Sat.Dec 28, 2024 - Fri.Jan 03, 2025

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Navigating Virtual Prescribing Policy Changes in 2025

MedCity News

Through collaboration between regulators and healthcare stakeholders, telehealth prescribing can continue to expand treatment access while maintaining proven safety standards. The post Navigating Virtual Prescribing Policy Changes in 2025 appeared first on MedCity News.

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Opdivo's subcutaneous PD-1 inhibitor cleared in US

pharmaphorum

BMS beats MSD to the US subcutaneous PD-1 inhibitor market after Opdivo Qvantiq is cleared across nearly all the indications of the IV form

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Pharma Commerce’s Most Popular Patient Support Articles

Pharmaceutical Commerce

A dive into the top articles in this sector making waves this year.

Pharma 52
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Specification Equivalence—A Practical Approach

PharmaTech

In this first of a four-part series, the authors provide an introduction to a practical approach for establishing specification equivalence. The regulatory basis and compliance examples from FDA observations and warning letters are included to support the need for an effective process.

FDA 52
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AI Strategies for Sales Managers: How to Cut Down on Tedious Admin Work

What if you could help your sellers stop wasting 72% of their day on non-selling activities and focus on bringing in revenue? Incorporating AI in your enablement workflows can help you cut down on busy work, get projects done faster, and let your team (and you!) focus on making a bigger impact. We put together this guide to show you how to use AI to cut time and costs for projects, including collateral creation, development of training videos, and automating tedious processes.

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Remodel Health Secures Over $100M to Fuel Expansion in the ICHRA Market

MedCity News

Remodel Health received $100 million in funding from Oak HC/FT and Hercules Capital. The post Remodel Health Secures Over $100M to Fuel Expansion in the ICHRA Market appeared first on MedCity News.

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FDA approves BMS’ Opdivo Qvantig for solid tumour indications

Pharmaceutical Technology

The US FDA has granted approval for Bristol Myers Squibbs (BMS) Opdivo Qvantig for subcutaneous use to treat various solid tumours.

FDA 52

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How automation and digital technologies will unlock the full potential of advanced therapies

European Pharmaceutical Review

The use of advanced therapies using cells or genes to achieve significant leaps in medical treatment was perceived as a niche sector just a decade ago, but it has now started to garner a greater level of understanding and recognition in the pharmaceutical industry. Numerous groundbreaking advances have shown these therapies hold potential to revolutionise how we treat, and potentially cure, many conditions, including for patients with underlying genetic or cellular causes of disease that have

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2025 Trends to Watch in Patient Payments

MedCity News

While worries about the affordability of care are sure to persist for many Americans over the coming year, here are some other patient payment trends for providers to watch The post 2025 Trends to Watch in Patient Payments appeared first on MedCity News.

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BeiGene’s Tevimbra approved in US for first-line gastric cancer treatment

Pharmaceutical Technology

Tevimbra is already approved in the US for the treatment of unresectable or metastatic oesophageal squamous cell carcinoma (ESCC).

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Our Top 5 Social Media Posts of 2024

PharmExec

OncLive serves as the connection to oncology, including groundbreaking cancer news and interviews with top oncologists in multimedia formats.

Media 52
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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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First global approval for Daiichi Sankyo's Dato-DXd

pharmaphorum

Daiichi Sankyo has claimed its first approval, in Japan, for TROP2-targeting antibody-drug conjugate (ADC) datopotamab deruxtecan

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The Same Processes that Make Smartphones a Risk for Young People Must Be Harnessed to Provide Beneficial Digital Medical Treatments For All

MedCity News

Addressing difficult-to-treat diseases and disorders, quickly, safely, and with little to no side effects is a positive boon to our overburdened health system. The post The Same Processes that Make Smartphones a Risk for Young People Must Be Harnessed to Provide Beneficial Digital Medical Treatments For All appeared first on MedCity News.

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Nelistotug by GSK for Recurrent Head And Neck Squamous Cell Carcinoma: Likelihood of Approval

Pharmaceutical Technology

Nelistotug is under clinical development by GSK and currently in Phase II for Recurrent Head And Neck Squamous Cell Carcinoma.

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Updated BNT162b2 XBB COVID-19 Vaccine Protects Against Hospitalization in Children Aged 5 to 17

Pharmacy Times

Study results show that the updated BNT162b2 XBB vaccine is effective in preventing hospitalizations or emergency department visits associated with COVID-19 complications.

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

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Trastuzumab rezetecan by Jiangsu Hengrui Medicine for Head And Neck Cancer: Likelihood of Approval

Pharmaceutical Technology

Trastuzumab rezetecan is under clinical development by Jiangsu Hengrui Medicine and currently in Phase I for Head And Neck Cancer.

