Mon.Nov 25, 2024

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Sustainability in biopharma: Collaboration and technology light the way forward

Pharmaceutical Technology

The biopharmaceutical industry is being called to take its sustainability efforts to the next level. A new report sheds light on the topic.

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Biohaven muscle drug misses goal of SMA study, but advances in obesity

Bio Pharma Dive

The setback likely removes one competitor to an emerging spinal muscular atrophy medicine from Scholar Rock, but sets the stage for a pair of readouts with implications for weight loss research.

Medicine 167
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November 25, 2024: NIH Collaboratory Trial Investigators Share Lessons From Using Electronic Health Records in Pragmatic Trials

Rethinking Clinical Trials

Drawing on experiences from the NIH Collaboratory Trials, authors of a new article in Contemporary Clinical Trials describe the challenges they encountered when relying on data from the electronic health record (EHR) to monitor outcomes and deliver interventions in pragmatic clinical trials embedded in healthcare systems. “Teams need to be aware of—and perhaps proactively investigate—possible changes to EHR systems and data that will affect the delivery of interventions and the integrity and saf

Trials 147
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New data could help Merck expand use of cardiovascular drug

Bio Pharma Dive

Positive results from a study of Winrevair could help the drugmaker achieve sales growth past top-seller Keytruda’s upcoming patent expirations this decade.

Sales 167
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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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A Rare, Fatal Skin Disease Has Been Cured in Patients For The First Time

AuroBlog - Aurous Healthcare Clinical Trials blog

Illustrative example of damaged skin, in this case from sunburn. (Jennifer A Smith/Getty Images) A rare and potentially fatal skin infection with nightmarish outcomes may soon have a cure.

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GSK gains approval in Japan for extended indication of RSV vaccine

Pharmaceutical Technology

GSK has received approval from Japan's MHLW for its application to extend the indication of its RSV vaccine, Arexvy.

More Trending

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MSD’s WELIREG approved by NMPA to treat VHL disease-associated tumours

Pharmaceutical Technology

China’s NMPA has approved MSD’s WELIREG (belzutifan) to treat adult individuals with certain types of VHL disease-associated tumours.

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Bioengineering is the new frontier in advanced technology: Kiran Mazumdar Shaw

AuroBlog - Aurous Healthcare Clinical Trials blog

Digital technologies have transformed biology research to provide in-depth insights into unravelling the mysteries of living systems. Bioengineering is the new frontier in advanced technology, said Kiran Mazumdar-Shaw, chairperson, Biocon Group and Association of Biotechnology Led Enterprises (ABLE). Genetic engineering has unleashed a power house of bio manufacturing in the fermentation industry.

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GSK eyes up combo approval for previously withdrawn myeloma drug

Pharmaceutical Technology

The US Food and Drug Administration (FDA) is expected to make a Prescription Drug User Fee Act (PDUFA) decision by mid-2025.

Drugs 130
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Look out, Pfizer: BridgeBio scores 'best-case' FDA nod for Attruby in cardiomyopathy

Fierce Pharma

On a Zoom call last month from California, BridgeBio CEO Neil Kumar needled a colleague about the remote possibility of the New York Yankees rallying to win the World Series as they trailed the Los | The FDA has signed off on BridgeBio's Attruby (acoramidis), a potential blockbuster to treat patients with the rare heart disease transthyretin amyloid cardiomyopathy.

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

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Exploring drug shortages in European markets: the causes, analysis, and response

Pharmaceutical Technology

Since 2023, the pharmaceutical industry operating in Europe has faced an unprecedented challenge related to drug shortages.

Drugs 130
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UK digital health funding should be ringfenced, says report

pharmaphorum

IT industry group techUK has called on the government to guarantee funding for digital transformation and cyber resilience in health and social care.

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FDA approves BridgeBio’s Attruby for ATTR-CM treatment

Pharmaceutical Technology

The US FDA has approved BridgeBio Pharma’s Attruby (acoramidis) for treating adult individuals with ATTR-CM.

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Merck preps filings after blockbuster-in-waiting Winrevair succeeds in severe PAH study

Fierce Pharma

Eight months after snaring an inaugural FDA green light, Merck & Co. is bolstering the case for the chief asset in its $11.5 billion Acceleron acquisition. | In the phase 3 ZENITH study, Merck’s activin signaling inhibitor Winrevair met its primary endpoint of time to first morbidity or mortality event, which included all-cause death, lung transplantation, or hospitalization for at least 24 hours linked to disease worsening in patients with PAH.

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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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Adcendo raises $135m as ADC funding frenzy continues 

Pharmaceutical Technology

This latest raise is intended to accelerate the development of the biotech’s four antibody-drug conjugates.

Antibody 130
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ASH: Incyte's Monjuvi triumphs in follicular lymphoma phase 3, teeing up FDA filing

Fierce Pharma

Incyte’s previously disclosed phase 3 win in relapsed or refract | In the phase 3 inMIND study, Monjuvi—added to Bristol Myers Squibb's Revlimid and Roche's Rituxan—triggered a 57% reduction in the risk of disease progression, relapse or death in R/R FL patients compared with those who were treated with placebo, Revlimid and Rituxan.

