

Research 130
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Examining Healthcare Spending Across US Counties

Pharmaceutical Commerce

What drivers impact the differences in expenditures?

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Optimizing Clinical Supply Strategy: Navigating Challenges & Finding Your Ideal Model

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Sermonix and Regor to enhance breast cancer treatment options

Pharmaceutical Technology

Sermonix Pharmaceuticals and Regor have announced a strategic partnership aimed at developing therapeutics in the breast oncology area.

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Pharma Pulse 3/25/25: Identifying Affordability Issues with Predictive Analytics, Novo Nordisk Extends Lowered Wegovy Price to Retail Pharmacies & more

Pharmaceutical Commerce

The latest news for pharma industry insiders.

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MSD licenses Lp(a) heart drug from Hengrui in $2bn deal

pharmaphorum

MSD has fleshed out its cardiovascular disease pipeline by licensing an oral Lp(a) inhibitor from China's Jiangsu Hengrui Pharma for $200m upfront

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Expert Reveals 8 ‘Essential’ Ways to Reduce Your Risk of Stroke

AuroBlog - Aurous Healthcare Clinical Trials blog

Strokes are caused by a blockage in the brain’s blood vessels. (piyaset/iStock/Getty Images Plus) As a nurse working in a neurocritical care, I witnessed the sudden and devastating effects of stroke on survivors and their carers. Following my nursing career, I became a researcher specializing in stroke.

Nurses 147
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The New Age of Decentralized Clinical Trials

White paper that delves into the complex topic of Decentralized Clinical Trials and how to master them within the confines of FDA Regulations

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5 ways to address pricing and access challenges across the European landscape

pharmaphorum

EVERSANA discuss 5 effective strategies for overcoming pricing and access challenges in the European healthcare landscape. Learn about HTA, risk-sharing, data utilisation, orphan drugs, and more.

Drugs 52
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Ayush and herbal products exports report growth of 10% in first nine months of FY25

AuroBlog - Aurous Healthcare Clinical Trials blog

Exports of Ayush and herbal products for the first nine months of the current fiscal have reported a 9.9 per cent growth, while the third quarter of the fiscal reported growth of 9 per cent compared to the same period of previous fiscal year.

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The Advantages of an All-in-One eClinical Tool for Clinical Trials: How Integrated CTMS and eTMF Enhances Efficiency and Compliance

Pharma Mirror

Clinical trials have grown increasingly complex and now require robust solutions to manage data, documentation, and workflows. Traditionally, organizations have relied on separate systems for Clinical Trial Management Systems (CTMS) and Electronic Trial Master Files (eTMF), often leading to inefficiencies, compliance risks, and administrative burdens.

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Is my Pharma Marketing Job Going to Be Eliminated?

Pharma Marketing Network

Automation, AI, budget cuts, and evolving digital strategies have prompted a growing question among pharmaceutical marketing teams: Is my pharma marketing job at risk? As companies adapt to more agile workflows and redefine what modern commercialization looks like, the roles of marketing professionals are being evaluated more critically than ever before.

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European Clinical Supply Planning: Balancing Cost, Flexibility and Time

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Can mRNA Integrity and 5’ Capping Efficiency be Assessed Using a Single Assay?

XTalks

The development of mRNA vaccines has revolutionized the field of immunization, offering a rapid, adaptable and effective approach to combating infectious diseases. However, ensuring their safety, efficacy and stability requires precise characterization throughout the development and manufacturing process. Characterizing mRNA vaccines involves evaluating molecular integrity, purity, potency and immunogenicity, as well as ensuring consistent large-scale production.

Vaccine 59
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How to Reach HCP’s In Pharma Marketing

Pharma Marketing Network

Healthcare professionals (HCPs) are the cornerstone of pharmaceutical success, yet reaching them has never been more complex. Between digital saturation, regulatory scrutiny, and shifting engagement preferences, marketers must be both strategic and adaptable. Understanding how to effectively engage HCPs in pharma marketing is essential for driving brand awareness, product education, and ultimately, prescription behavior.

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How Do You Engage Pediatric Participants When Developing Clinical Trial Materials?

Imperical Blog

Creating materials for pediatric participants, whether in digital or printed formats, presents unique challenges. This is due to the need to communicate complex ideas in simpler terms as well as create documents that appeal to that audience. Read on for tips to engage pediatric participants… The post How Do You Engage Pediatric Participants When Developing Clinical Trial Materials?

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Top 10 Clinical Trial Trends in the US in 2025

XTalks

Clinical trials in the US are undergoing rapid transformation in 2025. Driven by advances in digital technology, regulatory updates and growing emphasis on patient-centric design, sponsors and research organizations are rethinking how studies are designed, conducted and analyzed. From the rise of decentralized trial models and wearable technology to the integration of real-world evidence and AI-powered data management, these trends are reshaping timelines, accessibility and efficiency.

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The New Age of Decentralized Clinical Trials

This new white paper defines and details the impact of Decentralized Clinical Trials on the Pharmaceutical industry and how the impact can be measured along with steps companies can take to ensure adoption.

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Competing in the Generic Drug Market: Strategies for Success

Drug Patent Watch

Breaking into the Generic Drug Market: Strategies for Success As a pharmaceutical professional, you know that the generic drug market is a highly competitive space. With new generic drugs entering the market every year, it can be challenging to stand out from the crowd and achieve success. But what sets the successful generic drug companies apart from the rest?

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Reflections and Photos from the Inaugural Drug Channels Leadership Forum 2025

Drug Channels

Wow! What an absolutely incredible time at the inaugural Drug Channels Leadership Forum (DCLF)! Paula and I are beyond grateful to everyone who took the stage to share their insights and to all who participated in making this event so impactful. (Even Paula got on the main stage!) The event was packed with thought-provoking discussions, candid insights, and dynamic exchanges.

Drugs 52
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1 in 10: Understanding Endometriosis

My Local Study

March is Endometriosis Awareness Month, a time to bring attention to a condition that affects an estimated 1 in 10 women of reproductive age worldwide. Endometriosis. The word itself can feel heavy, echoing the weight of a condition often shrouded in silence, misunderstood, and frequently dismissed. Yet, for millions, it’s a daily reality of debilitating.

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Trump tariffs drive pharma manufacturing to US but risk inflation and disruption

Pharmaceutical Technology

Trump hinted that the US will impose a 25%+ tariff on pharmaceuticals after giving US companies time to build more manufacturing capacity.

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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