Fri.Jun 13, 2025

article thumbnail

Bharat Biotech acquires licence for GSK’s Shigella vaccine development

Pharmaceutical Technology

Skip to site menu Skip to page content Switch language: translate --> PT Menu Search Sections Home News Analysis Features Comment & Opinion Projects Data Insights Sectors Clinical Trials Drug Manufacturers Therapy Area Cardiovascular Central Nervous System Immunology Infectious Disease Oncology Respiratory Pricing and Market Access Themes Artificial Intelligence Corporate Governance Cloud Cybersecurity Environmental Sustainability Internet of Things Robotics Social Responsibility Covid-19 Insigh

Vaccine 219
article thumbnail

AstraZeneca forms an AI deal in China; Third Harmonic advances liquidation plans

Bio Pharma Dive

AstraZeneca could spend up to $5.3 billion in a deal to develop oral medicines with CSPC Pharmaceutical. Elsewhere, Insmed cashed in on a stock surge and Third Harmonic kicked off a drug auction.

Medicine 161
Insiders

Sign Up for our Newsletter

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

article thumbnail

Opinion: STAT+: Don’t cut NIH and NSF budgets — let the government invest like a venture capitalist

STAT News

Congress is floating a 40% cut to the National Science Foundation and deep reductions to the National Institutes of Health — America’s two flagship research engines. The justification? A $2 trillion deficit. But cutting science to fix the deficit is like burning your seed corn because you’re low on groceries. It’s fiscally shortsighted and strategically self-defeating.

Engineer 119
article thumbnail

Rewrite New AI method makes cancer tracking faster and easier using blood tests this news headline for the science magazine post

Scienmag

Singapore – Scientists from the A*STAR Genome Institute of Singapore (A*STAR GIS) have developed a new artificial intelligence (AI)-based method called “Fragle” that makes tracking cancer easier and faster using blood tests. Requiring only a small blood sample, this method analyses the size of DNA fragments in the blood to reveal distinct patterns that differentiate cancer DNA from healthy DNA, helping doctors track cancer treatment response more accurately and frequently.

DNA 59
article thumbnail

How to Turn “Check-the-Box” Compliance Trainings Into Real Learning

Speaker: Brian Richardson, Brian Richardson, Founder and CEO of Richardson Consulting Group

Let’s face it—most ethics and compliance training programs aren’t winning awards for engagement. But that doesn’t mean they can’t be effective, captivating, and maybe even enjoyable! Join learning design expert Brian Richardson for a dynamic session on how to breathe new life into your ethics and compliance training. We'll explore innovative strategies to bring traditionally dry topics to life, making them resonate with learners and drive tangible change.

article thumbnail

ACRP Journal Contributors Dive into Promising Applications of AI for Clinical Trial Sites

ACRP blog

The U.S. Food and Drug Administration’s (FDA’s) recent launch of an agency-wide large language model–powered artificial intelligence (AI) tool known Elsa and ongoing efforts to have another AI tool known as CDRH-GPT in place for speeding up reviews and approvals of medical devices by the end of June have attracted their share of both supporters and detractors.

article thumbnail

Rewrite FDA approves immune checkpoint inhibitor drug for patients with resectable locally advanced head and neck cancer, backed by Dana-Farber research this news headline for the science magazine post

Scienmag

image: Dr. Ravindra Uppaluri, director of Head and Neck Surgical Oncology at Dana-Farber and Brigham and Women’s Hospital view more Credit: Courtesy of Dana-Farber Cancer Institute BOSTON, June 13, 2025 — Pembrolizumab, an immune checkpoint inhibitor, has been approved by the U.S. Food and Drug Administration (FDA) for the treatment of patients with resectable locally advanced head and neck squamous cell carcinoma whose tumors express PD-L1 [Combined Positive Score (CPS) ≥1] as determined by an

More Trending

article thumbnail

Rewrite Researchers develop a rapid method for building vascular organoids this news headline for the science magazine post

