Sat.Apr 26, 2025 - Fri.May 02, 2025

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Why Is Faba Bean Protein Gaining Popularity in the Food Industry?

XTalks

Faba bean protein, derived from Vicia faba , is emerging as a high-quality, sustainable plant-based protein that is rapidly gaining traction in the food industry. Faba beans contain up to 30% protein and an impressive amino acid profile that rivals that of both soy and animal proteins. This makes it a versatile alternative for formulations ranging from bakery and dairy alternatives to meat substitutes.

Protein 64
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Rare Disease Day 2025: Rally for Rare Event Recap

Worldwide Clinical Trials

On the last day of February every year is Rare Disease Day , a dedicated day to celebrate the rare disease community, including patients, families, caregivers, clinicians, researchers, regulators, and more. The day inspires multiple events, such as fundraisers and scientific symposia, to bring together all the critical stakeholders who tirelessly work to make life better for those affected by rare diseases.

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Amgen’s Stelara biosimilar gets off to fast start

Bio Pharma Dive

Sales of the company’s copycat to J&J’s blockbuster medicine reached $150 million in the first quarter, adding to a surge in revenue for Amgen's biosimilar business.

Sales 179
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ICMR-NICPR announces DHR sponsored training course on omics technologies

AuroBlog - Aurous Healthcare Clinical Trials blog

In a significant leap towards advancing Indias capabilities in cancer research and personalized healthcare, the Indian Council of Medical Research (ICMR)-National Institute of Cancer Prevention and Research (NICPR) under the Department of Health Research (DHR) has announced a DHR-sponsored intensive training course titled Advent of Omics Technologies in Precision Diagnostics and Targeted Therapeutics.

Research 185
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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 trainings aren’t winning awards for engagement. But that doesn’t mean they can’t be effective, relevant, and maybe even enjoyable! Join expert Brian Richardson for a dynamic session on how to breathe new life into your ethics and compliance training programs. You’ll discover creative strategies to turn traditionally dry topics into meaningful learning experiences that resonate and drive real change.

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PTSD market expected to reach $5.5bn across the 7MM by 2034

Pharmaceutical Technology

The post-traumatic stress disorder (PTSD) market is expected to grow at a high compound annual growth rate of 16.1% from $1.2bn in 2024 to $5.5bn by 2034 across the seven major markets (7MM: the US, France, Germany, Italy, Spain, the UK, and Australia), according to leading data and analytics company GlobalDatas recent report, Post-Traumatic Stress Disorder: Opportunity Assessment and Forecast.

Marketing 173
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April 30, 2025: The FRESH-UP Study of Fluid Restriction in Heart Failure, in This Week’s PCT Grand Rounds

Rethinking Clinical Trials

In this Friday’s PCT Grand Rounds, Roland RJ van Kimmenade will present “Fluid Restriction in Heart Failure Versus Liberal Fluid Uptake: The FRESH-UP Study.” The Grand Rounds session will be held on Friday, May 2, 2025, at 1:00 pm eastern. Van Kimmenade is a cardiologist at Radboud University Medical Center in Nijmegen, Netherlands.

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Boehringer’s Zongertinib Shows Promising Durability in HER2-Mutated NSCLC

XTalks

New data for Boehringer Ingelheims investigational oncology candidate, zongertinib, shows sustained clinical benefits in non-small cell lung cancer (NSCLC) patients with HER2 mutations in the tyrosine kinase domain (TKD). Updated findings from the Phase Ib Beamion LUNG-1 trial included durability of response, building on the clinical evidence supporting zongertinibs efficacy.

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Entering the era of prenatal gene therapies 

Pharmaceutical Technology

As scientists explore treating genetic disorders before birth, the promise of foetal gene therapy is growingbut there are hurdles to overcome.

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Clinical Research Practices, Professionals, and Participants in the Spotlight at ACRP 2025

ACRP blog

Signature Series speakers took on more of the clinical research enterprises big picture topics at ACRP 2025 on Saturday (April 26), focusing in the morning on the implications for clinical trials teams of the recently updated ICH E6(R3) Guideline for Good Clinical Practice (GCP) from the International Council for Harmonization , and in the afternoon on how seasoned professionals are enacting meaningful change in their organizations for the betterment of trial implementation and management.

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AstraZeneca quietly exits neuroscience

Bio Pharma Dive

The company removed experimental drugs for Alzheimer’s, migraine and pain from its pipeline to focus more resources on “core therapeutic areas” and “high value” programs.

Drugs 275
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Clinical Research White Paper – Enhancing Transparency & Efficiency Throughout the Trial Lifecycle

Enhancing Transparency & Efficiency Throughout the Trial Lifecycle for AI Readiness

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Grand Rounds April 25, 2025: Automated Response Technology Integrated into EMR and Physician-Patient Communication (Ming Tai-Seale, PhD, MPH)

Rethinking Clinical Trials

Speaker Ming Tai-Seale, PhD, MPH Professor Departments of Family Medicine and Medicine (Bioinformatics) University of California San Diego School of Medicine Director of UC San Diego Learning Health Systems Science Center Slides Keywords Electronic Health Record; Artificial Intelligence; MyChart; Patient Messages; Large Language Models; Clinician Well-Being; Mental Health Key Points Physician work is increasingly centered around the electronic health record (EHR).

