
As pharmaceutical R&D policies evolve, the authors argue it is crucial to embed American patient values in reimbursement deliberations and frameworks.

Julie A. Patterson, PharmD, PhD, is Vice President of Research and Director of the Enterprise Lab at the National Pharmaceutical Council (NPC), which conducts policy-relevant research and communicates it with impact.
Prior to joining NPC, she served as faculty at the Virginia Commonwealth University (VCU) School of Pharmacy. In her academic role, she directed an extensive research program in pharmacoeconomics, drug value and pricing, and patient preferences, in addition to teaching Doctor of Pharmacy and graduate students. Dr Patterson earned her Doctor of Pharmacy and PhD from the VCU School of Pharmacy.

As pharmaceutical R&D policies evolve, the authors argue it is crucial to embed American patient values in reimbursement deliberations and frameworks.

This commentary explores how 2 recently published studies evaluating the clinical benefit of the FDA’s accelerated approval program for oncology drugs came to different conclusions.

This study examined employers’ understanding of rebate guarantees, dependency upon rebate dollars, and the role that pharmaceutical rebates or employer benefits consultants play in their pharmacy benefits manager selection.

The Inflation Reduction Act will likely change incentives surrounding single-indication launches and postapproval research for additional indications in small molecule drugs, affecting patient access.

July 19th 2024