Scienmag

Blood vessels are essential to nearly all tissues, delivering nutrients and oxygen, regulating hemostasis, and modulating inflammation. Recreating functional vascular networks is foundational to both basic and translational vascular biology, however current methods to make blood vessels from stem cells are often slow, inefficient, or lack the complexity needed for therapy.

article thumbnail

J&J’s Dual-Target CAR T-Cell Therapy Shows Promise in Large B-Cell Lymphoma

The Pharma Data

Johnson & Johnson’s Dual-Targeting CAR T-Cell Therapy Shows Encouraging First Clinical Results in Large B-Cell Lymphoma Johnson & Johnson recently presented promising first-in-human data from its ongoing Phase 1b study evaluating JNJ-90014496 (JNJ-4496) — an investigational, dual-targeting, autologous chimeric antigen receptor (CAR) T-cell therapy — in patients with relapsed or refractory large B-cell lymphoma (R/R LBCL) who have not previously received a CAR T-cell therapy.

article thumbnail

Inside the FDA: Staff Morale and Public Health Concerns

World of DTC Marketing

What are FDA staffers thinking? In recent months, Kennedy’s involvement in high-level decisions—especially those seen as overly friendly to industry interests—has become a growing concern. And while the outside world may only see the final decisions and policy announcements, it’s the rank-and-file FDA staffers who live with the day-to-day fallout.

Doctor 157
article thumbnail

Novo, searching for a spark, plans late-stage trials for amylin drug

Bio Pharma Dive

The Danish drugmaker, which is grappling with a share decline and competition from Eli Lilly, unveiled planned trials of an obesity medication that works differently than its popular Wegovy.

Trials 177
article thumbnail

Clinical Research White Paper – Enhancing Transparency & Efficiency Throughout the Trial Lifecycle

Enhancing Transparency & Efficiency Throughout the Trial Lifecycle for AI Readiness

article thumbnail

FDA Approves KEYTRUDA for Neoadjuvant and Adjuvant Treatment of PD-L1+ Resectable Head & Neck Cancer

The Pharma Data

FDA Approves KEYTRUDA® (Pembrolizumab) for Perioperative Treatment of Resectable Locally Advanced Head and Neck Squamous Cell Carcinoma Merck known as MSD outside the United States and Canada, recently announced that the U.S. Food and Drug Administration (FDA) has approved KEYTRUDA® (pembrolizumab), its flagship anti-PD-1 therapy, for the treatment of adult patients with resectable, locally advanced head and neck squamous cell carcinoma (HNSCC) whose tumors express PD-L1 (Combined Positive Score

article thumbnail

Rewrite University of Cincinnati structural biology research published in prestigious PNAS this news headline for the science magazine post

Scienmag

Two key protein structures in the body are being visualized for the first time, thanks in part to the latest technology in the University of Cincinnati’s Center for Advanced Structural Biology — potentially opening the door for better designed therapeutics. The research of a trio of UC structural biologists was published today in the Proceedings of the National Academy of Sciences ( PNAS ).

article thumbnail

Debiopharm and Alkyon link for radioligand therapies development

Pharmaceutical Technology

Skip to site menu Skip to page content Switch language: translate --> PT Menu Search Sections Home News Analysis Features Comment & Opinion Projects Data Insights Sectors Clinical Trials Drug Manufacturers Therapy Area Cardiovascular Central Nervous System Immunology Infectious Disease Oncology Respiratory Pricing and Market Access Themes Artificial Intelligence Corporate Governance Cloud Cybersecurity Environmental Sustainability Internet of Things Robotics Social Responsibility Covid-19 Insigh

article thumbnail

Astellas, Mitsubishi Research Institute Team Up to Support Japanese Pharma Startups

The Pharma Data

Mitsubishi Research Institute and Astellas Forge Collaborative Initiative to Support Japanese Drug Discovery Startups and Boost Global Innovation Mitsubishi Research Institute, Inc. (MRI) and Astellas Pharma Inc. (Astellas) today announced a significant new collaboration aimed at strengthening Japan’s role as a global hub for innovative drug discovery and fostering the growth of its biotechnology startups.

article thumbnail

Can Your Organization Spot a Conflict Before It’s a Crisis?