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Relief for AZ as Truqap hits the spot in prostate cancer

pharmaphorum

After a disappointing result with Truqap in triple-negative breast cancer, AstraZeneca chalks up a win in prostate cancer.

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Bristol Myers Squibb hands pink slips to 195 workers in NJ as cost-cutting effort rolls on

Fierce Pharma

Bristol Myers Squibb has executed another round of layoffs in its ongoing cost-savings push. | Bristol Myers Squibb has executed another round of layoffs in its ongoing cost-savings push. The company has handed pink slips to 195 more employees, according to a New Jersey Worker Adjustment and Retraining Notification (WARN) update.

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European Clinical Supply Planning: Balancing Cost, Flexibility and Time

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Imkeldi (Imatinib): Shorla Oncology Adds Another Accessible Solution to Its Leukemia Pipeline

XTalks

Shorla Oncology has received US Food and Drug Administration (FDA) approval for Imkeldi, an oral solution of imatinib designed to treat specific forms of leukemia and other cancers. Imkeldi introduces an accessible alternative to traditional tablets, particularly for those who struggle with swallowing or require customized dosing. Imkeldi’s innovative formulation provides consistent dosing accuracy while offering a palatable strawberry flavor and stable storage without refrigeration.

In-Vivo 59
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AZ's Truqap delivers phase 3 win in prostate cancer subtype after recent breast cancer miss

Fierce Pharma

After a recent failed showing in a breast cancer subgroup raised doubts around AstraZeneca’s Truqap, the first-in-class AKT inhibitor is making inroads in a prostate cancer subtype. | The AKT inhibitor's early win in a prostate cancer subtype follows a recent surprise flop in a breast cancer study. AZ has been working to grow Truqap beyond its current limited approval in a niche breast cancer category.

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Health Innovators: Lori Fletcher and Amber Beimer, Advanced Clinical

pharmaphorum

Watch this exclusive interview with health innovators Lori Fletcher and Amber Beimer from Advanced Clinical as they discuss the latest trends and advancements in the Functional Service Provider (FSP) field.

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Peer Exchange: RFID Technological Obstacles (Episode 2)

Pharmaceutical Commerce

In the second part of this roundtable discussion, key opinion leaders discuss the potential technological challenges surrounding RFID, and the likelihood of not only utilizing this tech at the item level but for product security purposes as well.

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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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Halozyme abandons its €2bn pursuit of Evotec

pharmaphorum

Halozyme Therapeutics has withdrawn its offer to acquire Evotec, saying that the German company had been unwilling to engage with negotiations.

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Celebrating National Caregivers Month: Recognizing the Vital Role of Caregivers in Patient Care and Clinical Trials

Antidote

November is National Caregivers Month, a time to celebrate and acknowledge the often-unseen heroes who provide vital support to individuals with chronic illnesses, disabilities, or age-related conditions. Whether they are family members, friends, or professional aides, caregivers offer essential day-to-day assistance that helps their loved ones maintain their health and quality of life.

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From Imaging to Analysis: 5 Steps for Success with TrialKit PACS

Crucial Data Soutions

When it comes to managing imaging data in clinical trials, researchers find many challenges. Disjointed systems that don’t talk to. The post From Imaging to Analysis: 5 Steps for Success with TrialKit PACS appeared first on Crucial Data Solutions.

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DDW Highlights: 25 November 2024

Drug Discovery World podcast

The latest episode of the DDW Highlights podcast is now available to listen to and watch below. DDW’s Megan Thomas narrates five key stories of the week to keep DDW subscribers up-to-date on the latest industry updates. This week’s most exciting news stories all represent innovative solutions to the treatment of disease, proving that ‘thinking outside the box’ can by the key to success in drug discovery.

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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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BridgeBio poised to challenge Pfizer after Attruby approval

pharmaphorum

BridgeBio grabs FDA approval for its ATTR cardiomyopathy drug Attruby, setting up a challenge to market leader Pfizer

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Mikkel Wandahl Pedersen

Pharma Times

Commit Biologics has appointed Mikkel Wandahl Pedersen as CSO

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Drug Channels News Roundup, November 2024: Employers & Their PBMs, Medicaid vs. 340B, U.S. Drug Prices, and Dr. G Shops for Health Plans

Drug Channels

Happy Thanksgiving, everyone! Before you stretch your stomach, stretch your mind with our extra-stuffed helping of food for thought. In this issue: Intriguing data on how employers oversee their PBMs State Medicaid programs carve out PBMs—and get a 340B windfall Are U.S. drug prices really higher than other countries? Plus, Dr. Glaucomflecken gets us ready for the open enrollment season.

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GBI Biomanufacturing Grows Drug Product Services

Pharmaceutical Commerce

The CDMO’s offerings will now feature automated fill-finish.

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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.