Mon.Dec 25, 2023

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Why US Healthcare Billing Needs an Overhaul

MedCity News

Current billing practices do not adequately meet the needs of consumers, providers or payers. While there is no magic wand, reinventing billing processes in the US will require measures that strengthen consumer protection, and continued policy change towards fairer drug pricing and increased price transparency of provider service costs.

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Opaganib by RedHill Biopharma for Bile Duct Cancer (Cholangiocarcinoma): Likelihood of Approval

Pharmaceutical Technology

Opaganib is under clinical development by RedHill Biopharma and currently in Phase II for Bile Duct Cancer (Cholangiocarcinoma).

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Who Spearheads Employee Retention Strategies At AdventHealth? Get This — The Employees

MedCity News

Last month at a conference, AdventHealth CEO Terry Shaw shared some employee retention strategies used at his health system. He stressed the importance of gathering employee feedback and using it to give them the changes they need. This month, MedCity News followed up with AdventHealth to get a better picture of what these strategies look like in practice.

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Ribociclib succinate by Novartis for Oligodendroglioma: Likelihood of Approval

Pharmaceutical Technology

Ribociclib succinate is under clinical development by Novartis and currently in Phase II for Oligodendroglioma.

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European Clinical Supply Planning: Balancing Cost, Flexibility and Time

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One VC Firm’s 5 Healthcare Predictions for 2024

MedCity News

Executives at LRVHealth expect to see a continued focus on generative AI, increased enrollment in Medicare Advantage and more in 2024.

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Efineptakin alfa by NeoImmuneTech for Solid Tumor: Likelihood of Approval

Pharmaceutical Technology

Efineptakin alfa is under clinical development by NeoImmuneTech and currently in Phase II for Solid Tumor.

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More Trending

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Disitamab vedotin by RemeGen for Cervical Cancer: Likelihood of Approval

Pharmaceutical Technology

Disitamab vedotin is under clinical development by RemeGen and currently in Phase I for Cervical Cancer.

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Top 3 Podcast Episodes of the Year

Pharmaceutical Commerce

This year’s PC Podcast episodes ranged in topic, from DSCSA compliance to pharmacovigilance.

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HCW-9218 by HCW Biologics for Ovarian Cancer: Likelihood of Approval

Pharmaceutical Technology

HCW-9218 is under clinical development by HCW Biologics and currently in Phase I for Ovarian Cancer.

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The Cover Stories of 2023

PharmExec

These stories graced the cover of Pharmaceutical Executive this year

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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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Cabometyx by Exelixis for Gastric Cancer: Likelihood of Approval

Pharmaceutical Technology

Cabometyx is under clinical development by Exelixis and currently in Phase II for Gastric Cancer.

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Top 5 Pharmacy Times Alzheimer Disease Articles of 2023

Pharmacy Times

From newsworthy moments to groundbreaking research, these were the most-read Alzheimer disease-related articles on Pharmacy Times in 2023.

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ZB-131 by ZielBio for Gallbladder Cancer: Likelihood of Approval

Pharmaceutical Technology

ZB-131 is under clinical development by ZielBio and currently in Phase II for Gallbladder Cancer.

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Top 5 Pharmacy Times Pharmacy Technician Articles of 2023

Pharmacy Times

From newsworthy moments to groundbreaking research, these were the most-read pharmacy technician-related articles on Pharmacy Times in 2023.

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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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ION-537 by Ionis Pharmaceuticals for Metastatic Castration-Resistant Prostate Cancer (mCRPC): Likelihood of Approval

Pharmaceutical Technology

ION-537 is under clinical development by Ionis Pharmaceuticals and currently in Phase I for Metastatic Castration-Resistant Prostate Cancer (mCRPC).

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Top 5 Pharmacy Times Biosimilar Articles of 2023

Pharmacy Times

From newsworthy moments to groundbreaking research, these were the most-read biosimilar-related articles on Pharmacy Times in 2023.

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Cusatuzumab by OncoVerity for Acute Myelocytic Leukemia (AML, Acute Myeloblastic Leukemia): Likelihood of Approval

Pharmaceutical Technology

Cusatuzumab is under clinical development by OncoVerity and currently in Phase II for Acute Myelocytic Leukemia (AML, Acute Myeloblastic Leukemia).

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Durvalumab by AstraZeneca for Acute Myelocytic Leukemia (AML, Acute Myeloblastic Leukemia): Likelihood of Approval

Pharmaceutical Technology

Durvalumab is under clinical development by AstraZeneca and currently in Phase II for Acute Myelocytic Leukemia (AML, Acute Myeloblastic Leukemia).

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Deliver Fast, Flexible Clinical Trial Insights with Spotfire

Clinical research has entered a new era, one that requires real-time analytics and visualization to allow trial leaders to work collaboratively and to develop, at the click of a mouse, deep insights that enable proactive study management. Learn how Revvity Signals helps drug developers deliver clinical trial data insights in real-time using a fast and flexible data and analytics platform to empower data-driven decision-making.