Speaker: Amie Phillips Pablo, VP, Corporate Compliance & Privacy Officer at Novo Nordisk

In today’s complex healthcare environment, navigating third-party relationships has become even more challenging—whether it’s vendor relationships, employee activities, or patient-facing interactions. Left unmanaged, these conflicts can compromise trust, regulatory compliance, and even organizational reputation. So, how can healthcare teams stay ahead?

article thumbnail

AstraZeneca taps Chinese biotech in $5.2bn chronic disease research deal

Pharmaceutical Technology

Skip to site menu Skip to page content Switch language: translate --> PT Menu Search Sections Home News Analysis Features Comment & Opinion Projects Data Insights Sectors Clinical Trials Drug Manufacturers Therapy Area Cardiovascular Central Nervous System Immunology Infectious Disease Oncology Respiratory Pricing and Market Access Themes Artificial Intelligence Corporate Governance Cloud Cybersecurity Environmental Sustainability Internet of Things Robotics Social Responsibility Covid-19 Insigh

Research 239
article thumbnail

How is AI Changing Pharma Marketing Strategies?

Pharma Marketing Network

Artificial intelligence is rapidly transforming industries, and the pharmaceutical sector is no exception. When it comes to marketing strategies , AI is reshaping how pharma companies reach healthcare professionals (HCPs), engage patients, and optimize campaign performance. But what exactly does this mean for pharma marketers in 2025? Are we merely adding tools to the toolkit—or rewriting the entire playbook?

article thumbnail

Elanco’s Zenrelia Wins Positive CVMP Opinion

The Pharma Data

Elanco’s Zenrelia (ilunocitinib) Wins Positive CVMP Opinion, Paving the Way for EU Approval and Market Release Elanco Animal Health Incorporated (NYSE: ELAN) today announces a significant milestone in its ongoing expansion into veterinary care: the Committee for Veterinary Medicinal Products (CVMP) of the European Medicines Agency (EMA) has issued a positive opinion for Zenrelia™ (ilunocitinib).

article thumbnail

What Clinical Trial Listings Say About Who’s Hiring Legal Help Next

Drug Patent Watch

"The Hiring Spree You Didn't See Coming: 3 Industries Where Clinical Trials Are Fueling a Surge in Legal Support As the pharmaceutical industry continues to navigate a complex landscape of patent expirations and emerging treatments, a new trend is emerging: companies are hiring lawyers at an unprecedented rate to protect their interests in the face of clinical trial data.

article thumbnail

White Paper - A Roadmap to AI Data Readiness in R&D Labs

Download this comprehensive guide to AI and ML in the R&D Laboratory Setting.

article thumbnail

Amgen & Barry Sanders Spotlight Bad Cholesterol Risks in Documentary

The Pharma Data

Amgen and Barry Sanders Raise Awareness About “Bad Cholesterol” in Documentary Highlighting Cardiovascular Disease Crisis in America Amgen today announced the launch of The Making of a Heart Attack , a powerful documentary that aims to illuminate the growing cardiovascular disease crisis in the United States — a condition that strikes someone nearly every 40 seconds with a heart attack or stroke.

Doctor 40
article thumbnail

Merck’s Enflonsia Gets FDA Nod for Infant RSV Protection to Rival Sanofi and AstraZeneca’s Beyfortus

XTalks

The FDA has approved Merck’s Enflonsia (clesrovimab-cfor), a long-acting monoclonal antibody, for the prevention of respiratory syncytial virus (RSV) lower respiratory tract disease in infants born during or entering their first RSV season. The once-per-season injection offers a new option to safeguard infants from RSV-related illness, a major cause of pediatric hospitalizations in the US.

article thumbnail

Starting with the End in Mind: How Pharma Can Build a Smarter Path to Commercialization

Drug Channels

Today’s guest post comes from Sean Wagner, VP of Client Partnerships and Carolyn Zele, Advisor, Solution Consulting at MMIT. Sean and Carolyn argue that planning for a successful drug launch must begin early—often well before Phase III. In this article, they present a six-step framework to help manufacturers align clinical development with payer expectations, patient needs, and real-world access dynamics.

article thumbnail

US lawmakers seek ban on DTC advertising

pharmaphorum

US Senators Bernie Sanders and Angus King have introduced a bill that seeks to ban direct-to-consumer (DTC) advertising by the pharma industry.

