Thu.Dec 19, 2024

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Leveraging a Drug Patent Portfolio for Success

Drug Patent Watch

A robust drug patent portfolio is not just an assetit’s a critical tool for success. As companies invest billions in research and development, protecting their innovations through strategic patent management has become more important than ever. This comprehensive guide will explore how pharmaceutical companies can leverage their drug patent portfolios to maximize value, maintain market dominance, and drive innovation.

Drugs 54
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MSD makes obesity play in up to $2bn deal for Hansoh’s GLP-1RA asset

Pharmaceutical Technology

MSD has entered an exclusive global licence agreement with Hansoh Pharma for a preclinical oral small molecule GLP-1RA.

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Zepbound, Mounjaro shortages are resolved, FDA confirms

Bio Pharma Dive

The FDA’s decision will close a lucrative market opportunity for compounding pharmacies, although the agency will give a limited grace period before taking any enforcement actions.

Pharmacy 216
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Vertex’s stock hurt after non-opioid pain drug shows benefit similar to placebo

Pharmaceutical Technology

Vertex said the Phase II trial met its primary endpoint, however there was only a minor difference to placebo.

Trials 147
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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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Vertex ‘ends the year in pain’ as latest non-opioid drug data disappoint

Bio Pharma Dive

Mixed results from a study focused on lower back pain left analysts wanting as well as confused about Vertex's plans to forge ahead in the indication.

Drugs 173
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FDA approves Mesoblast’s Ryoncil for SR-aGvHD treatment

Pharmaceutical Technology

Mesoblast has gained US FDA approval for its mesenchymal stromal cell (MSC) therapy, Ryoncil (remestemcel-L), to treat SR-aGvHD.

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BioAge and Novartis seek drug targets for ageing-related diseases

Pharmaceutical Technology

BioAge Labs has entered a multi-year research partnership with Novartis to seek therapeutic drug targets for ageing-related conditions.

Drugs 147
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Roche sticks with Parkinson’s drug despite second study failure

Bio Pharma Dive

Even with another mid-stage setback, Roche believes there were enough positive signs to “merit further exploration” of the drug, which it’s been developing with Prothena for more than a decade.

Drugs 147
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Novo Holdings completes Catalent acquisition for $16.5bn

Pharmaceutical Technology

Novo Holdings has completed the previously announced acquisition of Catalent in an all-cash transaction valued at around $16.5bn.

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Regeneron says study data support big bet on new blood thinners

Bio Pharma Dive

The company is planning a “broad Phase 3 program” for two anticoagulants after they outperformed marketed medicines in a pair of mid-stage trials.

Medicine 147
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Optimizing Clinical Supply Strategy: Navigating Challenges & Finding Your Ideal Model

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World Orphan Drug Congresses Europe vs. The US: Global Perspectives on Genetic Testing

Worldwide Clinical Trials

At the recent World Orphan Drug Congresses (WODC) in Europe and the United States, Worldwide Clinical Trials Derek Ansel , Vice President, Therapeutic Strategy Lead, Rare Disease, facilitated roundtable discussions to explore the operational challenges and ethical barriers surrounding genetic testing. While the agenda remained the same across both events, the conversations revealed key regional distinctions and global perspectives on how genetic testing, ethics, and operational challenges are ad

Genetics 130
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Novartis shutters MorphoSys sites, lays off staff

Bio Pharma Dive

While the pharma is still developing a MorphoSys drug acquired in its $2.9 billion deal for the biotech, it is closing down sites in the U.S. and Germany.

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Magazine: US reproductive laws could limit women’s participation in clinical trials

Pharmaceutical Technology

In this issue: Recent US reproductive laws could limit womens participation in trials, how Pfizer outplayed Starboard, PreP therapies come to the fore, and more.

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Psychiatry Clinical Trials: Inclusive, Patient-Centric Approaches for Mental Health Research

XTalks

Mental health problems represent a critical area of unmet need worldwide, affecting an estimated one in eight people globally, according to the World Health Organization (WHO). These issues carry substantial personal and societal costs, impacting daily life and productivity. In fact, mental health conditions are associated with a 10- to 25-year reduction in life expectancy , emphasizing the need for effective and accessible treatments.

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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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Neuralink rival Precision raises $102m, and other financings

pharmaphorum

Neuralink rival Precision Neurosciences raises $102m for its brain-computer interface tech, plus financings for Redesign, DeepLife, TG0 and Tuva.

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FDA Approves Ensacove (Ensartinib) for Advanced NSCLC in Crowded ALK Inhibitor Market

XTalks

The US Food and Drug Administration (FDA) has approved ensartinib, a next-generation anaplastic lymphoma kinase (ALK) inhibitor, as a first-line treatment for patients with ALK-positive locally advanced or metastatic non-small cell lung cancer (NSCLC). Ensartinibs approval, granted under the commercial name Ensacove, was awarded to Xcovery Holdings, a subsidiary of Chinas Betta Pharmaceuticals.

