Thu.Mar 20, 2025

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March 20, 2025: iPATH Team Explores Integration of Artificial Intelligence Into Analysis of Qualitative Data

Rethinking Clinical Trials

Dr. Sara Singer, principal investigator for iPATH Researchers from iPATH, an NIH Collaboratory Trial, described key considerations for integrating artificial intelligence tools into analyses of qualitative data. The report was posted this month on the AcademyHealth Blog. The iPATH trial, led by principal investigator Sara Singer at Stanford University, will test the implementation of a practice transformation strategy for type 2 diabetes in federally qualified health centers in California, Massa

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Alnylam drug gets long-awaited FDA approval in deadly heart disease

Bio Pharma Dive

Amvuttra’s clearance in a rare form of cardiomyopathy could help Alnylam turn a regular profit — if it can wrest control of a competitive and fast-changing market.

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Panel recommends programme for uniform high standard drug regulation nationwide

AuroBlog - Aurous Healthcare Clinical Trials blog

A Parliamentary Panel has recommended implementation of a comprehensive, nationwide and phased Medicines Regulatory Maturity Enhancement Programme on the lines of World Health Organisation’s (WHO) vaccine benchmarking process to ensure a consistently high standard of drug regulation across the country.

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Oxford BioTherapeutics and Roche link on antibody cancer treatments

Pharmaceutical Technology

OBT has entered a multi-year partnership with Roche to discover antibody-based therapeutics for cancer treatment.

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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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Novartis builds case for new SMA gene therapy

Bio Pharma Dive

To Novartis, fresh late-stage data support the idea that its intrathecal drug, which has the same active ingredient as Zolgensma, could be approved for a broad range of spinal muscular atrophy patients.

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Just 5 Days of Junk Food Can Trigger Obesity’s Hold on Your Brain

AuroBlog - Aurous Healthcare Clinical Trials blog

After a long, stressful day at work, or when pressed for time, the temptation to have a quick, satisfying snack like crisps or a chocolate bar can be strong.

More Trending

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Pfizer sells 7.3% stake in Haleon for $3.3bn

Pharmaceutical Technology

Pfizer has divested its residual shareholding in Haleon, representing 7.3% of the company's share capital, for a total of $3.3bn.

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Top Pharma and Biotech Companies to Work for in the US in 2025, According to Forbes

XTalks

The pharmaceutical and biotechnology industries offer some of the most rewarding career opportunities in the US. Find out the top pharma and biotech companies to work for in the US in 2025. Whether youre a scientist developing life-saving treatments, a regulatory expert ensuring drug safety or a business professional driving strategic growth, the right workplace makes a difference.

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International Reference Pricing (IRP) 2024: A year in review

Pharmaceutical Technology

A key trend seen in 2024 and recent years is the simplification of basket sizes, as countries look to streamline and simplify.

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Strategies for effective biosimilar regulatory agency interactions

Drug Patent Watch

Navigating the Complex World of Biosimilar Regulatory Agency Interactions As a biosimilar developer, you know that getting your product to market can be a long and arduous process. One of the most critical components of this journey is interacting with regulatory agencies. But how can you ensure that these interactions are effective and set your product up for success?

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

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Funding drought: how can biotech and biopharma keep trials running?

Pharmaceutical Technology

Biotech and biopharma companies have battled with a drought of private investment in recent years but could now face government funding cuts.

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The Advantages of Using a CDMO

Drug Patent Watch

Unlock the Full Potential of Your Pharmaceutical Product: The Power of a CDMO As a pharmaceutical professional, you're constantly looking for ways to bring innovative products to market faster and more efficiently. One key strategy that can help you achieve this goal is partnering with a Contract Development and Manufacturing Organization (CDMO). But what exactly is a CDMO, and how can it benefit your business?

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Sanofi outlays $1.9bn to purchase Dren Bio’s bispecific antibody

Pharmaceutical Technology

Sanofis move for Dren Bios clinical asset boosts its immunology-focused strategy of becoming a leader in the field.

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SXSW 2025: A Mandate, A Path, A Tool

Intouch Solutions

Every March, South by Southwest takes over Austin, TX, with a conference-festival hybrid showcasing the latest in tech-driven creativity. EVERSANA INTOUCH has been there every year for more than a decade, engaging with leaders and distilling our experiences into actionable insights for our clients. At SXSW 2025, we heard loud and clear: Pharma marketers are facing the biggest challenge of our careers.