66
article thumbnail

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!

article thumbnail

City of Hope Developed a Foundational Map of Tumor Cells for Personalized Brain Cancer Treatments

BioTech 365

City of Hope Developed a Foundational Map of Tumor Cells for Personalized Brain Cancer Treatments City of Hope Developed a Foundational Map of Tumor Cells for Personalized Brain Cancer Treatments Scientists developed a new framework to improve the ability of … Continue reading →

article thumbnail

Treating primary bone cancer: The potential of listeria-based bioengineered bacterial immunotherapy

pharmaphorum

Treating primary bone cancer: The potential of listeria-based bioengineered bacterial immunotherapy Nicole.

52
article thumbnail

Ethris Signs Strategic Collaboration with Thermo Fisher Scientific to Provide Access to mRNA Technology Platforms

BioTech 365

Ethris Signs Strategic Collaboration with Thermo Fisher Scientific to Provide Access to mRNA Technology Platforms Ethris Signs Strategic Collaboration with Thermo Fisher Scientific to Provide Access to mRNA Technology Platforms Partnership further validates Ethris’ novel technology platform based on stabilized … Continue reading →

52
article thumbnail

Pfizer Provides Update on U.S. Regulatory Review of TALZENNA in Combination with XTANDI for Broader Use in Metastatic Castration-Resistant Prostate Cancer

Pfizer

Pfizer Provides Update on U.S. Regulatory Review of TALZENNA in Combination with XTANDI for Broader Use in Metastatic Castration-Resistant Prostate Cancer skaarj Fri, 06/13/2025 - 16:20 Pfizer Provides Update on U.S. Regulatory Review of TALZENNA in Combination with XTANDI for Broader Use in Metastatic Castration-Resistant Prostate Cancer Friday, June 13, 2025 - 04:23pm Share New York, June 13, 2025 – Pfizer Inc.

Gene 40
article thumbnail

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

article thumbnail

STAT+: In fight over research overhead funding, universities propose alternatives to Trump’s cuts

STAT News

Facing billions of dollars in proposed cuts to research overhead payments from the Trump administration, a coalition of academic groups has devised plans it believes could be more sensible, measured ways to revamp how the federal government pays for scientific research. STAT obtained a copy of the proposals, which were developed by the Joint Associations Group, or JAG, a collection of 10 organizations that represent universities, medical centers, and other research institutions.

Research 135
article thumbnail

Addressing the Threat of Prescription Abandonment

Pharmaceutical Commerce

As the rising cost of prescription medications in the United States becomes an increasing barrier for millions of people, how can we effectively address and improve patient adherence?

52
article thumbnail

Tiziana Life Sciences Expands Phase 2 Clinical Trial of Intranasal Foralumab with Commencement of First Patient Dosing at Weill Cornell Multiple Sclerosis Center

BioTech 365

Tiziana Life Sciences Expands Phase 2 Clinical Trial of Intranasal Foralumab with Commencement of First Patient Dosing at Weill Cornell Multiple Sclerosis Center Tiziana Life Sciences Expands Phase 2 Clinical Trial of Intranasal Foralumab with Commencement of First Patient Dosing … Continue reading →

article thumbnail

Moderna’s mRNA RSV vaccine wins expanded FDA approval for younger adults

Pharmaceutical Technology

Skip to site menu Skip to page content Switch language: translate --> PT Menu Search Sections Home News Analysis Features Comment & Opinion Projects Data Insights Sectors Clinical Trials Drug Manufacturers Therapy Area Cardiovascular Central Nervous System Immunology Infectious Disease Oncology Respiratory Pricing and Market Access Themes Artificial Intelligence Corporate Governance Cloud Cybersecurity Environmental Sustainability Internet of Things Robotics Social Responsibility Covid-19 Insigh

article thumbnail

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