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MHRA authorises Bavarian Nordic’s chikungunya virus vaccine

Pharmaceutical Technology

The UK MHRA has granted marketing authorisation to Bavarian Nordic's Vimkunya vaccine for preventing the chikungunya virus.

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“Where Does Clinical Research Go from Here?” and Foundational Lessons for the Workforce

ACRP blog

With recent federal actions upending business as usual for many stakeholders in the clinical research enterprise, some of its thought leaders pondered the big question of Where does clinical research go from here? during Fridays (April 25) first Signature Series gathering at ACRP 2025 in New Orleans. After the heartfelt session closed with a Big Easy-style second line jazz band sendoff, an expert lineup of educational session presenters held forth on an array of vital topics for members of the i

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How integrated real-world data helps identify and improve outcomes for rare disease patients

Bio Pharma Dive

Pharmaceutical companies are turning to integrated RWD approaches to overcome challenges in rare disease research.

Research 276
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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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How the HeartBeam 12-Lead ECG Stacks Up: New Data Shows Clinical Promise

XTalks

HeartBeams synthesized 12-lead electrocardiogram (ECG) technology has met its clinical endpoints in the VALID-ECG pivotal study, a key step toward FDA clearance. The results, presented by Dr. Thomas Deering of Piedmont Heart Institute, lent credence to HeartBeams ability to deliver clinically reliable ECG data through a portable, patient-operated system.

Trials 82
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Pliant cuts workforce by 45% following lung trial termination 

Pharmaceutical Technology

Pliant is slashing 45% of its workforce in a move to minimise costs and preserve cash reserves.

Trials 130
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Lilly hit as PBM drops Zepbound, but retains Wegovy

pharmaphorum

Shares in Eli Lilly have weakened after pharmacy benefit manager CVS Health said it would no longer cover its weight-loss therapy Zepbound.

Pharmacy 100
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CVS strikes Wegovy deal with Novo Nordisk

Bio Pharma Dive

The deal could expand access to its in-demand obesity drug at the expense of Eli Lilly, whose shares fell by double digits on Thursday.

Drugs 238
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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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The Kinds of People You Can Meet at ACRP 2025

ACRP blog

From the moment one begins immersing oneself in the full education, networking, and workforce development advocacy experience that an Association of Clinical Research Professionals (ACRP) conference encompasses, theres almost limitless possibilities for meeting and learning from the new and exciting personalities one may encounter. Did you know that at ACRP 2025 (going on right now in New Orleans), you could meet such attendeeswhether they are ACRP members, certificants, presenters, leaders, ex

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FDA awards RMAT status to 4DMT diabetic macular oedema therapy

Pharmaceutical Technology

4D Molecular Therapeutics (4DMT) has received the regenerative medicine advanced therapy (RMAT) designation from the FDA for 4D-150.

Medicine 130
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List of Drug patent expiration 2025

Pharma Tutor

List of Drug patent expiration 2025 admin Fri, 05/02/2025 - 14:05 Drug patent expiration presents a significant opportunity for the launch of generic medications, which can dramatically alter market dynamics. When a branded drug's patent expires, it opens the door for generic manufacturers to produce and sell bioequivalent versions at a lower cost, leading to increased competition and reduced prices.

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Siren, a gene therapy startup, tests unconventional alternative to venture funding

Bio Pharma Dive

Siren Biotechnology is trying to raise $5 million via the type of crowdfunding round that’s rarely used by young drugmakers.

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

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

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Study offers new hope for babies born with opioid withdrawal syndrome

Medical Xpress

As the opioid crisis continues, the number of babies born with neonatal opioid withdrawal syndrome (NOWS)a condition that affects infants whose mothers used opioids during pregnancyhas risen 5-fold over the past 20 years. According to the Centers for Disease Control (CDC), there are 20,000 infants a year in the United States born with signs of NOWS.

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HHS launches $500m universal vaccines initiative

Pharmaceutical Technology

The US HHS has launched a $500m initiative to accelerate the development of universal vaccines targeting viruses with pandemic potential.

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NIH is pulling the plug on foreign research grants

pharmaphorum

A new policy from the NIH in the US will cut billions of dollars of funding for research organisations and hospitals outside the US.

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FDA misses approval deadline for a biotech’s rare disease drug

Bio Pharma Dive

The delay for Stealth Biotherapeutics comes amid a heightened focus on the impact FDA job cuts might have on drug reviews.

Drugs 202
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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.

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What makes an effective clinical trial project manager?

Imperical Blog

Effective clinical trial project managers do more than just keep tasks on schedule; they play a crucial role in ensuring project success and operational efficiency. Organizations that adopt project management practices achieve a 92% success rate in meeting their project goals and experience 28 times… The post What makes an effective clinical trial project manager?

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Repare signs out-licensing deal with DCx Biotherapeutics

Pharmaceutical Technology

Repare Therapeutics has entered into an out-licensing agreement with Canadian biotechnology firm DCx for discovery platforms and IP.

Licensing 130
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Backers submit plans for £1bn cancer district in London

pharmaphorum

A planning application has been filed to invest 1bn in "the world's leading centre for cancer research and treatment" in London.

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Top Republican calls for 340B reform in long-awaited investigation

Bio Pharma Dive

Sen. Bill Cassidy’s report calls on Congress to improve the transparency of the drug discount program in a move praised by pharmaceutical companies and criticized by hospitals.

Drugs 185
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Optimizing Clinical Supply Strategy: Navigating Challenges & Finding Your Ideal Model