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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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Servier and Black Diamond sign deal for solid tumours therapy

Pharmaceutical Technology

Servier and Black Diamond Therapeutics have signed a licencing agreement for targeted therapy, BDTX-4933, aimed at addressing solid tumours.

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Critical tools that support drug discovery and development

Drug Discovery World podcast

This is the latest episode of the free DDW narrated podcast, titled Critical tools that support drug discovery and development, which covers two articles written for DDW Volume 24 Issue 3, Summer 2023.They are called: You think you need an ELN but are you asking the right questions? and Big data: Charting a new path to drug discovery and development .

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Roche’s discontinued Alzheimer’s drug shows signs of preventing onset

Pharmaceutical Technology

Investigators said that the OLE study showed Roches gantenerumab dropped the risk of developing Alzheimer's symptoms by 50%.

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Bring Your Own Device (BYOD) Clinical Trials: How They Transform Decentralized Data Capture

Crucial Data Soutions

What Is BYOD in Clinical Trials? Bring Your Own Device (BYOD) is changing the way clinical trials collect and manage. The post Bring Your Own Device (BYOD) Clinical Trials: How They Transform Decentralized Data Capture appeared first on Crucial Data Solutions.

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European Clinical Supply Planning: Balancing Cost, Flexibility and Time

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Blood cancers dominate CAR-T pipeline

Pharmaceutical Technology

Among the 13 CAR-T therapeutics that have received regulatory approval are Gileads Yescarta and Immuneel Therapeutics Qartemi.

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Measuring Trials Transformation (MTT) Project Update: Tracking Progress Toward Transforming Clinical Trials

CTTI (Clinical Trials Transformation Initiative)

In September 2023, CTTI launched the Measuring Trials Transformation (MTT) Project to track progress toward CTTIs Transforming Trials 2030 (TT2030) vision. Introduced in 2021, this vision outlines how clinical trials should evolve by 2030 to become more efficient and inclusive, focusing on five key pillars: patient-centeredness, integration with health processes, trials designed with a quality approach, data-driven approaches, and improving population health.

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Gantenerumab 'shows sign of preventing Alzheimer's dementia'

pharmaphorum

A study has suggested early targeting of amyloid in the brains of people with inherited Alzheimer's can delay symptoms, but not all are convinced.

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UK expands mandatory infectious disease reporting requirements

Pharma Times

The update is aimed at strengthening local and national surveillance

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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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Synchron, Nvidia showcase AI for brain-computer interfaces

pharmaphorum

Brain-computer interface specialist Synchron has previewed an AI model that it believes will form the basis of a new generation of devices.

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Healthcare Marketing is Shifting Weekly, How to Prepare Your Team

Pharma Marketing Network

Introduction The landscape of healthcare marketing is evolving faster than ever, with new digital trends, regulatory updates, and consumer behaviors reshaping the industry on a weekly basis. For pharma marketing executives and their teams, staying ahead requires agility, data-driven decision-making, and a proactive approach. But how can marketing teams effectively navigate these rapid changes without losing efficiency?

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UK is becoming an 'outlier' for pharma, hitting investment

pharmaphorum

UK pharma leaders have renewed calls for a rethink by the government on levies imposed on medicine sales, saying investment is already being hit.

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PAP 2025: The Impact of Out-of-Pocket Costs on Patients with Rare Diseases

Pharmaceutical Commerce

Jonathan James, CEO, Hope Charities, discusses the critical importance of maintaining access to life-saving medications for patients with rare diseases to lead productive lives.

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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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CARGO offloads staff after abandoning lead CAR-T

pharmaphorum

Less than 18 months after its IPO, CAR-T developer CARGO has abandoned its development efforts and slashed around 90% of its staff

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PAP 2025: Understanding the Uninsured Landscape

Pharmaceutical Commerce

The session provides an overview of the uninsured population, and also tackles challenges faced by patients when it comes to accessing PAPs.

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Sanofi signs $1.9bn deal to buy Dren Bio autoimmune drug

pharmaphorum

Sanofi buys a drug from Dren Bio to claim a stake in the emerging field of deep B-cell depletion for autoimmune diseases.

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Pharma Pulse 3/20/25: New Ways of Targeting Cancer, How Employers Can Support Employee Well-Being and Mental Health & more

Pharmaceutical Commerce

The latest news for pharma industry insiders.

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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.