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Trastuzumab rezetecan by Jiangsu Hengrui Medicine for Transitional Cell Carcinoma (Urothelial Cell Carcinoma): Likelihood of Approval

Pharmaceutical Technology

Trastuzumab rezetecan is under clinical development by Jiangsu Hengrui Medicine and currently in Phase I for Transitional Cell Carcinoma (Urothelial Cell Carcinoma).

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GCC-4001 by Artiva Biotherapeutics for Hodgkin Lymphoma (B-Cell Hodgkin Lymphoma): Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase II for Hodgkin Lymphoma (B-Cell Hodgkin Lymphoma).

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GCC-4001 by Artiva Biotherapeutics for Diffuse Large B-Cell Lymphoma: Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase II for Diffuse Large B-Cell Lymphoma.

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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.

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GCC-4001 by Artiva Biotherapeutics for Lupus Nephritis: Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase I for Lupus Nephritis.

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GCC-4001 by Artiva Biotherapeutics for Follicular Lymphoma: Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase II for Follicular Lymphoma.

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GCC-4001 by Artiva Biotherapeutics for Waldenstrom Macroglobulinemia (Lymphoplasmacytic Lymphoma): Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase II for Waldenstrom Macroglobulinemia (Lymphoplasmacytic Lymphoma).

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GCC-4001 by Artiva Biotherapeutics for Angioimmunoblastic T-Cell Lymphoma (AITL)/Immunoblastic Lymphadenopathy: Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase II for Angioimmunoblastic T-Cell Lymphoma (AITL)/Immunoblastic Lymphadenopathy.

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How to Prove Marketing Value: Demonstrate Content ROI and Contribution to Sales

Every marketer knows how important it is to prove their efforts drive sales opportunities, but that’s easier said than done. When problems like sales and marketing misalignment, lack of data, and wasted efforts persist, marketers can’t measure, prove, or increase their impact on revenue at a time when demonstrating marketing value is critical. Using analyst and expert data, this guide to marketing impact and content attribution explains: How B2B buyers use content The most common types of conten

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GCC-4001 by Artiva Biotherapeutics for Peripheral T-Cell Lymphomas (PTCL): Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase II for Peripheral T-Cell Lymphomas (PTCL).

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Nelistotug by GSK for Recurrent Head And Neck Squamous Cell Carcinoma: Likelihood of Approval

Pharmaceutical Technology

Nelistotug is under clinical development by GSK and currently in Phase II for Recurrent Head And Neck Squamous Cell Carcinoma.

40
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Trastuzumab rezetecan by Jiangsu Hengrui Medicine for Head And Neck Cancer: Likelihood of Approval

Pharmaceutical Technology

Trastuzumab rezetecan is under clinical development by Jiangsu Hengrui Medicine and currently in Phase I for Head And Neck Cancer.

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Trastuzumab rezetecan by Jiangsu Hengrui Medicine for Transitional Cell Carcinoma (Urothelial Cell Carcinoma): Likelihood of Approval

Pharmaceutical Technology

Trastuzumab rezetecan is under clinical development by Jiangsu Hengrui Medicine and currently in Phase I for Transitional Cell Carcinoma (Urothelial Cell Carcinoma).

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How to Stay Competitive in the Evolving State of Martech

Marketing technology is essential for B2B marketers to stay competitive in a rapidly changing digital landscape — and with 53% of marketers experiencing legacy technology issues and limitations, they’re researching innovations to expand and refine their technology stacks. To help practitioners keep up with the rapidly evolving martech landscape, this special report will discuss: How practitioners are integrating technologies and systems to encourage information-sharing between departments and pr

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GCC-4001 by Artiva Biotherapeutics for Hodgkin Lymphoma (B-Cell Hodgkin Lymphoma): Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase II for Hodgkin Lymphoma (B-Cell Hodgkin Lymphoma).

40
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GCC-4001 by Artiva Biotherapeutics for Diffuse Large B-Cell Lymphoma: Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase II for Diffuse Large B-Cell Lymphoma.

40
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GCC-4001 by Artiva Biotherapeutics for Lupus Nephritis: Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase I for Lupus Nephritis.

40
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GCC-4001 by Artiva Biotherapeutics for Follicular Lymphoma: Likelihood of Approval

Pharmaceutical Technology

GCC-4001 is under clinical development by Artiva Biotherapeutics and currently in Phase II for Follicular Lymphoma.

40
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European Clinical Supply Planning: Balancing Cost, Flexibility and Time