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Ottimo raises $140m for its PD-1/VEGF cancer drug

pharmaphorum

Ottimo raises $140m for PD-1 and VEGF-targeting jankistomig, which the startup says is differentiated from bispecific antibodies in the class.

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FDA Issues Complete Response Letter to J&J for Subcutaneous Rybrevant Filing

XTalks

The US Food and Drug Administration (FDA) has rejected Johnson & Johnsons (J&J) application for a subcutaneous formulation of Rybrevant (amivantamab). J&J was seeking FDA approval for the subcutaneous version of Rybrevant, a bispecific antibody that targets the epidermal growth factor receptor (EGFR) and the MET receptor (also known as hepatocyte growth factor receptor, HGFR) for non-small cell lung cancer (NSCLC) with EGFR exon 20 insertion mutations.

Sales 97
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European Clinical Supply Planning: Balancing Cost, Flexibility and Time

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Novartis sheds MorphoSys staff, sites after pelabresib delay

pharmaphorum

Novartis has confirmed it will shut down two MorphoSys sites in Germany and the US, with the loss of around 330 jobs, by the end of next year.

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Playing catch-up with Pfizer and Roche, China-made ALK drug clears FDA in lung cancer

Fierce Pharma

Following in the footsteps of several Big Pharma companies, another ALK inhibitor has made its entry into the U.S. | Following in the footsteps of Pfizer, Roche and Takeda, another ALK inhibitor has made its belated entry into the U.S. The FDA nod comes four years after its initial approval in China.

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Vertex weakens after neuropathic pain trial reads out

pharmaphorum

A trial of Vertex's suzetrigine in neuropathic back pain met its primary objective, but shares in the company fell as investors reacted to the data

Trials 97
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FDA reaffirms decision to erase Eli Lilly's tirzepatide from shortage list, halting future flow of knockoffs

Fierce Pharma

The FDA has doubled down on its decision to remove Eli Lillys tirzepatide from its list of products that are in shortage. | The FDA has doubled down on its decision to remove Eli Lillys tirzepatide from its list of products that are in shortage. The agencys move means that compounding pharmacies will have to halt production of their knockoff versions of diabetes drug Mounjaro and obesity treatment Zepbound.

Pharmacy 103
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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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Mesoblast finally pushes GvHD cell therapy over finish line

pharmaphorum

At its third attempt, Mesoblast has secured FDA approval for the first-ever mesenchymal stem cell (MSC) therapy, Ryoncil for acute GvHD in children.

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Gilead recruits Terray in AI-driven drug discovery pact

Outsourcing Pharma

Gilead teams up with Terray for AI-powered drug discovery, leveraging Terrays tNova platform to accelerate the development of innovative treatments through generative AI and lab experiments.

Drugs 56
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Novo completes $16.5bn takeover of Catalent

pharmaphorum

Novo Holdings' $16.

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Pharma Brands: An Overview of Leading Names and Trends

Pharma Marketing Network

Table of Contents Sr# Headings 1 Introduction: Understanding Pharma Brands 2 Top Pharma Brands and Their Strategies 3 Trends Transforming the Pharma Industry 4 Conclusion: Adapting to the Pharma Future Introduction: Understanding Pharma Brands Pharma brands are the cornerstones of the healthcare industry, serving as the bridge between groundbreaking innovation and patient care.

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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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Why a healthy search strategy can power pharma brand growth

pharmaphorum

Discover how implementing a healthy and effective search strategy, focusing on Google, can significantly boost growth and success for pharmaceutical brands.

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Healthcare Social Media Marketing: Strategies for Pharma Success

Pharma Marketing Network

Table of Contents Sr# Headings 1 Introduction: Why Social Media Matters in Healthcare 2 The Unique Challenges of Healthcare Social Media Marketing 3 Effective Social Media Strategies for Pharma Success 4 Conclusion: Elevating Your Social Media Game Introduction: Why Social Media Matters in Healthcare In todays fast-paced digital landscape, healthcare social media marketing has become a game-changer for pharma brands.

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How small molecule-focused CDMOs can navigate the impact of the Inflation Reduction Act

pharmaphorum

Explore how small molecule-focused Contract Development and Manufacturing Organisations (CDMOs) are adapting to the impact of the Inflation Reduction Act (IRA), shifting legislative landscape, and changes in the investment landscape.

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Programmatic Advertising: Transforming Pharma Marketing Strategies

Pharma Marketing Network

Table of Contents Sr# Headings 1 Introduction: Why Programmatic Advertising Matters 2 How Programmatic Advertising Works 3 Benefits for Pharma Marketing Strategies 4 Overcoming Challenges in Programmatic Advertising 5 Conclusion: Embracing the Future of Advertising Introduction: Why Programmatic Advertising Matters In the fast-paced world of digital marketing, programmatic advertising is changing the game for pharma marketers.

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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.