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Magrolimab by Gilead Sciences for Metastatic Transitional (Urothelial) Tract Cancer: Likelihood of Approval

Pharmaceutical Technology

Magrolimab is under clinical development by Gilead Sciences and currently in Phase II for Metastatic Transitional (Urothelial) Tract Cancer.

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Sym-023 by Les Laboratoires Servier for Esophageal Squamous Cell Carcinoma (ESCC): Likelihood of Approval

Pharmaceutical Technology

Sym-023 is under clinical development by Les Laboratoires Servier and currently in Phase I for Esophageal Squamous Cell Carcinoma (ESCC).

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BDTX-4933 by Black Diamond Therapeutics for Central Nervous System (CNS) Tumor: Likelihood of Approval

Pharmaceutical Technology

BDTX-4933 is under clinical development by Black Diamond Therapeutics and currently in Phase I for Central Nervous System (CNS) Tumor.

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Y-101D by Wuhan YZY Biopharma for Metastatic Hepatocellular Carcinoma (HCC): Likelihood of Approval

Pharmaceutical Technology

Y-101D is under clinical development by Wuhan YZY Biopharma and currently in Phase II for Metastatic Hepatocellular Carcinoma (HCC).

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Roles and Responsibilities of Specialized Clinical Supply Experts

When selecting a clinical supply provider, consideration often focuses upon the manufacturing, packaging, storage and distribution capabilities available that will, at face-value, be sufficient to meet the needs of the sponsor and their trial. However, there are human-based and knowledge-driven factors that are often overlooked that go beyond these basic physical capabilities and are integral to the development and delivery of high performing clinical supply chains.

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Dabrafenib mesylate by Novartis for Gastrointestinal Stromal Tumor (GIST): Likelihood of Approval

Pharmaceutical Technology

Dabrafenib mesylate is under clinical development by Novartis and currently in Phase II for Gastrointestinal Stromal Tumor (GIST).

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BDTX-4933 by Black Diamond Therapeutics for Metastatic Colorectal Cancer: Likelihood of Approval

Pharmaceutical Technology

BDTX-4933 is under clinical development by Black Diamond Therapeutics and currently in Phase I for Metastatic Colorectal Cancer.

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Zanidatamab by Jazz Pharmaceuticals for Metastatic Biliary Tract Cancer: Likelihood of Approval

Pharmaceutical Technology

Zanidatamab is under clinical development by Jazz Pharmaceuticals and currently in Phase II for Metastatic Biliary Tract Cancer.

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Dupilumab by Regeneron Pharmaceuticals for Atopic Keratoconjunctivitis: Likelihood of Approval

Pharmaceutical Technology

Dupilumab is under clinical development by Regeneron Pharmaceuticals and currently in Phase II for Atopic Keratoconjunctivitis.

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Clinical Data Like You´ve Never Seen It Before: Why Spotfire Is the Leading Tool for Clinical Analytics

Clinical development organizations face a wide array of challenges when it comes to data, many of which can impact the operational effectiveness of their clinical trials. In this whitepaper, experts from Revvity Signals explore how solutions like TIBCO® Spotfire® enable better, more streamlined studies. The whitepaper also features a success story from Ambrx, a leading biopharmaceutical company, detailing how it has leveraged Spotfire to tackle data quality and collaboration challenges in clinic

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BDTX-4933 by Black Diamond Therapeutics for Non-Small Cell Lung Cancer: Likelihood of Approval

Pharmaceutical Technology

BDTX-4933 is under clinical development by Black Diamond Therapeutics and currently in Phase I for Non-Small Cell Lung Cancer.

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Capivasertib by AstraZeneca for Triple-Negative Breast Cancer (TNBC): Likelihood of Approval

Pharmaceutical Technology

Capivasertib is under clinical development by AstraZeneca and currently in Phase III for Triple-Negative Breast Cancer (TNBC).

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Taladegib by Endeavor BioMedicines for Idiopathic Pulmonary Fibrosis: Likelihood of Approval

Pharmaceutical Technology

Taladegib is under clinical development by Endeavor BioMedicines and currently in Phase II for Idiopathic Pulmonary Fibrosis.

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ADCT-901 by ADC Therapeutics for Triple-Negative Breast Cancer (TNBC): Likelihood of Approval

Pharmaceutical Technology

ADCT-901 is under clinical development by ADC Therapeutics and currently in Phase I for Triple-Negative Breast Cancer (TNBC).

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Accelerating Clinical Supply Through Integrated Drug Development

As the development pipeline for new drugs continues to grow, biopharmaceutical companies are re-evaluating how to best manage and balance resources across an increasing number of development projects and complex clinical trials. There are two approaches that can be used to speed a drug from development to clinic faster: timeline compression and parallel processing, but only one that considers the benefits of integrating clinical supply into the overall drug development process.